Analyze Diet
International journal of molecular sciences2020; 21(4); 1432; doi: 10.3390/ijms21041432

Persistent Breeding-Induced Endometritis in Mares – a Multifaceted Challenge: From Clinical Aspects to Immunopathogenesis and Pathobiology.

Abstract: Post-breeding endometritis (i.e., inflammation/infection of the endometrium), is a physiological reaction taking place in the endometrium of mares within 48 hours post-breeding, aimed to clear seminal plasma, excess sperm, microorganisms, and debris from the uterine lumen in preparation for the arrival of an embryo. Mares are classified as susceptible or resistant to persistent breeding-induced endometritis (PBIE) based on their ability to clear this inflammation/infection by 48 hours post-breeding. Mares susceptible to PBIE, or those with difficulty clearing infection/inflammation, have a deficient immune response and compromised physical mechanisms of defense against infection. Molecular pathways of the innate immune response known to be involved in PBIE are discussed herein. The role of the adaptive uterine immune response on PBIE remains to be elucidated in horses. Advances in the pathobiology of microbes involved in PBIE are also revised here. Traditional and non-traditional therapeutic modalities for endometritis are contrasted and described in the context of clinical and molecular aspects. In recent years, the lack of efficacy of traditional therapeutic modalities, alongside the ever-increasing incidence of antibiotic-resistant microorganisms, has enforced the development of non-traditional therapies. Novel biological products capable of modulating the endometrial inflammatory response are also discussed here as part of the non-traditional therapies for endometritis.
Publication Date: 2020-02-20 PubMed ID: 32093296PubMed Central: PMC7073041DOI: 10.3390/ijms21041432Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Review

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This study explores the challenge of persistent post-breeding endometritis in mares, investigating the infection’s clinical aspects, immunopathogenesis, and pathobiology. It also evaluates available, evolving therapeutic modalities for treating the condition.

Persistent Breeding-Induced Endometritis (PBIE)

  • The article starts by detailing persistent post-breeding endometritis (PBIE). This is a physiological reaction within a mare’s endometrium, that usually occurs within 48 hours of breeding. Its purpose is to flush out seminal plasma, surplus sperm, microorganisms, and debris from the horse’s uterine lumen in readiness for incoming embryos.
  • According to the article, mares are grouped as either susceptible or resistant to PBIE, depending on their ability to eliminate the resultant inflammation/infection within 48 hours following breeding. Those mares that are susceptible to PBIE generally have a poor immune response and compromised defense mechanisms against the infection.

Innate and Adaptive Immune Response

  • The study then examines the role of the innate and adaptive immune response involved in PBIE. It delves into the molecular pathways of the innate immune response known to participate in PBIE.
  • Interestingly, the adaptive uterine immune response’s actual role in PBIE remains inconclusive and is an area that requires further exploration.

Pathobiology of Microbes

  • The researchers also delve into the role of microbes in PBIE. They discuss recent developments in understanding the pathobiology of these microorganisms and their involvement in endometritis.

Therapeutic Modalities for Endometritis

  • The paper contrasts traditional and unconventional therapeutic modalities for endometritis, providing essential context in terms of both clinical and molecular aspects.
  • Recently, the rising incidence of antibiotic-resistant microorganisms and the ineffectiveness of traditional therapeutic methods have driven the development of atypical therapeutic approaches.
  • The article points to novel biological products capable of modulating the endometrial inflammatory reaction as elements of these non-traditional therapies. These are presented as potential solutions to the ever-evolving challenge of endometritis in mares.

Cite This Article

APA
Canisso IF, Segabinazzi LGTM, Fedorka CE. (2020). Persistent Breeding-Induced Endometritis in Mares – a Multifaceted Challenge: From Clinical Aspects to Immunopathogenesis and Pathobiology. Int J Mol Sci, 21(4), 1432. https://doi.org/10.3390/ijms21041432

Publication

ISSN: 1422-0067
NlmUniqueID: 101092791
Country: Switzerland
Language: English
Volume: 21
Issue: 4
PII: 1432

Researcher Affiliations

Canisso, Igor F
  • Department of Veterinary Clinical Medicine, College of Veterinary Medicine, University of Illinois Urbana-Champaign, Champaign, IL 61802, USA.
Segabinazzi, Lorenzo G T M
  • Department of Veterinary Clinical Medicine, College of Veterinary Medicine, University of Illinois Urbana-Champaign, Champaign, IL 61802, USA.
  • Department of Animal Reproduction and Veterinary Radiology, Faculty of Veterinary Medicine and Animal Science, São Paulo State University (UNESP), Botucatu 18618-000, São Paulo, Brazil.
Fedorka, Carleigh E
  • The Maxwell H. Gluck Equine Research Center, University of Kentucky, Lexington, KY 40503, USA.

MeSH Terms

  • Animals
  • Breeding
  • Endometritis / immunology
  • Endometritis / pathology
  • Endometritis / therapy
  • Endometritis / veterinary
  • Female
  • Horse Diseases / immunology
  • Horse Diseases / pathology
  • Horse Diseases / therapy
  • Horses / immunology

Conflict of Interest Statement

The authors declare no conflicts of interest.

References

This article includes 348 references
  1. Traub-Dargatz JL, Salman MD, Voss JL. Medical problems of adult horses, as ranked by equine practitioners.. J Am Vet Med Assoc 1991 May 15;198(10):1745-7.
    pubmed: 2071472
  2. Troedsson MH. Uterine clearance and resistance to persistent endometritis in the mare.. Theriogenology 1999 Aug;52(3):461-71.
    doi: 10.1016/S0093-691X(99)00143-0pubmed: 10734380google scholar: lookup
  3. LeBlanc MM, Neuwirth L, Asbury AC, Tran T, Mauragis D, Klapstein E. Scintigraphic measurement of uterine clearance in normal mares and mares with recurrent endometritis.. Equine Vet J 1994 Mar;26(2):109-13.
  4. Troedsson M.H.T., Desvousges A., Macpherson M.L., Pozor M.P.. Persistent breeding-induced endometritis. Pferdeheilkunde 1994;24:56–60.
    doi: 10.21836/PEM20080112google scholar: lookup
  5. Scoggin CF. Not just a number: effect of age on fertility, pregnancy and offspring vigour in thoroughbred brood-mares.. Reprod Fertil Dev 2015 Jul;27(6):872-9.
    doi: 10.1071/RD14390pubmed: 25786411google scholar: lookup
  6. Woodward EM, Christoffersen M, Campos J, Squires EL, Troedsson MH. Susceptibility to persistent breeding-induced endometritis in the mare: relationship to endometrial biopsy score and age, and variations between seasons.. Theriogenology 2012 Aug;78(3):495-501.
  7. Allen WE, Pycock JF. Cyclical accumulation of uterine fluid in mares with lowered resistance to endometritis.. Vet Rec 1988 May 14;122(20):489-90.
    doi: 10.1136/vr.122.20.489pubmed: 3420771google scholar: lookup
  8. Zent W.W., Troedsson M.H.T., Xue J.-L.. Postbreeding uterine fluid accumulation in a normal population of Thoroughbred mares: A field study. Proceedings of the 40th Annual Convention of the American Association of Equine Practitioners Baltimore, MD, USA. 6 December 1998; pp. 64–65.
  9. Troedsson MH, Liu IK, Crabo BG. Sperm transport and survival in the mare.. Theriogenology 1998 Apr 1;49(5):905-15.
    doi: 10.1016/S0093-691X(98)00040-5pubmed: 10732099google scholar: lookup
  10. Alghamdi AS, Foster DN, Carlson CS, Troedsson MH. Nitric oxide levels and nitric oxide synthase expression in uterine samples from mares susceptible and resistant to persistent breeding-induced endometritis.. Am J Reprod Immunol 2005 May;53(5):230-7.
  11. Katila T.. Onset and duration of uterine inflammatory response of mares after insemination with fresh semen. Biol. Reprod. 1995;52:515–517.
  12. Troedsson M.H.T.. Therapeutic considerations for mating-induced endometritis. Pferdeheilkunde 1997;13:516–520.
    doi: 10.21836/PEM19970515google scholar: lookup
  13. Troedsson MH, Liu IK. Uterine clearance of non-antigenic markers (51Cr) in response to a bacterial challenge in mares potentially susceptible and resistant to chronic uterine infections.. J Reprod Fertil Suppl 1991;44:283-8.
    pubmed: 1795272
  14. Carnevale EM, Ramirez RJ, Squires EL, Alvarenga MA, Vanderwall DK, McCue PM. Factors affecting pregnancy rates and early embryonic death after equine embryo transfer.. Theriogenology 2000 Oct 1;54(6):965-79.
    doi: 10.1016/S0093-691X(00)00405-2pubmed: 11097048google scholar: lookup
  15. Bucca S, Carli A, Buckley T, Dolci G, Fogarty U. The use of dexamethasone administered to mares at breeding time in the modulation of persistent mating induced endometritis.. Theriogenology 2008 Oct 15;70(7):1093-100.
  16. Woodward EM, Christoffersen M, Campos J, Betancourt A, Horohov D, Scoggin KE, Squires EL, Troedsson MH. Endometrial inflammatory markers of the early immune response in mares susceptible or resistant to persistent breeding-induced endometritis.. Reproduction 2013 Mar 1;145(3):289-96.
    doi: 10.1530/REP-12-0452pubmed: 23580950google scholar: lookup
  17. Freeman DA, Weber JA, Geary RT, Woods GL. Time of embryo transport through the mare oviduct.. Theriogenology 1991 Nov;36(5):823-30.
    doi: 10.1016/0093-691X(91)90348-Hpubmed: 16727051google scholar: lookup
  18. Robertson SA, Chin PY, Femia JG, Brown HM. Embryotoxic cytokines-Potential roles in embryo loss and fetal programming.. J Reprod Immunol 2018 Feb;125:80-88.
    doi: 10.1016/j.jri.2017.12.003pubmed: 29306096google scholar: lookup
  19. Squires E.L.. Embryo transfer challenges and perspectives. Rev. Bras. Reprod. Anim. 2013;37:105–107.
  20. Canisso IF, Stewart J, Coutinho da Silva MA. Endometritis: Managing Persistent Post-Breeding Endometritis.. Vet Clin North Am Equine Pract 2016 Dec;32(3):465-480.
    doi: 10.1016/j.cveq.2016.08.004pubmed: 27810036google scholar: lookup
  21. Scoggin CF. Endometritis: Nontraditional Therapies.. Vet Clin North Am Equine Pract 2016 Dec;32(3):499-511.
    doi: 10.1016/j.cveq.2016.08.002pubmed: 27726985google scholar: lookup
  22. Troedsson MH. Breeding-induced endometritis in mares.. Vet Clin North Am Equine Pract 2006 Dec;22(3):705-12.
    doi: 10.1016/j.cveq.2006.07.003pubmed: 17129798google scholar: lookup
  23. Liu IK, Troedsson MH. The diagnosis and treatment of endometritis in the mare: yesterday and today.. Theriogenology 2008 Aug;70(3):415-20.
  24. Troedsson MH. Mating-induced endometritis: physiology or pathology?. Vet J 2014 Jan;199(1):9-10.
    doi: 10.1016/j.tvjl.2013.10.012pubmed: 24280587google scholar: lookup
  25. Troedsson MH, Woodward EM. Our current understanding of the pathophysiology of equine endometritis with an emphasis on breeding-induced endometritis.. Reprod Biol 2016 Mar;16(1):8-12.
    doi: 10.1016/j.repbio.2016.01.003pubmed: 26952748google scholar: lookup
  26. Katila T. Evaluation of diagnostic methods in equine endometritis.. Reprod Biol 2016 Sep;16(3):189-196.
    doi: 10.1016/j.repbio.2016.06.002pubmed: 27692361google scholar: lookup
  27. Woodward EM, Troedsson MH. Inflammatory mechanisms of endometritis.. Equine Vet J 2015 Jul;47(4):384-9.
    doi: 10.1111/evj.12403pubmed: 25537084google scholar: lookup
  28. Marth CD, Firestone SM, Hanlon D, Glenton LY, Browning GF, Young ND, Krekeler N. Innate immune genes in persistent mating-induced endometritis in horses.. Reprod Fertil Dev 2018 Mar;30(3):533-545.
    doi: 10.1071/RD17157pubmed: 28834688google scholar: lookup
  29. Marth CD, Young ND, Glenton LY, Noden DM, Browning GF, Krekeler N. Deep sequencing of the uterine immune response to bacteria during the equine oestrous cycle.. BMC Genomics 2015 Nov 14;16:934.
    doi: 10.1186/s12864-015-2139-3pmc: PMC4647707pubmed: 26572250google scholar: lookup
  30. Nash DM, Sheldon IM, Herath S, Lane EA. Markers of the uterine innate immune response of the mare.. Anim Reprod Sci 2010 May;119(1-2):31-9.
  31. Fumuso EA, Aguilar J, Giguère S, Rivulgo M, Wade J, Rogan D. Immune parameters in mares resistant and susceptible to persistent post-breeding endometritis: effects of immunomodulation.. Vet Immunol Immunopathol 2007 Jul 15;118(1-2):30-9.
    doi: 10.1016/j.vetimm.2007.04.009pubmed: 17559943google scholar: lookup
  32. Fumuso E, Giguère S, Wade J, Rogan D, Videla-Dorna I, Bowden RA. Endometrial IL-1beta, IL-6 and TNF-alpha, mRNA expression in mares resistant or susceptible to post-breeding endometritis. Effects of estrous cycle, artificial insemination and immunomodulation.. Vet Immunol Immunopathol 2003 Nov 15;96(1-2):31-41.
    doi: 10.1016/S0165-2427(03)00137-5pubmed: 14522132google scholar: lookup
  33. Christoffersen M, Woodward EM, Bojesen AM, Petersen MR, Squires EL, Lehn-Jensen H, Troedsson MH. Effect of immunomodulatory therapy on the endometrial inflammatory response to induced infectious endometritis in susceptible mares.. Theriogenology 2012 Sep 15;78(5):991-1004.
  34. Woodward EM, Christoffersen M, Horohov D, Squires EL, Troedsson MH. The effect of treatment with immune modulators on endometrial cytokine expression in mares susceptible to persistent breeding-induced endometritis.. Equine Vet J 2015 Mar;47(2):235-9.
    doi: 10.1111/evj.12266pubmed: 24645833google scholar: lookup
  35. Woodward EM, Christoffersen M, Campos J, Horohov DW, Scoggin KE, Squires E, Troedsson MH. An investigation of uterine nitric oxide production in mares susceptible and resistant to persistent breeding-induced endometritis and the effects of immunomodulation.. Reprod Domest Anim 2013 Aug;48(4):554-61.
    doi: 10.1111/rda.12124pubmed: 23228000google scholar: lookup
  36. Troedsson M.H.T., Crabo B.G., Ibrahim N., Scott M., Ing M. M.. Mating-induced endometritis: Mechanisms, clinical importance and consequences. Proc. 40th Am. Assoc. Equine Pract. 1994;41:11–12.
  37. Kotilainen T, Huhtinen M, Katila T. Sperm-induced leukocytosis in the equine uterus.. Theriogenology 1994 Feb 2;41(3):629-36.
    doi: 10.1016/0093-691X(94)90173-Gpubmed: 16727418google scholar: lookup
  38. Trotter GW, McKinnon AO. Surgery for abnormal vulvar and perineal conformation in the mare.. Vet Clin North Am Equine Pract 1988 Dec;4(3):389-405.
    doi: 10.1016/S0749-0739(17)30618-1pubmed: 3061601google scholar: lookup
  39. Christoffersen M, Söderlind M, Rí»ºlk SR, Pedersen HG, Allen J, Krekeler N. Risk factors associated with uterine fluid after breeding caused by Streptococcus zooepidemicus.. Theriogenology 2015 Nov;84(8):1283-90.
  40. Riddle WT, LeBlanc MM, Stromberg AJ. Relationships between uterine culture, cytology and pregnancy rates in a Thoroughbred practice.. Theriogenology 2007 Aug;68(3):395-402.
  41. Wingfield Digby NJ, Ricketts SW. Results of concurrent bacteriological and cytological examinations of the endometrium of mares in routine stud farm practice 1978-1981.. J Reprod Fertil Suppl 1982;32:181-5.
    pubmed: 6962852
  42. LeBlanc MM, Causey RC. Clinical and subclinical endometritis in the mare: both threats to fertility.. Reprod Domest Anim 2009 Sep;44 Suppl 3:10-22.
  43. Overbeck W, Witte TS, Heuwieser W. Comparison of three diagnostic methods to identify subclinical endometritis in mares.. Theriogenology 2011 Apr 15;75(7):1311-8.
  44. Ricketts SW, Mackintosh ME. Role of anaerobic bacteria in equine endometritis.. J Reprod Fertil Suppl 1987;35:343-51.
    pubmed: 3479588
  45. Collins S.. A study of the incidence of cervical and uterine infection in Thoroughbred mares in Ireland. Vet. Rec. 1964;66:673–676.
  46. Bain AM. The rôle of infection in infertility in the thoroughbred mare.. Vet Rec 1966 Jan 29;78(5):168-73.
    doi: 10.1136/vr.78.5.168pubmed: 5948366google scholar: lookup
  47. Walter J, Neuberg KP, Failing K, Wehrend A. Cytological diagnosis of endometritis in the mare: investigations of sampling techniques and relation to bacteriological results.. Anim Reprod Sci 2012 Jun;132(3-4):178-86.
  48. LeBlanc MM, Magsig J, Stromberg AJ. Use of a low-volume uterine flush for diagnosing endometritis in chronically infertile mares.. Theriogenology 2007 Aug;68(3):403-12.
  49. Beltaire KA, Cheong SH, Coutinho da Silva MA. Retrospective study on equine uterine fungal isolates and antifungal susceptibility patterns (1999-2011).. Equine Vet J Suppl 2012 Dec;(43):84-7.
  50. Frontoso R, De Carlo E, Pasolini MP, van der Meulen K, Pagnini U, Iovane G, De Martino L. Retrospective study of bacterial isolates and their antimicrobial susceptibilities in equine uteri during fertility problems.. Res Vet Sci 2008 Feb;84(1):1-6.
    doi: 10.1016/j.rvsc.2007.02.008pubmed: 17434193google scholar: lookup
  51. Albihn A, Båverud V, Magnusson U. Uterine microbiology and antimicrobial susceptibility in isolated bacteria from mares with fertility problems.. Acta Vet Scand 2003;44(3-4):121-9.
    doi: 10.1186/1751-0147-44-121pmc: PMC1831563pubmed: 15074625google scholar: lookup
  52. Petersen MR, Skive B, Christoffersen M, Lu K, Nielsen JM, Troedsson MH, Bojesen AM. Activation of persistent Streptococcus equi subspecies zooepidemicus in mares with subclinical endometritis.. Vet Microbiol 2015 Aug 31;179(1-2):119-25.
    doi: 10.1016/j.vetmic.2015.06.006pubmed: 26123371google scholar: lookup
  53. Coutinho da Silva M.A., Alvarenga M.A.. Fungal endometritis. Equine Reproduction Blackwell Publishing Ltd.; Hoboken, NJ, USA: 2011. pp. 2643–2651.
  54. Dascanio J.J., Schweizer C., Ley W.B.. Equine fungal endometritis. Equine Vet. Educ. 2010;13:324–329.
  55. Hinrichs K, Spensley MS, McDonough PL. Evaluation of progesterone treatment to create a model for equine endometritis.. Equine Vet J 1992 Nov;24(6):457-61.
  56. Stout T.A.E.. Fungal endometritis in the mare. Pferdeheilkunde 2008;24:83–87.
    doi: 10.21836/PEM20080117google scholar: lookup
  57. Ferris R.A.. Current understanding of bacterial biofilms and latent infections: A clinical perspective. Rev. Bras. Reprod. Anim. 2017;41:74–80.
  58. Beehan D.P., Wolfsdorf K., Elam J., Krekeler N., Paccamonti D., Lyle S.K.. The evaluation of biofilm-forming potential of escherichia coli collected from the equine female reproductive tract. J. Equine Vet. Sci. 2015;35:935–939.
  59. Ferris R.A.. Bacterial endometritis: A focus on biofilms. Clin. Theriogenol. 2014;6:315–319.
  60. Stoodley P, Sauer K, Davies DG, Costerton JW. Biofilms as complex differentiated communities.. Annu Rev Microbiol 2002;56:187-209.
  61. Shah D, Zhang Z, Khodursky A, Kaldalu N, Kurg K, Lewis K. Persisters: a distinct physiological state of E. coli.. BMC Microbiol 2006 Jun 12;6:53.
    doi: 10.1186/1471-2180-6-53pmc: PMC1557402pubmed: 16768798google scholar: lookup
  62. Jensen ET, Kharazmi A, Lam K, Costerton JW, Høiby N. Human polymorphonuclear leukocyte response to Pseudomonas aeruginosa grown in biofilms.. Infect Immun 1990 Jul;58(7):2383-5.
  63. Thurlow LR, Hanke ML, Fritz T, Angle A, Aldrich A, Williams SH, Engebretsen IL, Bayles KW, Horswill AR, Kielian T. Staphylococcus aureus biofilms prevent macrophage phagocytosis and attenuate inflammation in vivo.. J Immunol 2011 Jun 1;186(11):6585-96.
    doi: 10.4049/jimmunol.1002794pmc: PMC3110737pubmed: 21525381google scholar: lookup
  64. Mustoe T. Understanding chronic wounds: a unifying hypothesis on their pathogenesis and implications for therapy.. Am J Surg 2004 May;187(5A):65S-70S.
    doi: 10.1016/S0002-9610(03)00306-4pubmed: 15147994google scholar: lookup
  65. Mah TF, O'Toole GA. Mechanisms of biofilm resistance to antimicrobial agents.. Trends Microbiol 2001 Jan;9(1):34-9.
    doi: 10.1016/S0966-842X(00)01913-2pubmed: 11166241google scholar: lookup
  66. Brown MR, Allison DG, Gilbert P. Resistance of bacterial biofilms to antibiotics: a growth-rate related effect?. J Antimicrob Chemother 1988 Dec;22(6):777-80.
    doi: 10.1093/jac/22.6.777pubmed: 3072331google scholar: lookup
  67. Anwar H, Strap JL, Costerton JW. Establishment of aging biofilms: possible mechanism of bacterial resistance to antimicrobial therapy.. Antimicrob Agents Chemother 1992 Jul;36(7):1347-51.
    doi: 10.1128/AAC.36.7.1347pmc: PMC191585pubmed: 1510427google scholar: lookup
  68. Römling U, Galperin MY, Gomelsky M. Cyclic di-GMP: the first 25 years of a universal bacterial second messenger.. Microbiol Mol Biol Rev 2013 Mar;77(1):1-52.
    doi: 10.1128/MMBR.00043-12pmc: PMC3591986pubmed: 23471616google scholar: lookup
  69. Hickman JW, Tifrea DF, Harwood CS. A chemosensory system that regulates biofilm formation through modulation of cyclic diguanylate levels.. Proc Natl Acad Sci U S A 2005 Oct 4;102(40):14422-7.
    doi: 10.1073/pnas.0507170102pmc: PMC1234902pubmed: 16186483google scholar: lookup
  70. Merighi M, Lee VT, Hyodo M, Hayakawa Y, Lory S. The second messenger bis-(3'-5')-cyclic-GMP and its PilZ domain-containing receptor Alg44 are required for alginate biosynthesis in Pseudomonas aeruginosa.. Mol Microbiol 2007 Aug;65(4):876-95.
  71. Hay ID, Remminghorst U, Rehm BH. MucR, a novel membrane-associated regulator of alginate biosynthesis in Pseudomonas aeruginosa.. Appl Environ Microbiol 2009 Feb;75(4):1110-20.
    doi: 10.1128/AEM.02416-08pmc: PMC2643583pubmed: 19088322google scholar: lookup
  72. Kuchma SL, Connolly JP, O'Toole GA. A three-component regulatory system regulates biofilm maturation and type III secretion in Pseudomonas aeruginosa.. J Bacteriol 2005 Feb;187(4):1441-54.
  73. Ma L, Jackson KD, Landry RM, Parsek MR, Wozniak DJ. Analysis of Pseudomonas aeruginosa conditional psl variants reveals roles for the psl polysaccharide in adhesion and maintaining biofilm structure postattachment.. J Bacteriol 2006 Dec;188(23):8213-21.
    doi: 10.1128/JB.01202-06pmc: PMC1698210pubmed: 16980452google scholar: lookup
  74. Ghafoor A, Hay ID, Rehm BH. Role of exopolysaccharides in Pseudomonas aeruginosa biofilm formation and architecture.. Appl Environ Microbiol 2011 Aug;77(15):5238-46.
    doi: 10.1128/AEM.00637-11pmc: PMC3147449pubmed: 21666010google scholar: lookup
  75. Jennings LK, Storek KM, Ledvina HE, Coulon C, Marmont LS, Sadovskaya I, Secor PR, Tseng BS, Scian M, Filloux A, Wozniak DJ, Howell PL, Parsek MR. Pel is a cationic exopolysaccharide that cross-links extracellular DNA in the Pseudomonas aeruginosa biofilm matrix.. Proc Natl Acad Sci U S A 2015 Sep 8;112(36):11353-8.
    doi: 10.1073/pnas.1503058112pmc: PMC4568648pubmed: 26311845google scholar: lookup
  76. Chew SC, Kundukad B, Seviour T, van der Maarel JR, Yang L, Rice SA, Doyle P, Kjelleberg S. Dynamic remodeling of microbial biofilms by functionally distinct exopolysaccharides.. mBio 2014 Aug 5;5(4):e01536-14.
    doi: 10.1128/mBio.01536-14pmc: PMC4128364pubmed: 25096883google scholar: lookup
  77. Vasseur P, Vallet-Gely I, Soscia C, Genin S, Filloux A. The pel genes of the Pseudomonas aeruginosa PAK strain are involved at early and late stages of biofilm formation.. Microbiology (Reading) 2005 Mar;151(Pt 3):985-997.
    doi: 10.1099/mic.0.27410-0pubmed: 15758243google scholar: lookup
  78. Ferris R.A., Wittstock S.M., McCue P.M., Borlee B.R.. Evaluation of biofilms in gram-negative bacteria isolated from the equine uterus. J. Equine Vet. Sci. 2014;34:121.
  79. Ferris RA, McCue PM, Borlee GI, Loncar KD, Hennet ML, Borlee BR. In Vitro Efficacy of Nonantibiotic Treatments on Biofilm Disruption of Gram-Negative Pathogens and an In Vivo Model of Infectious Endometritis Utilizing Isolates from the Equine Uterus.. J Clin Microbiol 2016 Mar;54(3):631-9.
    doi: 10.1128/JCM.02861-15pmc: PMC4768000pubmed: 26719448google scholar: lookup
  80. Morse DJ, Wilson MJ, Wei X, Lewis MAO, Bradshaw DJ, Murdoch C, Williams DW. Denture-associated biofilm infection in three-dimensional oral mucosal tissue models.. J Med Microbiol 2018 Mar;67(3):364-375.
    doi: 10.1099/jmm.0.000677pmc: PMC5882079pubmed: 29458673google scholar: lookup
  81. Berger D, Rakhamimova A, Pollack A, Loewy Z. Oral Biofilms: Development, Control, and Analysis.. High Throughput 2018 Aug 31;7(3).
    pmc: PMC6163956pubmed: 30200379doi: 10.3390/ht7030024google scholar: lookup
  82. Ferris RA, McCue PM, Borlee GI, Glapa KE, Martin KH, Mangalea MR, Hennet ML, Wolfe LM, Broeckling CD, Borlee BR. Model of Chronic Equine Endometritis Involving a Pseudomonas aeruginosa Biofilm.. Infect Immun 2017 Dec;85(12).
    doi: 10.1128/IAI.00332-17pmc: PMC5695105pubmed: 28970274google scholar: lookup
  83. Moreno I, Franasiak JM. Endometrial microbiota-new player in town.. Fertil Steril 2017 Jul;108(1):32-39.
  84. Verstraelen H, Vilchez-Vargas R, Desimpel F, Jauregui R, Vankeirsbilck N, Weyers S, Verhelst R, De Sutter P, Pieper DH, Van De Wiele T. Characterisation of the human uterine microbiome in non-pregnant women through deep sequencing of the V1-2 region of the 16S rRNA gene.. PeerJ 2016;4:e1602.
    doi: 10.7717/peerj.1602pmc: PMC4730988pubmed: 26823997google scholar: lookup
  85. Baker JM, Chase DM, Herbst-Kralovetz MM. Uterine Microbiota: Residents, Tourists, or Invaders?. Front Immunol 2018;9:208.
    doi: 10.3389/fimmu.2018.00208pmc: PMC5840171pubmed: 29552006google scholar: lookup
  86. Pelzer E, Gomez-Arango LF, Barrett HL, Nitert MD. Review: Maternal health and the placental microbiome.. Placenta 2017 Jun;54:30-37.
  87. Heil B.A., Thompson S.K., Kearns T.A., Davolli G.M., King G., Sones J.L.. Metagenetic characterization of the resident equine uterine microbiome using multiple techniques. J. Equine Vet. Sci. 2018;66:111.
  88. Heil BA, Paccamonti DL, Sones JL. Role for the mammalian female reproductive tract microbiome in pregnancy outcomes.. Physiol Genomics 2019 Aug 1;51(8):390-399.
  89. Rock K., Love B., DeSilva U., Rezabek G., Carrington S., Holyoak G., Carroll B., Gragg D.. Detectable differences in the endometrial microbiome between normal and susceptible mares using metagenomic profiling and conventional bacterial culture. Proceedings of the Society of Theriogenology Milwaukee, WI, USA. 11 August 2011.
  90. Subramaniam A, Ptacek T, Lobashevsky E, Cliver S, Lefkowitz EJ, Morrow CD, Biggio JR Jr, Edwards RK. Midtrimester Cervicovaginal Microbiota: Identification of Microbial Variations Associated with Puerperal Infection at Term.. Am J Perinatol 2016 Oct;33(12):1165-75.
    pmc: PMC6941171pubmed: 27441565doi: 10.1055/s-0036-1585467google scholar: lookup
  91. Swartz JD, Lachman M, Westveer K, O'Neill T, Geary T, Kott RW, Berardinelli JG, Hatfield PG, Thomson JM, Roberts A, Yeoman CJ. Characterization of the Vaginal Microbiota of Ewes and Cows Reveals a Unique Microbiota with Low Levels of Lactobacilli and Near-Neutral pH.. Front Vet Sci 2014;1:19.
    doi: 10.3389/fvets.2014.00019pmc: PMC4672155pubmed: 26664918google scholar: lookup
  92. Benner M, Ferwerda G, Joosten I, van der Molen RG. How uterine microbiota might be responsible for a receptive, fertile endometrium.. Hum Reprod Update 2018 Jul 1;24(4):393-415.
    doi: 10.1093/humupd/dmy012pubmed: 29668899google scholar: lookup
  93. Canisso IF, Ball BA, Cray C, Williams NM, Scoggin KE, Davolli GM, Squires EL, Troedsson MH. Serum amyloid A and haptoglobin concentrations are increased in plasma of mares with ascending placentitis in the absence of changes in peripheral leukocyte counts or fibrinogen concentration.. Am J Reprod Immunol 2014 Oct;72(4):376-85.
    doi: 10.1111/aji.12278pubmed: 24916762google scholar: lookup
  94. Troedsson MH, Loset K, Alghamdi AM, Dahms B, Crabo BG. Interaction between equine semen and the endometrium: the inflammatory response to semen.. Anim Reprod Sci 2001 Dec 3;68(3-4):273-8.
    doi: 10.1016/S0378-4320(01)00164-6pubmed: 11744271google scholar: lookup
  95. Lieberman J. The ABCs of granule-mediated cytotoxicity: new weapons in the arsenal.. Nat Rev Immunol 2003 May;3(5):361-70.
    doi: 10.1038/nri1083pubmed: 12766758google scholar: lookup
  96. Muraille E, Goriely S. The nonspecific face of adaptive immunity.. Curr Opin Immunol 2017 Oct;48:38-43.
    doi: 10.1016/j.coi.2017.08.002pubmed: 28823577google scholar: lookup
  97. Janeway CA Jr, Medzhitov R. Innate immune recognition.. Annu Rev Immunol 2002;20:197-216.
  98. Medzhitov R, Janeway C Jr. Innate immune recognition: mechanisms and pathways.. Immunol Rev 2000 Feb;173:89-97.
  99. Medzhitov R, Janeway CA Jr. Innate immune recognition and control of adaptive immune responses.. Semin Immunol 1998 Oct;10(5):351-3.
    doi: 10.1006/smim.1998.0136pubmed: 9799709google scholar: lookup
  100. Moldenhauer LM, Diener KR, Thring DM, Brown MP, Hayball JD, Robertson SA. Cross-presentation of male seminal fluid antigens elicits T cell activation to initiate the female immune response to pregnancy.. J Immunol 2009 Jun 15;182(12):8080-93.
    doi: 10.4049/jimmunol.0804018pubmed: 19494334google scholar: lookup
  101. Schjenken JE, Robertson SA. Seminal Fluid Signalling in the Female Reproductive Tract: Implications for Reproductive Success and Offspring Health.. Adv Exp Med Biol 2015;868:127-58.
    pubmed: 26178848doi: 10.1007/978-3-319-18881-2_6google scholar: lookup
  102. Jørgensen N, Persson G, Hviid TVF. The Tolerogenic Function of Regulatory T Cells in Pregnancy and Cancer.. Front Immunol 2019;10:911.
    doi: 10.3389/fimmu.2019.00911pmc: PMC6517506pubmed: 31134056google scholar: lookup
  103. Sakaguchi S. Regulatory T cells: key controllers of immunologic self-tolerance.. Cell 2000 May 26;101(5):455-8.
    doi: 10.1016/S0092-8674(00)80856-9pubmed: 10850488google scholar: lookup
  104. Shevach EM. CD4+ CD25+ suppressor T cells: more questions than answers.. Nat Rev Immunol 2002 Jun;2(6):389-400.
    doi: 10.1038/nri821pubmed: 12093005google scholar: lookup
  105. Somerset DA, Zheng Y, Kilby MD, Sansom DM, Drayson MT. Normal human pregnancy is associated with an elevation in the immune suppressive CD25+ CD4+ regulatory T-cell subset.. Immunology 2004 May;112(1):38-43.
  106. Aluvihare VR, Kallikourdis M, Betz AG. Regulatory T cells mediate maternal tolerance to the fetus.. Nat Immunol 2004 Mar;5(3):266-71.
    doi: 10.1038/ni1037pubmed: 14758358google scholar: lookup
  107. Hori S, Nomura T, Sakaguchi S. Control of regulatory T cell development by the transcription factor Foxp3.. Science 2003 Feb 14;299(5609):1057-61.
    doi: 10.1126/science.1079490pubmed: 12522256google scholar: lookup
  108. Khattri R, Cox T, Yasayko SA, Ramsdell F. Pillars Article: An Essential Role for Scurfin in CD4+CD25+ T Regulatory Cells. Nat. Immunol. 2003. 4: 337-342.. J Immunol 2017 Feb 1;198(3):993-998.
    doi: 10.1038/ni909pubmed: 28115588google scholar: lookup
  109. Fontenot JD, Gavin MA, Rudensky AY. Foxp3 programs the development and function of CD4+CD25+ regulatory T cells.. Nat Immunol 2003 Apr;4(4):330-6.
    doi: 10.1038/ni904pubmed: 12612578google scholar: lookup
  110. Fedorka CE, Loux SL, Scoggin KE, Adams AA, Troedsson MHT, Ball BA. Alterations in T cell-related transcripts at the feto-maternal interface throughout equine gestation.. Placenta 2020 Jan 1;89:78-87.
  111. Baratelli F, Lin Y, Zhu L, Yang SC, Heuzé-Vourc'h N, Zeng G, Reckamp K, Dohadwala M, Sharma S, Dubinett SM. Prostaglandin E2 induces FOXP3 gene expression and T regulatory cell function in human CD4+ T cells.. J Immunol 2005 Aug 1;175(3):1483-90.
    doi: 10.4049/jimmunol.175.3.1483pubmed: 16034085google scholar: lookup
  112. Chen W, Jin W, Hardegen N, Lei KJ, Li L, Marinos N, McGrady G, Wahl SM. Conversion of peripheral CD4+CD25- naive T cells to CD4+CD25+ regulatory T cells by TGF-beta induction of transcription factor Foxp3.. J Exp Med 2003 Dec 15;198(12):1875-86.
    doi: 10.1084/jem.20030152pmc: PMC2194145pubmed: 14676299google scholar: lookup
  113. Kumar V. The complement system, toll-like receptors and inflammasomes in host defense: three musketeers' one target.. Int Rev Immunol 2019;38(4):131-156.
    doi: 10.1080/08830185.2019.1609962pubmed: 31066339google scholar: lookup
  114. Hakansson A, Albihn A, Magnusson U. The contribution of complement to opsonic activity in the uterine secretions of mares free of endometritis.. Theriogenology 1993 Mar;39(3):601-9.
    doi: 10.1016/0093-691X(93)90247-3pubmed: 16727239google scholar: lookup
  115. Grossman TR, Hettrick LA, Johnson RB, Hung G, Peralta R, Watt A, Henry SP, Adamson P, Monia BP, McCaleb ML. Inhibition of the alternative complement pathway by antisense oligonucleotides targeting complement factor B improves lupus nephritis in mice.. Immunobiology 2016 Jun;221(6):701-8.
    doi: 10.1016/j.imbio.2015.08.001pubmed: 26307001google scholar: lookup
  116. Weiler JM, Daha MR, Austen KF, Fearon DT. Control of the amplification convertase of complement by the plasma protein beta1H.. Proc Natl Acad Sci U S A 1976 Sep;73(9):3268-72.
    doi: 10.1073/pnas.73.9.3268pmc: PMC431003pubmed: 1067618google scholar: lookup
  117. Conrad DH, Carlo JR, Ruddy S. Interaction of beta1H globulin with cell-bound C3b: quantitative analysis of binding and influence of alternative pathway components on binding.. J Exp Med 1978 Jun 1;147(6):1792-1805.
    doi: 10.1084/jem.147.6.1792pmc: PMC2184316pubmed: 567241google scholar: lookup
  118. Pangburn MK, Schreiber RD, Müller-Eberhard HJ. Human complement C3b inactivator: isolation, characterization, and demonstration of an absolute requirement for the serum protein beta1H for cleavage of C3b and C4b in solution.. J Exp Med 1977 Jul 1;146(1):257-70.
    doi: 10.1084/jem.146.1.257pmc: PMC2180748pubmed: 301546google scholar: lookup
  119. Ahearn JM, Fearon DT. Structure and function of the complement receptors, CR1 (CD35) and CR2 (CD21).. Adv Immunol 1989;46:183-219.
    pubmed: 2551147doi: 10.1016/s0065-2776(08)60654-9google scholar: lookup
  120. Krych-Goldberg M, Atkinson JP. Structure-function relationships of complement receptor type 1.. Immunol Rev 2001 Apr;180:112-22.
  121. Nonaka M. Evolution of the complement system.. Subcell Biochem 2014;80:31-43.
    pubmed: 24798006doi: 10.1007/978-94-017-8881-6_3google scholar: lookup
  122. Walport MJ. Complement. First of two parts.. N Engl J Med 2001 Apr 5;344(14):1058-66.
    doi: 10.1056/NEJM200104053441406pubmed: 11287977google scholar: lookup
  123. Rus H, Cudrici C, Niculescu F. The role of the complement system in innate immunity.. Immunol Res 2005;33(2):103-12.
    doi: 10.1385/IR:33:2:103pubmed: 16234578google scholar: lookup
  124. Meri S. Self-nonself discrimination by the complement system.. FEBS Lett 2016 Aug;590(15):2418-34.
    doi: 10.1002/1873-3468.12284pubmed: 27393384google scholar: lookup
  125. Watson ED, Stokes CR, Bourne FJ. Influence of arachidonic acid metabolites in vitro and in uterine washings on migration of equine neutrophils under agarose.. Res Vet Sci 1987 Sep;43(2):203-7.
    doi: 10.1016/S0034-5288(18)30774-4pubmed: 2825309google scholar: lookup
  126. Pycock JF, Allen WE. Pre-chemotactic and chemotactic properties of uterine fluid from mares with experimentally induced endometritis.. Vet Rec 1988 Aug 20;123(8):193-5.
    doi: 10.1136/vr.123.8.193pubmed: 3176271google scholar: lookup
  127. Pycock JF, Allen WE. Inflammatory components in uterine fluid from mares with experimentally induced bacterial endometritis.. Equine Vet J 1990 Nov;22(6):422-5.
  128. Watson ED, Stokes CR, Bourne FJ. Cellular and humoral defence mechanisms in mares susceptible and resistant to persistent endometritis.. Vet Immunol Immunopathol 1987 Sep;16(1-2):107-21.
    doi: 10.1016/0165-2427(87)90178-4pubmed: 3314110google scholar: lookup
  129. Asbury AC, Gorman NT, Foster GW. Uterine defense mechanisms in the mare: Serum opsonins affecting phagocytosis of Streptococcus zooepidemicus by equine neutrophils.. Theriogenology 1984 Feb;21(2):375-85.
    doi: 10.1016/0093-691X(84)90422-9pubmed: 16725887google scholar: lookup
  130. Watson ED. Opsonins in uterine washings influencing in vitro activity of equine neutrophils.. Equine Vet J 1988 Nov;20(6):435-7.
  131. Asbury AC, Halliwell RE, Foster GW, Longino SJ. Immunoglobulins in uterine secretions of mares with differing resistance to endometritis.. Theriogenology 1980 Oct;14(4):299-308.
    doi: 10.1016/0093-691X(80)90079-5pubmed: 16725526google scholar: lookup
  132. Mitchell G, Liu IK, Perryman LE, Stabenfeldt GH, Hughes JP. Preferential production and secretion of immunoglobulins by the equine endometrium--a mucosal immune system.. J Reprod Fertil Suppl 1982;32:161-8.
    pubmed: 6762437
  133. Troedsson MH, Liu IK, Thurmond M. Immunoglobulin (IgG and IgA) and complement (C3) concentrations in uterine secretion following an intrauterine challenge of Streptococcus zooepidemicus in mares susceptible to versus resistant to chronic uterine infection.. Biol Reprod 1993 Sep;49(3):502-6.
    doi: 10.1095/biolreprod49.3.502pubmed: 8399842google scholar: lookup
  134. Widders PR, Stokes CR, David JS, Bourne FJ. Quantitation of the immunoglobulins in reproductive tract secretions of the mare.. Res Vet Sci 1984 Nov;37(3):324-30.
    doi: 10.1016/S0034-5288(18)31872-1pubmed: 6522826google scholar: lookup
  135. Williamson P., Dunning A., O’Connor J., Penhale W.J.. Immunoglobulin levels, protein concentrations and alkaline phosphatase activity in uterine flushings from mares with endometritis. Theriogenology 1983;19:441–448.
  136. Dell’Aqua J.A., Jr., Papa F.O., Lopes M.D., Alvarenga M.A., Macedo L.P., Melo C.M.. Modulation of acute uterine inflammatory response after artificial insemination with equine frozen semen. Anim. Reprod. Sci. 2006;94:270–273.
  137. Kawai T, Akira S. The role of pattern-recognition receptors in innate immunity: update on Toll-like receptors.. Nat Immunol 2010 May;11(5):373-84.
    doi: 10.1038/ni.1863pubmed: 20404851google scholar: lookup
  138. Cronin JG, Turner ML, Goetze L, Bryant CE, Sheldon IM. Toll-like receptor 4 and MYD88-dependent signaling mechanisms of the innate immune system are essential for the response to lipopolysaccharide by epithelial and stromal cells of the bovine endometrium.. Biol Reprod 2012 Feb;86(2):51.
  139. Kitaya K, Yamada H. Pathophysiological roles of chemokines in human reproduction: an overview.. Am J Reprod Immunol 2011 May;65(5):449-59.
  140. Wira CR, Fahey JV, Sentman CL, Pioli PA, Shen L. Innate and adaptive immunity in female genital tract: cellular responses and interactions.. Immunol Rev 2005 Aug;206:306-35.
  141. Farage M.A., Miller K.W., Gerberick G.F., Saito F.H., Ledger W.J., Witkin S.S.. Innate Immunity in the Lower Female Mucosal Tract. J. Steroids Horm. Sci. 2011;2:2.
    doi: 10.4172/2157-7536.1000106google scholar: lookup
  142. An H, Yu Y, Zhang M, Xu H, Qi R, Yan X, Liu S, Wang W, Guo Z, Guo J, Qin Z, Cao X. Involvement of ERK, p38 and NF-kappaB signal transduction in regulation of TLR2, TLR4 and TLR9 gene expression induced by lipopolysaccharide in mouse dendritic cells.. Immunology 2002 May;106(1):38-45.
  143. Chen C, Zibiao H, Ming Z, Shiyi C, Ruixia L, Jie W, SongJia L. Expression pattern of Toll-like receptors (TLRs) in different organs and effects of lipopolysaccharide on the expression of TLR 2 and 4 in reproductive organs of female rabbit.. Dev Comp Immunol 2014 Oct;46(2):341-8.
    doi: 10.1016/j.dci.2014.05.008pubmed: 24858029google scholar: lookup
  144. Silva E, Leitão S, Henriques S, Kowalewski MP, Hoffmann B, Ferreira-Dias G, da Costa LL, Mateus L. Gene transcription of TLR2, TLR4, LPS ligands and prostaglandin synthesis enzymes are up-regulated in canine uteri with cystic endometrial hyperplasia-pyometra complex.. J Reprod Immunol 2010 Jan;84(1):66-74.
    doi: 10.1016/j.jri.2009.10.004pubmed: 19945173google scholar: lookup
  145. Swangchan-Uthai T, Lavender CR, Cheng Z, Fouladi-Nashta AA, Wathes DC. Time course of defense mechanisms in bovine endometrium in response to lipopolysaccharide.. Biol Reprod 2012 Jun;87(6):135.
    doi: 10.1095/biolreprod.112.102376pubmed: 23077171google scholar: lookup
  146. Turner ML, Healey GD, Sheldon IM. Immunity and inflammation in the uterus.. Reprod Domest Anim 2012 Aug;47 Suppl 4:402-9.
  147. Souza-Fonseca-Guimaraes F, Adib-Conquy M, Cavaillon JM. Natural killer (NK) cells in antibacterial innate immunity: angels or devils?. Mol Med 2012 Mar 30;18(1):270-85.
    doi: 10.2119/molmed.2011.00201pmc: PMC3324953pubmed: 22105606google scholar: lookup
  148. Takeda K, Akira S. TLR signaling pathways.. Semin Immunol 2004 Feb;16(1):3-9.
    doi: 10.1016/j.smim.2003.10.003pubmed: 14751757google scholar: lookup
  149. Chow JC, Young DW, Golenbock DT, Christ WJ, Gusovsky F. Toll-like receptor-4 mediates lipopolysaccharide-induced signal transduction.. J Biol Chem 1999 Apr 16;274(16):10689-92.
    doi: 10.1074/jbc.274.16.10689pubmed: 10196138google scholar: lookup
  150. Sheldon IM, Cronin J, Goetze L, Donofrio G, Schuberth HJ. Defining postpartum uterine disease and the mechanisms of infection and immunity in the female reproductive tract in cattle.. Biol Reprod 2009 Dec;81(6):1025-32.
  151. Fujita Y, Mihara T, Okazaki T, Shitanaka M, Kushino R, Ikeda C, Negishi H, Liu Z, Richards JS, Shimada M. Toll-like receptors (TLR) 2 and 4 on human sperm recognize bacterial endotoxins and mediate apoptosis.. Hum Reprod 2011 Oct;26(10):2799-806.
    doi: 10.1093/humrep/der234pmc: PMC3174031pubmed: 21775336google scholar: lookup
  152. Akthar I, Suarez SS, Morillo VA, Sasaki M, Ezz MA, Takahashi KI, Shimada M, Marey MA, Miyamoto A. Sperm enter glands of preovulatory bovine endometrial explants and initiate inflammation.. Reproduction 2020 Feb;159(2):181-192.
    doi: 10.1530/REP-19-0414pubmed: 31794421google scholar: lookup
  153. Ezz MA, Marey MA, Elweza AE, Kawai T, Heppelmann M, Pfarrer C, Balboula AZ, Montaser A, Imakawa K, Zaabel SM, Shimada M, Miyamoto A. TLR2/4 signaling pathway mediates sperm-induced inflammation in bovine endometrial epithelial cells in vitro.. PLoS One 2019;14(4):e0214516.
  154. Elweza AE, Ezz MA, Acosta TJ, Talukder AK, Shimizu T, Hayakawa H, Shimada M, Imakawa K, Zaghloul AH, Miyamoto A. A proinflammatory response of bovine endometrial epithelial cells to active sperm in vitro.. Mol Reprod Dev 2018 Mar;85(3):215-226.
    doi: 10.1002/mrd.22955pubmed: 29337420google scholar: lookup
  155. Franchi L, Warner N, Viani K, Nuñez G. Function of Nod-like receptors in microbial recognition and host defense.. Immunol Rev 2009 Jan;227(1):106-28.
  156. Inohara, Chamaillard, McDonald C, Nuñez G. NOD-LRR proteins: role in host-microbial interactions and inflammatory disease.. Annu Rev Biochem 2005;74:355-83.
  157. Mariathasan S, Weiss DS, Newton K, McBride J, O'Rourke K, Roose-Girma M, Lee WP, Weinrauch Y, Monack DM, Dixit VM. Cryopyrin activates the inflammasome in response to toxins and ATP.. Nature 2006 Mar 9;440(7081):228-32.
    doi: 10.1038/nature04515pubmed: 16407890google scholar: lookup
  158. Barbé F, Douglas T, Saleh M. Advances in Nod-like receptors (NLR) biology.. Cytokine Growth Factor Rev 2014 Dec;25(6):681-97.
    doi: 10.1016/j.cytogfr.2014.07.001pubmed: 25070125google scholar: lookup
  159. Schroder K, Tschopp J. The inflammasomes.. Cell 2010 Mar 19;140(6):821-32.
    doi: 10.1016/j.cell.2010.01.040pubmed: 20303873google scholar: lookup
  160. Benko S, Magalhaes JG, Philpott DJ, Girardin SE. NLRC5 limits the activation of inflammatory pathways.. J Immunol 2010 Aug 1;185(3):1681-91.
    doi: 10.4049/jimmunol.0903900pubmed: 20610642google scholar: lookup
  161. Cui J, Zhu L, Xia X, Wang HY, Legras X, Hong J, Ji J, Shen P, Zheng S, Chen ZJ, Wang RF. NLRC5 negatively regulates the NF-kappaB and type I interferon signaling pathways.. Cell 2010 Apr 30;141(3):483-96.
    doi: 10.1016/j.cell.2010.03.040pmc: PMC3150216pubmed: 20434986google scholar: lookup
  162. Lawrence T. The nuclear factor NF-kappaB pathway in inflammation.. Cold Spring Harb Perspect Biol 2009 Dec;1(6):a001651.
    doi: 10.1101/cshperspect.a001651pmc: PMC2882124pubmed: 20457564google scholar: lookup
  163. Karin M, Ben-Neriah Y. Phosphorylation meets ubiquitination: the control of NF-[kappa]B activity.. Annu Rev Immunol 2000;18:621-63.
  164. Zandi E, Rothwarf DM, Delhase M, Hayakawa M, Karin M. The IkappaB kinase complex (IKK) contains two kinase subunits, IKKalpha and IKKbeta, necessary for IkappaB phosphorylation and NF-kappaB activation.. Cell 1997 Oct 17;91(2):243-52.
    doi: 10.1016/S0092-8674(00)80406-7pubmed: 9346241google scholar: lookup
  165. Yamamoto Y, Gaynor RB. IkappaB kinases: key regulators of the NF-kappaB pathway.. Trends Biochem Sci 2004 Feb;29(2):72-9.
    doi: 10.1016/j.tibs.2003.12.003pubmed: 15102433google scholar: lookup
  166. Senftleben U, Cao Y, Xiao G, Greten FR, Krähn G, Bonizzi G, Chen Y, Hu Y, Fong A, Sun SC, Karin M. Activation by IKKalpha of a second, evolutionary conserved, NF-kappa B signaling pathway.. Science 2001 Aug 24;293(5534):1495-9.
    doi: 10.1126/science.1062677pubmed: 11520989google scholar: lookup
  167. Dejardin E, Droin NM, Delhase M, Haas E, Cao Y, Makris C, Li ZW, Karin M, Ware CF, Green DR. The lymphotoxin-beta receptor induces different patterns of gene expression via two NF-kappaB pathways.. Immunity 2002 Oct;17(4):525-35.
    doi: 10.1016/S1074-7613(02)00423-5pubmed: 12387745google scholar: lookup
  168. Bonizzi G, Bebien M, Otero DC, Johnson-Vroom KE, Cao Y, Vu D, Jegga AG, Aronow BJ, Ghosh G, Rickert RC, Karin M. Activation of IKKalpha target genes depends on recognition of specific kappaB binding sites by RelB:p52 dimers.. EMBO J 2004 Oct 27;23(21):4202-10.
    doi: 10.1038/sj.emboj.7600391pmc: PMC524385pubmed: 15470505google scholar: lookup
  169. Novack DV, Yin L, Hagen-Stapleton A, Schreiber RD, Goeddel DV, Ross FP, Teitelbaum SL. The IkappaB function of NF-kappaB2 p100 controls stimulated osteoclastogenesis.. J Exp Med 2003 Sep 1;198(5):771-81.
    doi: 10.1084/jem.20030116pmc: PMC2194184pubmed: 12939342google scholar: lookup
  170. Matsushima A, Kaisho T, Rennert PD, Nakano H, Kurosawa K, Uchida D, Takeda K, Akira S, Matsumoto M. Essential role of nuclear factor (NF)-kappaB-inducing kinase and inhibitor of kappaB (IkappaB) kinase alpha in NF-kappaB activation through lymphotoxin beta receptor, but not through tumor necrosis factor receptor I.. J Exp Med 2001 Mar 5;193(5):631-6.
    doi: 10.1084/jem.193.5.631pmc: PMC2193391pubmed: 11238593google scholar: lookup
  171. Bonizzi G, Karin M. The two NF-kappaB activation pathways and their role in innate and adaptive immunity.. Trends Immunol 2004 Jun;25(6):280-8.
    doi: 10.1016/j.it.2004.03.008pubmed: 15145317google scholar: lookup
  172. Girling JE, Hedger MP. Toll-like receptors in the gonads and reproductive tract: emerging roles in reproductive physiology and pathology.. Immunol Cell Biol 2007 Aug-Sep;85(6):481-9.
    doi: 10.1038/sj.icb.7100086pubmed: 17592495google scholar: lookup
  173. Chandrasekharan NV, Simmons DL. The cyclooxygenases.. Genome Biol 2004;5(9):241.
    doi: 10.1186/gb-2004-5-9-241pmc: PMC522864pubmed: 15345041google scholar: lookup
  174. Gohda J, Matsumura T, Inoue J. Cutting edge: TNFR-associated factor (TRAF) 6 is essential for MyD88-dependent pathway but not toll/IL-1 receptor domain-containing adaptor-inducing IFN-beta (TRIF)-dependent pathway in TLR signaling.. J Immunol 2004 Sep 1;173(5):2913-7.
    doi: 10.4049/jimmunol.173.5.2913pubmed: 15322147google scholar: lookup
  175. Lu YC, Yeh WC, Ohashi PS. LPS/TLR4 signal transduction pathway.. Cytokine 2008 May;42(2):145-151.
    doi: 10.1016/j.cyto.2008.01.006pubmed: 18304834google scholar: lookup
  176. Sato S, Sanjo H, Takeda K, Ninomiya-Tsuji J, Yamamoto M, Kawai T, Matsumoto K, Takeuchi O, Akira S. Essential function for the kinase TAK1 in innate and adaptive immune responses.. Nat Immunol 2005 Nov;6(11):1087-95.
    doi: 10.1038/ni1255pubmed: 16186825google scholar: lookup
  177. Van de Craen M, Declercq W, Van den brande I, Fiers W, Vandenabeele P. The proteolytic procaspase activation network: an in vitro analysis.. Cell Death Differ 1999 Nov;6(11):1117-24.
    doi: 10.1038/sj.cdd.4400589pubmed: 10578181google scholar: lookup
  178. Hazuda DJ, Strickler J, Kueppers F, Simon PL, Young PR. Processing of precursor interleukin 1 beta and inflammatory disease.. J Biol Chem 1990 Apr 15;265(11):6318-22.
    pubmed: 2156847
  179. Black RA, Kronheim SR, Cantrell M, Deeley MC, March CJ, Prickett KS, Wignall J, Conlon PJ, Cosman D, Hopp TP. Generation of biologically active interleukin-1 beta by proteolytic cleavage of the inactive precursor.. J Biol Chem 1988 Jul 5;263(19):9437-42.
    pubmed: 3288634
  180. Ito A, Mukaiyama A, Itoh Y, Nagase H, Thogersen IB, Enghild JJ, Sasaguri Y, Mori Y. Degradation of interleukin 1beta by matrix metalloproteinases.. J Biol Chem 1996 Jun 21;271(25):14657-60.
    doi: 10.1074/jbc.271.25.14657pubmed: 8663297google scholar: lookup
  181. Boerboom D, Brown KA, Vaillancourt D, Poitras P, Goff AK, Watanabe K, Doré M, Sirois J. Expression of key prostaglandin synthases in equine endometrium during late diestrus and early pregnancy.. Biol Reprod 2004 Feb;70(2):391-9.
    doi: 10.1095/biolreprod.103.020800pubmed: 14561653google scholar: lookup
  182. Palm F, Walter I, Budik S, Kolodziejek J, Nowotny N, Aurich C. Influence of different semen extenders and seminal plasma on PMN migration and on expression of IL-1beta, IL-6, TNF-alpha and COX-2 mRNA in the equine endometrium.. Theriogenology 2008 Sep 15;70(5):843-51.
  183. Contran R.S., Kumar V., Collins T., Robbins S.L.. Robbins Pathologic Basic of Disease. 6th ed. W.B. Saunders; Philadelphia, PA, USA: 1999.
  184. Fumuso E., Aguilar J., Gigu S.. Interleukin-8 (IL-8) and 10 (IL-10) mRNA transcriptions in the endometrium of normal mares and mares susceptible to persistent post-breeding endometritis. Anim. Reprod. Sci. 2006;94:282–285.
  185. Doré M, Sirois J. Regulation of P-selectin expression by inflammatory mediators in canine jugular endothelial cells.. Vet Pathol 1996 Nov;33(6):662-71.
    doi: 10.1177/030098589603300605pubmed: 8952025google scholar: lookup
  186. Tizard I.R.. Veterinary Immunology. 9th ed. Volume 1. Elsevier Saunders; St. Louis, MI, USA: 2009. Innate immunity: The recognition of invaders; pp. 11–20.
  187. Troedsson M.H.T., Liu I.K.M., Ing M., Pascoe J.. Smooth muscle electrical activity in the oviduct, and the effect of oxytocin, prostaglandin F2α, and prostaglandin E2 on the myometrium and the oviduct of the cycling mare. Biol. Reprod. 1995;52:475–488.
  188. Lögters T, Margraf S, Altrichter J, Cinatl J, Mitzner S, Windolf J, Scholz M. The clinical value of neutrophil extracellular traps.. Med Microbiol Immunol 2009 Nov;198(4):211-9.
    doi: 10.1007/s00430-009-0121-xpubmed: 19653000google scholar: lookup
  189. Fuchs TA, Abed U, Goosmann C, Hurwitz R, Schulze I, Wahn V, Weinrauch Y, Brinkmann V, Zychlinsky A. Novel cell death program leads to neutrophil extracellular traps.. J Cell Biol 2007 Jan 15;176(2):231-41.
    doi: 10.1083/jcb.200606027pmc: PMC2063942pubmed: 17210947google scholar: lookup
  190. Garcia-Romo GS, Caielli S, Vega B, Connolly J, Allantaz F, Xu Z, Punaro M, Baisch J, Guiducci C, Coffman RL, Barrat FJ, Banchereau J, Pascual V. Netting neutrophils are major inducers of type I IFN production in pediatric systemic lupus erythematosus.. Sci Transl Med 2011 Mar 9;3(73):73ra20.
  191. Brinkmann V, Reichard U, Goosmann C, Fauler B, Uhlemann Y, Weiss DS, Weinrauch Y, Zychlinsky A. Neutrophil extracellular traps kill bacteria.. Science 2004 Mar 5;303(5663):1532-5.
    doi: 10.1126/science.1092385pubmed: 15001782google scholar: lookup
  192. Brinkmann V.. Neutrophil extracellular traps in microbial infections. Neutrophils Ininfectious Diseases Bentham eBooks; Dubais, UAE: 2011. pp. 3–10.
  193. Weinrauch Y, Drujan D, Shapiro SD, Weiss J, Zychlinsky A. Neutrophil elastase targets virulence factors of enterobacteria.. Nature 2002 May 2;417(6884):91-4.
    doi: 10.1038/417091apubmed: 12018205google scholar: lookup
  194. Wartha F, Beiter K, Albiger B, Fernebro J, Zychlinsky A, Normark S, Henriques-Normark B. Capsule and D-alanylated lipoteichoic acids protect Streptococcus pneumoniae against neutrophil extracellular traps.. Cell Microbiol 2007 May;9(5):1162-71.
  195. van der Windt D, Bootsma HJ, Burghout P, van der Gaast-de Jongh CE, Hermans PW, van der Flier M. Nonencapsulated Streptococcus pneumoniae resists extracellular human neutrophil elastase- and cathepsin G-mediated killing.. FEMS Immunol Med Microbiol 2012 Dec;66(3):445-8.
  196. Marin-Esteban V, Turbica I, Dufour G, Semiramoth N, Gleizes A, Gorges R, Beau I, Servin AL, Lievin-Le Moal V, Sandré C, Chollet-Martin S. Afa/Dr diffusely adhering Escherichia coli strain C1845 induces neutrophil extracellular traps that kill bacteria and damage human enterocyte-like cells.. Infect Immun 2012 May;80(5):1891-9.
    doi: 10.1128/IAI.00050-12pmc: PMC3347451pubmed: 22371374google scholar: lookup
  197. Rebordão MR, Carneiro C, Alexandre-Pires G, Brito P, Pereira C, Nunes T, Galvão A, Leitão A, Vilela C, Ferreira-Dias G. Neutrophil extracellular traps formation by bacteria causing endometritis in the mare.. J Reprod Immunol 2014 Dec;106:41-9.
    doi: 10.1016/j.jri.2014.08.003pubmed: 25218891google scholar: lookup
  198. Opal SM, DePalo VA. Anti-inflammatory cytokines.. Chest 2000 Apr;117(4):1162-72.
    doi: 10.1378/chest.117.4.1162pubmed: 10767254google scholar: lookup
  199. Christoffersen M, Woodward E, Bojesen AM, Jacobsen S, Petersen MR, Troedsson MH, Lehn-Jensen H. Inflammatory responses to induced infectious endometritis in mares resistant or susceptible to persistent endometritis.. BMC Vet Res 2012 Mar 29;8:41.
    doi: 10.1186/1746-6148-8-41pmc: PMC3368729pubmed: 22458733google scholar: lookup
  200. Arend WP, Guthridge CJ. Biological role of interleukin 1 receptor antagonist isoforms.. Ann Rheum Dis 2000 Nov;59 Suppl 1(Suppl 1):i60-4.
    doi: 10.1136/ard.59.suppl_1.i60pmc: PMC1766634pubmed: 11053091google scholar: lookup
  201. Couper KN, Blount DG, Riley EM. IL-10: the master regulator of immunity to infection.. J Immunol 2008 May 1;180(9):5771-7.
    doi: 10.4049/jimmunol.180.9.5771pubmed: 18424693google scholar: lookup
  202. Dripps DJ, Brandhuber BJ, Thompson RC, Eisenberg SP. Interleukin-1 (IL-1) receptor antagonist binds to the 80-kDa IL-1 receptor but does not initiate IL-1 signal transduction.. J Biol Chem 1991 Jun 5;266(16):10331-6.
    pubmed: 1828071
  203. Cassatella MA, Meda L, Gasperini S, Calzetti F, Bonora S. Interleukin 10 (IL-10) upregulates IL-1 receptor antagonist production from lipopolysaccharide-stimulated human polymorphonuclear leukocytes by delaying mRNA degradation.. J Exp Med 1994 May 1;179(5):1695-9.
    doi: 10.1084/jem.179.5.1695pmc: PMC2191489pubmed: 8163946google scholar: lookup
  204. Fiorentino DF, Zlotnik A, Mosmann TR, Howard M, O'Garra A. IL-10 inhibits cytokine production by activated macrophages.. J Immunol 1991 Dec 1;147(11):3815-22.
    pubmed: 1940369
  205. Troedsson MH, Liu IK, Ing M, Pascoe J, Thurmond M. Multiple site electromyography recordings of uterine activity following an intrauterine bacterial challenge in mares susceptible and resistant to chronic uterine infection.. J Reprod Fertil 1993 Nov;99(2):307-13.
    doi: 10.1530/jrf.0.0990307pubmed: 8107011google scholar: lookup
  206. Griscavage JM, Wilk S, Ignarro LJ. Inhibitors of the proteasome pathway interfere with induction of nitric oxide synthase in macrophages by blocking activation of transcription factor NF-kappa B.. Proc Natl Acad Sci U S A 1996 Apr 16;93(8):3308-12.
    doi: 10.1073/pnas.93.8.3308pmc: PMC39603pubmed: 8622934google scholar: lookup
  207. Liu I., Rakestraw P., Coit C., Harmon F., Snyder J.. An in vitro investigation of the mechanism of neuromuscular regulation in myometrial contractility. Pferdeheilkunde 1997;13:557.
  208. Khan FA, Chenier TS, Murrant CL, Foster RA, Hewson J, Scholtz EL. Dose-dependent inhibition of uterine contractility by nitric oxide: A potential mechanism underlying persistent breeding-induced endometritis in the mare.. Theriogenology 2017 Mar 1;90:59-64.
  209. Khan FA, Chenier TS, Foster RA, Hewson J, Scholtz EL. Endometrial nitric oxide synthase activity in mares susceptible or resistant to persistent breeding-induced endometritis and the effect of a specific iNOS inhibitor in vitro.. Reprod Domest Anim 2018 Jun;53(3):718-724.
    doi: 10.1111/rda.13162pubmed: 29537110google scholar: lookup
  210. Evans MJ, Hamer JM, Gason LM, Graham CS, Asbury AC, Irvine CH. Clearance of bacteria and non-antigenic markers following intra-uterine inoculation into maiden mares: Effect of steroid hormone environment.. Theriogenology 1986 Jul;26(1):37-50.
    doi: 10.1016/0093-691X(86)90110-Xpubmed: 16726168google scholar: lookup
  211. Bowdish DM, Davidson DJ, Hancock RE. Immunomodulatory properties of defensins and cathelicidins.. Curr Top Microbiol Immunol 2006;306:27-66.
    pmc: PMC7121507pubmed: 16909917doi: 10.1007/3-540-29916-5_2google scholar: lookup
  212. Oddsdóttir C., Riley S.C., Leask R., Edwards D.R.. Activities of matrix metalloproteinases-9 and -2 in uterine fluid during induced equine endometritis. Pferdeheilkunde 2008;24:70–73.
  213. Chakraborti S, Mandal M, Das S, Mandal A, Chakraborti T. Regulation of matrix metalloproteinases: an overview.. Mol Cell Biochem 2003 Nov;253(1-2):269-85.
    doi: 10.1023/A:1026028303196pubmed: 14619979google scholar: lookup
  214. Curry TE Jr, Osteen KG. The matrix metalloproteinase system: changes, regulation, and impact throughout the ovarian and uterine reproductive cycle.. Endocr Rev 2003 Aug;24(4):428-65.
    doi: 10.1210/er.2002-0005pubmed: 12920150google scholar: lookup
  215. Rebordão MR, Galvão A, Szóstek A, Amaral A, Mateus L, Skarzynski DJ, Ferreira-Dias G. Physiopathologic mechanisms involved in mare endometrosis.. Reprod Domest Anim 2014 Oct;49 Suppl 4:82-7.
    doi: 10.1111/rda.12397pubmed: 25277436google scholar: lookup
  216. Alpoim-Moreira J, Fernandes C, Rebordão MR, Amaral A, Pinto-Bravo P, Bliebernicht M, Skarzynski DJ, Ferreira-Dias G. Collagens and DNA methyltransferases in mare endometrosis.. Reprod Domest Anim 2019 Sep;54 Suppl 3:46-52.
    doi: 10.1111/rda.13515pubmed: 31512314google scholar: lookup
  217. Hoffmann C, Ellenberger C, Mattos RC, Aupperle H, Dhein S, Stief B, Schoon HA. The equine endometrosis: new insights into the pathogenesis.. Anim Reprod Sci 2009 Apr;111(2-4):261-78.
  218. Rawdanowicz TJ, Hampton AL, Nagase H, Woolley DE, Salamonsen LA. Matrix metalloproteinase production by cultured human endometrial stromal cells: identification of interstitial collagenase, gelatinase-A, gelatinase-B, and stromelysin-1 and their differential regulation by interleukin-1 alpha and tumor necrosis factor-alpha.. J Clin Endocrinol Metab 1994 Aug;79(2):530-6.
    pubmed: 8045973doi: 10.1210/jcem.79.2.8045973google scholar: lookup
  219. Singer CF, Marbaix E, Lemoine P, Courtoy PJ, Eeckhout Y. Local cytokines induce differential expression of matrix metalloproteinases but not their tissue inhibitors in human endometrial fibroblasts.. Eur J Biochem 1999 Jan;259(1-2):40-5.
  220. Braundmeier AG, Nowak RA. Cytokines regulate matrix metalloproteinases in human uterine endometrial fibroblast cells through a mechanism that does not involve increases in extracellular matrix metalloproteinase inducer.. Am J Reprod Immunol 2006 Sep;56(3):201-14.
  221. Amaral A, Fernandes C, Lukasik K, Szóstek-Mioduchowska A, Baclawska A, Rebordão MR, Aguiar-Silva J, Pinto-Bravo P, Skarzynski DJ, Ferreira-Dias G. Elastase inhibition affects collagen transcription and prostaglandin secretion in mare endometrium during the estrous cycle.. Reprod Domest Anim 2018 Sep;53 Suppl 2:66-69.
    doi: 10.1111/rda.13258pubmed: 30238664google scholar: lookup
  222. Rebordão MR, Amaral A, Lukasik K, Szóstek-Mioduchowska A, Pinto-Bravo P, Galvão A, Skarzynski DJ, Ferreira-Dias G. Constituents of neutrophil extracellular traps induce in vitro collagen formation in mare endometrium.. Theriogenology 2018 Jun;113:8-18.
  223. Szóstek-Mioduchowska AZ, Lukasik K, Skarzynski DJ, Okuda K. Effect of transforming growth factor -β1 on α-smooth muscle actin and collagen expression in equine endometrial fibroblasts.. Theriogenology 2019 Jan 15;124:9-17.
  224. Szóstek AZ, Lukasik K, Galvão AM, Ferreira-Dias GM, Skarzynski DJ. Impairment of the interleukin system in equine endometrium during the course of endometrosis.. Biol Reprod 2013 Oct;89(4):79.
    doi: 10.1095/biolreprod.113.109447pubmed: 23946535google scholar: lookup
  225. Vesey DA, Cheung C, Cuttle L, Endre Z, Gobe G, Johnson DW. Interleukin-1beta stimulates human renal fibroblast proliferation and matrix protein production by means of a transforming growth factor-beta-dependent mechanism.. J Lab Clin Med 2002 Nov;140(5):342-50.
    doi: 10.1067/mlc.2002.128468pubmed: 12434136google scholar: lookup
  226. Xiao H, Ji AM, Li ZL, Song XD, Su D, Chen AH. Interleukin-1β inhibits collagen synthesis and promotes its decomposition in cultured cardiac fibroblasts.. Sheng Li Xue Bao 2008 Jun 25;60(3):355-61.
    pubmed: 18560726
  227. Szóstek-Mioduchowska AZ, Baclawska A, Okuda K, Skarzynski DJ. Effect of proinflammatory cytokines on endometrial collagen and metallopeptidase expression during the course of equine endometrosis.. Cytokine 2019 Nov;123:154767.
    doi: 10.1016/j.cyto.2019.154767pubmed: 31265984google scholar: lookup
  228. Wiesner J, Vilcinskas A. Antimicrobial peptides: the ancient arm of the human immune system.. Virulence 2010 Sep-Oct;1(5):440-64.
    doi: 10.4161/viru.1.5.12983pubmed: 21178486google scholar: lookup
  229. Linde A, Ross CR, Davis EG, Dib L, Blecha F, Melgarejo T. Innate immunity and host defense peptides in veterinary medicine.. J Vet Intern Med 2008 Mar-Apr;22(2):247-65.
  230. Nevalainen TJ, Graham GG, Scott KF. Antibacterial actions of secreted phospholipases A2. Review.. Biochim Biophys Acta 2008 Jan-Feb;1781(1-2):1-9.
    doi: 10.1016/j.bbalip.2007.12.001pubmed: 18177747google scholar: lookup
  231. Tomee JF, Koëter GH, Hiemstra PS, Kauffman HF. Secretory leukoprotease inhibitor: a native antimicrobial protein presenting a new therapeutic option?. Thorax 1998 Feb;53(2):114-6.
    doi: 10.1136/thx.53.2.114pmc: PMC1758711pubmed: 9624296google scholar: lookup
  232. Couto MA, Harwig SS, Lehrer RI. Selective inhibition of microbial serine proteases by eNAP-2, an antimicrobial peptide from equine neutrophils.. Infect Immun 1993 Jul;61(7):2991-4.
  233. Couto MA, Harwig SS, Cullor JS, Hughes JP, Lehrer RI. eNAP-2, a novel cysteine-rich bactericidal peptide from equine leukocytes.. Infect Immun 1992 Dec;60(12):5042-7.
  234. Kolm G, Klein D, Knapp E, Watanabe K, Walter I. Lactoferrin expression in the horse endometrium: relevance in persisting mating-induced endometritis.. Vet Immunol Immunopathol 2006 Nov 15;114(1-2):159-67.
    doi: 10.1016/j.vetimm.2006.08.005pubmed: 16973221google scholar: lookup
  235. Hultén C, Grönlund U, Hirvonen J, Tulamo RM, Suominen MM, Marhaug G, Forsberg M. Dynamics in serum of the inflammatory markers serum amyloid A (SAA), haptoglobin, fibrinogen and alpha2-globulins during induced noninfectious arthritis in the horse.. Equine Vet J 2002 Nov;34(7):699-704.
    doi: 10.2746/042516402776250405pubmed: 12455841google scholar: lookup
  236. Hultén C, Sandgren B, Skiöldebrand E, Klingeborn B, Marhaug G, Forsberg M. The acute phase protein serum amyloid A (SAA) as an inflammatory marker in equine influenza virus infection.. Acta Vet Scand 1999;40(4):323-33.
    pmc: PMC8043133pubmed: 10918902doi: 10.1186/bf03547012google scholar: lookup
  237. Nunokawa Y, Fujinaga T, Taira T, Okumura M, Yamashita K, Tsunoda N, Hagio M. Evaluation of serum amyloid A protein as an acute-phase reactive protein in horses.. J Vet Med Sci 1993 Dec;55(6):1011-6.
    doi: 10.1292/jvms.55.1011pubmed: 7509640google scholar: lookup
  238. Tuppits U, Orro T, Einarsson S, Kask K, Kavak A. Influence of the uterine inflammatory response after insemination with frozen-thawed semen on serum concentrations of acute phase proteins in mares.. Anim Reprod Sci 2014 May;146(3-4):182-6.
  239. Berg LC, Thomsen PD, Andersen PH, Jensen HE, Jacobsen S. Serum amyloid A is expressed in histologically normal tissues from horses and cattle.. Vet Immunol Immunopathol 2011 Nov 15;144(1-2):155-9.
    doi: 10.1016/j.vetimm.2011.06.037pubmed: 21783263google scholar: lookup
  240. Christoffersen M, Baagoe CD, Jacobsen S, Bojesen AM, Petersen MR, Lehn-Jensen H. Evaluation of the systemic acute phase response and endometrial gene expression of serum amyloid A and pro- and anti-inflammatory cytokines in mares with experimentally induced endometritis.. Vet Immunol Immunopathol 2010 Nov 15;138(1-2):95-105.
    doi: 10.1016/j.vetimm.2010.07.011pubmed: 20728224google scholar: lookup
  241. Nielsen JM. Endometritis in the mare: a diagnostic study comparing cultures from swab and biopsy.. Theriogenology 2005 Aug;64(3):510-8.
  242. Ferris R.A., Bohn A., McCue P.M.. Equine endometrial cytology: Collection techniques and interpretation. Equine Vet. Educ. 2015;27:316–322.
    doi: 10.1111/eve.12280google scholar: lookup
  243. Bohn AA, Ferris RA, McCue PM. Comparison of equine endometrial cytology samples collected with uterine swab, uterine brush, and low-volume lavage from healthy mares.. Vet Clin Pathol 2014 Dec;43(4):594-600.
    doi: 10.1111/vcp.12194pubmed: 25208767google scholar: lookup
  244. Cocchia N, Paciello O, Auletta L, Uccello V, Silvestro L, Mallardo K, Paraggio G, Pasolini MP. Comparison of the cytobrush, cottonswab, and low-volume uterine flush techniques to evaluate endometrial cytology for diagnosing endometritis in chronically infertile mares.. Theriogenology 2012 Jan 1;77(1):89-98.
  245. Christoffersen M, Brandis L, Samuelsson J, Bojesen AM, Troedsson MH, Petersen MR. Diagnostic double-guarded low-volume uterine lavage in mares.. Theriogenology 2015 Jan 15;83(2):222-7.
  246. Nielsen J.M., Nielsen F.H., Petersen M.R., Dyrehospital A.. Diagnosis of equine endometritis-Microbiology, cytology and histology of endometrial biopsies and the correlation to fertility. Pferdeheilkunde 2012;28:8–13.
  247. Nielsen J.M., Troedsson M.H., Pedersen M.R., Bojesen A.M., Lehn-Jensen H., Zent W.W.. Diagnosis of endometritis in the mare based on bacteriological and cytological examinations of the endometrium: Comparison of results obtained by swabs and biopsies. J. Equine Vet. Sci. 2010;30:27–30.
  248. Ball B.A., Shin S.J., Patten V.H., Lein D.H., Woods G.L.. Use of a low-volume uterine flush for microbiologic and cytologic examination of the mare’s endometrium. Theriogenology 1988;29:1269–1283.
  249. Ferris RA. Endometritis: Diagnostic Tools for Infectious Endometritis.. Vet Clin North Am Equine Pract 2016 Dec;32(3):481-498.
    doi: 10.1016/j.cveq.2016.08.001pubmed: 27810037google scholar: lookup
  250. Ferris RA, Dern K, Veir JK, Hawley JR, Lappin MR, McCue PM. Development of a broad-range quantitative polymerase chain reaction assay to detect and identify fungal DNA in equine endometrial samples.. Am J Vet Res 2013 Jan;74(1):161-5.
    doi: 10.2460/ajvr.74.1.161pubmed: 23270362google scholar: lookup
  251. Kenney RM. Prognostic value of endometrial biopsy of the mare.. J Reprod Fertil Suppl 1975 Oct;(23):347-8.
    pubmed: 1060804
  252. Doig PA, McKnight JD, Miller RB. The use of endometrial biopsy in the infertile mare.. Can Vet J 1981 Mar;22(3):72-6.
    pmc: PMC1789874pubmed: 7026016
  253. Ricketts SW, Alonso S. Assessment of the breeding prognosis of mares using paired endometrial biopsy techniques.. Equine Vet J 1991 May;23(3):185-8.
  254. Kenney R.M., Doig P.A.. Equine endometrial biopsy. Current Therapy in Theriogenology W.B. Saunders Company; Philadelphia, PA, USA: 1986. pp. 723–729.
  255. Cadario M.E., Thatcher M.J.D., Leblanc M.M.. Relationship between prostaglandin and uterine clearance of radiocolloid in the mare. Biol. Reprod. 1995;52:495–500.
  256. Rasch K, Schoon HA, Sieme H, Klug E. Histomorphological endometrial status and influence of oxytocin on the uterine drainage and pregnancy rate in mares.. Equine Vet J 1996 Nov;28(6):455-60.
  257. Allen WE. Investigations into the use of exogenous oxytocin for promoting uterine drainage in mares susceptible to endometritis.. Vet Rec 1991 Jun 22;128(25):593-4.
    doi: 10.1136/vr.128.25.593pubmed: 1897091google scholar: lookup
  258. Brinsko S.P., Varner D.D., Blanchard T.L.. The effect of uterine lavage performed four hours post insemination on pregnancy rate in mares. Theriogenology 1991;35:1111–1119.
  259. Cadario ME, Thatcher WW, Klapstein E, Merrit AM, Archbald LF, Thatcher MJ, LeBlanc MM. Dynamics of prostaglandin secretion, intrauterine fluid and uterine clearance in reproductively normal mares and mares with delayed uterine clearance.. Theriogenology 1999 Nov;52(7):1181-92.
    doi: 10.1016/S0093-691X(99)00210-1pubmed: 10735096google scholar: lookup
  260. Madill S., Troedsson M.H.T., Santschi E.M., Malone E.D.. Dose-response effect of intramuscular oxytocin treatment on myometrial contraction of reproductively normal mares during estrus. Theriogenology 2002;58:479–481.
  261. Campbell M.L.H., England G.C.W.. A comparison of the ecbolic efficacy of intravenous and intrauterine oxytocin treatments. Theriogenology 2002;58:473–477.
  262. Brendemuehl J.P.. Effect of oxytocin and PGF2α on luteal formation, function and pregnancy rates in mares. Theriogenology 2002;58:623–626.
  263. LeBlanc M.M.. Persistent Mating-Induced Endometritis. Current Therapy in Equine Medicine 5th ed. Elsevier Saunders; St. Louis, MI, USA: 2003. pp. 234–237.
  264. Irvine CH, McKeough VL, Turner JE, Alexander SL, Taylor TB. Effectiveness of a two-dose regimen of prostaglandin administration in inducing luteolysis without adverse side effects in mares.. Equine Vet J 2002 Mar;34(2):191-4.
    doi: 10.2746/042516402776767240pubmed: 11905437google scholar: lookup
  265. Nie G.J., Johnson K.E., Wenzel J.G.W., Braden T.D.. Effect of periovulatory ecbolics on luteal function and fertility. Theriogenology 2002;58:461–463.
  266. Schramme AR, Pinto CR, Davis J, Whisnant CS, Whitacre MD. Pharmacokinetics of carbetocin, a long-acting oxytocin analogue, following intravenous administration in horses.. Equine Vet J 2008 Nov;40(7):658-61.
    doi: 10.2746/042516408X334343pubmed: 19165935google scholar: lookup
  267. Steckler D, Naidoo V, Gerber D, Kähn W. Ex vivo influence of carbetocin on equine myometrial muscles and comparison with oxytocin.. Theriogenology 2012 Aug;78(3):502-9.
  268. Dascanio J.J.. How and When to Treat Endometritis With Systemic or Local Antibiotics. Proceedings of the 57th American Association of Equine Practitioners San Antonio, TX, USA. 1 January 2011; p. 57.
  269. Benko T., Boldizar M., Novotny F., Hura V., Valocky I., Dudrikova K., Karamanova M., Petrovic V.. Incidence of bacterial pathogens in equine uterine swabs, their antibiotic resistance patterns, and selected reproductive indices in English thoroughbred mares during the foal heat cycle. Vet. Med. 2015;60:613–620.
    doi: 10.17221/8529-VETMEDgoogle scholar: lookup
  270. Giguère S., Prescott J.F., Dowling P.M.. Antimicrobial drug action and interaction: An introduction. Antimicrobial Therapy in Veterinary Medicine 5th ed. John Wiley & Sons, Inc.; Hoboken, NJ, USA: 2013. pp. 3–10.
  271. Vila J, Martí S, Sánchez-Céspedes J. Porins, efflux pumps and multidrug resistance in Acinetobacter baumannii.. J Antimicrob Chemother 2007 Jun;59(6):1210-5.
    doi: 10.1093/jac/dkl509pubmed: 17324960google scholar: lookup
  272. Alekshun MN, Levy SB. Molecular mechanisms of antibacterial multidrug resistance.. Cell 2007 Mar 23;128(6):1037-50.
    doi: 10.1016/j.cell.2007.03.004pubmed: 17382878google scholar: lookup
  273. Rodriguez J.S., Han S., Nielsen S., Pearson L.K., Gay J.M., Tibary A.. Consequences of intrauterine enrofloxacin infusion on mare endometrium. J. Equine Vet. Sci. 2012;32:106–111.
  274. Schnobrich M.R., Pearson L.K., Barber B.K., Bradecamp E., Tibary A.. Effects of intrauterine infusion of a water-based suspension of enrofloxacin on mare endometrium. J. Equine Vet. Sci. 2015;35:662–667.
  275. Leblanc M.. The current status of antibiotic use in equine reproduction. Equine Vet. Educ. 2009;21:156–167.
    doi: 10.2746/095777308X357621google scholar: lookup
  276. Giguère S., Prescott J.F., Dowling P.M.. Antifungal chemotherapy. Antimicrobial Therapy in Veterinary Medicine John Wiley & Sons, Inc.; Hoboken, NJ, USA: 2013. pp. 333–355.
  277. Brinsko S.P., Rigby S.L., Varner D., Blanchard T.L.. A practical method for recognizing mares susceptible to post-breeding endometritis. AAEP Proc. 2003;49:363–365.
  278. Vanderwall DK, Woods GL. Effect on fertility of uterine lavage performed immediately prior to insemination in mares.. J Am Vet Med Assoc 2003 Apr 15;222(8):1108-10.
    doi: 10.2460/javma.2003.222.1108pubmed: 12710775google scholar: lookup
  279. Hua Q, Joyce AR, Palsson BØ, Fong SS. Metabolic characterization of Escherichia coli strains adapted to growth on lactate.. Appl Environ Microbiol 2007 Jul;73(14):4639-47.
    doi: 10.1128/AEM.00527-07pmc: PMC1932837pubmed: 17513588google scholar: lookup
  280. Eisenberg RC, Dobrogosz WJ. Gluconate metabolism in Escherichia coli.. J Bacteriol 1967 Mar;93(3):941-9.
    doi: 10.1128/JB.93.3.941-949.1967pmc: PMC276539pubmed: 5337840google scholar: lookup
  281. Knutti B., Pycock J.F., Weijden G.C., Küpfer U.. The influence of early postbreeding uterine lavage on pregnancy rate in mares with intrauterine fluid accumulations after breeding. Equine Vet. Educ. 2010;12:267–270.
  282. Brinsko SP, Varner DD, Blanchard TL, Meyers SA. The effect of postbreeding uterine lavage on pregnancy rate in mares.. Theriogenology 1990 Feb;33(2):465-75.
    doi: 10.1016/0093-691X(90)90504-Mpubmed: 16726743google scholar: lookup
  283. Fiala SM, Pimentel CA, Mattos AL, Gregory RM, Mattos RC. Effect of sperm numbers and concentration on sperm transport and uterine inflammatory response in the mare.. Theriogenology 2007 Feb;67(3):556-62.
  284. LeBlanc M.M.. Effects of oxytocin, prostaglandin and phenylbutazone on uterine clearance of radiocolloid. Pferdeheilkunde 1997;13:483–485.
    doi: 10.21836/PEM19970509google scholar: lookup
  285. Reilas T., Risco A.M., Kareskoski M., Katila T.. Effect of flunixin meglumine and oxytocin on uterine response to insemination in mares. Anim. Reprod. Sci. 2006;94:252–253.
  286. Cuervo-Arango J. The effect of treatment with flunixin meglumine at different times relative to hCG administration on ovulation failure and luteal function in mares.. Anim Reprod Sci 2011 Aug;127(1-2):84-90.
  287. Armstrong DT. Prostaglandins and follicular functions.. J Reprod Fertil 1981 May;62(1):283-91.
    doi: 10.1530/jrf.0.0620283pubmed: 6262509google scholar: lookup
  288. Donnelly CG, Sones JL, Dockweiler JC, Norberg LA, Norberg LE, Cheong SH, Gilbert RO. Effects of flunixin meglumine on postponement of ovulation in mares.. Am J Vet Res 2019 Mar;80(3):306-310.
    doi: 10.2460/ajvr.80.3.306pubmed: 30801209google scholar: lookup
  289. Aurich C., Rojer H., Walter I.. Treatment of estrous mares with the non-steroidal anti-inflammatory drug vedaprofen reduces the inflammatory response of the endometrium to insemination. Anim. Reprod. Sci. 2010;121:104–106.
  290. Cook VL, Blikslager AT. The use of nonsteroidal anti-inflammatory drugs in critically ill horses.. J Vet Emerg Crit Care (San Antonio) 2015 Jan-Feb;25(1):76-88.
    doi: 10.1111/vec.12271pubmed: 25521286google scholar: lookup
  291. Friso AM, Segabinazzi LGTM, Cyrino M, Correal SB, Freitas-Dell'Aqua CP, Teoro do Carmo M, Dell'Aqua JA Jr, Miró J, Papa FO, Alvarenga MA. Periovulatory administration of firocoxib did not alter ovulation rates and mitigated post-breeding inflammatory response in mares.. Theriogenology 2019 Oct 15;138:24-30.
  292. Rojer H, Aurich C. Treatment of persistent mating-induced endometritis in mares with the non-steroid anti-inflammatory drug vedaprofen.. Reprod Domest Anim 2010 Dec;45(6):e458-60.
  293. Papa F.O., Dell’Aqua J.A., Jr., Alvarenga M.A., Melo-Oña C.M., Zahn F., Lopes M.D.. Use of corticosteroid therapy on the modulation of uterine inflammatory response in mares after artificial insemination with frozen semen. Pferdeheilkunde 2007;24:79–82.
    doi: 10.21836/PEM20080116google scholar: lookup
  294. Ruijter-Villani M., de Grauw J.C., de Stout T.A.E.. Post-breeding endometritis: Effect of dexamethasone treatment on the expression of inflammatory markers. 7th International Conference on Equine Reproductive Medicine Leipzig, Germany. 20–21 January 2012; Leipziger blaue Hefte Band 2; pp. 286–288.
  295. Arlas TR, Wolf CA, Petrucci BP, Estanislau JF, Gregory RM, Jobim MI, Mattos RC. Proteomics of endometrial fluid after dexamethasone treatment in mares susceptible to endometritis.. Theriogenology 2015 Sep 1;84(4):617-23.
  296. Ohman T., Klein C., Doty A., Troedsson M.H.T.. The phagocytic function of blood-derived polymorphonuclear neutrophils after administration of dexamethasone for the modulation of post-breeding endometritis in the mare. Pferdeheilkunde 2011;27:267–270.
    doi: 10.21836/PEM20110310google scholar: lookup
  297. Wolf CA, Maslchitzky E, Gregory RM, Jobim MI, Mattos RC. Effect of corticotherapy on proteomics of endometrial fluid from mares susceptible to persistent postbreeding endometritis.. Theriogenology 2012 Apr 15;77(7):1351-9.
  298. Ferris RA, McCue PM. The effects of dexamethasone and prednisolone on pituitary and ovarian function in the mare.. Equine Vet J 2010 Jul;42(5):438-43.
  299. McNeill-Wiest DR, Thompson DL Jr, Wiest JJ. Gonadotropin secretion in ovariectomized pony mares treated with dexamethasone or progesterone and subsequently with dihydrotestosterone.. Domest Anim Endocrinol 1988 Apr;5(2):149-55.
    doi: 10.1016/0739-7240(88)90015-Xpubmed: 3147167google scholar: lookup
  300. Thompson DL Jr, Garza F Jr, St George RL, Rabb MH, Barry BE, French DD. Relationships among LH, FSH and prolactin secretion, storage and response to secretagogue and hypothalamic GnRH content in ovariectomized pony mares administered testosterone, dihydrotestosterone, estradiol, progesterone, dexamethasone or follicular fluid.. Domest Anim Endocrinol 1991 Apr;8(2):189-99.
    doi: 10.1016/0739-7240(91)90055-Opubmed: 1906388google scholar: lookup
  301. Andrews RV. Influence of the adrenal gland on gonadal function.. Adv Sex Horm Res 1977;3:197-215.
    pubmed: 188322
  302. Schreiber JR, Nakamura K, Erickson GF. Rat ovary glucocorticoid receptor: identification and characterization.. Steroids 1982 May;39(5):569-84.
    doi: 10.1016/0039-128X(82)90057-5pubmed: 6890727google scholar: lookup
  303. Hsueh AJ, Erickson GF. Glucocorticoid inhibition of FSH-induced estrogen production in cultured rat granulosa cells.. Steroids 1978 Dec;32(5):639-48.
    doi: 10.1016/0039-128X(78)90074-0pubmed: 734698google scholar: lookup
  304. Rogan D., Fumuso E., Rodríguez E., Wade J., Sánchez Bruni S.F.. Use of a Mycobacterial cell wall extract (MCWE) in susceptible mares to clear experimentally induced endometritis with Streptococcus zooepidemicus. J. Equine Vet. Sci. 2007;27:112–117.
  305. Rohrbach BW, Sheerin PC, Cantrell CK, Matthews PM, Steiner JV, Dodds LE. Effect of adjunctive treatment with intravenously administered Propionibacterium acnes on reproductive performance in mares with persistent endometritis.. J Am Vet Med Assoc 2007 Jul 1;231(1):107-13.
    doi: 10.2460/javma.231.1.107pubmed: 17605673google scholar: lookup
  306. Suzuki YA, Lopez V, Lönnerdal B. Mammalian lactoferrin receptors: structure and function.. Cell Mol Life Sci 2005 Nov;62(22):2560-75.
    doi: 10.1007/s00018-005-5371-1pubmed: 16261254google scholar: lookup
  307. Ammons MC, Copié V. Mini-review: Lactoferrin: a bioinspired, anti-biofilm therapeutic.. Biofouling 2013;29(4):443-55.
  308. Fedorka C.E., Woodward E.M., Scoggin K.E., Esteller-Vico A., Squires E.L., Ball B.A., Troedsson M.H.T.. The effect of cysteine-rich secretory protein-3 and lactoferrin on endometrial cytokine mRNA expression after breeding in the horse. J. Equine Vet. Sci. 2017;48:136–142.
  309. Coutinho da Silva M.A., Darr C.R., Moraes L.E., Forshey B.S.. Lactoferrin modulates uterine inflammation postbreeding in the mare. J. Equine Vet. Sci. 2017;56:63–67.
  310. Fedorka CE, Scoggin KE, Woodward EM, Squires EL, Ball BA, Troedsson M. The effect of select seminal plasma proteins on endometrial mRNA cytokine expression in mares susceptible to persistent mating-induced endometritis.. Reprod Domest Anim 2017 Feb;52(1):89-96.
    doi: 10.1111/rda.12813pubmed: 27686063google scholar: lookup
  311. Fedorka CE, Scoggin KE, Boakari YL, Hoppe NE, Squires EL, Ball BA, Troedsson MHT. The anti-inflammatory effect of exogenous lactoferrin on breeding-induced endometritis when administered post-breeding in susceptible mares.. Theriogenology 2018 Jul 1;114:63-69.
  312. Ammons MC, Ward LS, Fisher ST, Wolcott RD, James GA. In vitro susceptibility of established biofilms composed of a clinical wound isolate of Pseudomonas aeruginosa treated with lactoferrin and xylitol.. Int J Antimicrob Agents 2009 Mar;33(3):230-6.
  313. Ammons MC, Ward LS, James GA. Anti-biofilm efficacy of a lactoferrin/xylitol wound hydrogel used in combination with silver wound dressings.. Int Wound J 2011 Jun;8(3):268-73.
  314. Pereira RCDF, De La Côrte FD, Brass KE, da Silva Azevedo M, Gallio M, Cantarelli C, Dau SL, Cezar AS, Inkelmann MA. Evaluation of Three Methods of Platelet-Rich Plasma for Treatment of Equine Distal Limb Skin Wounds.. J Equine Vet Sci 2019 Jan;72:1-7.
    doi: 10.1016/j.jevs.2017.10.009pubmed: 30929771google scholar: lookup
  315. Carmona J.U., Argüelles D., Climent F., Prades M.. Autologous platelet concentrates as a treatment of horses with osteoarthritis: A preliminary pilot clinical study. J. Equine Vet. Sci. 2007;27:167–170.
  316. Argüelles D, Carmona JU, Climent F, Muñoz E, Prades M. Autologous platelet concentrates as a treatment for musculoskeletal lesions in five horses.. Vet Rec 2008 Feb 16;162(7):208-11.
    doi: 10.1136/vr.162.7.208pubmed: 18281627google scholar: lookup
  317. Georg R, Maria C, Gisela A, Bianca C. Autologous conditioned plasma as therapy of tendon and ligament lesions in seven horses.. J Vet Sci 2010 Jun;11(2):173-5.
    doi: 10.4142/jvs.2010.11.2.173pmc: PMC2873820pubmed: 20458161google scholar: lookup
  318. Pascoe D.R.. Effect of Adding Autologous Plasma to an intrauterine antibiotic therapy after breeding on pregnancy rates in mares. Biol. Reprod. 1995;52:539–543.
  319. Kim HJ, Yeom JS, Koh YG, Yeo JE, Kang KT, Kang YM, Chang BS, Lee CK. Anti-inflammatory effect of platelet-rich plasma on nucleus pulposus cells with response of TNF-α and IL-1.. J Orthop Res 2014 Apr;32(4):551-6.
    doi: 10.1002/jor.22532pubmed: 24338609google scholar: lookup
  320. Sundman EA, Cole BJ, Karas V, Della Valle C, Tetreault MW, Mohammed HO, Fortier LA. The anti-inflammatory and matrix restorative mechanisms of platelet-rich plasma in osteoarthritis.. Am J Sports Med 2014 Jan;42(1):35-41.
    doi: 10.1177/0363546513507766pubmed: 24192391google scholar: lookup
  321. Wu CC, Chen WH, Zao B, Lai PL, Lin TC, Lo HY, Shieh YH, Wu CH, Deng WP. Regenerative potentials of platelet-rich plasma enhanced by collagen in retrieving pro-inflammatory cytokine-inhibited chondrogenesis.. Biomaterials 2011 Sep;32(25):5847-54.
  322. Woodell-May J, Matuska A, Oyster M, Welch Z, O'Shaughnessey K, Hoeppner J. Autologous protein solution inhibits MMP-13 production by IL-1β and TNFα-stimulated human articular chondrocytes.. J Orthop Res 2011 Sep;29(9):1320-6.
    doi: 10.1002/jor.21384pubmed: 21437966google scholar: lookup
  323. Mazzocca AD, McCarthy MB, Intravia J, Beitzel K, Apostolakos J, Cote MP, Bradley J, Arciero RA. An in vitro evaluation of the anti-inflammatory effects of platelet-rich plasma, ketorolac, and methylprednisolone.. Arthroscopy 2013 Apr;29(4):675-83.
    doi: 10.1016/j.arthro.2012.12.005pubmed: 23395471google scholar: lookup
  324. Cieslik-Bielecka A, Bielecki T, Gazdzik TS, Arendt J, Król W, Szczepanski T. Autologous platelets and leukocytes can improve healing of infected high-energy soft tissue injury.. Transfus Apher Sci 2009 Aug;41(1):9-12.
    doi: 10.1016/j.transci.2009.05.006pubmed: 19524487google scholar: lookup
  325. Trowbridge CC, Stammers AH, Woods E, Yen BR, Klayman M, Gilbert C. Use of platelet gel and its effects on infection in cardiac surgery.. J Extra Corpor Technol 2005 Dec;37(4):381-6.
    pmc: PMC4680831pubmed: 16524157
  326. Yuan T, Zhang C, Zeng B. Treatment of chronic femoral osteomyelitis with platelet-rich plasma (PRP): a case report.. Transfus Apher Sci 2008 Apr;38(2):167-73.
    doi: 10.1016/j.transci.2008.01.006pubmed: 18343727google scholar: lookup
  327. Anitua E, Alonso R, Girbau C, Aguirre JJ, Muruzabal F, Orive G. Antibacterial effect of plasma rich in growth factors (PRGF®-Endoret®) against Staphylococcus aureus and Staphylococcus epidermidis strains.. Clin Exp Dermatol 2012 Aug;37(6):652-7.
  328. Álvarez M., López C., Giraldo C., Samudio I., Carmona J.. In vitro bactericidal activity of equine platelet concentrates, platelet poor plasma, and plasma against methicillin-resistant Staphylococcus aureus. Arch. Med. Vet. 2011;43:155–161.
  329. Bielecki TM, Gazdzik TS, Arendt J, Szczepanski T, Król W, Wielkoszynski T. Antibacterial effect of autologous platelet gel enriched with growth factors and other active substances: an in vitro study.. J Bone Joint Surg Br 2007 Mar;89(3):417-20.
    doi: 10.1302/0301-620X.89B3.18491pubmed: 17356164google scholar: lookup
  330. Burnouf T, Chou ML, Wu YW, Su CY, Lee LW. Antimicrobial activity of platelet (PLT)-poor plasma, PLT-rich plasma, PLT gel, and solvent/detergent-treated PLT lysate biomaterials against wound bacteria.. Transfusion 2013 Jan;53(1):138-46.
  331. Moojen DJ, Everts PA, Schure RM, Overdevest EP, van Zundert A, Knape JT, Castelein RM, Creemers LB, Dhert WJ. Antimicrobial activity of platelet-leukocyte gel against Staphylococcus aureus.. J Orthop Res 2008 Mar;26(3):404-10.
    doi: 10.1002/jor.20519pubmed: 17960651google scholar: lookup
  332. Reghini MF, Ramires Neto C, Segabinazzi LG, Castro Chaves MM, Dell'Aqua Cde P, Bussiere MC, Dell'Aqua JA Jr, Papa FO, Alvarenga MA. Inflammatory response in chronic degenerative endometritis mares treated with platelet-rich plasma.. Theriogenology 2016 Jul 15;86(2):516-22.
  333. Segabinazzi LG, Friso AM, Correal SB, Crespilho AM, Dell'Aqua JA Jr, Miró J, Papa FO, Alvarenga MA. Uterine clinical findings, fertility rate, leucocyte migration, and COX-2 protein levels in the endometrial tissue of susceptible mares treated with platelet-rich plasma before and after AI.. Theriogenology 2017 Dec;104:120-126.
  334. Metcalf E.S.. The effect of Platelet-Rich Plasma (PRP) on intraluminal fluid and pregnancy rates in mares susceptible to persistent mating-induced endometritis (PMIE). J. Equine Vet. Sci. 2014;34:128.
  335. Metcalf E.S., Scoggin K., Troedsson M.H.T.. The effect of platelet-rich plasma on endometrial pro-inflammatory cytokines in susceptible mares following semen deposition. J. Equine Vet. Sci. 2012;32:498.
  336. Timmers L, Lim SK, Hoefer IE, Arslan F, Lai RC, van Oorschot AA, Goumans MJ, Strijder C, Sze SK, Choo A, Piek JJ, Doevendans PA, Pasterkamp G, de Kleijn DP. Human mesenchymal stem cell-conditioned medium improves cardiac function following myocardial infarction.. Stem Cell Res 2011 May;6(3):206-14.
    doi: 10.1016/j.scr.2011.01.001pubmed: 21419744google scholar: lookup
  337. Barrachina L, Remacha AR, Romero A, Vázquez FJ, Albareda J, Prades M, Ranera B, Zaragoza P, Martín-Burriel I, Rodellar C. Effect of inflammatory environment on equine bone marrow derived mesenchymal stem cells immunogenicity and immunomodulatory properties.. Vet Immunol Immunopathol 2016 Mar;171:57-65.
    doi: 10.1016/j.vetimm.2016.02.007pubmed: 26964718google scholar: lookup
  338. Grove JE, Bruscia E, Krause DS. Plasticity of bone marrow-derived stem cells.. Stem Cells 2004;22(4):487-500.
    doi: 10.1634/stemcells.22-4-487pubmed: 15277695google scholar: lookup
  339. Du H, Taylor HS. Contribution of bone marrow-derived stem cells to endometrium and endometriosis.. Stem Cells 2007 Aug;25(8):2082-6.
    doi: 10.1634/stemcells.2006-0828pubmed: 17464086google scholar: lookup
  340. Alvarenga M.A., do Carmo M.T., Segabinazzi L.G., Guastali M.D., Maia L., Landim-Alvarenga F.C.. Feasibility and safety of endometrial injection of autologous bone marrow mesenchymal stem cells in mares. J. Equine Vet. Sci. 2016;42:12–18.
  341. Mambelli LI, Mattos RC, Winter GH, Madeiro DS, Morais BP, Malschitzky E, Miglino MA, Kerkis A, Kerkis I. Changes in expression pattern of selected endometrial proteins following mesenchymal stem cells infusion in mares with endometrosis.. PLoS One 2014;9(6):e97889.
  342. Ferris RA, Frisbie DD, McCue PM. Use of mesenchymal stem cells or autologous conditioned serum to modulate the inflammatory response to spermatozoa in mares.. Theriogenology 2014 Jul 1;82(1):36-42.
  343. Rink BE, Beyer T, French HM, Watson E, Aurich C, Donadeu FX. The Fate of Autologous Endometrial Mesenchymal Stromal Cells After Application in the Healthy Equine Uterus.. Stem Cells Dev 2018 Aug 1;27(15):1046-1052.
    doi: 10.1089/scd.2018.0056pmc: PMC6067096pubmed: 29790424google scholar: lookup
  344. Mambelli LI, Winter GH, Kerkis A, Malschitzky E, Mattos RC, Kerkis I. A novel strategy of mesenchymal stem cells delivery in the uterus of mares with endometrosis.. Theriogenology 2013 Mar 15;79(5):744-50.
  345. Zhao J, Zhang Q, Wang Y, Li Y. Uterine infusion with bone marrow mesenchymal stem cells improves endometrium thickness in a rat model of thin endometrium.. Reprod Sci 2015 Feb;22(2):181-8.
    doi: 10.1177/1933719114537715pmc: PMC4287599pubmed: 24947483google scholar: lookup
  346. Mao F, Xu WR, Qian H, Zhu W, Yan YM, Shao QX, Xu HX. Immunosuppressive effects of mesenchymal stem cells in collagen-induced mouse arthritis.. Inflamm Res 2010 Mar;59(3):219-25.
    doi: 10.1007/s00011-009-0090-ypubmed: 19763787google scholar: lookup
  347. Bai L, Lennon DP, Eaton V, Maier K, Caplan AI, Miller SD, Miller RH. Human bone marrow-derived mesenchymal stem cells induce Th2-polarized immune response and promote endogenous repair in animal models of multiple sclerosis.. Glia 2009 Aug 15;57(11):1192-203.
    doi: 10.1002/glia.20841pmc: PMC2706928pubmed: 19191336google scholar: lookup
  348. Achache H, Revel A. Endometrial receptivity markers, the journey to successful embryo implantation.. Hum Reprod Update 2006 Nov-Dec;12(6):731-46.
    doi: 10.1093/humupd/dml004pubmed: 16982667google scholar: lookup

Citations

This article has been cited 57 times.
  1. Mazzuchini MP, Canisso IF. The Apparent pH Stability of Antibiotic Preparations Used for Uterine Infusions in Mares. Animals (Basel) 2026 Jan 26;16(3).
    doi: 10.3390/ani16030382pubmed: 41681363google scholar: lookup
  2. Dabiri M, Goss DM, Ramasamy R, Bhakat M, Gardner DK, de Graaf SP, Ebrahimi Warkiani M. Sperm DNA fragmentation and its influence on mammalian reproduction. Nat Rev Urol 2026 Jan 28;.
    doi: 10.1038/s41585-025-01123-6pubmed: 41606137google scholar: lookup
  3. Ferreira CSC, Pinna AE, Dos Santos IPF, Dias MCR, Dos Santos NSL, Bragueroli SDS, Quintino PM, Almeida GB, Penna BA, da Rocha EMDS, de Souza GN, Barbosa CG, de Jesus VLT, Jacob JCF. Powerflow Doppler Ultrasonography in the Evaluation of Mares with and Without Endometritis. Vet Sci 2025 Sep 28;12(10).
    doi: 10.3390/vetsci12100941pubmed: 41150081google scholar: lookup
  4. Köhne M, Hüsch R, Peh E, Hirnet J, Tönissen A, Müsken M, Plötz M, Kittler S, Sieme H. Newly isolated bacteriophages show efficacy and phage-antibiotic synergy in vitro against the equine genital pathogens Klebsiella pneumoniae and Pseudomonas aeruginosa. BMC Vet Res 2025 Oct 3;21(1):568.
    doi: 10.1186/s12917-025-04989-1pubmed: 41044673google scholar: lookup
  5. Alfatlawy HJ. Microbial profile of post-breeding endometritis in Arabian mares from the Al-Hira District, Iraq. Open Vet J 2025;15(8):3670-3676.
    doi: 10.5455/OVJ.2025.v15.i8.30pubmed: 41035988google scholar: lookup
  6. Beckers KF, Liu CC, Gomes VCL, Schulz CJ, Childers GW, Fedorka CE, Sones JL. Effects of Intra-uterine Ceftiofur on the Equine Uterine Microbiome. Vet Sci 2025 Aug 30;12(9).
    doi: 10.3390/vetsci12090837pubmed: 41012762google scholar: lookup
  7. Yáñez Ramil U, Jezierska S, Krupa M, Bogado Pascottini O. Fundamentals of microbiome-based therapies for reproductive tract inflammatory diseases in domestic animals. Anim Reprod 2025;22(3):e20250030.
    doi: 10.1590/1984-3143-AR2025-0030pubmed: 40933872google scholar: lookup
  8. Hardefeldt L, Thomas K, Page S, Norris J, Browning G, El Hage C, Stewart A, Gilkerson J, Muscatello G, Verwilghen D, van Galen G, Bauquier J, Cuming R, Reynolds B, Whittaker C, Wilkes E, Clulow J, Burden C, Begg L. Antimicrobial prescribing guidelines for horses in Australia. Aust Vet J 2025 Dec;103(12):781-889.
    doi: 10.1111/avj.70003pubmed: 40903020google scholar: lookup
  9. Fehin B, Scott CJ, Arango-Sabogal JC, de Mestre AM, Mouncey R. Associations between endometrial swab bacteriology and cytology findings and live foal rates in Thoroughbred broodmares in the United Kingdom. Equine Vet J 2026 Mar;58(2):348-358.
    doi: 10.1111/evj.70086pubmed: 40888035google scholar: lookup
  10. Nash DM, Giles JL. Uterine inflammation and lessons from large animal models of endometritis. Nat Rev Immunol 2025 Dec;25(12):934-946.
    doi: 10.1038/s41577-025-01200-2pubmed: 40696155google scholar: lookup
  11. Del Prete C, Attolini E, Merlo B, Iacono E, Nocera FP, De Martino L, Longobardi C, Damiano S, Longobardi V, Cocchia N, Pasolini MP. Post-Insemination Infusion of Wharton's Jelly Mesenchymal Stromal/Stem Cells-Derived Conditioned Medium: A Novel Approach for Improving Pregnancy Outcomes in Problem Mares. Vet Sci 2025 May 16;12(5).
    doi: 10.3390/vetsci12050482pubmed: 40431575google scholar: lookup
  12. Piotrowska-Tomala KK, Szóstek-Mioduchowska A, Jonczyk AW, Drzewiecka EM, Wrobel MH, Hojo T, Ferreira-Dias G, Skarzynski DJ. The effect of lysophosphatidic acid on myometrial contractility and the mRNA transcription of its receptors in the myometrium at different stages of endometrosis in mares. BMC Vet Res 2024 Dec 19;20(1):571.
    doi: 10.1186/s12917-024-04384-2pubmed: 39696406google scholar: lookup
  13. Köhne M, Hüsch R, Tönissen A, Schmidt M, Müsken M, Böttcher D, Hirnet J, Plötz M, Kittler S, Sieme H. Isolation and characterization of bacteriophages specific to Streptococcus equi subspecies zooepidemicus and evaluation of efficacy ex vivo. Front Microbiol 2024;15:1448958.
    doi: 10.3389/fmicb.2024.1448958pubmed: 39529671google scholar: lookup
  14. Mazzuchini MP, Lisboa FP, de Castro JI, Alvarenga MA, Segabinazzi LGTM, Canisso IF. In vitro antimicrobial activity of non-traditional therapies for infectious endometritis in mares. Equine Vet J 2025 Jul;57(4):1118-1126.
    doi: 10.1111/evj.14423pubmed: 39431554google scholar: lookup
  15. Wang Z, Zeng S, Wang Y, Wang T, Qu H, Zhu Y, Li J. Reproductive Disorders in Donkeys: Current Evidence and Update. Animals (Basel) 2024 Aug 28;14(17).
    doi: 10.3390/ani14172494pubmed: 39272279google scholar: lookup
  16. Novello G, Souza FF, Canisso IF. Platelet-Rich Plasma Proteome of Mares Susceptible to Persistent-Breeding-Induced Endometritis Differs from Resistant Mares. Animals (Basel) 2024 Jul 18;14(14).
    doi: 10.3390/ani14142100pubmed: 39061562google scholar: lookup
  17. Gil-Miranda A, Macnicol J, Orellana-Guerrero D, Samper JC, Gomez DE. Reproductive Tract Microbiota of Mares. Vet Sci 2024 Jul 18;11(7).
    doi: 10.3390/vetsci11070324pubmed: 39058008google scholar: lookup
  18. Gil-Miranda A, Caddey B, Orellana-Guerrero D, Smith H, Samper JC, Gomez DE. Vaginal and Uterine Microbiota of Healthy Maiden Mares during Estrus. Vet Sci 2024 Jul 18;11(7).
    doi: 10.3390/vetsci11070323pubmed: 39058007google scholar: lookup
  19. Prete CD, Nocera FP, Piegari G, Palumbo V, Martino L, Cocchia N, Paciello O, Montano C, Pasolini MP. Use of cytobrush for bacteriological and cytological diagnosis of endometritis in mares. Vet World 2024 Feb;17(2):398-406.
  20. Silva JA, Castañares M, Mouguelar H, Valenciano JA, Pellegrino MS. Isolation of lactic acid bacteria from the reproductive tract of mares as potentially beneficial strains to prevent equine endometritis. Vet Res Commun 2024 Jun;48(3):1353-1366.
    doi: 10.1007/s11259-024-10295-2pubmed: 38233700google scholar: lookup
  21. Heil BA, van Heule M, Thompson SK, Kearns TA, Oberhaus EL, King G, Daels P, Dini P, Sones JL. Effect of Sampling Method on Detection of the Equine Uterine Microbiome during Estrus. Vet Sci 2023 Nov 8;10(11).
    doi: 10.3390/vetsci10110644pubmed: 37999467google scholar: lookup
  22. Wong YS, Mançanares AC, Navarrete FI, Poblete PM, Méndez-Pérez L, Ferreira-Dias GML, Rodriguez-Alvarez L, Castro FO. Mare stromal endometrial cells differentially modulate inflammation depending on oestrus cycle status: an in vitro study. Front Vet Sci 2023;10:1271240.
    doi: 10.3389/fvets.2023.1271240pubmed: 37869492google scholar: lookup
  23. Reddy LS, Jaiswal A, Reddy K, Jyotsna G, Yadav P. Retained Intrauterine Fetal Bone Fragments Causing Secondary Infertility: A Review. Cureus 2023 Aug;15(8):e44005.
    doi: 10.7759/cureus.44005pubmed: 37746402google scholar: lookup
  24. Nocera FP, Maurizi L, Masullo A, Nicoletti M, Conte AL, Brunetti F, De Martino L, Zagaglia C, Longhi C. Genotypic and Phenotypic Characterization of Escherichia coli Isolates Recovered from the Uterus of Mares with Fertility Problems. Animals (Basel) 2023 May 14;13(10).
    doi: 10.3390/ani13101639pubmed: 37238068google scholar: lookup
  25. Ezz MA, Mansouri A, Akthar I, Yousef MS, Kowsar R, Miyamoto A. Hyaluronan regulates sperm-induced inflammatory response by enhancing sperm attachment to bovine endometrial epithelial cells via CD44: in-silico and in-vitro approaches. Front Endocrinol (Lausanne) 2023;14:1134868.
    doi: 10.3389/fendo.2023.1134868pubmed: 37234812google scholar: lookup
  26. Tyrnenopoulou P, Fthenakis GC. Clinical Aspects of Bacterial Distribution and Antibiotic Resistance in the Reproductive System of Equids. Antibiotics (Basel) 2023 Mar 28;12(4).
    doi: 10.3390/antibiotics12040664pubmed: 37107026google scholar: lookup
  27. Scarlet D, Malama E, Fischer S, Knutti B, Bollwein H. Relationship between Clinical Uterine Findings, Therapy, and Fertility in the Mare. Vet Sci 2023 Mar 29;10(4).
    doi: 10.3390/vetsci10040259pubmed: 37104414google scholar: lookup
  28. Lange-Consiglio A, Gaspari G, Funghi F, Capra E, Cretich M, Frigerio R, Bosi G, Cremonesi F. Amniotic Mesenchymal-Derived Extracellular Vesicles and Their Role in the Prevention of Persistent Post-Breeding Induced Endometritis. Int J Mol Sci 2023 Mar 8;24(6).
    doi: 10.3390/ijms24065166pubmed: 36982240google scholar: lookup
  29. Amaral A, Cebola N, Szóstek-Mioduchowska A, Rebordão MR, Kordowitzki P, Skarzynski D, Ferreira-Dias G. Inhibition of Myeloperoxidase Pro-Fibrotic Effect by Noscapine in Equine Endometrium. Int J Mol Sci 2023 Feb 10;24(4).
    doi: 10.3390/ijms24043593pubmed: 36835008google scholar: lookup
  30. Köhne M, Hofbauer L, Böttcher D, Tönissen A, Hegger A, Görgens A, Ulrich R, Sieme H. Comparison of systemic trimethoprim-sulfadimethoxine treatment and intrauterine ozone application as possible therapies for bacterial endometritis in equine practice. Front Vet Sci 2023;10:1102149.
    doi: 10.3389/fvets.2023.1102149pubmed: 36777673google scholar: lookup
  31. Ashraf R, Rashid S, Rasheed I, Asif S. Early embryonic death in equines and camelids. Open Vet J 2022 Nov-Dec;12(6):903-909.
    doi: 10.5455/OVJ.2022.v12.i6.16pubmed: 36777062google scholar: lookup
  32. Cecchini Gualandi S, Di Palma T, Boni R. Serological and Uterine Biomarkers for Detecting Endometritis in Mares. Animals (Basel) 2023 Jan 11;13(2).
    doi: 10.3390/ani13020253pubmed: 36670793google scholar: lookup
  33. Freccero F, Mislei B, Bucci D, Dondi F, Mari G. Effects of Intra-Uterine Fluid Accumulation after Artificial Insemination on Luteal Function in Mares. Animals (Basel) 2022 Dec 23;13(1).
    doi: 10.3390/ani13010067pubmed: 36611677google scholar: lookup
  34. Garner C, Stephen C, Pant SD, Ghorashi SA. Comparison of PCR-HRM, colorimetric LAMP and culture based diagnostic assays in the detection of endometritis caused by Streptococcus equi subsp. zooepidemicus in mares. Vet Res Commun 2023 Jun;47(2):495-509.
    doi: 10.1007/s11259-022-10047-0pubmed: 36538151google scholar: lookup
  35. Lee S, Yoo I, Cheon Y, Ka H. Conceptus-derived cytokines interleukin-1β and interferon-γ induce the expression of acute phase protein serum amyloid A3 in endometrial epithelia at the time of conceptus implantation in pigs. Anim Biosci 2023 Mar;36(3):441-450.
    doi: 10.5713/ab.22.0334pubmed: 36397697google scholar: lookup
  36. Boni R, Cecchini Gualandi S. Relationship between Oxidative Stress and Endometritis: Exploiting Knowledge Gained in Mares and Cows. Animals (Basel) 2022 Sep 13;12(18).
    doi: 10.3390/ani12182403pubmed: 36139263google scholar: lookup
  37. Magnusson U. Antimicrobial use and resistance in food-producing animals-How can we protect the efficacy of antibiotics for reproductive diseases?. Reprod Domest Anim 2022 Sep;57 Suppl 4(Suppl 4):13-20.
    doi: 10.1111/rda.14170pubmed: 35668646google scholar: lookup
  38. Mahmoud SF, Fayez M, Swelum AA, Alswat AS, Alkafafy M, Alzahrani OM, Alsunaini SJ, Almuslem A, Al Amer AS, Yusuf S. Genetic Diversity, Biofilm Formation, and Antibiotic Resistance of Pseudomonas aeruginosa Isolated from Cow, Camel, and Mare with Clinical Endometritis. Vet Sci 2022 May 16;9(5).
    doi: 10.3390/vetsci9050239pubmed: 35622767google scholar: lookup
  39. Smieszek A, Marcinkowska K, Pielok A, Sikora M, Valihrach L, Carnevale E, Marycz K. Obesity Affects the Proliferative Potential of Equine Endometrial Progenitor Cells and Modulates Their Molecular Phenotype Associated with Mitochondrial Metabolism. Cells 2022 Apr 24;11(9).
    doi: 10.3390/cells11091437pubmed: 35563743google scholar: lookup
  40. Katila T, Ferreira-Dias G. Evolution of the Concepts of Endometrosis, Post Breeding Endometritis, and Susceptibility of Mares. Animals (Basel) 2022 Mar 19;12(6).
    doi: 10.3390/ani12060779pubmed: 35327176google scholar: lookup
  41. Bazzano M, Marchegiani A, Troisi A, McLean A, Laus F. Serum Amyloid A as a Promising Biomarker in Domestic Animals' Reproduction: Current Knowledge and Future Perspective. Animals (Basel) 2022 Feb 25;12(5).
    doi: 10.3390/ani12050589pubmed: 35268158google scholar: lookup
  42. Zhao Y, Zhu Y, Liu B, Mi J, Li N, Zhao W, Wu R, Holyoak GR, Li J, Liu D, Zeng S, Wang Y. Antimicrobial Susceptibility of Bacterial Isolates from Donkey Uterine Infections, 2018-2021. Vet Sci 2022 Feb 5;9(2).
    doi: 10.3390/vetsci9020067pubmed: 35202320google scholar: lookup
  43. Morrell JM, Rocha A. A Novel Approach to Minimising Acute Equine Endometritis That May Help to Prevent the Development of the Chronic State. Front Vet Sci 2021;8:799619.
    doi: 10.3389/fvets.2021.799619pubmed: 35071389google scholar: lookup
  44. Nocera FP, D'Eletto E, Ambrosio M, Fiorito F, Pagnini U, De Martino L. Occurrence and Antimicrobial Susceptibility Profiles of Streptococcus equi subsp. zooepidemicus Strains Isolated from Mares with Fertility Problems. Antibiotics (Basel) 2021 Dec 27;11(1).
    doi: 10.3390/antibiotics11010025pubmed: 35052902google scholar: lookup
  45. Bottrel M, Ortiz I, Hidalgo M, Díaz-Jiménez M, Pereira B, Consuegra C, Yousef MS, Dorado J. Hormonal Management for the Induction of Luteolysis and Ovulation in Andalusian Jennies: Effect on Reproductive Performance, Embryo Quality and Recovery Rate. Animals (Basel) 2022 Jan 8;12(2).
    doi: 10.3390/ani12020143pubmed: 35049767google scholar: lookup
  46. Ibrahim S, Hedia M, Taqi MO, Derbala MK, Mahmoud KGM, Ahmed Y, Sosa AS, Saber YHA, Hasanain MH, Nawito MF, Seidel GE. Extracellular vesicles in low volume uterine lavage and serum: novel and promising biomarker for endometritis in Arabian mares. BMC Vet Res 2022 Jan 18;18(1):42.
    doi: 10.1186/s12917-022-03137-3pubmed: 35042518google scholar: lookup
  47. Karam KM, Alebady AS, Alhilfi HO, Al-Delemi DH. Comparative study utilizing different post-breeding treatment regimens in cyclic Arabian mares. Vet World 2021 Nov;14(11):2863-2868.
  48. Amaral A, Fernandes C, Szóstek-Mioduchowska A, Lukasik K, Rebordão MR, Pinto-Bravo P, Skarzynski DJ, Ferreira-Dias G. The Inhibitory Effect of Noscapine on the In Vitro Cathepsin G-Induced Collagen Expression in Equine Endometrium. Life (Basel) 2021 Oct 19;11(10).
    doi: 10.3390/life11101107pubmed: 34685478google scholar: lookup
  49. Ibrahim S, Hedia M, Taqi MO, Derbala MK, Mahmoud KGM, Ahmed Y, Ismail S, El-Belely M. Alterations in the Expression Profile of Serum miR-155, miR-223, miR-17, miR-200a, miR-205, as well as Levels of Interleukin 6, and Prostaglandins during Endometritis in Arabian Mares. Vet Sci 2021 Jun 4;8(6).
    doi: 10.3390/vetsci8060098pubmed: 34199703google scholar: lookup
  50. Borlee GI, Lakin SM, Kapuscinski ML, Abdo Z, Stenglein MD, McCue PM, Borlee BR. Complete Genome Sequences of Eight Streptococcus equi subsp. zooepidemicus Strains Isolated from Mares in Estrus with Endometritis. Microbiol Resour Announc 2021 Jul;10(26):e0132120.
    doi: 10.1128/MRA.01321-20pubmed: 34197198google scholar: lookup
  51. Amaral A, Fernandes C, Szóstek-Mioduchowska A, Rebordão MR, Skarzynski DJ, Ferreira-Dias G. Noscapine Acts as a Protease Inhibitor of In Vitro Elastase-Induced Collagen Deposition in Equine Endometrium. Int J Mol Sci 2021 May 19;22(10).
    doi: 10.3390/ijms22105333pubmed: 34069423google scholar: lookup
  52. Segabinazzi LGTM, Podico G, Rosser MF, Nanjappa SG, Alvarenga MA, Canisso IF. Three Manual Noncommercial Methods to Prepare Equine Platelet-Rich Plasma. Animals (Basel) 2021 May 21;11(6).
    doi: 10.3390/ani11061478pubmed: 34063777google scholar: lookup
  53. Segabinazzi LGTM, Canisso IF, Podico G, Cunha LL, Novello G, Rosser MF, Loux SC, Lima FS, Alvarenga MA. Intrauterine Blood Plasma Platelet-Therapy Mitigates Persistent Breeding-Induced Endometritis, Reduces Uterine Infections, and Improves Embryo Recovery in Mares. Antibiotics (Basel) 2021 Apr 23;10(5).
    doi: 10.3390/antibiotics10050490pubmed: 33922743google scholar: lookup
  54. Dawod A, Miro J, Elbaz HT, Fahmy H, Abdoon AS. Effect of Intrauterine Infusion of Equine Fresh Platelets-Rich Plasma (PRP) or Lyophilized PRP (L-GF(equina)) on Ovarian Activity and Pregnancy Rate in Repeat Breeder Purebred Arabian Mares. Animals (Basel) 2021 Apr 14;11(4).
    doi: 10.3390/ani11041123pubmed: 33919901google scholar: lookup
  55. Cequier A, Sanz C, Rodellar C, Barrachina L. The Usefulness of Mesenchymal Stem Cells beyond the Musculoskeletal System in Horses. Animals (Basel) 2021 Mar 25;11(4).
    doi: 10.3390/ani11040931pubmed: 33805967google scholar: lookup
  56. Köhne M, Kuhlmann M, Tönißen A, Martinsson G, Sieme H. Diagnostic and Treatment Practices of Equine Endometritis-A Questionnaire. Front Vet Sci 2020;7:547.
    doi: 10.3389/fvets.2020.00547pubmed: 32984410google scholar: lookup
  57. Bauersachs S, Almiñana C. Embryo-Maternal Interactions Underlying Reproduction in Mammals. Int J Mol Sci 2020 Jul 10;21(14).
    doi: 10.3390/ijms21144872pubmed: 32664189google scholar: lookup