Evaluation of progesterone treatment to create a model for equine endometritis.
Abstract: To investigate a model for equine endometritis, 12 mares with normal reproductive tracts were divided into 2 groups. All mares received progesterone in oil, 250 mg im, daily. At 5 days after initiation of progesterone administration, the uteri were inoculated with 10(6) colony forming units of Pseudomonas aeruginosa. The day of inoculation was designated Day 0. On Day 6, endometrial swab samples yielded P. aeruginosa in 5 mares; samples from the other 7 mares yielded heavy growth of Escherichia coli, Streptococcus zooepidemicus, Klebsiella pneumoniae, Enterobacter spp., Citrobacter diversus, Staphylococcus epidermidis and Streptococcus morbillorum. On Days 6, 7 and 8, Group A mares received intrauterine infusions of 6 g ticarcillin disodium and 0.2 g clavulanate potassium in 100 ml sterile saline. Group B mares received infusions of saline only. The incidence of swab specimens yielding no bacterial growth was significantly higher in Group A than Group B mares on Days 8 and 13 (4/6 vs 0/6). Swab samples from 5 of the 6 mares in Group A yielded growth of fungi on Days 13 and 19. Mares in Group B were then similarly treated with ticarcillin/clavulanate infusions, on Days 19, 20 and 21. The incidence of swab specimens yielding no bacterial growth was 2/6 and 1/6 on Days 21 and 26, respectively; fungi were not recovered from these mares at any time. The incidence of no-growth swabs after antibiotic treatment tended to be higher in Group A and incidence of fungal recovery after antibiotic treatment was significantly higher in Group A.(ABSTRACT TRUNCATED AT 250 WORDS)
Publication Date: 1992-11-01 PubMed ID: 1459059DOI: 10.1111/j.2042-3306.1992.tb02876.xGoogle Scholar: Lookup
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- Journal Article
Summary
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This study proposes a model to understand endometritis in horses based on the action of the hormone progesterone. Researchers used two groups of mares, giving one group supplementary antibiotic treatment alongside a hormone injection and then comparing bacterial growth in the two groups.
Overview of Research Methodology
- The experiment compiled data from 12 mares with healthy reproductive tracts.
- These mares were split into two groups, with all mares receiving a daily dose of progesterone.
- Five days later, a bacterium known as Pseudomonas aeruginosa was introduced into their uteri. The day this was done is referred to as Day 0 in the study.
Observations and Results
- On Day 6, endometrial swab samples from five mares showed the presence of the Pseudomonas aeruginosa bacteria, while swabs from the other seven mares showed the growth of various other bacteria.
- Starting from Day 6, the mares in Group A were given an antibiotic infusion of ticarcillin disodium and clavulanate potassium. The mares in Group B, on the other hand, were only given infusions of saline solution.
- By comparing bacterial growth in the two groups on Days 8 and 13, it was found that a higher number of swabs from Group A mares resulted in no bacterial growth as compared to swabs from Group B mares.
- Furthermore, swabs from five out of the six mares in Group A showed an increase in fungal growth on Days 13 and 19. In response, the mares in Group B were also given the antibiotic infusions on Days 19, 20 and 21.
Conclusion
- In summary, the study found that progesterone treatment combined with antibiotic infusions might inhibit bacterial growth in the uterus but could also potentially induce fungal growth. This suggests that this process could be leveraged as a model to understand equine endometritis better, although the findings need to be complemented by further research.
Cite This Article
APA
Hinrichs K, Spensley MS, McDonough PL.
(1992).
Evaluation of progesterone treatment to create a model for equine endometritis.
Equine Vet J, 24(6), 457-461.
https://doi.org/10.1111/j.2042-3306.1992.tb02876.x Publication
Researcher Affiliations
- Department of Medicine, Tufts University School of Veterinary Medicine, North Grafton, Massachusetts 01536.
MeSH Terms
- Animals
- Clitoris / microbiology
- Disease Models, Animal
- Disease Susceptibility
- Endometritis / immunology
- Endometritis / microbiology
- Endometritis / veterinary
- Female
- Horse Diseases / immunology
- Horse Diseases / microbiology
- Horses
- Progesterone
- Pseudomonas Infections / immunology
- Pseudomonas Infections / microbiology
- Pseudomonas Infections / veterinary
- Pseudomonas aeruginosa / isolation & purification
- Random Allocation
- Ultrasonography
- Uterus / diagnostic imaging
- Uterus / microbiology
- Uterus / pathology
- Vaginal Smears / veterinary
- Vulva / pathology
Citations
This article has been cited 7 times.- Ding X, Cui X, Shi J, Cheng X, Yao D, Gao Y, Zhang Y. Construction of a model of endometritis in domestic rabbits using equine-derived pathogens and evaluation of therapeutic effect of sensitive drugs. Front Vet Sci 2023;10:1064522.
- 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.
- Canisso IF, Segabinazzi LGTM, Fedorka CE. Persistent Breeding-Induced Endometritis in Mares - a Multifaceted Challenge: From Clinical Aspects to Immunopathogenesis and Pathobiology. Int J Mol Sci 2020 Feb 20;21(4).
- Zhu H, Li W, Wang Z, Chen J, Ding M, Han L. TREM-1 deficiency attenuates the inflammatory responses in LPS-induced murine endometritis. Microb Biotechnol 2019 Nov;12(6):1337-1345.
- 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).
- Guidi EE, Thomas A, Cadoré JL, Smith AB. Citrobacter freundii induced endocarditis in a yearling colt. Can Vet J 2016 Jul;57(7):767-70.
- 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.
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