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Pathogens (Basel, Switzerland)2021; 10(6); 707; doi: 10.3390/pathogens10060707

Equid herpesvirus-1 Distribution in Equine Lymphoid and Neural Tissues 70 Days Post Infection.

Abstract: Equid herpesvirus-1 (EHV-1) causes respiratory disease, abortion and myeloencephalopathy in horses worldwide. As member of the , latency is key to EHV-1 epidemiology. EHV-1 latent infection has been detected in the trigeminal ganglion (TG), respiratory associated lymphoid tissue (RALT) and peripheral blood mononuclear cells (PBMC) but additional locations are likely. The aim of this study was to investigate the distribution of viral DNA throughout the equine body. Twenty-five horses divided into three groups were experimentally infected via intranasal instillation with one of three EHV-1 viruses and euthanized on Day 70, post infection. During necropsy, TG, various sympathetic/parasympathetic ganglia of head, neck, thorax and abdomen, spinal cord dorsal root ganglia, RALT, mesenteric lymph nodes, spleen and PBMC of each horse were collected. Genomic viral loads and L-(late) gene transcriptional activity in each tissue and PBMC were measured using qPCR. In addition, immunohistochemistry (IHC) was applied on neural parenchyma tissue sections. EHV-1 DNA was detected in many neural and lymphoid tissue sections, but not in PBMC. L-gene transcriptional activity was not detected in any sample, and translational activity was not apparent on IHC. Tissue tropism differed between the Ab4 wild type and the two mutant viruses.
Publication Date: 2021-06-05 PubMed ID: 34198884PubMed Central: PMC8228440DOI: 10.3390/pathogens10060707Google Scholar: Lookup
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  • Journal Article

Summary

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The research studied the distribution of Equid herpesvirus-1 (EHV-1) in horses’ bodies, specifically in lymphoid and neural tissues, at 70 days after infection. It found the presence of the virus across many different parts of the body but none in peripheral blood mononuclear cells.

Objective

The objective of this research was to investigate the distribution of EHV-1, a herpes virus that can cause several health problems in horses, including respiratory disease, abortion, and myeloencephalopathy. The study aimed to expand the understanding of the virus’s distribution in horses’ bodies, particularly in the lymphoid and neural tissues, approximately 70 days post infection. This is a crucial area of study since EHV-1’s latency in different body parts plays a significant role in its spread and epidemiology.

Methodology

  • Twenty-five horses, divided into three groups, were intranasally infected with the virus and euthanized about two months post infection.
  • Different body parts and tissues from these horses, including ganglia from the head, neck, thorax, and abdomen, dorsal root ganglia of the spinal cord, lymph nodes, spleen, and PBMC, were collected.
  • The collected tissues and PBMC were then analyzed for the presence of viral DNA.
  • Detection methods included qPCR to measure genomic viral loads and L-gene transcriptional activity and immunohistochemistry (IHC) on neural parenchyma tissue sections.

Findings

  • The results of this study reveal the distribution of EHV-1 in horses’ bodies. The virus was found in many neural and lymphoid tissues, but not in peripheral blood mononuclear cells (PBMCs).
  • No transcriptional activity of the L-gene, a late gene of the virus, was detected from any of the samples taken. Immunohistochemistry also found no translational activity.
  • The study found that tissue tropism, or the specific cells and tissues that a virus targets, differed between the wild type EHV-1 and its two mutant strains.

Impact

These findings shed light on the behavior of EHV-1 in horses’ bodies, particularly considering its potential to establish latent infections in different tissues. Understanding this distribution can help inform approaches to diagnose, manage, and treat various health conditions caused by EHV-1 in horses.

Cite This Article

APA
Samoilowa S, Giessler KS, Torres CEM, Hussey GS, Allum A, Fux R, Jerke C, Kiupel M, Matiasek K, Sledge DG, Goehring LS. (2021). Equid herpesvirus-1 Distribution in Equine Lymphoid and Neural Tissues 70 Days Post Infection. Pathogens, 10(6), 707. https://doi.org/10.3390/pathogens10060707

Publication

ISSN: 2076-0817
NlmUniqueID: 101596317
Country: Switzerland
Language: English
Volume: 10
Issue: 6
PII: 707

Researcher Affiliations

Samoilowa, Susanna
  • Equine Hospital, Division of Medicine and Reproduction, Center for Clinical Veterinary Medicine, Ludwig-Maximilians University, 80539 Munich, Germany.
Giessler, Kim S
  • Equine Hospital, Division of Medicine and Reproduction, Center for Clinical Veterinary Medicine, Ludwig-Maximilians University, 80539 Munich, Germany.
  • Department of Pathobiology and Diagnostic Investigation, College of Veterinary Medicine, Michigan State University, East Lansing, MI 48824, USA.
Torres, Carlos E Medina
  • Equine Hospital, Division of Medicine and Reproduction, Center for Clinical Veterinary Medicine, Ludwig-Maximilians University, 80539 Munich, Germany.
Hussey, Gisela Soboll
  • Department of Pathobiology and Diagnostic Investigation, College of Veterinary Medicine, Michigan State University, East Lansing, MI 48824, USA.
Allum, Allison
  • Department of Pathobiology and Diagnostic Investigation, College of Veterinary Medicine, Michigan State University, East Lansing, MI 48824, USA.
Fux, Robert
  • Division of Virology, Institute for Infectious Diseases and Zoonoses, Department of Veterinary Sciences, Ludwig-Maximilians University, 80539 Munich, Germany.
Jerke, Christin
  • Equine Hospital, Division of Medicine and Reproduction, Center for Clinical Veterinary Medicine, Ludwig-Maximilians University, 80539 Munich, Germany.
Kiupel, Matti
  • Department of Pathobiology and Diagnostic Investigation, College of Veterinary Medicine, Michigan State University, East Lansing, MI 48824, USA.
  • Veterinary Diagnostic Laboratory, College of Veterinary Medicine, Michigan State University, Lansing, MI 48824, USA.
Matiasek, Kaspar
  • Section of Clinical and Comparative Neuropathology, Centre for Clinical Veterinary Medicine, Ludwig-Maximilians Universitaet München, 80539 Munich, Germany.
Sledge, Dodd G
  • Veterinary Diagnostic Laboratory, College of Veterinary Medicine, Michigan State University, Lansing, MI 48824, USA.
Goehring, Lutz S
  • Equine Hospital, Division of Medicine and Reproduction, Center for Clinical Veterinary Medicine, Ludwig-Maximilians University, 80539 Munich, Germany.

Grant Funding

  • 2016#306 / Grayson-Jockey Club Research Foundation

Conflict of Interest Statement

The authors declare no conflict of interest.

References

This article includes 44 references
  1. Slater J. Equine Herpesviruses. In: Long M., editor. Equine Infectious Diseases. Elsevier; St. Louis, MO, USA: 2014. pp. 151–168.e158.
  2. Efstathiou S, Preston CM. Towards an understanding of the molecular basis of herpes simplex virus latency.. Virus Res 2005 Aug;111(2):108-19.
  3. Slater JD, Borchers K, Thackray AM, Field HJ. The trigeminal ganglion is a location for equine herpesvirus 1 latency and reactivation in the horse.. J Gen Virol 1994 Aug;75 ( Pt 8):2007-16.
    doi: 10.1099/0022-1317-75-8-2007pubmed: 8046404google scholar: lookup
  4. Pusterla N, Mapes S, David Wilson W. Prevalence of latent alpha-herpesviruses in Thoroughbred racing horses.. Vet J 2012 Aug;193(2):579-82.
    doi: 10.1016/j.tvjl.2012.01.030pubmed: 22405721google scholar: lookup
  5. Chesters PM, Allsop R, Purewal A, Edington N. Detection of latency-associated transcripts of equid herpesvirus 1 in equine leukocytes but not in trigeminal ganglia.. J Virol 1997 May;71(5):3437-43.
  6. Giessler KS, Samoilowa S, Soboll Hussey G, Kiupel M, Matiasek K, Sledge DG, Liesche F, Schlegel J, Fux R, Goehring LS. Viral Load and Cell Tropism During Early Latent Equid Herpesvirus 1 Infection Differ Over Time in Lymphoid and Neural Tissue Samples From Experimentally Infected Horses.. Front Vet Sci 2020;7:621.
    doi: 10.3389/fvets.2020.00621pmc: PMC7499125pubmed: 33102556google scholar: lookup
  7. Gilden DH, Gesser R, Smith J, Wellish M, Laguardia JJ, Cohrs RJ, Mahalingam R. Presence of VZV and HSV-1 DNA in human nodose and celiac ganglia.. Virus Genes 2001;23(2):145-7.
    doi: 10.1023/A:1011883919058pubmed: 11724266google scholar: lookup
  8. Parzefall B, Schmahl W, Fischer A, Blutke A, Truyen U, Matiasek K. Evidence of feline herpesvirus-1 DNA in the vestibular ganglion of domestic cats.. Vet J 2010 Jun;184(3):371-2.
    doi: 10.1016/j.tvjl.2009.03.030pubmed: 19394881google scholar: lookup
  9. Townsend WM, Jacobi S, Tai SH, Kiupel M, Wise AG, Maes RK. Ocular and neural distribution of feline herpesvirus-1 during active and latent experimental infection in cats.. BMC Vet Res 2013 Sep 22;9:185.
    doi: 10.1186/1746-6148-9-185pmc: PMC4016492pubmed: 24053192google scholar: lookup
  10. Winkler MT, Doster A, Jones C. Persistence and reactivation of bovine herpesvirus 1 in the tonsils of latently infected calves.. J Virol 2000 Jun;74(11):5337-46.
  11. Brockmeier SL, Lager KM, Mengeling WL. Comparison of in vivo reactivation, in vitro reactivation, and polymerase chain reaction for detection of latent pseudorabies virus infection in swine.. J Vet Diagn Invest 1993 Oct;5(4):505-9.
    doi: 10.1177/104063879300500401pubmed: 8286446google scholar: lookup
  12. Perez S, Inman M, Doster A, Jones C. Latency-related gene encoded by bovine herpesvirus 1 promotes virus growth and reactivation from latency in tonsils of infected calves.. J Clin Microbiol 2005 Jan;43(1):393-401.
  13. Romero CH, Meade PN, Homer BL, Shultz JE, Lollis G. Potential sites of virus latency associated with indigenous pseudorabies viruses in feral swine.. J Wildl Dis 2003 Jul;39(3):567-75.
    doi: 10.7589/0090-3558-39.3.567pubmed: 14567217google scholar: lookup
  14. Nugent J, Birch-Machin I, Smith KC, Mumford JA, Swann Z, Newton JR, Bowden RJ, Allen GP, Davis-Poynter N. Analysis of equid herpesvirus 1 strain variation reveals a point mutation of the DNA polymerase strongly associated with neuropathogenic versus nonneuropathogenic disease outbreaks.. J Virol 2006 Apr;80(8):4047-60.
  15. Azab W, Osterrieder N. Glycoproteins D of equine herpesvirus type 1 (EHV-1) and EHV-4 determine cellular tropism independently of integrins.. J Virol 2012 Feb;86(4):2031-44.
    doi: 10.1128/JVI.06555-11pmc: PMC3302398pubmed: 22171258google scholar: lookup
  16. Holz CL, Nelli RK, Wilson ME, Zarski LM, Azab W, Baumgardner R, Osterrieder N, Pease A, Zhang L, Hession S, Goehring LS, Hussey SB, Soboll Hussey G. Viral genes and cellular markers associated with neurological complications during herpesvirus infections.. J Gen Virol 2017 Jun;98(6):1439-1454.
    doi: 10.1099/jgv.0.000773pubmed: 28631601google scholar: lookup
  17. Mweene AS, Okazaki K, Kida H. Detection of viral genome in non-neural tissues of cattle experimentally infected with bovine herpesvirus 1.. Jpn J Vet Res 1996 Dec;44(3):165-74.
    pubmed: 8997877
  18. Butcher EC, Picker LJ. Lymphocyte homing and homeostasis.. Science 1996 Apr 5;272(5258):60-6.
    doi: 10.1126/science.272.5258.60pubmed: 8600538google scholar: lookup
  19. Wilsterman S, Soboll-Hussey G, Lunn DP, Ashton LV, Callan RJ, Hussey SB, Rao S, Goehring LS. Equine herpesvirus-1 infected peripheral blood mononuclear cell subpopulations during viremia.. Vet Microbiol 2011 Apr 21;149(1-2):40-7.
    doi: 10.1016/j.vetmic.2010.10.004pubmed: 21093993google scholar: lookup
  20. Gilden DH, Vafai A, Shtram Y, Becker Y, Devlin M, Wellish M. Varicella-zoster virus DNA in human sensory ganglia.. Nature 1983 Dec 1-7;306(5942):478-80.
    doi: 10.1038/306478a0pubmed: 6316159google scholar: lookup
  21. Gilden DH, Rozenman Y, Murray R, Devlin M, Vafai A. Detection of varicella-zoster virus nucleic acid in neurons of normal human thoracic ganglia.. Ann Neurol 1987 Sep;22(3):377-80.
    doi: 10.1002/ana.410220315pubmed: 2823688google scholar: lookup
  22. Furuta Y, Takasu T, Fukuda S, Sato-Matsumura KC, Inuyama Y, Hondo R, Nagashima K. Detection of varicella-zoster virus DNA in human geniculate ganglia by polymerase chain reaction.. J Infect Dis 1992 Nov;166(5):1157-9.
    doi: 10.1093/infdis/166.5.1157pubmed: 1328403google scholar: lookup
  23. Mahalingam R, Wellish MC, Dueland AN, Cohrs RJ, Gilden DH. Localization of herpes simplex virus and varicella zoster virus DNA in human ganglia.. Ann Neurol 1992 Apr;31(4):444-8.
    doi: 10.1002/ana.410310417pubmed: 1316733google scholar: lookup
  24. Kennedy PG, Grinfeld E, Gow JW. Latent varicella-zoster virus is located predominantly in neurons in human trigeminal ganglia.. Proc Natl Acad Sci U S A 1998 Apr 14;95(8):4658-62.
    doi: 10.1073/pnas.95.8.4658pmc: PMC22546pubmed: 9539794google scholar: lookup
  25. Kennedy PG, Grinfeld E, Gow JW. Latent Varicella-zoster virus in human dorsal root ganglia.. Virology 1999 Jun 5;258(2):451-4.
    doi: 10.1006/viro.1999.9745pubmed: 10366583google scholar: lookup
  26. Hyman RW, Ecker JR, Tenser RB. Varicella-zoster virus RNA in human trigeminal ganglia.. Lancet 1983 Oct 8;2(8354):814-6.
    doi: 10.1016/S0140-6736(83)90736-5pubmed: 6137648google scholar: lookup
  27. Grigoryan S, Yee MB, Glick Y, Gerber D, Kepten E, Garini Y, Yang IH, Kinchington PR, Goldstein RS. Direct transfer of viral and cellular proteins from varicella-zoster virus-infected non-neuronal cells to human axons.. PLoS One 2015;10(5):e0126081.
  28. Zerboni L, Arvin AM. The Pathogenesis of Varicella-Zoster Virus Neurotropism and Infection. Springer International Publishing; Cham, Switzerland: 2016. pp. 135–173.
  29. Depledge DP, Sadaoka T, Ouwendijk WJD. Molecular Aspects of Varicella-Zoster Virus Latency.. Viruses 2018 Jun 28;10(7).
    doi: 10.3390/v10070349pmc: PMC6070824pubmed: 29958408google scholar: lookup
  30. Goehring LS, Hussey GS, Ashton LV, Schenkel AR, Lunn DP. Infection of central nervous system endothelial cells by cell-associated EHV-1.. Vet Microbiol 2011 Mar 24;148(2-4):389-95.
    doi: 10.1016/j.vetmic.2010.08.030pubmed: 20884134google scholar: lookup
  31. Smith KC, Borchers K. A study of the pathogenesis of equid herpesvirus-1 (EHV-1) abortion by DNA in-situ hybridization.. J Comp Pathol 2001 Nov;125(4):304-10.
    doi: 10.1053/jcpa.2001.0513pubmed: 11798247google scholar: lookup
  32. Stierstorfer B, Eichhorn W, Schmahl W, Brandmüller C, Kaaden OR, Neubauer A. Equine herpesvirus type 1 (EHV-1) myeloencephalopathy: a case report.. J Vet Med B Infect Dis Vet Public Health 2002 Feb;49(1):37-41.
  33. Pusterla N, Wilson WD, Mapes S, Finno C, Isbell D, Arthur RM, Ferraro GL. Characterization of viral loads, strain and state of equine herpesvirus-1 using real-time PCR in horses following natural exposure at a racetrack in California.. Vet J 2009 Feb;179(2):230-9.
    doi: 10.1016/j.tvjl.2007.09.018pubmed: 18024200google scholar: lookup
  34. Abdelgawad A, Damiani A, Ho SY, Strauss G, Szentiks CA, East ML, Osterrieder N, Greenwood AD. Zebra Alphaherpesviruses (EHV-1 and EHV-9): Genetic Diversity, Latency and Co-Infections.. Viruses 2016 Sep 20;8(9).
    doi: 10.3390/v8090262pmc: PMC5035975pubmed: 27657113google scholar: lookup
  35. Baxi MK, Efstathiou S, Lawrence G, Whalley JM, Slater JD, Field HJ. The detection of latency-associated transcripts of equine herpesvirus 1 in ganglionic neurons.. J Gen Virol 1995 Dec;76 ( Pt 12):3113-8.
    doi: 10.1099/0022-1317-76-12-3113pubmed: 8847517google scholar: lookup
  36. Pusterla N, Mapes S, Wilson WD. Prevalence of equine herpesvirus type 1 in trigeminal ganglia and submandibular lymph nodes of equids examined postmortem.. Vet Rec 2010 Sep 4;167(10):376-8.
    doi: 10.1136/vr.c3748pubmed: 20817899google scholar: lookup
  37. Slater J. Personal Communication. 2017.
  38. Quintana AM, Landolt GA, Annis KM, Hussey GS. Immunological characterization of the equine airway epithelium and of a primary equine airway epithelial cell culture model.. Vet Immunol Immunopathol 2011 Apr 15;140(3-4):226-36.
    doi: 10.1016/j.vetimm.2010.12.008pubmed: 21292331google scholar: lookup
  39. Soboll Hussey G, Ashton LV, Quintana AM, Van de Walle GR, Osterrieder N, Lunn DP. Equine herpesvirus type 1 pUL56 modulates innate responses of airway epithelial cells.. Virology 2014 Sep;464-465:76-86.
    doi: 10.1016/j.virol.2014.05.023pubmed: 25046270google scholar: lookup
  40. Breathnach CC, Yeargan MR, Timoney JF, Allen GP. Detection of equine herpesvirus-specific effector and memory cytotoxic immunity in the equine upper respiratory tract.. Vet Immunol Immunopathol 2006 May 15;111(1-2):117-25.
    doi: 10.1016/j.vetimm.2006.01.014pubmed: 16472871google scholar: lookup
  41. Holz CL, Sledge DG, Kiupel M, Nelli RK, Goehring LS, Soboll Hussey G. Histopathologic Findings Following Experimental Equine Herpesvirus 1 Infection of Horses.. Front Vet Sci 2019;6:59.
    doi: 10.3389/fvets.2019.00059pmc: PMC6409500pubmed: 30886853google scholar: lookup
  42. Pusterla N, Wilson WD, Conrad PA, Barr BC, Ferraro GL, Daft BM, Leutenegger CM. Cytokine gene signatures in neural tissue of horses with equine protozoal myeloencephalitis or equine herpes type 1 myeloencephalopathy.. Vet Rec 2006 Sep 9;159(11):341-6.
    doi: 10.1136/vr.159.11.341pubmed: 16963713google scholar: lookup
  43. Hussey SB, Clark R, Lunn KF, Breathnach C, Soboll G, Whalley JM, Lunn DP. Detection and quantification of equine herpesvirus-1 viremia and nasal shedding by real-time polymerase chain reaction.. J Vet Diagn Invest 2006 Jul;18(4):335-42.
    doi: 10.1177/104063870601800403pubmed: 16921871google scholar: lookup
  44. Allen G, Kydd J, Slater J, Smith K. Equid Herpesvirus-1 (EHV-1) and-4 (EHV-4) Infections. Infectious Diseases of Livestock. 2nd ed. Oxford Press; Cape Town, South Africa: 2004. pp. 829–859.

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