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Archives of virology2017; 162(8); 2329-2335; doi: 10.1007/s00705-017-3376-3

Genetic characterization of equid herpesvirus type 1 from cases of abortion in Poland.

Abstract: Equid herpesvirus type 1 (EHV-1) is a common viral infection associated with varied clinical outcomes including respiratory disease, abortion and neurological disease. We have characterized EHV-1 sequences (n = 38) obtained from cases of equine abortion in Poland between 1999 and 2016, based on sequencing of PCR products from open reading frames (ORF) 30 and 68 of the EHV-1 genome. The majority (81.6%) of sequences were not classified into any of the previously described groups based on the ORF68 sequence. The remaining sequences belonged to ORF68 group III (7.9%) or IV (10.5%). A haplotype network analysis did not show any obvious structure within networks of local Polish sequences, nor within a global network of 215 EHV-1 sequences when these networks were coloured based on the geographical origin of viruses or date of detection. Our data suggest that ORF68 does not provide a reliable molecular marker for epidemiological studies of EHV-1, at least in a global sense. Its usefulness to aid local investigations of individual outbreaks remains to be established. All but two Polish EHV-1 sequences belonged to the ORF30 N genotype. The two ORF30 D viruses were obtained from abortion cases in 2009 and 2010. Hence, abortion cases that occurred in Poland between 1999 and 2016 were caused predominantly by EHV-1 with the ORF30 N genotype, with no indication of an increase in the prevalence of the ORF30 D variant.
Publication Date: 2017-04-27 PubMed ID: 28451902PubMed Central: PMC5506511DOI: 10.1007/s00705-017-3376-3Google Scholar: Lookup
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  • Journal Article

Summary

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The research article focuses on the genetic characterization of Equid herpesvirus type 1 (EHV-1), a common virus causing various clinical illnesses in horses. It analyses EHV-1 sequences obtained from equine abortion cases in Poland from 1999 to 2016, addressing its classification, distribution, and its role in epidemiological studies.

Research Methodology

  • The research was based on the characterization of EHV-1 sequences. These sequences were taken from cases of equine abortions that occurred in Poland between 1999 and 2016.
  • PCR (Polymerase chain reaction) products from open reading frames (ORF) 30 and 68 of the EHV-1 genome were sequenced.
  • A total of 38 EHV-1 sequences were obtained and examined.

Findings of the research

  • The researchers found out that the majority (about 82%) of the sequences did not belong to any of the previously described groups based on the ORF68 part of the genome.
  • The remaining sequences belonged either to ORF68 group III (8%) or to group IV (around 11%).
  • A haplotype network analysis did not reveal any clear structure within the networks of local Polish sequences, nor in a global network of 215 EHV-1 sequences.
  • The characteristics of these networks were not affected significantly by the geographical origin of the viruses or the date of detection.

Implications of the Research

  • The study suggests that ORF68 does not act as a reliable molecular marker in epidemiological studies of EHV-1 on a global scale.
  • The ability of ORF68 to aid local investigations of individual outbreaks is yet to be determined.
  • Most of the Polish EHV-1 sequences belonged to the ORF30 N genotype barring two sequences that belonged to the ORF30 D genotype.
  • The two sequences classified under the ORF30 D genotype were obtained during the years 2009 and 2010.
  • It was observed that the abortion cases that happened in Poland from 1999 to 2016 were predominantly caused by EHV-1 with the ORF30 N genotype.
  • The study did not indicate an increase in prevalence of the ORF30 D variant within that period.

Cite This Article

APA
Stasiak K, Dunowska M, Hills SF, Rola J. (2017). Genetic characterization of equid herpesvirus type 1 from cases of abortion in Poland. Arch Virol, 162(8), 2329-2335. https://doi.org/10.1007/s00705-017-3376-3

Publication

ISSN: 1432-8798
NlmUniqueID: 7506870
Country: Austria
Language: English
Volume: 162
Issue: 8
Pages: 2329-2335

Researcher Affiliations

Stasiak, Karol
  • Department of Virology, National Veterinary Research Institute, Al. Partyzantow 57, 24-100, Pulawy, Poland.
Dunowska, Magdalena
  • Institute of Veterinary, Animal and Biomedical Sciences, Massey University, Palmerston North, New Zealand.
Hills, Simon F
  • Institute of Agriculture and Environment, Massey University, Palmerston North, New Zealand.
Rola, Jerzy
  • Department of Virology, National Veterinary Research Institute, Al. Partyzantow 57, 24-100, Pulawy, Poland. jrola@piwet.pulawy.pl.

MeSH Terms

  • Abortion, Veterinary / epidemiology
  • Abortion, Veterinary / virology
  • Animals
  • Disease Outbreaks / veterinary
  • Female
  • Genotype
  • Herpesviridae Infections / veterinary
  • Herpesviridae Infections / virology
  • Herpesvirus 1, Equid / genetics
  • Horse Diseases / diagnosis
  • Horse Diseases / virology
  • Horses / virology
  • Open Reading Frames
  • Poland / epidemiology
  • Polymerase Chain Reaction / veterinary
  • Pregnancy
  • Sequence Analysis, DNA

Conflict of Interest Statement

The authors declare no conflict of interest.

References

This article includes 31 references
  1. Slater J. Equine herpesviruses. In: Sellon DC, Long MT (ed) Equine infectious diseases. Saunders Elsevier, New York, pp 134–153.
  2. Davison AJ, Eberle R, Ehlers B, Hayward GS, McGeoch DJ, Minson AC, Pellett PE, Roizman B, Studdert MJ, Thiry E. The order Herpesvirales.. Arch Virol 2009;154(1):171-7.
    doi: 10.1007/s00705-008-0278-4pmc: PMC3552636pubmed: 19066710google scholar: lookup
  3. Lunn DP, Davis-Poynter N, Flaminio MJ, Horohov DW, Osterrieder K, Pusterla N, Townsend HG. Equine herpesvirus-1 consensus statement.. J Vet Intern Med 2009 May-Jun;23(3):450-61.
  4. Dunowska M. A review of equid herpesvirus 1 for the veterinary practitioner. Part A: clinical presentation, diagnosis and treatment.. N Z Vet J 2014 Jul;62(4):171-8.
    doi: 10.1080/00480169.2014.899945pubmed: 24597778google scholar: lookup
  5. Kydd JH, Slater J, Osterrieder N, Lunn DP, Antczak DF, Azab W, Balasuriya U, Barnett C, Brosnahan M, Cook C, Damiani A, Elton D, Frampton A, Gilkerson J, Goehring L, Horohov D, Maxwell L, Minke J, Morley P, Nauwynck H, Newton R, Perkins G, Pusterla N, Soboll-Hussey G, Traub-Dargatz J, Townsend H, Van de Walle GR, Wagner B. Third International Havemeyer Workshop on Equine Herpesvirus type 1.. Equine Vet J 2012 Sep;44(5):513-7.
  6. Gardiner DW, Lunn DP, Goehring LS, Chiang YW, Cook C, Osterrieder N, McCue P, Del Piero F, Hussey SB, Hussey GS. Strain impact on equine herpesvirus type 1 (EHV-1) abortion models: viral loads in fetal and placental tissues and foals.. Vaccine 2012 Oct 12;30(46):6564-72.
    doi: 10.1016/j.vaccine.2012.08.046pubmed: 22944628google scholar: lookup
  7. Patel JR, Edington N, Mumford JA. Variation in cellular tropism between isolates of equine herpesvirus-1 in foals.. Arch Virol 1982;74(1):41-51.
    doi: 10.1007/BF01320781pubmed: 6297429google scholar: lookup
  8. Tearle JP, Smith KC, Platt AJ, Hannant D, Davis-Poynter NJ, Mumford JA. In vitro characterisation of high and low virulence isolates of equine herpesvirus-1 and -4.. Res Vet Sci 2003 Aug;75(1):83-6.
    doi: 10.1016/S0034-5288(03)00031-6pubmed: 12801466google scholar: lookup
  9. Wagner B, Wimer C, Freer H, Osterrieder N, Erb HN. Infection of peripheral blood mononuclear cells with neuropathogenic equine herpesvirus type-1 strain Ab4 reveals intact interferon-α induction and induces suppression of anti-inflammatory interleukin-10 responses in comparison to other viral strains.. Vet Immunol Immunopathol 2011 Sep 15;143(1-2):116-24.
    doi: 10.1016/j.vetimm.2011.06.032pubmed: 21764140google scholar: lookup
  10. Goodman LB, Loregian A, Perkins GA, Nugent J, Buckles EL, Mercorelli B, Kydd JH, Palù G, Smith KC, Osterrieder N, Davis-Poynter N. A point mutation in a herpesvirus polymerase determines neuropathogenicity.. PLoS Pathog 2007 Nov;3(11):e160.
  11. Gryspeerdt AC, Vandekerckhove AP, Garré B, Barbé F, Van de Walle GR, Nauwynck HJ. Differences in replication kinetics and cell tropism between neurovirulent and non-neurovirulent EHV1 strains during the acute phase of infection in horses.. Vet Microbiol 2010 May 19;142(3-4):242-53.
    doi: 10.1016/j.vetmic.2009.10.015pubmed: 19926232google scholar: lookup
  12. 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.
  13. Cuxson JL, Hartley CA, Ficorilli NP, Symes SJ, Devlin JM, Gilkerson JR. Comparing the genetic diversity of ORF30 of Australian isolates of 3 equid alphaherpesviruses.. Vet Microbiol 2014 Feb 21;169(1-2):50-7.
    doi: 10.1016/j.vetmic.2013.12.007pubmed: 24418044google scholar: lookup
  14. Pronost S, Cook RF, Fortier G, Timoney PJ, Balasuriya UB. Relationship between equine herpesvirus-1 myeloencephalopathy and viral genotype.. Equine Vet J 2010 Nov;42(8):672-4.
  15. Malik P, Bálint A, Dán A, Pálfi V. Molecular characterisation of the ORF68 region of equine herpesvirus-1 strains isolated from aborted fetuses in Hungary between 1977 and 2008.. Acta Vet Hung 2012 Mar;60(1):175-87.
    doi: 10.1556/AVet.2012.015pubmed: 22366142google scholar: lookup
  16. Stasiak K, Rola J, Ploszay G, Socha W, Zmudzinski JF. Detection of the neuropathogenic variant of equine herpesvirus 1 associated with abortions in mares in Poland.. BMC Vet Res 2015 May 1;11:102.
    doi: 10.1186/s12917-015-0416-7pmc: PMC4416348pubmed: 25929692google scholar: lookup
  17. Stasiak K, Rola J, Zmudzinski JF. Application of real-time PCR for evaluation of distribution of equine herpesvirus type 1 in tissues of aborted fetuses.. Pol J Vet Sci 2015;18(4):833-9.
    pubmed: 26812827doi: 10.1515/pjvs-2015-0108google scholar: lookup
  18. Kirisawa R, Endo A, Iwai H, Kawakami Y. Detection and identification of equine herpesvirus-1 and -4 by polymerase chain reaction.. Vet Microbiol 1993 Jul;36(1-2):57-67.
    doi: 10.1016/0378-1135(93)90128-Tpubmed: 8236780google scholar: lookup
  19. Diallo IS, Hewitson G, Wright L, Rodwell BJ, Corney BG. Detection of equine herpesvirus type 1 using a real-time polymerase chain reaction.. J Virol Methods 2006 Jan;131(1):92-8.
  20. Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S. MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods.. Mol Biol Evol 2011 Oct;28(10):2731-9.
    doi: 10.1093/molbev/msr121pmc: PMC3203626pubmed: 21546353google scholar: lookup
  21. Perkins GA, Goodman LB, Tsujimura K, Van de Walle GR, Kim SG, Dubovi EJ, Osterrieder N. Investigation of the prevalence of neurologic equine herpes virus type 1 (EHV-1) in a 23-year retrospective analysis (1984-2007).. Vet Microbiol 2009 Nov 18;139(3-4):375-8.
    doi: 10.1016/j.vetmic.2009.06.033pubmed: 19615831google scholar: lookup
  22. Smith KL, Allen GP, Branscum AJ, Frank Cook R, Vickers ML, Timoney PJ, Balasuriya UB. The increased prevalence of neuropathogenic strains of EHV-1 in equine abortions.. Vet Microbiol 2010 Feb 24;141(1-2):5-11.
    doi: 10.1016/j.vetmic.2009.07.030pubmed: 19733451google scholar: lookup
  23. Dunowska M, Gopakumar G, Perrott MR, Kendall AT, Waropastrakul S, Hartley CA, Carslake HB. Virological and serological investigation of Equid herpesvirus 1 infection in New Zealand.. Vet Microbiol 2015 Apr 17;176(3-4):219-28.
    doi: 10.1016/j.vetmic.2015.01.016pubmed: 25666453google scholar: lookup
  24. Pusterla N, David Wilson W, Madigan JE, Ferraro GL. Equine herpesvirus-1 myeloencephalopathy: a review of recent developments.. Vet J 2009 Jun;180(3):279-89.
    doi: 10.1016/j.tvjl.2008.08.004pubmed: 18805030google scholar: lookup
  25. Vaz PK, Horsington J, Hartley CA, Browning GF, Ficorilli NP, Studdert MJ, Gilkerson JR, Devlin JM. Evidence of widespread natural recombination among field isolates of equine herpesvirus 4 but not among field isolates of equine herpesvirus 1.. J Gen Virol 2016 Mar;97(3):747-755.
    doi: 10.1099/jgv.0.000378pmc: PMC5381393pubmed: 26691326google scholar: lookup
  26. Gryspeerdt A, Vandekerckhove A, Van Doorsselaere J, Van de Walle G, Nauwynck H. Description of an unusually large outbreak of nervous system disorders caused by equine herpesvirus 1 (EHV1) in 2009 in Belgium. Vlaams Diergeneeskd Tijdschr 2011;80(2):147–153.
  27. Telford EA, Watson MS, McBride K, Davison AJ. The DNA sequence of equine herpesvirus-1.. Virology 1992 Jul;189(1):304-16.
    doi: 10.1016/0042-6822(92)90706-Upubmed: 1318606google scholar: lookup
  28. Garré B, van der Meulen K, Nugent J, Neyts J, Croubels S, De Backer P, Nauwynck H. In vitro susceptibility of six isolates of equine herpesvirus 1 to acyclovir, ganciclovir, cidofovir, adefovir, PMEDAP and foscarnet.. Vet Microbiol 2007 May 16;122(1-2):43-51.
    doi: 10.1016/j.vetmic.2007.01.004pubmed: 17276631google scholar: lookup
  29. Negussie H, Gizaw D, Tessema TS, Nauwynck HJ. Equine Herpesvirus-1 Myeloencephalopathy, an Emerging Threat of Working Equids in Ethiopia.. Transbound Emerg Dis 2017 Apr;64(2):389-397.
    doi: 10.1111/tbed.12377pubmed: 26010868google scholar: lookup
  30. Damiani AM, de Vries M, Reimers G, Winkler S, Osterrieder N. A severe equine herpesvirus type 1 (EHV-1) abortion outbreak caused by a neuropathogenic strain at a breeding farm in northern Germany.. Vet Microbiol 2014 Aug 27;172(3-4):555-62.
    doi: 10.1016/j.vetmic.2014.06.023pubmed: 25042527google scholar: lookup
  31. Anagha G, Gulati BR, Riyesh T, Virmani N. Genetic characterization of equine herpesvirus 1 isolates from abortion outbreaks in India.. Arch Virol 2017 Jan;162(1):157-163.
    doi: 10.1007/s00705-016-3097-zpubmed: 27699511google scholar: lookup

Citations

This article has been cited 9 times.
  1. Chau VQ, Kolb AW, Miller DL, Yannuzzi NA, Brandt CR. Phylogenetic and Genomic Characterization of Whole Genome Sequences of Ocular Herpes Simplex Virus Type 1 Isolates Identifies Possible Virulence Determinants in Humans. Invest Ophthalmol Vis Sci 2023 Jul 3;64(10):16.
    doi: 10.1167/iovs.64.10.16pubmed: 37450309google scholar: lookup
  2. Chodkowski M, Słońska A, Gregorczyk-Zboroch K, Nowak-Zyczynska Z, Golke A, Krzyżowska M, Bańbura MW, Cymerys J. Equid Alphaherpesvirus 1 (EHV-1) Influences Morphology and Function of Neuronal Mitochondria In Vitro. Pathogens 2022 Aug 3;11(8).
    doi: 10.3390/pathogens11080876pubmed: 36014997google scholar: lookup
  3. Kang HW, Lee EY, Lee KK, Ko MK, Park JY, Kim YH, Lee K, Choi EJ, Kim J, So B, Park CK, Jeoung HY. Evaluation of the Variability of the ORF34, ORF68, and MLST Genes in EHV-1 from South Korea. Pathogens 2021 Apr 2;10(4).
    doi: 10.3390/pathogens10040425pubmed: 33918404google scholar: lookup
  4. Stasiak K, Dunowska M, Rola J. Outbreak of equid herpesvirus 1 abortions at the Arabian stud in Poland. BMC Vet Res 2020 Oct 6;16(1):374.
    doi: 10.1186/s12917-020-02586-ypubmed: 33023592google scholar: lookup
  5. Preziuso S, Sgorbini M, Marmorini P, Cuteri V. Equid alphaherpesvirus 1 from Italian Horses: Evaluation of the Variability of the ORF30, ORF33, ORF34 and ORF68 Genes. Viruses 2019 Sep 13;11(9).
    doi: 10.3390/v11090851pubmed: 31540321google scholar: lookup
  6. Garvey M, Lyons R, Hector RD, Walsh C, Arkins S, Cullinane A. Molecular Characterisation of Equine Herpesvirus 1 Isolates from Cases of Abortion, Respiratory and Neurological Disease in Ireland between 1990 and 2017. Pathogens 2019 Jan 15;8(1).
    doi: 10.3390/pathogens8010007pubmed: 30650561google scholar: lookup
  7. Matczuk AK, Skarbek M, Jackulak NA, Bażanów BA. Molecular characterisation of equid alphaherpesvirus 1 strains isolated from aborted fetuses in Poland. Virol J 2018 Dec 3;15(1):186.
    doi: 10.1186/s12985-018-1093-5pubmed: 30509297google scholar: lookup
  8. Stasiak K, Dunowska M, Rola J. Prevalence and sequence analysis of equid herpesviruses from the respiratory tract of Polish horses. Virol J 2018 Jul 11;15(1):106.
    doi: 10.1186/s12985-018-1018-3pubmed: 29996858google scholar: lookup
  9. El Brini Z, Cullinane A, Garvey M, Fassi Fihri O, Fellahi S, Amraoui F, Loutfi C, Sebbar G, Paillot R, Piro M. First Molecular and Phylogenetic Characterization of Equine Herpesvirus-1 (EHV-1) and Equine Herpesvirus-4 (EHV-4) in Morocco. Animals (Basel) 2025 Jan 5;15(1).
    doi: 10.3390/ani15010102pubmed: 39795045google scholar: lookup