Analyze Diet
Journal of clinical microbiology1991; 29(5); 889-893; doi: 10.1128/jcm.29.5.889-893.1991

Analysis of serotypes and electropherotypes of equine rotaviruses isolated in the United States.

Abstract: Equine group A rotaviruses isolated over a 10-year period in New York State, New Jersey, Kentucky, and Texas were compared serotypically and electropherotypically. All isolates were determined to be serotype 3 by reaction with hyperimmune antiserum to the serotype 3 H-2 strain of equine rotavirus. All displayed RNA electrophoretic migration patterns related to that of the H-2 strain but distinct from that of serotype 5 strain H-1. A serologic survey of 184 mares in Kentucky, which was done to determine the incidence of H-1 and H-2 infections, showed geometric mean serum neutralizing titers to the H-2 strain of equine rotavirus to be significantly higher than those to the H-1 strain. These data suggest that the serotype 3 H-2 strain is the dominant equine rotavirus in Kentucky and perhaps elsewhere in the United States. We were unable to produce confirmational evidence that the H-1 strain occurs as a natural infection in the United States.
Publication Date: 1991-05-01 PubMed ID: 1647407PubMed Central: PMC269902DOI: 10.1128/jcm.29.5.889-893.1991Google 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
  • Research Support
  • Non-U.S. Gov't

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 research article discusses an analysis carried out on samples of equine rotaviruses collected in the US over a span of 10 years. The main finding of the study is that the serotype 3 H-2 strain is likely the dominant strain of equine rotavirus in the United States.

Analysis of Equine Rotaviruses

  • The study focuses on equine group A rotaviruses, which were isolated over a decade from various states in the United States – New York, New Jersey, Kentucky, and Texas.
  • The rotaviruses were studied and compared using their serotypes – classification based on their reaction to hyperimmune antiserum, and electropherotypes – classification based on their RNA migration patterns.

Dominance of Serotype 3

  • Findings from the study concluded all isolates to be serotype 3, struck by the reaction to the hyperimmune antiserum to the serotype 3 H-2 strain of equine rotavirus.
  • The RNA electrophoretic migration patterns of these isolates displayed resemblance to that of the H-2 strain but deviated significantly from the serotype 5 strain H-1.
  • Serotype 3’s dominance is reinforced by an associated serologic survey conducted amongst 184 mares in Kentucky. This survey aimed to gauge the incidence of H-1 and H-2 infections by comparing geometric mean serum neutralizing titers between both strains.
  • The results indicated higher titers for the H-2 strain in comparison to the H-1 strain, making its occurrence more prevalent and suggesting it to be the dominant strain in the Kentucky region and potentially other regions in the United States.

Lack of Evidence for H-1 Strain

  • The research was not able to provide strong evidence for the presence or the natural infection of the H-1 strain in the United States.
  • While the study did not entirely rule out the strain’s existence, the lack of confirmational evidence limits the study’s conclusions regarding the prevalence of this serotype.

Cite This Article

APA
Hardy ME, Woode GN, Xu ZC, Williams JD, Conner ME, Dwyer RM, Powell DG. (1991). Analysis of serotypes and electropherotypes of equine rotaviruses isolated in the United States. J Clin Microbiol, 29(5), 889-893. https://doi.org/10.1128/jcm.29.5.889-893.1991

Publication

ISSN: 0095-1137
NlmUniqueID: 7505564
Country: United States
Language: English
Volume: 29
Issue: 5
Pages: 889-893

Researcher Affiliations

Hardy, M E
  • Department of Veterinary Pathobiology, College of Veterinary Medicine, Texas A&M University, College Station 77843-4467.
Woode, G N
    Xu, Z C
      Williams, J D
        Conner, M E
          Dwyer, R M
            Powell, D G

              MeSH Terms

              • Animals
              • Electrophoresis, Polyacrylamide Gel
              • Female
              • Horse Diseases / microbiology
              • Horses / microbiology
              • Pregnancy
              • RNA, Viral / genetics
              • RNA, Viral / isolation & purification
              • Rotavirus / classification
              • Rotavirus / genetics
              • Rotavirus / isolation & purification
              • Rotavirus Infections / microbiology
              • Rotavirus Infections / veterinary
              • Serotyping
              • United States

              References

              This article includes 18 references
              1. Shaw RD, Vo PT, Offit PA, Coulson BS, Greenberg HB. Antigenic mapping of the surface proteins of rhesus rotavirus.. Virology 1986 Dec;155(2):434-51.
                pubmed: 2431540doi: 10.1016/0042-6822(86)90205-9google scholar: lookup
              2. Zheng SL, Woode GN, Melendy DR, Ramig RF. Comparative studies of the antigenic polypeptide species VP4, VP6, and VP7 of three strains of bovine rotavirus.. J Clin Microbiol 1989 Sep;27(9):1939-45.
              3. Hoshino Y, Wyatt RG, Greenberg HB, Flores J, Kapikian AZ. Serotypic similarity and diversity of rotaviruses of mammalian and avian origin as studied by plaque-reduction neutralization.. J Infect Dis 1984 May;149(5):694-702.
                pubmed: 6202807doi: 10.1093/infdis/149.5.694google scholar: lookup
              4. Hoshino Y, Wyatt RG, Greenberg HB, Kalica AR, Flores J, Kapikian AZ. Isolation, propagation, and characterization of a second equine rotavirus serotype.. Infect Immun 1983 Sep;41(3):1031-7.
              5. Greenberg HB, Valdesuso J, van Wyke K, Midthun K, Walsh M, McAuliffe V, Wyatt RG, Kalica AR, Flores J, Hoshino Y. Production and preliminary characterization of monoclonal antibodies directed at two surface proteins of rhesus rotavirus.. J Virol 1983 Aug;47(2):267-75.
                pubmed: 6312065doi: 10.1128/JVI.47.2.267-275.1983google scholar: lookup
              6. Woode GN, Kelso NE, Simpson TF, Gaul SK, Evans LE, Babiuk L. Antigenic relationships among some bovine rotaviruses: serum neutralization and cross-protection in gnotobiotic calves.. J Clin Microbiol 1983 Aug;18(2):358-64.
                pubmed: 6311873doi: 10.1128/jcm.18.2.358-364.1983google scholar: lookup
              7. Hoshino Y, Wyatt RG, Greenberg HB, Kalica AR, Flores J, Kapikian AZ. Isolation and characterization of an equine rotavirus.. J Clin Microbiol 1983 Sep;18(3):585-91.
                pubmed: 6313746doi: 10.1128/jcm.18.3.585-591.1983google scholar: lookup
              8. Gillespie J, Kalica A, Conner M, Schiff E, Barr M, Holmes D, Frey M. The isolation, propagation and characterization of tissue-cultured equine rotaviruses.. Vet Microbiol 1984 Feb;9(1):1-14.
                pubmed: 6326375doi: 10.1016/0378-1135(84)90074-9google scholar: lookup
              9. Theil KW, McCloskey CM, Saif LJ, Redman DR, Bohl EH, Hancock DD, Kohler EM, Moorhead PD. Rapid, simple method of preparing rotaviral double-stranded ribonucleic acid for analysis by polyacrylamide gel electrophoresis.. J Clin Microbiol 1981 Sep;14(3):273-80.
                pubmed: 6270190doi: 10.1128/jcm.14.3.273-280.1981google scholar: lookup
              10. Conner ME, Darlington RW. Rotavirus infection in foals.. Am J Vet Res 1980 Oct;41(10):1699-703.
                pubmed: 6261616
              11. Gaul SK, Simpson TF, Woode GN, Fulton RW. Antigenic relationships among some animal rotaviruses: virus neutralization in vitro and cross-protection in piglets.. J Clin Microbiol 1982 Sep;16(3):495-503.
                pubmed: 6290530doi: 10.1128/jcm.16.3.495-503.1982google scholar: lookup
              12. Beards GM. Polymorphism of genomic RNAs within rotavirus serotypes and subgroups.. Arch Virol 1982;74(1):65-70.
                pubmed: 6297431doi: 10.1007/BF01320783google scholar: lookup
              13. Durham PJ, Stevenson BJ, Farquharson BC. Rotavirus and coronavirus associated diarrhoea in domestic animals.. N Z Vet J 1979 Mar;27(3):30-2.
                pubmed: 221870doi: 10.1080/00480169.1979.34595google scholar: lookup
              14. Tzipori S, Walker M. Isolation of rotavirus from foals with diarrhoea.. Aust J Exp Biol Med Sci 1978 Aug;56(4):453-7.
                pubmed: 215112doi: 10.1038/icb.1978.51google scholar: lookup
              15. Woode GN, Bridger JC, Jones JM, Flewett TH, Davies HA, Davis HA, White GB. Morphological and antigenic relationships between viruses (rotaviruses) from acute gastroenteritis of children, calves, piglets, mice, and foals.. Infect Immun 1976 Sep;14(3):804-10.
                pubmed: 965097doi: 10.1128/iai.14.3.804-810.1976google scholar: lookup
              16. Offit PA, Clark HF, Blavat G, Greenberg HB. Reassortant rotaviruses containing structural proteins vp3 and vp7 from different parents induce antibodies protective against each parental serotype.. J Virol 1986 Nov;60(2):491-6.
                pubmed: 3021983doi: 10.1128/JVI.60.2.491-496.1986google scholar: lookup
              17. Woode GN, Zheng SL, Rosen BI, Knight N, Gourley NE, Ramig RF. Protection between different serotypes of bovine rotavirus in gnotobiotic calves: specificity of serum antibody and coproantibody responses.. J Clin Microbiol 1987 Jun;25(6):1052-8.
              18. Estes MK, Graham DY, Dimitrov DH. The molecular epidemiology of rotavirus gastroenteritis.. Prog Med Virol 1984;29:1-22.
                pubmed: 6199812

              Citations

              This article has been cited 15 times.
              1. Carossino M, Balasuriya UBR, Thieulent CJ, Barrandeguy ME, Vissani MA, Parreño V. Quadruplex Real-Time TaqMan(®) RT-qPCR Assay for Differentiation of Equine Group A and B Rotaviruses and Identification of Group A G3 and G14 Genotypes. Viruses 2023 Jul 26;15(8).
                doi: 10.3390/v15081626pubmed: 37631969google scholar: lookup
              2. Carossino M, Barrandeguy ME, Erol E, Li Y, Balasuriya UBR. Development and evaluation of a one-step multiplex real-time TaqMan(®) RT-qPCR assay for the detection and genotyping of equine G3 and G14 rotaviruses in fecal samples. Virol J 2019 Apr 25;16(1):49.
                doi: 10.1186/s12985-019-1149-1pubmed: 31023319google scholar: lookup
              3. Bailey KE, Gilkerson JR, Browning GF. Equine rotaviruses--current understanding and continuing challenges. Vet Microbiol 2013 Nov 29;167(1-2):135-44.
                doi: 10.1016/j.vetmic.2013.07.010pubmed: 23932076google scholar: lookup
              4. Gulati BR, Deepa R, Singh BK, Rao CD. Diversity in Indian equine rotaviruses: identification of genotype G10,P6[1] and G1 strains and a new VP7 genotype (G16) strain in specimens from diarrheic foals in India. J Clin Microbiol 2007 Mar;45(3):972-8.
                doi: 10.1128/JCM.01696-06pubmed: 17135436google scholar: lookup
              5. Ciarlet M, I a P, Conner ME, Liprandi F. Antigenic and molecular analyses reveal that the equine rotavirus strain H-1 is closely related to porcine, but not equine, rotaviruses: interspecies transmission from pigs to horses?. Virus Genes 2001 Jan;22(1):5-20.
                doi: 10.1023/a:1008175716816pubmed: 11210939google scholar: lookup
              6. Isa P, Wood AR, Netherwood T, Ciarlet M, Imagawa H, Snodgrass DR. Survey of equine rotaviruses shows conservation of one P genotype in background of two G genotypes. Arch Virol 1996;141(9):1601-12.
                doi: 10.1007/BF01718285pubmed: 8893784google scholar: lookup
              7. Browning GF, Begg AP. Prevalence of G and P serotypes among equine rotaviruses in the faeces of diarrhoeic foals. Arch Virol 1996;141(6):1077-89.
                doi: 10.1007/BF01718611pubmed: 8712925google scholar: lookup
              8. Imagawa H, Tanaka T, Sekiguchi K, Fukunaga Y, Anzai T, Minamoto N, Kamada M. Electropherotypes, serotypes, and subgroups of equine rotaviruses isolated in Japan. Arch Virol 1993;131(1-2):169-76.
                doi: 10.1007/BF01379088pubmed: 8392320google scholar: lookup
              9. Imagawa H, Ishida S, Uesugi S, Masanobu K, Fukunaga Y, Nakagomi O. Genetic analysis of equine rotavirus by RNA-RNA hybridization. J Clin Microbiol 1994 Aug;32(8):2009-12.
              10. Dwyer RM. Progress in identifying the aetiologies of infectious foal diarrhoea. Equine Vet J 1991 Nov;23(6):397-8.
              11. Browning GF, Chalmers RM, Fitzgerald TA, Snodgrass DR. Evidence for two serotype G3 subtypes among equine rotaviruses. J Clin Microbiol 1992 Feb;30(2):485-91.
                doi: 10.1128/jcm.30.2.485-491.1992pubmed: 1371520google scholar: lookup
              12. Rosen BI, Parwani AV, Gorziglia M, Larralde G, Saif LJ. Characterization of full-length and polymerase chain reaction-derived partial-length Gottfried and OSU gene 4 probes for serotypic differentiation of porcine rotaviruses. J Clin Microbiol 1992 Oct;30(10):2644-52.
              13. Browning GF, Chalmers RM, Fitzgerald TA, Corley KT, Campbell I, Snodgrass DR. Rotavirus serotype G3 predominates in horses. J Clin Microbiol 1992 Jan;30(1):59-62.
                doi: 10.1128/jcm.30.1.59-62.1992pubmed: 1310333google scholar: lookup
              14. Ghonaim AH, Rouby SR, Nageeb WM, Elgendy AA, Xu R, Jiang C, Ghonaim NH, He Q, Li W. Insights into recent advancements in human and animal rotavirus vaccines: Exploring new frontiers. Virol Sin 2025 Feb;40(1):1-14.
                doi: 10.1016/j.virs.2024.12.001pubmed: 39672271google scholar: lookup
              15. Carossino M, Vissani MA, Barrandeguy ME, Balasuriya UBR, Parreño V. Equine Rotavirus A under the One Health Lens: Potential Impacts on Public Health. Viruses 2024 Jan 16;16(1).
                doi: 10.3390/v16010130pubmed: 38257830google scholar: lookup