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Journal of clinical microbiology1992; 30(1); 59-62; doi: 10.1128/jcm.30.1.59-62.1992

Rotavirus serotype G3 predominates in horses.

Abstract: Foal fecal group A rotavirus strains were characterized by electropherotype, serotype, and subgroup and shown to be distinctly different from rotaviruses of other mammals. Of 86 strains that were electropherotyped, 98% had similar profiles, with gene segments 3 and 4 close together and segments 7, 8, and 9 widely spaced. Of 70 strains that had sufficient detectable VP7 antigen to be serotyped by enzyme-linked immunosorbent assays (ELISAs), 63% were serotype G3 (39% were subtype G3A and 24% were subtype G3B), 4% were serotype G13, and 33% were untypeable. Serotypes G1, G2, G4, G5, G6, G9, G10, and G14 were not detected, although G5 and G14 strains have been identified among cultivable equine strains. Of 50 strains that had sufficient detectable VP6 antigen to be subgrouped by ELISAs, only 12% were able to be assigned to either subgroup I or II, with the remaining 88% belonging to neither subgroup.
Publication Date: 1992-01-01 PubMed ID: 1310333PubMed Central: PMC264996DOI: 10.1128/jcm.30.1.59-62.1992Google Scholar: Lookup
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  • 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.

The research finds that serotype G3 is most prevalent in equine rotavirus strains commonly found in foal feces. Although other serotypes and subgroups exist, G3, specifically subtypes G3A and G3B, dramatically dominate in horse populations.

Overview of Research Methods

The researchers collected and examined foal fecal rotavirus strains. By using electropherotype, serotype, and subgroup characterization methods, they were able to identify the specific types of rotaviruses found in horses. The report outlines the results from characterizing 86 electropherotyped strains and 70 serotyped strains, which were analyzed for VP7 antigen presence, and 50 strains tested for VP6 antigen to be subgrouped.

  • Electropherotyping: This method differentiates virus strains based on patterns of RNA migration in an electric field.
  • Serotyping and Subgrouping: These techniques identify the serological differences among viral strains. In this case, researchers sought the presence of VP7 and VP6 antigens.

Key Findings from the Research

The studies found that rotavirus strains from horse populations are distinct from those discovered in other mammals.

  • 98% of the electropherotyped strains shared similar profiles, which identifies them as a specific and distinctive rotavirus strain in the horse population.
  • Within the serotyped strains, 63% were identified as serotype G3. More specifically, 39% belonged to subtype G3A and 24% to subtype G3B.
  • Other serotypes such as G1, G2, G4, G5, G6, G9, G10, and G14 were not detected in the samples, although G5 and G14 have previously been found among cultivable equine strains.
  • In subgrouping based on presence of VP6 antigen, only 12% of the strains could be assigned to either subgroup I or II, and 88% did not belong to either of those subgroups.

Implications of the Research

Understanding the dominant rotavirus strains in horses is critical for effective disease management and control. It is fundamental for the development of accurate diagnostic tools and effective vaccines. Moreover, this research also provides insights into the specific characteristics of equine rotaviruses, which could be beneficial in further studies mapping rotavirus evolution and cross-species transmission.

Cite This Article

APA
Browning GF, Chalmers RM, Fitzgerald TA, Corley KT, Campbell I, Snodgrass DR. (1992). Rotavirus serotype G3 predominates in horses. J Clin Microbiol, 30(1), 59-62. https://doi.org/10.1128/jcm.30.1.59-62.1992

Publication

ISSN: 0095-1137
NlmUniqueID: 7505564
Country: United States
Language: English
Volume: 30
Issue: 1
Pages: 59-62

Researcher Affiliations

Browning, G F
  • Mordun Research Institute, Edinburgh, Scotland.
Chalmers, R M
    Fitzgerald, T A
      Corley, K T
        Campbell, I
          Snodgrass, D R

            MeSH Terms

            • Animals
            • Diarrhea / microbiology
            • Diarrhea / veterinary
            • Enzyme-Linked Immunosorbent Assay
            • Feces / microbiology
            • Horse Diseases / microbiology
            • Horses
            • Rotavirus / classification
            • Rotavirus / immunology
            • Rotavirus / isolation & purification
            • Rotavirus Infections / microbiology
            • Rotavirus Infections / veterinary
            • Serotyping

            Grant Funding

            • Wellcome Trust

            References

            This article includes 29 references
            1. Browning GF, Fitzgerald TA, Chalmers RM, Snodgrass DR. A novel group A rotavirus G serotype: serological and genomic characterization of equine isolate FI23.. J Clin Microbiol 1991 Sep;29(9):2043-6.
            2. Fitzgerald TA, Browning GF. Increased sensitivity of a rotavirus serotyping enzyme-linked immunosorbent assay by the incorporation of CaCl2.. J Virol Methods 1991 Aug;33(3):299-304.
              pubmed: 1664432doi: 10.1016/0166-0934(91)90029-ygoogle scholar: lookup
            3. Gerna G, Sarasini A, Arista S, di Matteo A, Giovannelli L, Parea M, Halonen P. Prevalence of human rotavirus serotypes in some European countries 1981-1988.. Scand J Infect Dis 1990;22(1):5-10.
              pubmed: 2157276doi: 10.3109/00365549009023112google scholar: lookup
            4. Padilla-Noriega L, Arias CF, López S, Puerto F, Snodgrass DR, Taniguchi K, Greenberg HB. Diversity of rotavirus serotypes in Mexican infants with gastroenteritis.. J Clin Microbiol 1990 Jun;28(6):1114-9.
            5. Taniguchi K, Urasawa T, Kobayashi N, Gorziglia M, Urasawa S. Nucleotide sequence of VP4 and VP7 genes of human rotaviruses with subgroup I specificity and long RNA pattern: implication for new G serotype specificity.. J Virol 1990 Nov;64(11):5640-4.
            6. Hoshino Y, Gorziglia M, Valdesuso J, Askaa J, Glass RI, Kapikian AZ. An equine rotavirus (FI-14 strain) which bears both subgroup I and subgroup II specificities on its VP6.. Virology 1987 Apr;157(2):488-96.
              pubmed: 2435059doi: 10.1016/0042-6822(87)90291-1google scholar: lookup
            7. Mackow ER, Shaw RD, Matsui SM, Vo PT, Benfield DA, Greenberg HB. Characterization of homotypic and heterotypic VP7 neutralization sites of rhesus rotavirus.. Virology 1988 Aug;165(2):511-7.
              pubmed: 2457279doi: 10.1016/0042-6822(88)90595-8google scholar: lookup
            8. Unicomb LE, Coulson BS, Bishop RF. Experience with an enzyme immunoassay for serotyping human group A rotaviruses.. J Clin Microbiol 1989 Mar;27(3):586-8.
              pubmed: 2541171doi: 10.1128/jcm.27.3.586-588.1989google scholar: lookup
            9. Urasawa S, Urasawa T, Taniguchi K, Wakasugi F, Kobayashi N, Chiba S, Sakurada N, Morita M, Morita O, Tokieda M. Survey of human rotavirus serotypes in different locales in Japan by enzyme-linked immunosorbent assay with monoclonal antibodies.. J Infect Dis 1989 Jul;160(1):44-51.
              pubmed: 2543711doi: 10.1093/infdis/160.1.44google scholar: lookup
            10. Bellinzoni RC, Blackhall JO, Mattion NM, Estes MK, Snodgrass DR, LaTorre JL, Scodeller EA. Serological characterization of bovine rotaviruses isolated from dairy and beef herds in Argentina.. J Clin Microbiol 1989 Nov;27(11):2619-23.
            11. Ruiz AM, López IV, López S, Espejo RT, Arias CF. Molecular and antigenic characterization of porcine rotavirus YM, a possible new rotavirus serotype.. J Virol 1988 Nov;62(11):4331-6.
            12. Matsuno S, Hasegawa A, Mukoyama A, Inouye S. A candidate for a new serotype of human rotavirus.. J Virol 1985 May;54(2):623-4.
              pubmed: 2985825doi: 10.1128/JVI.54.2.623-624.1985google scholar: lookup
            13. Albert MJ, Unicomb LE, Tzipori SR, Bishop RF. Isolation and serotyping of animal rotaviruses and antigenic comparison with human rotaviruses. Brief report.. Arch Virol 1987;93(1-2):123-30.
              pubmed: 3028338doi: 10.1007/BF01313898google scholar: lookup
            14. Greenberg H, McAuliffe V, Valdesuso J, Wyatt R, Flores J, Kalica A, Hoshino Y, Singh N. Serological analysis of the subgroup protein of rotavirus, using monoclonal antibodies.. Infect Immun 1983 Jan;39(1):91-9.
              pubmed: 6185436doi: 10.1128/iai.39.1.91-99.1983google scholar: lookup
            15. 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
            16. 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
            17. 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
            18. Hardy ME, Woode GN, Xu ZC, Williams JD, Conner ME, Dwyer RM, Powell DG. Analysis of serotypes and electropherotypes of equine rotaviruses isolated in the United States.. J Clin Microbiol 1991 May;29(5):889-93.
              pubmed: 1647407doi: 10.1128/jcm.29.5.889-893.1991google scholar: lookup
            19. Browning GF, Chalmers RM, Fitzgerald TA, Snodgrass DR. Serological and genomic characterization of L338, a novel equine group A rotavirus G serotype.. J Gen Virol 1991 May;72 ( Pt 5):1059-64.
              pubmed: 1851806doi: 10.1099/0022-1317-72-5-1059google scholar: lookup
            20. Snodgrass DR, Fitzgerald T, Campbell I, Scott FM, Browning GF, Miller DL, Herring AJ, Greenberg HB. Rotavirus serotypes 6 and 10 predominate in cattle.. J Clin Microbiol 1990 Mar;28(3):504-7.
              pubmed: 2157736doi: 10.1128/jcm.28.3.504-507.1990google scholar: lookup
            21. 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
            22. Clark HF, Hoshino Y, Bell LM, Groff J, Hess G, Bachman P, Offit PA. Rotavirus isolate WI61 representing a presumptive new human serotype.. J Clin Microbiol 1987 Sep;25(9):1757-62.
            23. Hum CP, Dyall-Smith ML, Holmes IH. The VP7 gene of a new G serotype of human rotavirus (B37) is similar to G3 proteins in the antigenic c region.. Virology 1989 May;170(1):55-61.
              pubmed: 2541556doi: 10.1016/0042-6822(89)90351-6google scholar: lookup
            24. Ahmed MU, Taniguchi K, Kobayashi N, Urasawa T, Wakasugi F, Islam M, Shaikh H, Urasawa S. Characterization by enzyme-linked immunosorbent assay using subgroup- and serotype-specific monoclonal antibodies of human rotavirus obtained from diarrheic patients in Bangladesh.. J Clin Microbiol 1989 Jul;27(7):1678-81.
            25. Beards GM, Desselberger U, Flewett TH. Temporal and geographical distributions of human rotavirus serotypes, 1983 to 1988.. J Clin Microbiol 1989 Dec;27(12):2827-33.
            26. Shaw RD, Stoner-Ma DL, Estes MK, Greenberg HB. Specific enzyme-linked immunoassay for rotavirus serotypes 1 and 3.. J Clin Microbiol 1985 Aug;22(2):286-91.
              pubmed: 2993354doi: 10.1128/jcm.22.2.286-291.1985google scholar: lookup
            27. Coulson BS, Unicomb LE, Pitson GA, Bishop RF. Simple and specific enzyme immunoassay using monoclonal antibodies for serotyping human rotaviruses.. J Clin Microbiol 1987 Mar;25(3):509-15.
              pubmed: 3033013doi: 10.1128/jcm.25.3.509-515.1987google scholar: lookup
            28. 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.
            29. 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

            Citations

            This article has been cited 18 times.
            1. Gurgel RQ, Alvarez Ade J, Rodrigues A, Ribeiro RR, Dolabella SS, Da Mota NL, Santos VS, Iturriza-Gomara M, Cunliffe NA, Cuevas LE. Incidence of rotavirus and circulating genotypes in Northeast Brazil during 7 years of national rotavirus vaccination. PLoS One 2014;9(10):e110217.
              doi: 10.1371/journal.pone.0110217pubmed: 25360784google scholar: lookup
            2. 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
            3. 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
            4. 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
            5. Ciarlet M, Hoshino Y, Liprandi F. Single point mutations may affect the serotype reactivity of serotype G11 porcine rotavirus strains: a widening spectrum?. J Virol 1997 Nov;71(11):8213-20.
            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. Ciarlet M, Hidalgo M, Liprandi F. Cross-reactive, serotype- and monotype-specific neutralization epitopes on VP7 of serotype G3 and G5 porcine rotavirus strains. Arch Virol 1996;141(3-4):601-14.
              doi: 10.1007/BF01718320pubmed: 8645098google scholar: lookup
            9. 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
            10. Dwyer RM. Rotaviral diarrhea. Vet Clin North Am Equine Pract 1993 Aug;9(2):311-9.
              doi: 10.1016/s0749-0739(17)30398-xpubmed: 8358646google scholar: lookup
            11. 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.
            12. Takagi M, Taniguchi K, Urasawa T, Urasawa S, Shirahata T, Goto H. Characterization of a G14 equine rotavirus (strain CH3) isolated in Japan. Arch Virol 1994;139(1-2):209-15.
              doi: 10.1007/BF01309466pubmed: 7826211google scholar: lookup
            13. Ciarlet M, Reggeti F, Piña CI, Liprandi F. Equine rotaviruses with G14 serotype specificity circulate among venezuelan horses. J Clin Microbiol 1994 Oct;32(10):2609-12.
            14. Ciarlet M, Ludert JE, Liprandi F. Comparative amino acid sequence analysis of the major outer capsid protein (VP7) of porcine rotaviruses with G3 and G5 serotype specificities isolated in Venezuela and Argentina. Arch Virol 1995;140(3):437-51.
              doi: 10.1007/BF01718422pubmed: 7733818google scholar: lookup
            15. Fitzgerald TA, Munoz M, Wood AR, Snodgrass DR. Serological and genomic characterisation of group A rotaviruses from lambs. Arch Virol 1995;140(9):1541-8.
              doi: 10.1007/BF01322528pubmed: 7487486google scholar: lookup
            16. 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
            17. 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.
            18. Browning GF, Snodgrass DR, Nakagomi O, Kaga E, Sarasini A, Gerna G. Human and bovine serotype G8 rotaviruses may be derived by reassortment. Arch Virol 1992;125(1-4):121-8.
              doi: 10.1007/BF01309632pubmed: 1322648google scholar: lookup