Analyze Diet
Journal of clinical microbiology1994; 32(10); 2609-2612; doi: 10.1128/jcm.32.10.2609-2612.1994

Equine rotaviruses with G14 serotype specificity circulate among venezuelan horses.

Abstract: Two group A rotavirus strains isolated from diarrheic foals in Venezuela were classified as belonging to G14 serotype by cross-neutralization tests and on the basis of the homology of the sequenced VP7 gene. This report confirms that rotavirus strains of G14 serotype specificity circulate among equine populations.
Publication Date: 1994-10-01 PubMed ID: 7814511PubMed Central: PMC264117DOI: 10.1128/jcm.32.10.2609-2612.1994Google 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

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 article presents findings which confirm the presence of G14 serotype rotaviruses among horse populations in Venezuela, isolated from foals suffering from diarrhea.

Study Background

  • The research focuses on the investigation of rotavirus strains found in horse populations in Venezuela.
  • Rotaviruses are a type of virus that cause gastrointestinal illnesses, commonly diarrhea, which can be severe and life-threatening in young animals and humans.
  • These viruses are classified into different groups and subgroups, and one such classification is based on their “G” (glycoprotein) and “P” (protease-sensitive) types. The classification in this study was specifically on the “G” or glycoprotein type.
  • The G14 serotype of rotavirus has not been widely studied or identified as a common strain among equine populations.

Methodology

  • The researchers isolated rotavirus strains from foals (young horses) with diarrhea in Venezuela. Two Group A rotavirus strains were singled out for further study.
  • The classification of these strains as belonging to the G14 serotype was achieved through cross-neutralization tests – a method used to ascertain the identity of a virus by observing its reaction to antibodies that interact with specific viral types.
  • Furthermore, they also sequenced the VP7 gene of the isolated viruses and found homology (similarity) with the known sequence of the G14 serotype rotavirus. The VP7 gene codes for a glycoprotein which determines the “G” type of the rotavirus.

Findings and Significance

  • The research confirms that the G14 serotype rotavirus circulates among the horse populations in Venezuela.
  • This has significant implications as it expands the known diversity of rotaviruses affecting equines and may have potential impacts on diagnostic methods, treatments, and prevention strategies.
  • The discovery of G14 serotype in horses may also warrant further investigation to determine its prevalence in other equine populations around the world and to explore if the strain has possibilities of zoonotic transmission (transmission from animals to humans).

Cite This Article

APA
Ciarlet M, Reggeti F, Piña CI, Liprandi F. (1994). Equine rotaviruses with G14 serotype specificity circulate among venezuelan horses. J Clin Microbiol, 32(10), 2609-2612. https://doi.org/10.1128/jcm.32.10.2609-2612.1994

Publication

ISSN: 0095-1137
NlmUniqueID: 7505564
Country: United States
Language: English
Volume: 32
Issue: 10
Pages: 2609-2612

Researcher Affiliations

Ciarlet, M
  • Centro de Microbiología y Biología Celular, Instituto Venezolano de Investigaciones Cientificas, Caracas.
Reggeti, F
    Piña, C I
      Liprandi, F

        MeSH Terms

        • Amino Acid Sequence
        • Animals
        • Antigens, Viral
        • Capsid / genetics
        • Capsid Proteins
        • Diarrhea / veterinary
        • Diarrhea / virology
        • Horse Diseases / virology
        • Horses / virology
        • Molecular Sequence Data
        • Neutralization Tests
        • Rotavirus / classification
        • Rotavirus / immunology
        • Rotavirus / isolation & purification
        • Serotyping

        References

        This article includes 23 references
        1. Caust J, Dyall-Smith ML, Lazdins I, Holmes IH. Glycosylation, an important modifier of rotavirus antigenicity.. Arch Virol 1987;96(3-4):123-34.
          pubmed: 2444193doi: 10.1007/BF01320955google scholar: lookup
        2. Gorziglia M, Hoshino Y, Buckler-White A, Blumentals I, Glass R, Flores J, Kapikian AZ, Chanock RM. Conservation of amino acid sequence of VP8 and cleavage region of 84-kDa outer capsid protein among rotaviruses recovered from asymptomatic neonatal infection.. Proc Natl Acad Sci U S A 1986 Sep;83(18):7039-43.
          pubmed: 3018754doi: 10.1073/pnas.83.18.7039google scholar: lookup
        3. Nishikawa K, Hoshino Y, Taniguchi K, Green KY, Greenberg HB, Kapikian AZ, Chanock RM, Gorziglia M. Rotavirus VP7 neutralization epitopes of serotype 3 strains.. Virology 1989 Aug;171(2):503-15.
          pubmed: 2474892doi: 10.1016/0042-6822(89)90620-xgoogle scholar: lookup
        4. Kang SY, Saif LJ, Miller KL. Reactivity of VP4-specific monoclonal antibodies to a serotype 4 porcine rotavirus with distinct serotypes of human (symptomatic and asymptomatic) and animal rotaviruses.. J Clin Microbiol 1989 Dec;27(12):2744-50.
        5. Estes MK, Cohen J. Rotavirus gene structure and function.. Microbiol Rev 1989 Dec;53(4):410-49.
          pubmed: 2556635doi: 10.1128/mr.53.4.410-449.1989google scholar: lookup
        6. 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.
        7. 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
        8. 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.
        9. 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.
          pubmed: 1310333doi: 10.1128/jcm.30.1.59-62.1992google scholar: lookup
        10. 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.
          pubmed: 1371520doi: 10.1128/jcm.30.2.485-491.1992google scholar: lookup
        11. Kirkwood C, Masendycz PJ, Coulson BS. Characteristics and location of cross-reactive and serotype-specific neutralization sites on VP7 of human G type 9 rotaviruses.. Virology 1993 Sep;196(1):79-88.
          pubmed: 8395127doi: 10.1006/viro.1993.1456google scholar: lookup
        12. Hoshino Y, Nishikawa K, Benfield DA, Gorziglia M. Mapping of antigenic sites involved in serotype-cross-reactive neutralization on group A rotavirus outercapsid glycoprotein VP7.. Virology 1994 Feb 15;199(1):233-7.
          pubmed: 8116249doi: 10.1006/viro.1994.1117google scholar: lookup
        13. Ciarlet M, Liprandi F. Serological and genomic characterization of two porcine rotaviruses with serotype G1 specificity.. J Clin Microbiol 1994 Jan;32(1):269-72.
          pubmed: 8126197doi: 10.1128/jcm.32.1.269-272.1994google 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. 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
        16. Conner ME, Darlington RW. Rotavirus infection in foals.. Am J Vet Res 1980 Oct;41(10):1699-703.
          pubmed: 6261616
        17. 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
        18. 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.
        19. 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
        20. 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
        21. Glass RI, Keith J, Nakagomi O, Nakagomi T, Askaa J, Kapikian AZ, Chanock RM, Flores J. Nucleotide sequence of the structural glycoprotein VP7 gene of Nebraska calf diarrhea virus rotavirus: comparison with homologous genes from four strains of human and animal rotaviruses.. Virology 1985 Mar;141(2):292-8.
          pubmed: 2417410doi: 10.1016/0042-6822(85)90260-0google scholar: lookup
        22. Dyall-Smith ML, Lazdins I, Tregear GW, Holmes IH. Location of the major antigenic sites involved in rotavirus serotype-specific neutralization.. Proc Natl Acad Sci U S A 1986 May;83(10):3465-8.
          pubmed: 2422651doi: 10.1073/pnas.83.10.3465google scholar: lookup
        23. Green KY, Midthun K, Gorziglia M, Hoshino Y, Kapikian AZ, Chanock RM, Flores J. Comparison of the amino acid sequences of the major neutralization protein of four human rotavirus serotypes.. Virology 1987 Nov;161(1):153-9.
          pubmed: 2823458doi: 10.1016/0042-6822(87)90181-4google scholar: lookup

        Citations

        This article has been cited 18 times.
        1. Mao T, Wang M, Wang J, Ma Y, Liu X, Wang M, Sun X, Li L, Li H, Zhang Q, Li D, Duan Z. Phylogenetic analysis of the viral proteins VP4/VP7 of circulating human rotavirus strains in China from 2016 to 2019 and comparison of their antigenic epitopes with those of vaccine strains. Front Cell Infect Microbiol 2022;12:927490.
          doi: 10.3389/fcimb.2022.927490pubmed: 36004332google scholar: lookup
        2. Geletu US, Usmael MA, Bari FD. Rotavirus in Calves and Its Zoonotic Importance. Vet Med Int 2021;2021:6639701.
          doi: 10.1155/2021/6639701pubmed: 33968359google scholar: lookup
        3. Malakalinga JJ, Misinzo G, Msalya GM, Kazwala RR. Rotavirus Burden, Genetic Diversity and Impact of Vaccine in Children under Five in Tanzania. Pathogens 2019 Oct 29;8(4).
          doi: 10.3390/pathogens8040210pubmed: 31671824google scholar: lookup
        4. Umair M, Abbasi BH, Sharif S, Alam MM, Rana MS, Mujtaba G, Arshad Y, Fatmi MQ, Zaidi SZ. High prevalence of G3 rotavirus in hospitalized children in Rawalpindi, Pakistan during 2014. PLoS One 2018;13(4):e0195947.
          doi: 10.1371/journal.pone.0195947pubmed: 29708975google scholar: lookup
        5. 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
        6. Zeller M, Patton JT, Heylen E, De Coster S, Ciarlet M, Van Ranst M, Matthijnssens J. Genetic analyses reveal differences in the VP7 and VP4 antigenic epitopes between human rotaviruses circulating in Belgium and rotaviruses in Rotarix and RotaTeq. J Clin Microbiol 2012 Mar;50(3):966-76.
          doi: 10.1128/JCM.05590-11pubmed: 22189107google scholar: lookup
        7. Ciarlet M, Hoffmann C, Lorusso E, Baselga R, Cafiero MA, Bányai K, Matthijnssens J, Parreño V, de Grazia S, Buonavoglia C, Martella V. Genomic characterization of a novel group A lamb rotavirus isolated in Zaragoza, Spain. Virus Genes 2008 Oct;37(2):250-65.
          doi: 10.1007/s11262-008-0257-6pubmed: 18661221google scholar: lookup
        8. Matthijnssens J, Ciarlet M, Heiman E, Arijs I, Delbeke T, McDonald SM, Palombo EA, Iturriza-Gómara M, Maes P, Patton JT, Rahman M, Van Ranst M. Full genome-based classification of rotaviruses reveals a common origin between human Wa-Like and porcine rotavirus strains and human DS-1-like and bovine rotavirus strains. J Virol 2008 Apr;82(7):3204-19.
          doi: 10.1128/JVI.02257-07pubmed: 18216098google scholar: lookup
        9. 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
        10. 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
        11. 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.
        12. 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
        13. 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
        14. Vizzi E, Rosales RE, Piñeros O, Fernández R, Inaty D, López K, Peña L, De Freitas-Linares A, Navarro D, Neri S, Durán O, Liprandi F. Emergence of Equine-like G3P[8] Rotavirus Strains Infecting Children in Venezuela. Viruses 2025 Mar 13;17(3).
          doi: 10.3390/v17030410pubmed: 40143336google scholar: lookup
        15. Hosseini-Fakhr SS, Jalilvand S, Maleki A, Kachooei A, Behnezhad F, Mir-Hosseinian M, Taghvaei S, Marashi SM, Shoja Z. Genetic characterization of rotavirus A strains circulating in children under 5 years of age with acute gastroenteritis in Tehran, Iran, in 2023-2024: dissemination of the emerging equine-like G3P[8]-I2-E2 DS-1-like strains. J Gen Virol 2025 Mar;106(3).
          doi: 10.1099/jgv.0.002088pubmed: 40100090google scholar: lookup
        16. Díaz Alarcón RG, Salvatierra K, Gómez Quintero E, Liotta DJ, Parreño V, Miño SO. Complete Genome Classification System of Rotavirus alphagastroenteritidis: An Updated Analysis. Viruses 2025 Jan 31;17(2).
          doi: 10.3390/v17020211pubmed: 40006966google scholar: lookup
        17. Uprety T, Soni S, Sreenivasan C, Hause BM, Naveed A, Ni S, Graves AJ, Morrow JK, Meade N, Mellits KH, Adam E, Kennedy MA, Wang D, Li F. Genetic and antigenic characterization of two diarrhoeicdominant rotavirus A genotypes G3P[12] and G14P[12] circulating in the global equine population. J Gen Virol 2024 Aug;105(8).
          doi: 10.1099/jgv.0.002016pubmed: 39163114google scholar: lookup
        18. Jalilvand S, Latifi T, Kachooei A, Mirhoseinian M, Hoseini-Fakhr SS, Behnezhad F, Roohvand F, Shoja Z. Circulating rotavirus strains in children with acute gastroenteritis in Iran, 1986 to 2023 and their genetic/antigenic divergence compared to approved vaccines strains (Rotarix, RotaTeq, ROTAVAC, ROTASIIL) before mass vaccination: Clues for vaccination policy makers. Virus Res 2024 Aug;346:199411.