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Evidence for two serotype G3 subtypes among equine rotaviruses
Ten cultivable equine rotavirus isolates, two of North American, six of British, and two of Irish origin, were compared with standard rotavirus strains and with each other by cross neutralization, neutralization with a panel of monoclonal antibodies (MAbs), hybridization to a simian rotavirus (SA-11...
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Published in: | Journal of Clinical Microbiology 1992-02, Vol.30 (2), p.485-491 |
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description | Ten cultivable equine rotavirus isolates, two of North American, six of British, and two of Irish origin, were compared with standard rotavirus strains and with each other by cross neutralization, neutralization with a panel of monoclonal antibodies (MAbs), hybridization to a simian rotavirus (SA-11) VP7 gene probe, and reaction with rotavirus subgrouping and serotyping MAbs in enzyme-linked immunosorbent assays. Six isolates, two of which had previously been serotyped as G3 by other workers, were found to be serotype G3; one was confirmed to be G5, and three were not related to serotypes G1 to G10. The serotype G3 strains were divisible into two subtypes, G3A and G3B, on the basis of cross neutralization. This division was also apparent in reactions with neutralizing Vp7-specific MAbs and in the liquid hybridization assay. Two of the isolates were not bound by either subgroup MAb, six were bound by both subgroup I and II MAbs, and two were bound by only the subgroup I MAb. The assays used in this characterization provide a range of epidemiological information for use in future field investigations. |
doi_str_mv | 10.1128/jcm.30.2.485-491.1992 |
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Six isolates, two of which had previously been serotyped as G3 by other workers, were found to be serotype G3; one was confirmed to be G5, and three were not related to serotypes G1 to G10. The serotype G3 strains were divisible into two subtypes, G3A and G3B, on the basis of cross neutralization. This division was also apparent in reactions with neutralizing Vp7-specific MAbs and in the liquid hybridization assay. Two of the isolates were not bound by either subgroup MAb, six were bound by both subgroup I and II MAbs, and two were bound by only the subgroup I MAb. The assays used in this characterization provide a range of epidemiological information for use in future field investigations.</description><identifier>ISSN: 0095-1137</identifier><identifier>EISSN: 1098-660X</identifier><identifier>DOI: 10.1128/jcm.30.2.485-491.1992</identifier><identifier>PMID: 1371520</identifier><identifier>CODEN: JCMIDW</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>Animals ; Antibodies, Monoclonal ; Antigens, Viral ; Biological and medical sciences ; Capsid - immunology ; Capsid Proteins ; characterization ; Enzyme-Linked Immunosorbent Assay ; Epidemiologic Methods ; epidemiology ; Epitopes ; Fundamental and applied biological sciences. Psychology ; genetic variation ; Horse Diseases - epidemiology ; Horse Diseases - microbiology ; Horses ; isolation ; Microbiology ; Neutralization Tests ; Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains ; Rotavirus ; Rotavirus - classification ; Rotavirus - immunology ; Rotavirus - isolation & purification ; Rotavirus Infections - epidemiology ; Rotavirus Infections - microbiology ; Rotavirus Infections - veterinary ; Serotyping ; strains ; Virology</subject><ispartof>Journal of Clinical Microbiology, 1992-02, Vol.30 (2), p.485-491</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4952-d81b5e3cf8408aaa460a0e6aa2888cda50f3d6e15463fc987581883a19d77d293</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC265082/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC265082/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,3175,3176,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5067027$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1371520$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Browning, G.F</creatorcontrib><creatorcontrib>Chalmers, R.M</creatorcontrib><creatorcontrib>Fitzgerald, T.A</creatorcontrib><creatorcontrib>Snodgrass, D.R</creatorcontrib><title>Evidence for two serotype G3 subtypes among equine rotaviruses</title><title>Journal of Clinical Microbiology</title><addtitle>J Clin Microbiol</addtitle><description>Ten cultivable equine rotavirus isolates, two of North American, six of British, and two of Irish origin, were compared with standard rotavirus strains and with each other by cross neutralization, neutralization with a panel of monoclonal antibodies (MAbs), hybridization to a simian rotavirus (SA-11) VP7 gene probe, and reaction with rotavirus subgrouping and serotyping MAbs in enzyme-linked immunosorbent assays. Six isolates, two of which had previously been serotyped as G3 by other workers, were found to be serotype G3; one was confirmed to be G5, and three were not related to serotypes G1 to G10. The serotype G3 strains were divisible into two subtypes, G3A and G3B, on the basis of cross neutralization. This division was also apparent in reactions with neutralizing Vp7-specific MAbs and in the liquid hybridization assay. Two of the isolates were not bound by either subgroup MAb, six were bound by both subgroup I and II MAbs, and two were bound by only the subgroup I MAb. The assays used in this characterization provide a range of epidemiological information for use in future field investigations.</description><subject>Animals</subject><subject>Antibodies, Monoclonal</subject><subject>Antigens, Viral</subject><subject>Biological and medical sciences</subject><subject>Capsid - immunology</subject><subject>Capsid Proteins</subject><subject>characterization</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Epidemiologic Methods</subject><subject>epidemiology</subject><subject>Epitopes</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>genetic variation</subject><subject>Horse Diseases - epidemiology</subject><subject>Horse Diseases - microbiology</subject><subject>Horses</subject><subject>isolation</subject><subject>Microbiology</subject><subject>Neutralization Tests</subject><subject>Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains</subject><subject>Rotavirus</subject><subject>Rotavirus - classification</subject><subject>Rotavirus - immunology</subject><subject>Rotavirus - isolation & purification</subject><subject>Rotavirus Infections - epidemiology</subject><subject>Rotavirus Infections - microbiology</subject><subject>Rotavirus Infections - veterinary</subject><subject>Serotyping</subject><subject>strains</subject><subject>Virology</subject><issn>0095-1137</issn><issn>1098-660X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><recordid>eNp9kcFu1DAURS0EKkPhEyqyQOwS3rPjxF6AhKrSVqrEAiqxs944zoyrSTy1J1P17_GQUaEbVrZ8z_WzdRg7Q6gQufp0Z4dKQMWrWsmy1lih1vwFWyBoVTYN_HrJFgBaloiifc3epHQHgHUt5Qk7yUcoOSzYl4u979xoXdGHWOweQpFcDLvHrSsuRZGm5WGbChrCuCrc_eRHV-Sc9j5OyaW37FVPm-TeHddTdvvt4uf5VXnz_fL6_OtNaWstedkpXEonbK9qUERUN0DgGiKulLIdSehF1ziUdSN6q1UrFSolCHXXth3X4pR9nu_dTsvBddaNu0gbs41-oPhoAnnzPBn92qzC3vBGguK5__HYj-F-cmlnBp-s22xodGFKpuUKG_5n0P_BTKlWo8ygnEEbQ0rR9U-PQTAHQSYLMgIMN1mQyYLMQVDunf37k7-t2UjOPxxzSpY2faTR-vSESWha4G3Gihlb-9X6wUdnKA3PRmbk_Yz0FAytYr7l9gcHFICtBFAofgNuMq43</recordid><startdate>19920201</startdate><enddate>19920201</enddate><creator>Browning, G.F</creator><creator>Chalmers, R.M</creator><creator>Fitzgerald, T.A</creator><creator>Snodgrass, D.R</creator><general>American Society for Microbiology</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19920201</creationdate><title>Evidence for two serotype G3 subtypes among equine rotaviruses</title><author>Browning, G.F ; Chalmers, R.M ; Fitzgerald, T.A ; Snodgrass, D.R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4952-d81b5e3cf8408aaa460a0e6aa2888cda50f3d6e15463fc987581883a19d77d293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Animals</topic><topic>Antibodies, Monoclonal</topic><topic>Antigens, Viral</topic><topic>Biological and medical sciences</topic><topic>Capsid - immunology</topic><topic>Capsid Proteins</topic><topic>characterization</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Epidemiologic Methods</topic><topic>epidemiology</topic><topic>Epitopes</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>genetic variation</topic><topic>Horse Diseases - epidemiology</topic><topic>Horse Diseases - microbiology</topic><topic>Horses</topic><topic>isolation</topic><topic>Microbiology</topic><topic>Neutralization Tests</topic><topic>Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains</topic><topic>Rotavirus</topic><topic>Rotavirus - classification</topic><topic>Rotavirus - immunology</topic><topic>Rotavirus - isolation & purification</topic><topic>Rotavirus Infections - epidemiology</topic><topic>Rotavirus Infections - microbiology</topic><topic>Rotavirus Infections - veterinary</topic><topic>Serotyping</topic><topic>strains</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Browning, G.F</creatorcontrib><creatorcontrib>Chalmers, R.M</creatorcontrib><creatorcontrib>Fitzgerald, T.A</creatorcontrib><creatorcontrib>Snodgrass, D.R</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of Clinical Microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Browning, G.F</au><au>Chalmers, R.M</au><au>Fitzgerald, T.A</au><au>Snodgrass, D.R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evidence for two serotype G3 subtypes among equine rotaviruses</atitle><jtitle>Journal of Clinical Microbiology</jtitle><addtitle>J Clin Microbiol</addtitle><date>1992-02-01</date><risdate>1992</risdate><volume>30</volume><issue>2</issue><spage>485</spage><epage>491</epage><pages>485-491</pages><issn>0095-1137</issn><eissn>1098-660X</eissn><coden>JCMIDW</coden><abstract>Ten cultivable equine rotavirus isolates, two of North American, six of British, and two of Irish origin, were compared with standard rotavirus strains and with each other by cross neutralization, neutralization with a panel of monoclonal antibodies (MAbs), hybridization to a simian rotavirus (SA-11) VP7 gene probe, and reaction with rotavirus subgrouping and serotyping MAbs in enzyme-linked immunosorbent assays. Six isolates, two of which had previously been serotyped as G3 by other workers, were found to be serotype G3; one was confirmed to be G5, and three were not related to serotypes G1 to G10. The serotype G3 strains were divisible into two subtypes, G3A and G3B, on the basis of cross neutralization. This division was also apparent in reactions with neutralizing Vp7-specific MAbs and in the liquid hybridization assay. Two of the isolates were not bound by either subgroup MAb, six were bound by both subgroup I and II MAbs, and two were bound by only the subgroup I MAb. The assays used in this characterization provide a range of epidemiological information for use in future field investigations.</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>1371520</pmid><doi>10.1128/jcm.30.2.485-491.1992</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antibodies, Monoclonal Antigens, Viral Biological and medical sciences Capsid - immunology Capsid Proteins characterization Enzyme-Linked Immunosorbent Assay Epidemiologic Methods epidemiology Epitopes Fundamental and applied biological sciences. Psychology genetic variation Horse Diseases - epidemiology Horse Diseases - microbiology Horses isolation Microbiology Neutralization Tests Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains Rotavirus Rotavirus - classification Rotavirus - immunology Rotavirus - isolation & purification Rotavirus Infections - epidemiology Rotavirus Infections - microbiology Rotavirus Infections - veterinary Serotyping strains Virology |
title | Evidence for two serotype G3 subtypes among equine rotaviruses |
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