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In vitro characterization of an avian reovirus vaccine strain

dc.contributor.authorGouvea, Veraen_US
dc.contributor.authorHuang, Diana D.en_US
dc.contributor.authorRamos, Teresaen_US
dc.contributor.authorSchnitzer, Thomas J.en_US
dc.date.accessioned2006-04-07T18:43:26Z
dc.date.available2006-04-07T18:43:26Z
dc.date.issued1983-04-15en_US
dc.identifier.citationGouvea, Vera, Huang, Diana D., Ramos, Teresa, Schnitzer, Thomas J. (1983/04/15)."In vitro characterization of an avian reovirus vaccine strain." Virology 126(1): 240-247. <http://hdl.handle.net/2027.42/25241>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WXR-4C546Y3-M/2/aa0e4e7fb0264422d83d206ed3ae49caen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/25241
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=6845656&dopt=citationen_US
dc.description.abstractIn vitro studies were performed to characterize the vaccine strain, designated P100, derived from the arthrogenic reovirus isolate, S1133, by vold adaptation. P100 appeared to be temperature sensitive, shown by a marked drop in titer and efficiency of plaquing after incubation at 41[deg]. Studies indicated that genomic double-stranded RNA and protein synthesis were severely restricted at the elevated temperature. Differences in the growth behavior of P100 and S1133 at 37[deg] were also noted. The vaccine strain seemed to be more cell associated than S1133. Three outer coat proteins of P100 grown at 37[deg] displayed mobilities different from those of S1133 by PAGE. It is possible that alterations in these proteins may have some relationship to the growth characteristics observed for the P100 strain.en_US
dc.format.extent1817928 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleIn vitro characterization of an avian reovirus vaccine strainen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumRackham Arthritis Research Unit, Department of Internal Medicine, School of Medicine, University of Michigan, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumRackham Arthritis Research Unit, Department of Internal Medicine, School of Medicine, University of Michigan, Ann Arbor, Michigan 48109, USA; Rackham Arthritis Research Unit, Department of Internal Medicine, School of Medicine, University of Michigan, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumDepartment of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, Michigan 48109, USAen_US
dc.identifier.pmid6845656en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/25241/1/0000683.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0042-6822(83)90475-0en_US
dc.identifier.sourceVirologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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