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dc.contributor.authorCrawford N.W.en
dc.contributor.authorKirkwood C.D.en
dc.contributor.authorBishop R.F.en
dc.contributor.authorLyon M.en
dc.contributor.authorButtery J.P.en
dc.contributor.authorDonato C.M.en
dc.contributor.authorCh'Ng L.S.en
dc.contributor.authorBoniface K.F.en
dc.date.accessioned2021-05-14T09:29:32Zen
dc.date.available2021-05-14T09:29:32Zen
dc.date.copyright2012en
dc.date.created20120809en
dc.date.issued2012-08-09en
dc.identifier.citationJournal of Infectious Diseases. 206 (3) (pp 377-383), 2012. Date of Publication: 01 Aug 2012.en
dc.identifier.issn0022-1899en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/28187en
dc.description.abstractBackground. RotaTeq vaccine was introduced into the Australian National Immunisation Program in 2007. This study identified and characterised rotavirus strains excreted by infants who presented with symptoms of gastroenteritis following recent RotaTeq vaccination. Methods. Fecal samples (N = 61) from children who developed gastroenteritis following recent RotaTeq vaccination were forwarded to the Australian Rotavirus Surveillance Program (ARSP). RotaTeq-positive samples were genotyped and regions of the VP3, VP4, VP6, and VP7 genes were sequenced. Also, 460 rotavirus-positive ARSP routine surveillance samples were analyzed by dot-blot Northern hybridization to detect RotaTeq vaccine-derived strains circulating in the community. Results. Thirteen of the 61 samples collected from infants developing gastroenteritis after RotaTeq vaccination contained vaccine-derived (vd) rotavirus strains. Of these, 4 contained a vdG1P[8] strain derived by reassortment between the G1P[5] and G6P[8] parental vaccine strains. Northern hybridization analysis of 460 surveillance samples identified 3 samples that contained RotaTeq vaccine-derived strains, including 2 vdG1P[8] reassortant vaccine strains. Conclusions. During replication and excretion of RotaTeq vaccine, reassortment of parental strains can occur. Shedding of RotaTeq vaccine strains in 7 of 13 infants was associated with underlying medical conditions that may have altered their immune function. The benefits of vaccination outweigh any small risk of vaccine-associated gastroenteritis. © 2012 The Author.en
dc.languageenen
dc.languageEnglishen
dc.publisherOxford University Press (Great Clarendon Street, Oxford OX2 6DP, United Kingdom)en
dc.titleIdentification of strains of rotateq rotavirus vaccine in infants with gastroenteritis following routine vaccination.en
dc.typeArticleen
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1093/infdis/jis361en
dc.publisher.placeUnited Kingdomen
dc.identifier.pubmedid22615314 [http://www.ncbi.nlm.nih.gov/pubmed/?term=22615314]en
dc.identifier.source365259684en
dc.identifier.institution(Donato, Ch'Ng, Boniface, Bishop, Kirkwood) Enteric Virus Group, Murdoch Childrens Research Institute, Royal Children's Hospital, Melbourne, Australia (Donato, Kirkwood) Department of Microbiology, La Trobe University, Bundoora, Australia (Ch'Ng, Crawford, Bishop) Department of Paediatrics, University of Melbourne, Australia (Crawford, Buttery) Department of General Medicine, Murdoch Childrens Research Institute, Royal Children's Hospital, Melbourne, Australia (Buttery) Department of Paediatrics, Monash Children's Hospital, Monash University, Melbourne, Australia (Lyon) Public Health Virology Laboratory, Forensic and Scientific Services, Queensland Health, Flemington Road, Parkville, VIC 3052, Australiaen
dc.description.addressC.M. Donato, Enteric Virus Group, Murdoch Childrens Research Institute, Royal Children's Hospital, Melbourne, Australia. E-mail: cmdonato@students.latrobe.edu.auen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2013 Elsevier B.V., All rights reserved.en
dc.identifier.authoremailDonato C.M.; cmdonato@students.latrobe.edu.auen
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairetypeArticle-
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