Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/66865
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dc.contributor.authorDo, T.en
dc.contributor.authorStephens, C.en
dc.contributor.authorTownsend, K.en
dc.contributor.authorWu, X.en
dc.contributor.authorChapman, T.en
dc.contributor.authorChin, J.en
dc.contributor.authorMcCormick, B.en
dc.contributor.authorBara, M.en
dc.contributor.authorTrott, D.en
dc.date.issued2005en
dc.identifier.citationAustralian Veterinary Journal, 2005; 83(5):293-299en
dc.identifier.issn0005-0423en
dc.identifier.issn1751-0813en
dc.identifier.urihttp://hdl.handle.net/2440/66865-
dc.description.abstractOBJECTIVE:To identify virulence genes in enterotoxigenic E coli (ETEC) isolates associated with diarrhoea in neonatal, 1 to 3 week-old and weaned pigs in southeast Queensland. DESIGN:Multiplex PCR and serotyping were applied to E coli isolates obtained over a 5-year period (1998-2002) from cases diagnosed at Toowoomba Veterinary Laboratory. PROCEDURE:A total of 126 isolates from 25 different Queensland piggeries were tested for haemolytic activity on 5% sheep blood agar and by multiplex PCR for the presence of five commonly recognised fimbrial (F4, F5, F6, F41 and F18) and three enterotoxin genes (STa, STb, LT). A subset of 62 representative isolates were serotyped by slide agglutination. For comparative purposes, multiplex PCR was also performed on the DNA of 31 ETEC isolates from 9 serotypes originating from piggeries in southern New South Wales. RESULTS:A total of 113 (89.7%) of the isolates from Queensland possessed ETEC virulence genes, including 14 of 15 isolates from neonatal pigs (93.3%), 18 of 23 isolates from 1 to 3 week old pigs (78.3%) and 81 of 88 isolates from weaned pigs (92.1%). F4:STa:STb:LT (serotype O149) was the most prevalent pathotype in neonatal and 1-3 week old pigs and F4:STa:STb:LT (serotype O149) and F18:STa:STb:LT (serotype O141) were most prevalent in weaned pigs. In comparison, isolates obtained from neonatal pigs from New South Wales belonged to a more diverse range of pathotypes and serotypes. CONCLUSION:Multiplex PCR was a rapid and specific method for detecting the presence of ETEC virulence genes in porcine E coli isolates. For isolates obtained from cases of suspected colibacillosis in Queensland, growth of a heavy pure culture of haemolytic E coli was a sensitive prognostic indicator of the presence of ETEC virulence genes in the isolate. ETEC pathotypes and serotypes remained stable in Queensland piggeries over the five-year study period and appear to have changed little over the last three decades.en
dc.description.statementofresponsibilityT Do, C Stephens, K Townsend, X Wu, T Chapman, J Chin, B McCormick, M Bara and DJ Trotten
dc.language.isoenen
dc.publisherAustralian Veterinary Assnen
dc.rightsCopyright status unknownen
dc.subjectFimbriae, Bacterial; Animals; Animals, Newborn; Swine; Escherichia coli; Escherichia coli Infections; Swine Diseases; Diarrhea; Fimbriae Proteins; Escherichia coli Proteins; Bacterial Toxins; Enterotoxins; Serotyping; Sensitivity and Specificity; Polymerase Chain Reaction; Virulence; Genes, Bacterial; Time Factors; Queensland; Female; Maleen
dc.titleRapid identification of virulence genes in enterotoxigenic Escherichia coli isolates associated with diarrhoea in Queensland piggeriesen
dc.typeJournal articleen
dc.identifier.rmid0020106847en
dc.identifier.doi10.1111/j.1751-0813.2005.tb12745.xen
dc.identifier.pubid30493-
pubs.library.collectionAnimal and Veterinary Sciences publicationsen
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
Appears in Collections:Animal and Veterinary Sciences publications

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