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Microbiology 150 (2004), 1735-1740; DOI  10.1099/mic.0.26733-0
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Microbiology 150 (2004), 1735-1740; DOI  10.1099/mic.0.26733-0
© 2004 Society for General Microbiology

Diversity analysis of commensal porcine Escherichia coli – associations between genotypes and habitat in the porcine gastrointestinal tract

Sameer M. Dixit1,2, David M. Gordon3, Xi-Yang Wu1, Toni Chapman1, Kaila Kailasapathy2 and James J.-C. Chin1,{dagger}

1 Department of Immunology, Elizabeth Macarthur Agriculture Institute, Woodbridge Rd, Menangle, NSW 2568, Sydney, Australia
2 Center for Advanced Food Research, University of Western Sydney, Hawkesbury Campus, Penrith South DC, NSW 1797, Australia
3 School of Botany and Zoology, Australia National University, Canberra, ACT 0200, Australia

Correspondence
James J.-C. Chin
james.chin{at}agric.nsw.gov.au

Diversity studies of enteric Escherichia coli have relied almost entirely on faecal isolations on the assumption that they are representative of flora found throughout the gastrointestinal tract. The authors have addressed this belief by analysing isolates obtained from the duodenum, ileum, colon and faeces of pigs. E. coli isolates were obtained from eight pigs and characterized using multi-locus enzyme electrophoresis and PCR-based screening for a range of factors thought to be associated with intestinal and extra-intestinal disease. There are four main genetic groups of commensal E. coli (A, B1, B2, D). Group A strains represented 76 % of the isolates from the duodenum, ileum and colon compared to 58 % of the strains isolated from faeces. A nested molecular analysis of variance based on the allozyme and virulence factor screening results showed that differences among individual pigs accounted for 6 % of the observed genetic diversity, whilst 27 % of the genetic variation could be explained by clonal composition differences among gut regions. Finally, the absence of virulence genes in these commensals indicates that they may be suitable as a probiotic consortium, particularly if they also display increased adherence to enterocytes and antagonistic activity against pathogenic strains of E. coli.


Abbreviations: AMOVA, molecular analysis of variance; ECOR, E. coli Reference collection; GIT, gastrointestinal tract; MLEE, multi-locus enzyme electrophoresis

MLEE and virulence factor screening results for all E. coli isolates examined are available as supplementary data with the online version of this paper at http://mic.sgmjournals.org.

{dagger}Present address: NSW Agriculture, PMB 8, Camden, NSW 2570, Sydney, Australia.




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