E. coli as an All-Rounder: The Thin Line Between Commensalism and Pathogenicity View Full Text


Ontology type: schema:Chapter     


Chapter Info

DATE

2013

AUTHORS

Andreas Leimbach , Jörg Hacker , Ulrich Dobrindt

ABSTRACT

Escherichia coli is a paradigm for a versatile bacterial species which comprises harmless commensal as well as different pathogenic variants with the ability to either cause intestinal or extraintestinal diseases in humans and many animal hosts. Because of this broad spectrum of lifestyles and phenotypes, E. coli is a well-suited model organism to study bacterial evolution and adaptation to different growth conditions and niches. The geno- and phenotypic diversity, however, also hampers risk assessment and strain typing. A marked genome plasticity is the key to the great variability seen in this species. Acquisition of genetic information by horizontal gene transfer, gene loss as well as other genomic modifications, like DNA rearrangements and point mutations, can constantly alter the genome content and thus the fitness and competitiveness of individual variants in certain niches. Specific gene subsets and traits have been correlated with an increased potential of E. coli strains to cause intestinal or extraintestinal disease. Intestinal pathogenic E. coli strains can be reliably discriminated from non-pathogenic, commensal, or from extraintestinal E. coli pathogens based on genome content and phenotypic traits. An unambiguous distinction of extraintestinal pathogenic E. coli and commensals is, nevertheless, not so easy, as strains with the ability to cause extraintestinal infection are facultative pathogens and belong to the normal flora of many healthy individuals. Here, we compare insights into phylogeny, geno-, and phenotypic traits of commensal and pathogenic E. coli. We demonstrate that the borderline between extraintestinal virulence and intestinal fitness can be blurred as improved adaptability and competitiveness may promote intestinal colonization as well as extraintestinal infection by E. coli. More... »

PAGES

3-32

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  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1007/82_2012_303

    DOI

    http://dx.doi.org/10.1007/82_2012_303

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1020689042

    PUBMED

    https://www.ncbi.nlm.nih.gov/pubmed/23340801


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