Literature DB >> 17224306

Enterohaemorrhagic Escherichia coli O157 and non-O157 serovars differ in their mechanisms for iron supply.

Andreas U Kresse1, Ilse Rienäcker, Ana Maria Valle, Hartmut Steinrück, Hermann Claus, Shelley M Payne, Helmut Tschäpe, Peter H Williams, Rolf Reissbrodt.   

Abstract

Clinical isolates of enterohaemorrhagic Escherichia coli, both O157 and non-O157 serotypes, were investigated for siderophore production, for growth promotion by haem and esculetin in iron-restricted conditions, for production of enterohaemolysin and esculin hydrolase, and for the presence of the chuA and ehx genes by PCR. As expected, all the strains produced enterobactin, but the prevalence of other factors varied among the serovars tested. None of the O157 and O26 strains produced aerobactin or "colibactin", whereas among other enterohaemorrhagic E. coli non-O157 serovars the frequencies of aerobactin and "colibactin" production were similar to those of commensal E. coli strains. The ability to use ferric esculetin for growth in iron-limited media was markedly more prevalent among non-O157 serovars and less prevalent among O157 strains compared with commensal E. coli strains. Almost all O157, O26 and O103 strains expressed enterohaemolysin, compared with only 50% of other non-O157 strains. Similarly, almost all O157 and O26 strains utilised haem as a host iron source; the frequency of haem use by other non-O157 strains was generally lower and variable among serovars, such that none of the O103:H2 isolates tested used haem as an iron source. The gene chuA, which encodes the haem transport protein ChuA and which is prevalent in O157:H7 strains, was only rarely noted among non-O157 serovars of enterohaemorrhagic E. coli, even among isolates that could use haem as an iron source. Overall our data demonstrate that O157:H7 and non-O157 serovars, in particular O26:H(-)/H11 and O103:H2, use distinctly different strategies for obtaining iron, and suggest two evolutionary distinct lines of enterhaemorrhagic E. coli.

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Year:  2007        PMID: 17224306     DOI: 10.1016/j.ijmm.2006.11.002

Source DB:  PubMed          Journal:  Int J Med Microbiol        ISSN: 1438-4221            Impact factor:   3.473


  6 in total

1.  Molecular risk assessment and epidemiological typing of Shiga toxin-producing Escherichia coli by using a novel PCR binary typing system.

Authors:  Stephanie M Brandt; Nicola King; Angela J Cornelius; Aruni Premaratne; Thomas E Besser; Stephen L W On
Journal:  Appl Environ Microbiol       Date:  2011-02-04       Impact factor: 4.792

2.  OI-57, a genomic island of Escherichia coli O157, is present in other seropathotypes of Shiga toxin-producing E. coli associated with severe human disease.

Authors:  Lejla Imamovic; Rosangela Tozzoli; Valeria Michelacci; Fabio Minelli; Maria Luisa Marziano; Alfredo Caprioli; Stefano Morabito
Journal:  Infect Immun       Date:  2010-09-07       Impact factor: 3.441

3.  Chromosomal instability in enterohaemorrhagic Escherichia coli O157:H7: impact on adherence, tellurite resistance and colony phenotype.

Authors:  Martina Bielaszewska; Barbara Middendorf; Phillip I Tarr; Wenlan Zhang; Rita Prager; Thomas Aldick; Ulrich Dobrindt; Helge Karch; Alexander Mellmann
Journal:  Mol Microbiol       Date:  2011-01-04       Impact factor: 3.501

4.  Escherichia coli-derived outer membrane vesicles are genotoxic to human enterocyte-like cells.

Authors:  Peter C Tyrer; Frank A Frizelle; Jacqueline I Keenan
Journal:  Infect Agent Cancer       Date:  2014-01-10       Impact factor: 2.965

Review 5.  Iron, copper, zinc, and manganese transport and regulation in pathogenic Enterobacteria: correlations between strains, site of infection and the relative importance of the different metal transport systems for virulence.

Authors:  Gaëlle Porcheron; Amélie Garénaux; Julie Proulx; Mourad Sabri; Charles M Dozois
Journal:  Front Cell Infect Microbiol       Date:  2013-12-05       Impact factor: 5.293

6.  Comparative Transcriptomics of Shiga Toxin-Producing and Commensal Escherichia coli and Cytokine Responses in Colonic Epithelial Cell Culture Infections.

Authors:  Lisa M Harrison; David W Lacher; Mark K Mammel; Susan R Leonard
Journal:  Front Cell Infect Microbiol       Date:  2020-10-26       Impact factor: 5.293

  6 in total

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