Evidence map›Paper›PMID 22003022›Full record

ArticleApplied and environmental microbiology2011

Genetic background and mobility of variants of the gene nleA in attaching and effacing Escherichia coli.

Kristina Creuzburg, Sabine Heeren, Claudia M Lis, Markus Kranz, Michael Hensel, Herbert Schmidt

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Article in Applied and environmental microbiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Kristina CreuzburgDepartment of Food Microbiology, Institute of Food Science and Biotechnology, University of Hohenheim, 70599 Stuttgart, Germany.
Sabine Heeren
Claudia M Lis
Markus Kranz
Michael Hensel
Herbert Schmidt

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we characterized the genetic background of various nleA variants in 106 Shiga toxin-producing Escherichia coli (STEC) and enteropathogenic Escherichia coli (EPEC) strains. The flanking regions of eight nleA variants were analyzed by DNA sequencing and compared with the corresponding regions of five previously described NleA-encoding prophages. The analyzed nleA variants were all located downstream of the DNA region responsible for phage morphogenesis. In particular, the type III effector genes avrA, ospB, nleH, and nleG and IS elements were detected in the neighborhood of nleA. The structure of the eight analyzed regions flanking nleA primarily resembled the corresponding region of the NleA₄₇₉₅-encoding prophage BP-4795. Using PCR, the gene order flanking 13 nleA variants in strains of different serogroups was compared to the respective regions in reference strains. The analyses showed that strains which harbor prophages with conserved flanking regions of a particular nleA variant predominantly occurred, and IS elements were additionally detected in these regions. We were able to mobilize nleA by transduction in 20% of strains determined, which comprised in particular EPEC strains harboring an nleA variant, the gene encoding the protein known as "EspI-like." Plaque hybridization was used to identify phages that harbor the genes stx and nleA. However, only two strains harbored variant nleA₄₇₉₅ in the genome of an Stx1 prophage.

Indexed as

Gene Transfer, HorizontalAdhesins, BacterialDNA, BacterialEnteropathogenic Escherichia coliEscherichia coli ProteinsGene OrderMolecular Sequence DataProphagesSequence Analysis, DNAShiga-Toxigenic Escherichia coliSyntenyVirulence FactorsAdhesins, BacterialDNA, BacterialeaeA protein, E coliEscherichia coli ProteinsNleA protein, E coliVirulence Factors

Identifiers

PMID22003022
PMCPMC3233075

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