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    Intimate host attachment: enteropathogenic and enterohaemorrhagic Escherichia coli

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    Authors
    Lai, YuShuan (Cindy)
    Rosenshine, Ilan
    Leong, John M.
    Frankel, Gad
    UMass Chan Affiliations
    Department of Microbiology and Physiological Systems
    Document Type
    Journal Article
    Publication Date
    2013-11-01
    Keywords
    *Bacterial Adhesion
    Enterohemorrhagic Escherichia coli
    Enteropathogenic Escherichia coli
    Epithelial Cells
    *Host-Pathogen Interactions
    Bacteriology
    Microbial Physiology
    Pathogenic Microbiology
    
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    Link to Full Text
    http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4036124/
    Abstract
    Enteropathogenic and enterohaemorrhagic Escherichia coli use a novel infection strategy to colonize the gut epithelium, involving translocation of their own receptor, Tir, via a type III secretion system and subsequent formation of attaching and effecting (A/E) lesions. Following integration into the host cell plasma membrane of cultured cells, and clustering by the outer membrane adhesin intimin, Tir triggers multiple actin polymerization pathways involving host and bacterial adaptor proteins that converge on the host Arp2/3 actin nucleator. Although initially thought to be involved in A/E lesion formation, recent data have shown that the known Tir-induced actin polymerization pathways are dispensable for this activity, but can play other major roles in colonization efficiency, in vivo fitness and systemic disease. In this review we summarize the roadmap leading from the discovery of Tir, through the different actin polymerization pathways it triggers, to our current understanding of their physiological functions.
    Source
    Cell Microbiol. 2013 Nov;15(11):1796-808. doi: 10.1111/cmi.12179. Epub 2013 Sep 3. Link to article on publisher's site
    DOI
    10.1111/cmi.12179
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/30540
    PubMed ID
    23927593
    Related Resources
    Link to Article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1111/cmi.12179
    Scopus Count
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