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Dissecting virulence: systematic and functional analyses of a pathogenicity island.


ABSTRACT: Bacterial pathogenicity islands (PAI) often encode both effector molecules responsible for disease and secretion systems that deliver these effectors to host cells. Human enterohemorrhagic Escherichia coli (EHEC), enteropathogenic E. coli, and the mouse pathogen Citrobacter rodentium (CR) possess the locus of enterocyte effacement (LEE) PAI. We systematically mutagenized all 41 CR LEE genes and functionally characterized these mutants in vitro and in a murine infection model. We identified 33 virulence factors, including two virulence regulators and a hierarchical switch for type III secretion. In addition, 7 potential type III effectors encoded outside the LEE were identified by using a proteomics approach. These non-LEE effectors are encoded by three uncharacterized PAIs in EHEC O157, suggesting that these PAIs act cooperatively with the LEE in pathogenesis. Our findings provide significant insights into bacterial virulence mechanisms and disease.

SUBMITTER: Deng W 

PROVIDER: S-EPMC373508 | biostudies-literature | 2004 Mar

REPOSITORIES: biostudies-literature

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Dissecting virulence: systematic and functional analyses of a pathogenicity island.

Deng Wanyin W   Puente José L JL   Gruenheid Samantha S   Li Yuling Y   Vallance Bruce A BA   Vázquez Alejandra A   Barba Jeannette J   Ibarra J Antonio JA   O'Donnell Paul P   Metalnikov Pavel P   Ashman Keith K   Lee Sansan S   Goode David D   Pawson Tony T   Finlay B Brett BB  

Proceedings of the National Academy of Sciences of the United States of America 20040226 10


Bacterial pathogenicity islands (PAI) often encode both effector molecules responsible for disease and secretion systems that deliver these effectors to host cells. Human enterohemorrhagic Escherichia coli (EHEC), enteropathogenic E. coli, and the mouse pathogen Citrobacter rodentium (CR) possess the locus of enterocyte effacement (LEE) PAI. We systematically mutagenized all 41 CR LEE genes and functionally characterized these mutants in vitro and in a murine infection model. We identified 33 vi  ...[more]

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