Dissecting virulence: Systematic and functional analyses of a pathogenicity island

Wanyin Deng(Mount Sinai Hospital), José L. Puente(Mount Sinai Hospital), Samantha Gruenheid(Mount Sinai Hospital), Yuling Li(Mount Sinai Hospital), Bruce A. Vallance(Mount Sinai Hospital), Alejandra Vázquez(Mount Sinai Hospital), Jeannette Barba‐León(Mount Sinai Hospital), J. Antonio Ibarra(Mount Sinai Hospital), Paul O’Donnell(Mount Sinai Hospital), Pavel Metalnikov(Mount Sinai Hospital), Keith Ashman(Mount Sinai Hospital), Sansan Lee(Mount Sinai Hospital), David L. Goode(Mount Sinai Hospital), Tony Pawson(Mount Sinai Hospital), B. Brett Finlay(Mount Sinai Hospital)
Proceedings of the National Academy of Sciences
February 26, 2004
Cited by 618Open Access
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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.


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