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Enteropathogenic E. coli, Salmonella, and Shigella: masters of host cell cytoskeletal exploitation.

Bacterial pathogens have evolved numerous strategies to exploit their host's cellular processes so that they can survive and persist. Often, a bacterium must adhere very tightly to the cells and mediate its effects extracellularly, or it must find a way to invade the host's cells and survi...

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Detalles Bibliográficos
Autores principales: Goosney, D L, Knoechel, D G, Finlay, B B
Formato: Texto
Lenguaje:English
Publicado: Centers for Disease Control and Prevention 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2640686/
https://www.ncbi.nlm.nih.gov/pubmed/10221873
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author Goosney, D L
Knoechel, D G
Finlay, B B
author_facet Goosney, D L
Knoechel, D G
Finlay, B B
author_sort Goosney, D L
collection PubMed
description Bacterial pathogens have evolved numerous strategies to exploit their host's cellular processes so that they can survive and persist. Often, a bacterium must adhere very tightly to the cells and mediate its effects extracellularly, or it must find a way to invade the host's cells and survive intracellularly. In either case, the pathogen hijacks the host's cytoskeleton. The cytoskeleton provides a flexible framework for the cell and is involved in mediating numerous cellular functions, from cell shape and structure to programmed cell death. Altering the host cytoskeleton is crucial for mediating pathogen adherence, invasion, and intracellular locomotion. We highlight recent advances in the pathogenesis of enteropathogenic Escherichia coli, Salmonella Typhimurium, and Shigella flexneri. Each illustrates how bacterial pathogens can exert dramatic effects on the host cytoskeleton.
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spelling pubmed-26406862009-05-20 Enteropathogenic E. coli, Salmonella, and Shigella: masters of host cell cytoskeletal exploitation. Goosney, D L Knoechel, D G Finlay, B B Emerg Infect Dis Research Article Bacterial pathogens have evolved numerous strategies to exploit their host's cellular processes so that they can survive and persist. Often, a bacterium must adhere very tightly to the cells and mediate its effects extracellularly, or it must find a way to invade the host's cells and survive intracellularly. In either case, the pathogen hijacks the host's cytoskeleton. The cytoskeleton provides a flexible framework for the cell and is involved in mediating numerous cellular functions, from cell shape and structure to programmed cell death. Altering the host cytoskeleton is crucial for mediating pathogen adherence, invasion, and intracellular locomotion. We highlight recent advances in the pathogenesis of enteropathogenic Escherichia coli, Salmonella Typhimurium, and Shigella flexneri. Each illustrates how bacterial pathogens can exert dramatic effects on the host cytoskeleton. Centers for Disease Control and Prevention 1999 /pmc/articles/PMC2640686/ /pubmed/10221873 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited.
spellingShingle Research Article
Goosney, D L
Knoechel, D G
Finlay, B B
Enteropathogenic E. coli, Salmonella, and Shigella: masters of host cell cytoskeletal exploitation.
title Enteropathogenic E. coli, Salmonella, and Shigella: masters of host cell cytoskeletal exploitation.
title_full Enteropathogenic E. coli, Salmonella, and Shigella: masters of host cell cytoskeletal exploitation.
title_fullStr Enteropathogenic E. coli, Salmonella, and Shigella: masters of host cell cytoskeletal exploitation.
title_full_unstemmed Enteropathogenic E. coli, Salmonella, and Shigella: masters of host cell cytoskeletal exploitation.
title_short Enteropathogenic E. coli, Salmonella, and Shigella: masters of host cell cytoskeletal exploitation.
title_sort enteropathogenic e. coli, salmonella, and shigella: masters of host cell cytoskeletal exploitation.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2640686/
https://www.ncbi.nlm.nih.gov/pubmed/10221873
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