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Listeriolysin O: a genuine cytolysin optimized for an intracellular parasite

Cholesterol-dependent cytolysins (CDCs) are produced by a large number of pathogenic gram–positive bacteria. A member of this family, listeriolysin O (LLO), is produced by the intracellular pathogen Listeria monocytogenes. A unique feature of LLO is its low optimal pH activity (∼6) which permits esc...

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Detalles Bibliográficos
Autores principales: Dramsi, Shaynoor, Cossart, Pascale
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173465/
https://www.ncbi.nlm.nih.gov/pubmed/11901162
http://dx.doi.org/10.1083/jcb.200202121
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author Dramsi, Shaynoor
Cossart, Pascale
author_facet Dramsi, Shaynoor
Cossart, Pascale
author_sort Dramsi, Shaynoor
collection PubMed
description Cholesterol-dependent cytolysins (CDCs) are produced by a large number of pathogenic gram–positive bacteria. A member of this family, listeriolysin O (LLO), is produced by the intracellular pathogen Listeria monocytogenes. A unique feature of LLO is its low optimal pH activity (∼6) which permits escape of the bacterium from the phagosome into the host cell cytosol without damaging the plasma membrane of the infected cell. In a recent study (Glomski et al., 2002, this issue), Portnoy's group has addressed the molecular mechanism underlying the pH sensitivity of LLO. Unexpectedly, a single amino acid substitution in LLO L461T results in a molecule more active at neutral pH and promoting premature permeabilization of the infected cells, leading to attenuated virulence. This finding highlights how subtle changes in proteins can be exploited by bacterial pathogens to establish and maintain the integrity of their specific niches.
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spelling pubmed-21734652008-05-01 Listeriolysin O: a genuine cytolysin optimized for an intracellular parasite Dramsi, Shaynoor Cossart, Pascale J Cell Biol Comment Cholesterol-dependent cytolysins (CDCs) are produced by a large number of pathogenic gram–positive bacteria. A member of this family, listeriolysin O (LLO), is produced by the intracellular pathogen Listeria monocytogenes. A unique feature of LLO is its low optimal pH activity (∼6) which permits escape of the bacterium from the phagosome into the host cell cytosol without damaging the plasma membrane of the infected cell. In a recent study (Glomski et al., 2002, this issue), Portnoy's group has addressed the molecular mechanism underlying the pH sensitivity of LLO. Unexpectedly, a single amino acid substitution in LLO L461T results in a molecule more active at neutral pH and promoting premature permeabilization of the infected cells, leading to attenuated virulence. This finding highlights how subtle changes in proteins can be exploited by bacterial pathogens to establish and maintain the integrity of their specific niches. The Rockefeller University Press 2002-03-18 /pmc/articles/PMC2173465/ /pubmed/11901162 http://dx.doi.org/10.1083/jcb.200202121 Text en Copyright © 2002, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Comment
Dramsi, Shaynoor
Cossart, Pascale
Listeriolysin O: a genuine cytolysin optimized for an intracellular parasite
title Listeriolysin O: a genuine cytolysin optimized for an intracellular parasite
title_full Listeriolysin O: a genuine cytolysin optimized for an intracellular parasite
title_fullStr Listeriolysin O: a genuine cytolysin optimized for an intracellular parasite
title_full_unstemmed Listeriolysin O: a genuine cytolysin optimized for an intracellular parasite
title_short Listeriolysin O: a genuine cytolysin optimized for an intracellular parasite
title_sort listeriolysin o: a genuine cytolysin optimized for an intracellular parasite
topic Comment
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173465/
https://www.ncbi.nlm.nih.gov/pubmed/11901162
http://dx.doi.org/10.1083/jcb.200202121
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