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Kin cell lysis is a danger signal that activates antibacterial pathways of Pseudomonas aeruginosa

The perception and response to cellular death is an important aspect of multicellular eukaryotic life. For example, damage-associated molecular patterns activate an inflammatory cascade that leads to removal of cellular debris and promotion of healing. We demonstrate that lysis of Pseudomonas aerugi...

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Autores principales: LeRoux, Michele, Kirkpatrick, Robin L, Montauti, Elena I, Tran, Bao Q, Peterson, S Brook, Harding, Brittany N, Whitney, John C, Russell, Alistair B, Traxler, Beth, Goo, Young Ah, Goodlett, David R, Wiggins, Paul A, Mougous, Joseph D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4348357/
https://www.ncbi.nlm.nih.gov/pubmed/25643398
http://dx.doi.org/10.7554/eLife.05701
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author LeRoux, Michele
Kirkpatrick, Robin L
Montauti, Elena I
Tran, Bao Q
Peterson, S Brook
Harding, Brittany N
Whitney, John C
Russell, Alistair B
Traxler, Beth
Goo, Young Ah
Goodlett, David R
Wiggins, Paul A
Mougous, Joseph D
author_facet LeRoux, Michele
Kirkpatrick, Robin L
Montauti, Elena I
Tran, Bao Q
Peterson, S Brook
Harding, Brittany N
Whitney, John C
Russell, Alistair B
Traxler, Beth
Goo, Young Ah
Goodlett, David R
Wiggins, Paul A
Mougous, Joseph D
author_sort LeRoux, Michele
collection PubMed
description The perception and response to cellular death is an important aspect of multicellular eukaryotic life. For example, damage-associated molecular patterns activate an inflammatory cascade that leads to removal of cellular debris and promotion of healing. We demonstrate that lysis of Pseudomonas aeruginosa cells triggers a program in the remaining population that confers fitness in interspecies co-culture. We find that this program, termed P. aeruginosa response to antagonism (PARA), involves rapid deployment of antibacterial factors and is mediated by the Gac/Rsm global regulatory pathway. Type VI secretion, and, unexpectedly, conjugative type IV secretion within competing bacteria, induce P. aeruginosa lysis and activate PARA, thus providing a mechanism for the enhanced capacity of P. aeruginosa to target bacteria that elaborate these factors. Our finding that bacteria sense damaged kin and respond via a widely distributed pathway to mount a complex response raises the possibility that danger sensing is an evolutionarily conserved process. DOI: http://dx.doi.org/10.7554/eLife.05701.001
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spelling pubmed-43483572015-03-05 Kin cell lysis is a danger signal that activates antibacterial pathways of Pseudomonas aeruginosa LeRoux, Michele Kirkpatrick, Robin L Montauti, Elena I Tran, Bao Q Peterson, S Brook Harding, Brittany N Whitney, John C Russell, Alistair B Traxler, Beth Goo, Young Ah Goodlett, David R Wiggins, Paul A Mougous, Joseph D eLife Microbiology and Infectious Disease The perception and response to cellular death is an important aspect of multicellular eukaryotic life. For example, damage-associated molecular patterns activate an inflammatory cascade that leads to removal of cellular debris and promotion of healing. We demonstrate that lysis of Pseudomonas aeruginosa cells triggers a program in the remaining population that confers fitness in interspecies co-culture. We find that this program, termed P. aeruginosa response to antagonism (PARA), involves rapid deployment of antibacterial factors and is mediated by the Gac/Rsm global regulatory pathway. Type VI secretion, and, unexpectedly, conjugative type IV secretion within competing bacteria, induce P. aeruginosa lysis and activate PARA, thus providing a mechanism for the enhanced capacity of P. aeruginosa to target bacteria that elaborate these factors. Our finding that bacteria sense damaged kin and respond via a widely distributed pathway to mount a complex response raises the possibility that danger sensing is an evolutionarily conserved process. DOI: http://dx.doi.org/10.7554/eLife.05701.001 eLife Sciences Publications, Ltd 2015-02-02 /pmc/articles/PMC4348357/ /pubmed/25643398 http://dx.doi.org/10.7554/eLife.05701 Text en © 2015, LeRoux et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Microbiology and Infectious Disease
LeRoux, Michele
Kirkpatrick, Robin L
Montauti, Elena I
Tran, Bao Q
Peterson, S Brook
Harding, Brittany N
Whitney, John C
Russell, Alistair B
Traxler, Beth
Goo, Young Ah
Goodlett, David R
Wiggins, Paul A
Mougous, Joseph D
Kin cell lysis is a danger signal that activates antibacterial pathways of Pseudomonas aeruginosa
title Kin cell lysis is a danger signal that activates antibacterial pathways of Pseudomonas aeruginosa
title_full Kin cell lysis is a danger signal that activates antibacterial pathways of Pseudomonas aeruginosa
title_fullStr Kin cell lysis is a danger signal that activates antibacterial pathways of Pseudomonas aeruginosa
title_full_unstemmed Kin cell lysis is a danger signal that activates antibacterial pathways of Pseudomonas aeruginosa
title_short Kin cell lysis is a danger signal that activates antibacterial pathways of Pseudomonas aeruginosa
title_sort kin cell lysis is a danger signal that activates antibacterial pathways of pseudomonas aeruginosa
topic Microbiology and Infectious Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4348357/
https://www.ncbi.nlm.nih.gov/pubmed/25643398
http://dx.doi.org/10.7554/eLife.05701
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