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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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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 |
format | Online Article Text |
id | pubmed-4348357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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