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Discovery of coordinately regulated pathways that provide innate protection against interbacterial antagonism

Bacterial survival is fraught with antagonism, including that deriving from viruses and competing bacterial cells. It is now appreciated that bacteria mount complex antiviral responses; however, whether a coordinated defense against bacterial threats is undertaken is not well understood. Previously,...

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Autores principales: Ting, See-Yeun, LaCourse, Kaitlyn D, Ledvina, Hannah E, Zhang, Rutan, Radey, Matthew C, Kulasekara, Hemantha D, Somavanshi, Rahul, Bertolli, Savannah K, Gallagher, Larry A, Kim, Jennifer, Penewit, Kelsi M, Salipante, Stephen J, Xu, Libin, Peterson, S Brook, Mougous, Joseph D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8926400/
https://www.ncbi.nlm.nih.gov/pubmed/35175195
http://dx.doi.org/10.7554/eLife.74658
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author Ting, See-Yeun
LaCourse, Kaitlyn D
Ledvina, Hannah E
Zhang, Rutan
Radey, Matthew C
Kulasekara, Hemantha D
Somavanshi, Rahul
Bertolli, Savannah K
Gallagher, Larry A
Kim, Jennifer
Penewit, Kelsi M
Salipante, Stephen J
Xu, Libin
Peterson, S Brook
Mougous, Joseph D
author_facet Ting, See-Yeun
LaCourse, Kaitlyn D
Ledvina, Hannah E
Zhang, Rutan
Radey, Matthew C
Kulasekara, Hemantha D
Somavanshi, Rahul
Bertolli, Savannah K
Gallagher, Larry A
Kim, Jennifer
Penewit, Kelsi M
Salipante, Stephen J
Xu, Libin
Peterson, S Brook
Mougous, Joseph D
author_sort Ting, See-Yeun
collection PubMed
description Bacterial survival is fraught with antagonism, including that deriving from viruses and competing bacterial cells. It is now appreciated that bacteria mount complex antiviral responses; however, whether a coordinated defense against bacterial threats is undertaken is not well understood. Previously, we showed that Pseudomonas aeruginosa possess a danger-sensing pathway that is a critical fitness determinant during competition against other bacteria. Here, we conducted genome-wide screens in P. aeruginosa that reveal three conserved and widespread interbacterial antagonism resistance clusters (arc1-3). We find that although arc1-3 are coordinately activated by the Gac/Rsm danger-sensing system, they function independently and provide idiosyncratic defense capabilities, distinguishing them from general stress response pathways. Our findings demonstrate that Arc3 family proteins provide specific protection against phospholipase toxins by preventing the accumulation of lysophospholipids in a manner distinct from previously characterized membrane repair systems. These findings liken the response of P. aeruginosa to bacterial threats to that of eukaryotic innate immunity, wherein threat detection leads to the activation of specialized defense systems.
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spelling pubmed-89264002022-03-17 Discovery of coordinately regulated pathways that provide innate protection against interbacterial antagonism Ting, See-Yeun LaCourse, Kaitlyn D Ledvina, Hannah E Zhang, Rutan Radey, Matthew C Kulasekara, Hemantha D Somavanshi, Rahul Bertolli, Savannah K Gallagher, Larry A Kim, Jennifer Penewit, Kelsi M Salipante, Stephen J Xu, Libin Peterson, S Brook Mougous, Joseph D eLife Microbiology and Infectious Disease Bacterial survival is fraught with antagonism, including that deriving from viruses and competing bacterial cells. It is now appreciated that bacteria mount complex antiviral responses; however, whether a coordinated defense against bacterial threats is undertaken is not well understood. Previously, we showed that Pseudomonas aeruginosa possess a danger-sensing pathway that is a critical fitness determinant during competition against other bacteria. Here, we conducted genome-wide screens in P. aeruginosa that reveal three conserved and widespread interbacterial antagonism resistance clusters (arc1-3). We find that although arc1-3 are coordinately activated by the Gac/Rsm danger-sensing system, they function independently and provide idiosyncratic defense capabilities, distinguishing them from general stress response pathways. Our findings demonstrate that Arc3 family proteins provide specific protection against phospholipase toxins by preventing the accumulation of lysophospholipids in a manner distinct from previously characterized membrane repair systems. These findings liken the response of P. aeruginosa to bacterial threats to that of eukaryotic innate immunity, wherein threat detection leads to the activation of specialized defense systems. eLife Sciences Publications, Ltd 2022-02-17 /pmc/articles/PMC8926400/ /pubmed/35175195 http://dx.doi.org/10.7554/eLife.74658 Text en © 2022, Ting et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://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
Ting, See-Yeun
LaCourse, Kaitlyn D
Ledvina, Hannah E
Zhang, Rutan
Radey, Matthew C
Kulasekara, Hemantha D
Somavanshi, Rahul
Bertolli, Savannah K
Gallagher, Larry A
Kim, Jennifer
Penewit, Kelsi M
Salipante, Stephen J
Xu, Libin
Peterson, S Brook
Mougous, Joseph D
Discovery of coordinately regulated pathways that provide innate protection against interbacterial antagonism
title Discovery of coordinately regulated pathways that provide innate protection against interbacterial antagonism
title_full Discovery of coordinately regulated pathways that provide innate protection against interbacterial antagonism
title_fullStr Discovery of coordinately regulated pathways that provide innate protection against interbacterial antagonism
title_full_unstemmed Discovery of coordinately regulated pathways that provide innate protection against interbacterial antagonism
title_short Discovery of coordinately regulated pathways that provide innate protection against interbacterial antagonism
title_sort discovery of coordinately regulated pathways that provide innate protection against interbacterial antagonism
topic Microbiology and Infectious Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8926400/
https://www.ncbi.nlm.nih.gov/pubmed/35175195
http://dx.doi.org/10.7554/eLife.74658
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