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Competence remodels the pneumococcal cell wall exposing key surface virulence factors that mediate increased host adherence

Competence development in the human pathogen Streptococcus pneumoniae controls several features such as genetic transformation, biofilm formation, and virulence. Competent bacteria produce so-called “fratricins” such as CbpD that kill noncompetent siblings by cleaving peptidoglycan (PGN). CbpD is a...

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Autores principales: Minhas, Vikrant, Domenech, Arnau, Synefiaridou, Dimitra, Straume, Daniel, Brendel, Max, Cebrero, Gonzalo, Liu, Xue, Costa, Charlotte, Baldry, Mara, Sirard, Jean-Claude, Perez, Camilo, Gisch, Nicolas, Hammerschmidt, Sven, Håvarstein, Leiv Sigve, Veening, Jan-Willem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910801/
https://www.ncbi.nlm.nih.gov/pubmed/36716340
http://dx.doi.org/10.1371/journal.pbio.3001990
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author Minhas, Vikrant
Domenech, Arnau
Synefiaridou, Dimitra
Straume, Daniel
Brendel, Max
Cebrero, Gonzalo
Liu, Xue
Costa, Charlotte
Baldry, Mara
Sirard, Jean-Claude
Perez, Camilo
Gisch, Nicolas
Hammerschmidt, Sven
Håvarstein, Leiv Sigve
Veening, Jan-Willem
author_facet Minhas, Vikrant
Domenech, Arnau
Synefiaridou, Dimitra
Straume, Daniel
Brendel, Max
Cebrero, Gonzalo
Liu, Xue
Costa, Charlotte
Baldry, Mara
Sirard, Jean-Claude
Perez, Camilo
Gisch, Nicolas
Hammerschmidt, Sven
Håvarstein, Leiv Sigve
Veening, Jan-Willem
author_sort Minhas, Vikrant
collection PubMed
description Competence development in the human pathogen Streptococcus pneumoniae controls several features such as genetic transformation, biofilm formation, and virulence. Competent bacteria produce so-called “fratricins” such as CbpD that kill noncompetent siblings by cleaving peptidoglycan (PGN). CbpD is a choline-binding protein (CBP) that binds to phosphorylcholine residues found on wall and lipoteichoic acids (WTA and LTA) that together with PGN are major constituents of the pneumococcal cell wall. Competent pneumococci are protected against fratricide by producing the immunity protein ComM. How competence and fratricide contribute to virulence is unknown. Here, using a genome-wide CRISPRi-seq screen, we show that genes involved in teichoic acid (TA) biosynthesis are essential during competence. We demonstrate that LytR is the major enzyme mediating the final step in WTA formation, and that, together with ComM, is essential for immunity against CbpD. Importantly, we show that key virulence factors PspA and PspC become more surface-exposed at midcell during competence, in a CbpD-dependent manner. Together, our work supports a model in which activation of competence is crucial for host adherence by increased surface exposure of its various CBPs.
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spelling pubmed-99108012023-02-10 Competence remodels the pneumococcal cell wall exposing key surface virulence factors that mediate increased host adherence Minhas, Vikrant Domenech, Arnau Synefiaridou, Dimitra Straume, Daniel Brendel, Max Cebrero, Gonzalo Liu, Xue Costa, Charlotte Baldry, Mara Sirard, Jean-Claude Perez, Camilo Gisch, Nicolas Hammerschmidt, Sven Håvarstein, Leiv Sigve Veening, Jan-Willem PLoS Biol Research Article Competence development in the human pathogen Streptococcus pneumoniae controls several features such as genetic transformation, biofilm formation, and virulence. Competent bacteria produce so-called “fratricins” such as CbpD that kill noncompetent siblings by cleaving peptidoglycan (PGN). CbpD is a choline-binding protein (CBP) that binds to phosphorylcholine residues found on wall and lipoteichoic acids (WTA and LTA) that together with PGN are major constituents of the pneumococcal cell wall. Competent pneumococci are protected against fratricide by producing the immunity protein ComM. How competence and fratricide contribute to virulence is unknown. Here, using a genome-wide CRISPRi-seq screen, we show that genes involved in teichoic acid (TA) biosynthesis are essential during competence. We demonstrate that LytR is the major enzyme mediating the final step in WTA formation, and that, together with ComM, is essential for immunity against CbpD. Importantly, we show that key virulence factors PspA and PspC become more surface-exposed at midcell during competence, in a CbpD-dependent manner. Together, our work supports a model in which activation of competence is crucial for host adherence by increased surface exposure of its various CBPs. Public Library of Science 2023-01-30 /pmc/articles/PMC9910801/ /pubmed/36716340 http://dx.doi.org/10.1371/journal.pbio.3001990 Text en © 2023 Minhas et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Minhas, Vikrant
Domenech, Arnau
Synefiaridou, Dimitra
Straume, Daniel
Brendel, Max
Cebrero, Gonzalo
Liu, Xue
Costa, Charlotte
Baldry, Mara
Sirard, Jean-Claude
Perez, Camilo
Gisch, Nicolas
Hammerschmidt, Sven
Håvarstein, Leiv Sigve
Veening, Jan-Willem
Competence remodels the pneumococcal cell wall exposing key surface virulence factors that mediate increased host adherence
title Competence remodels the pneumococcal cell wall exposing key surface virulence factors that mediate increased host adherence
title_full Competence remodels the pneumococcal cell wall exposing key surface virulence factors that mediate increased host adherence
title_fullStr Competence remodels the pneumococcal cell wall exposing key surface virulence factors that mediate increased host adherence
title_full_unstemmed Competence remodels the pneumococcal cell wall exposing key surface virulence factors that mediate increased host adherence
title_short Competence remodels the pneumococcal cell wall exposing key surface virulence factors that mediate increased host adherence
title_sort competence remodels the pneumococcal cell wall exposing key surface virulence factors that mediate increased host adherence
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910801/
https://www.ncbi.nlm.nih.gov/pubmed/36716340
http://dx.doi.org/10.1371/journal.pbio.3001990
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