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Discovery of a Diverse Set of Bacteria That Build Their Cell Walls without the Canonical Peptidoglycan Polymerase aPBP
Peptidoglycan (PG) is a highly cross-linked peptide-glycan mesh that confers structural rigidity and shape to most bacterial cells. Polymerization of new PG is usually achieved by the concerted activity of two membrane-bound machineries, class-A penicillin binding proteins (aPBPs) and class-B penici...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406291/ https://www.ncbi.nlm.nih.gov/pubmed/34311584 http://dx.doi.org/10.1128/mBio.01342-21 |
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author | Atwal, Sharanjeet Chuenklin, Suthida Bonder, Edward M. Flores, Juan Gillespie, Joseph J. Driscoll, Timothy P. Salje, Jeanne |
author_facet | Atwal, Sharanjeet Chuenklin, Suthida Bonder, Edward M. Flores, Juan Gillespie, Joseph J. Driscoll, Timothy P. Salje, Jeanne |
author_sort | Atwal, Sharanjeet |
collection | PubMed |
description | Peptidoglycan (PG) is a highly cross-linked peptide-glycan mesh that confers structural rigidity and shape to most bacterial cells. Polymerization of new PG is usually achieved by the concerted activity of two membrane-bound machineries, class-A penicillin binding proteins (aPBPs) and class-B penicillin binding proteins (bPBPs) in complex with shape, elongation, division, and sporulation (SEDS) proteins. Here, we have identified four phylogenetically distinct groups of bacteria that lack any identifiable aPBPs. We performed experiments on a panel of species within one of these groups, the Rickettsiales, and found that bacteria lacking aPBPs build a PG-like cell wall with minimal abundance and rigidity relative to cell walls of aPBP-containing bacteria. This reduced cell wall may have evolved to minimize the activation of host responses to pathogens and endosymbionts while retaining the minimal PG-biosynthesis machinery required for cell elongation and division. We term these “peptidoglycan-intermediate” bacteria, a cohort of host-associated species that includes some human pathogens. |
format | Online Article Text |
id | pubmed-8406291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-84062912021-09-09 Discovery of a Diverse Set of Bacteria That Build Their Cell Walls without the Canonical Peptidoglycan Polymerase aPBP Atwal, Sharanjeet Chuenklin, Suthida Bonder, Edward M. Flores, Juan Gillespie, Joseph J. Driscoll, Timothy P. Salje, Jeanne mBio Research Article Peptidoglycan (PG) is a highly cross-linked peptide-glycan mesh that confers structural rigidity and shape to most bacterial cells. Polymerization of new PG is usually achieved by the concerted activity of two membrane-bound machineries, class-A penicillin binding proteins (aPBPs) and class-B penicillin binding proteins (bPBPs) in complex with shape, elongation, division, and sporulation (SEDS) proteins. Here, we have identified four phylogenetically distinct groups of bacteria that lack any identifiable aPBPs. We performed experiments on a panel of species within one of these groups, the Rickettsiales, and found that bacteria lacking aPBPs build a PG-like cell wall with minimal abundance and rigidity relative to cell walls of aPBP-containing bacteria. This reduced cell wall may have evolved to minimize the activation of host responses to pathogens and endosymbionts while retaining the minimal PG-biosynthesis machinery required for cell elongation and division. We term these “peptidoglycan-intermediate” bacteria, a cohort of host-associated species that includes some human pathogens. American Society for Microbiology 2021-07-27 /pmc/articles/PMC8406291/ /pubmed/34311584 http://dx.doi.org/10.1128/mBio.01342-21 Text en Copyright © 2021 Atwal et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Atwal, Sharanjeet Chuenklin, Suthida Bonder, Edward M. Flores, Juan Gillespie, Joseph J. Driscoll, Timothy P. Salje, Jeanne Discovery of a Diverse Set of Bacteria That Build Their Cell Walls without the Canonical Peptidoglycan Polymerase aPBP |
title | Discovery of a Diverse Set of Bacteria That Build Their Cell Walls without the Canonical Peptidoglycan Polymerase aPBP |
title_full | Discovery of a Diverse Set of Bacteria That Build Their Cell Walls without the Canonical Peptidoglycan Polymerase aPBP |
title_fullStr | Discovery of a Diverse Set of Bacteria That Build Their Cell Walls without the Canonical Peptidoglycan Polymerase aPBP |
title_full_unstemmed | Discovery of a Diverse Set of Bacteria That Build Their Cell Walls without the Canonical Peptidoglycan Polymerase aPBP |
title_short | Discovery of a Diverse Set of Bacteria That Build Their Cell Walls without the Canonical Peptidoglycan Polymerase aPBP |
title_sort | discovery of a diverse set of bacteria that build their cell walls without the canonical peptidoglycan polymerase apbp |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406291/ https://www.ncbi.nlm.nih.gov/pubmed/34311584 http://dx.doi.org/10.1128/mBio.01342-21 |
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