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Evidence of two differentially regulated elongasomes in Salmonella
Cell shape is genetically inherited by all forms of life. Some unicellular microbes increase niche adaptation altering shape whereas most show invariant morphology. A universal system of peptidoglycan synthases guided by cytoskeletal scaffolds defines bacterial shape. In rod-shaped bacteria, this sy...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10492807/ https://www.ncbi.nlm.nih.gov/pubmed/37689828 http://dx.doi.org/10.1038/s42003-023-05308-w |
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author | Castanheira, Sónia García-del Portillo, Francisco |
author_facet | Castanheira, Sónia García-del Portillo, Francisco |
author_sort | Castanheira, Sónia |
collection | PubMed |
description | Cell shape is genetically inherited by all forms of life. Some unicellular microbes increase niche adaptation altering shape whereas most show invariant morphology. A universal system of peptidoglycan synthases guided by cytoskeletal scaffolds defines bacterial shape. In rod-shaped bacteria, this system consists of two supramolecular complexes, the elongasome and divisome, which insert cell wall material along major and minor axes. Microbes with invariant shape are thought to use a single morphogenetic system irrespective of the occupied niche. Here, we provide evidence for two elongasomes that generate (rod) shape in the same bacterium. This phenomenon was unveiled in Salmonella, a pathogen that switches between extra- and intracellular lifestyles. The two elongasomes can be purified independently, respond to different environmental cues, and are directed by distinct peptidoglycan synthases: the canonical PBP2 and the pathogen-specific homologue PBP2(SAL). The PBP2-elongasome responds to neutral pH whereas that directed by PBP2(SAL) assembles in acidic conditions. Moreover, the PBP2(SAL)-elongasome moves at a lower speed. Besides Salmonella, other human, animal, and plant pathogens encode alternative PBPs with predicted morphogenetic functions. Therefore, contrasting the view of morphological plasticity facilitating niche adaptation, some pathogens may have acquired alternative systems to preserve their shape in the host. |
format | Online Article Text |
id | pubmed-10492807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104928072023-09-11 Evidence of two differentially regulated elongasomes in Salmonella Castanheira, Sónia García-del Portillo, Francisco Commun Biol Article Cell shape is genetically inherited by all forms of life. Some unicellular microbes increase niche adaptation altering shape whereas most show invariant morphology. A universal system of peptidoglycan synthases guided by cytoskeletal scaffolds defines bacterial shape. In rod-shaped bacteria, this system consists of two supramolecular complexes, the elongasome and divisome, which insert cell wall material along major and minor axes. Microbes with invariant shape are thought to use a single morphogenetic system irrespective of the occupied niche. Here, we provide evidence for two elongasomes that generate (rod) shape in the same bacterium. This phenomenon was unveiled in Salmonella, a pathogen that switches between extra- and intracellular lifestyles. The two elongasomes can be purified independently, respond to different environmental cues, and are directed by distinct peptidoglycan synthases: the canonical PBP2 and the pathogen-specific homologue PBP2(SAL). The PBP2-elongasome responds to neutral pH whereas that directed by PBP2(SAL) assembles in acidic conditions. Moreover, the PBP2(SAL)-elongasome moves at a lower speed. Besides Salmonella, other human, animal, and plant pathogens encode alternative PBPs with predicted morphogenetic functions. Therefore, contrasting the view of morphological plasticity facilitating niche adaptation, some pathogens may have acquired alternative systems to preserve their shape in the host. Nature Publishing Group UK 2023-09-09 /pmc/articles/PMC10492807/ /pubmed/37689828 http://dx.doi.org/10.1038/s42003-023-05308-w Text en © The Author(s) 2023, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Castanheira, Sónia García-del Portillo, Francisco Evidence of two differentially regulated elongasomes in Salmonella |
title | Evidence of two differentially regulated elongasomes in Salmonella |
title_full | Evidence of two differentially regulated elongasomes in Salmonella |
title_fullStr | Evidence of two differentially regulated elongasomes in Salmonella |
title_full_unstemmed | Evidence of two differentially regulated elongasomes in Salmonella |
title_short | Evidence of two differentially regulated elongasomes in Salmonella |
title_sort | evidence of two differentially regulated elongasomes in salmonella |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10492807/ https://www.ncbi.nlm.nih.gov/pubmed/37689828 http://dx.doi.org/10.1038/s42003-023-05308-w |
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