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Rv0954 Is a Member of the Mycobacterial Cell Division Complex

Proper control of cell division in the intracellular pathogen Mycobacterium tuberculosis is central to its growth, survival, pathogenesis, and resistance to antibiotics. Nevertheless, the divisome components and mechanisms by which mycobacteria regulate their cell cycle are not entirely understood....

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Detalles Bibliográficos
Autores principales: Wang, Ruojun, Ehrt, Sabine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8093794/
https://www.ncbi.nlm.nih.gov/pubmed/33959103
http://dx.doi.org/10.3389/fmicb.2021.626461
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author Wang, Ruojun
Ehrt, Sabine
author_facet Wang, Ruojun
Ehrt, Sabine
author_sort Wang, Ruojun
collection PubMed
description Proper control of cell division in the intracellular pathogen Mycobacterium tuberculosis is central to its growth, survival, pathogenesis, and resistance to antibiotics. Nevertheless, the divisome components and mechanisms by which mycobacteria regulate their cell cycle are not entirely understood. Here we demonstrate that the previously uncharacterized Rv0954 protein localizes to the mid-cell during cell division and interacts with the division-related proteins LamA, PbpA, and PknH. Deletion of rv0954 did not result in alterations in cell morphology or sensitivity to cell wall-targeting antibiotics but transposon mutagenesis demonstrated genetic interactions with genes related to cell division. This work suggests that Rv0954 participates in cell division and reveals potential components of the mycobacterial divisome for future investigation.
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spelling pubmed-80937942021-05-05 Rv0954 Is a Member of the Mycobacterial Cell Division Complex Wang, Ruojun Ehrt, Sabine Front Microbiol Microbiology Proper control of cell division in the intracellular pathogen Mycobacterium tuberculosis is central to its growth, survival, pathogenesis, and resistance to antibiotics. Nevertheless, the divisome components and mechanisms by which mycobacteria regulate their cell cycle are not entirely understood. Here we demonstrate that the previously uncharacterized Rv0954 protein localizes to the mid-cell during cell division and interacts with the division-related proteins LamA, PbpA, and PknH. Deletion of rv0954 did not result in alterations in cell morphology or sensitivity to cell wall-targeting antibiotics but transposon mutagenesis demonstrated genetic interactions with genes related to cell division. This work suggests that Rv0954 participates in cell division and reveals potential components of the mycobacterial divisome for future investigation. Frontiers Media S.A. 2021-04-20 /pmc/articles/PMC8093794/ /pubmed/33959103 http://dx.doi.org/10.3389/fmicb.2021.626461 Text en Copyright © 2021 Wang and Ehrt. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Wang, Ruojun
Ehrt, Sabine
Rv0954 Is a Member of the Mycobacterial Cell Division Complex
title Rv0954 Is a Member of the Mycobacterial Cell Division Complex
title_full Rv0954 Is a Member of the Mycobacterial Cell Division Complex
title_fullStr Rv0954 Is a Member of the Mycobacterial Cell Division Complex
title_full_unstemmed Rv0954 Is a Member of the Mycobacterial Cell Division Complex
title_short Rv0954 Is a Member of the Mycobacterial Cell Division Complex
title_sort rv0954 is a member of the mycobacterial cell division complex
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8093794/
https://www.ncbi.nlm.nih.gov/pubmed/33959103
http://dx.doi.org/10.3389/fmicb.2021.626461
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