Journal
FRONTIERS IN MICROBIOLOGY
Volume 12, Issue -, Pages -Publisher
FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2021.626461
Keywords
Mycobacterium tuberculosis; cell division; divisome; phosphorylation; Tnseq
Categories
Funding
- NIH [U19 AI111143, P01 AI143575]
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The previously uncharacterized Rv0954 protein was found to localize to the mid-cell during cell division in Mycobacterium tuberculosis, interacting with division-related proteins LamA, PbpA, and PknH. Deletion of rv0954 did not affect cell morphology or sensitivity to antibiotics targeting cell wall, but transposon mutagenesis showed genetic interactions with genes related to cell division. This study suggests that Rv0954 is involved in cell division and identifies potential components of the mycobacterial divisome for further investigation.
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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