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Toxin-antitoxin vapBC locus participates in formation of the dormant state in Mycobacterium smegmatis.
- Source :
-
FEMS microbiology letters [FEMS Microbiol Lett] 2014 Mar; Vol. 352 (1), pp. 69-77. Date of Electronic Publication: 2014 Feb 26. - Publication Year :
- 2014
-
Abstract
- Toxin-antitoxin (TA) loci are widely spread in bacterial plasmids and chromosomes. Toxins affect important functions of bacterial cells such as translation, replication and cell-wall synthesis, whereas antitoxins are toxin inhibitors. Participation in formation of the dormant state in bacteria is suggested to be a possible function of toxins. Here we show that overexpression of VapC toxin in Mycobacterium smegmatis results in development of morphologically distinct ovoid cells. The ovoid cells were nonreplicating and revealed a low level of uracil incorporation and respiration that indicated their dormant status. To validate the role of VapBC in dormancy formation, we used a model of dormant, 'nonculturable' (NC) M. smegmatis cells obtained in potassium-limited conditions. Overexpression of VapB antitoxin prevented transition to dormancy, presumably due to a decreased level of the free VapC protein. Indeed, this effect of the VapB was neutralized by coexpression of the cognate VapC as a part of the vapBC operon. In summary, these findings reveal participation of vapBC products in formation of the dormant state in M. smegmatis.<br /> (© 2014 Federation of European Microbiological Societies. Published by John Wiley & Sons Ltd. All rights reserved.)
- Subjects :
- Antitoxins metabolism
Bacterial Proteins genetics
Bacterial Toxins genetics
DNA-Binding Proteins genetics
Gene Expression Regulation, Bacterial
Membrane Glycoproteins genetics
Mycobacterium smegmatis genetics
Bacterial Proteins metabolism
Bacterial Toxins metabolism
DNA-Binding Proteins metabolism
Membrane Glycoproteins metabolism
Mycobacterium smegmatis growth & development
Mycobacterium smegmatis metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1574-6968
- Volume :
- 352
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- FEMS microbiology letters
- Publication Type :
- Report
- Accession number :
- 24417293
- Full Text :
- https://doi.org/10.1111/1574-6968.12380