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Proc Natl Acad Sci U S A. 2012 Jul 31;109(31):12497-502. doi: 10.1073/pnas.1121217109. Epub 2012 Jul 16.

Additional role for the ccd operon of F-plasmid as a transmissible persistence factor.

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1
Molecular Biophysics Unit, Indian Institute of Science, Bangalore 560 012, India.

Abstract

Toxin-antitoxin (TA) systems are found on both bacterial plasmids and chromosomes, but in most cases their functional role is unclear. Gene knockouts often yield limited insights into functions of individual TA systems because of their redundancy. The well-characterized F-plasmid-based CcdAB TA system is important for F-plasmid maintenance. We have isolated several point mutants of the toxin CcdB that fail to bind to its cellular target, DNA gyrase, but retain binding to the antitoxin, CcdA. Expression of such mutants is shown to result in release of the WT toxin from a functional preexisting TA complex as well as derepression of the TA operon. One such inactive, active-site mutant of CcdB was used to demonstrate the contribution of CcdB to antibiotic persistence. Transient activation of WT CcdB either by coexpression of the mutant or by antibiotic/heat stress was shown to enhance the generation of drug-tolerant persisters in a process dependent on Lon protease and RecA. An F-plasmid containing a ccd locus can, therefore, function as a transmissible persistence factor.

PMID:
22802647
PMCID:
PMC3412025
DOI:
10.1073/pnas.1121217109
[Indexed for MEDLINE]
Free PMC Article
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