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A Type III protein-RNA toxin-antitoxin system from Bacillus thuringiensis promotes plasmid retention during spore development. | LitMetric

AI Article Synopsis

  • - Members of the Bacillus cereus sensu lato group possess large plasmids that may include virulence factors, and these species can form spores when under stress, leading to genomic changes.
  • - During spore formation, bacteria might lose extrachromosomal elements unless they have strong systems for stabilization and segregation, like toxin-antitoxin (TA) systems, which are widespread in prokaryotes.
  • - This study highlights how a Type III TA system from Bacillus thuringiensis can enhance the retention of plasmids during sporulation by eliminating plasmid-free forespores, suggesting a mechanism for maintaining plasmids under stress within these bacterial groups.

Article Abstract

Members of the Bacillus cereus sensu lato group of bacteria often contain multiple large plasmids, including those encoding virulence factors in B. anthracis. Bacillus species can develop into spores in response to stress. During sporulation the genomic content of the cell is heavily compressed, which could result in counterselection of extrachromosomal genomic elements, unless they have robust stabilization and segregation systems. Toxin-antitoxin (TA) systems are near-ubiquitous in prokaryotes and have multiple biological roles, including plasmid stabilization during vegetative growth. Here, we have shown that a Type III TA system, based on an RNA antitoxin and endoribonuclease toxin, from plasmid pAW63 in Bacillus thuringiensis serovar kurstaki HD-73 can dramatically promote plasmid retention in populations undergoing sporulation and germination, and we provide evidence that this occurs through the post-segregational killing of plasmid-free forespores. Our findings show how an extremely common genetic module can be used to ensure plasmid maintenance during stress-induced developmental transitions, with implications for plasmid dynamics in B. cereus s.l. bacteria.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4615649PMC
http://dx.doi.org/10.1080/15476286.2015.1073438DOI Listing

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