Cargando…

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

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, whi...

Descripción completa

Detalles Bibliográficos
Autores principales: Short, Francesca L, Monson, Rita E, Salmond, George PC
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4615649/
https://www.ncbi.nlm.nih.gov/pubmed/26274022
http://dx.doi.org/10.1080/15476286.2015.1073438
_version_ 1782396501313454080
author Short, Francesca L
Monson, Rita E
Salmond, George PC
author_facet Short, Francesca L
Monson, Rita E
Salmond, George PC
author_sort Short, Francesca L
collection PubMed
description 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.
format Online
Article
Text
id pubmed-4615649
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-46156492016-02-03 A Type III protein-RNA toxin-antitoxin system from Bacillus thuringiensis promotes plasmid retention during spore development Short, Francesca L Monson, Rita E Salmond, George PC RNA Biol Brief Communication 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. Taylor & Francis 2015-08-14 /pmc/articles/PMC4615649/ /pubmed/26274022 http://dx.doi.org/10.1080/15476286.2015.1073438 Text en © 2015 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License http://creativecommons.org/licenses/by-nc/3.0/, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Brief Communication
Short, Francesca L
Monson, Rita E
Salmond, George PC
A Type III protein-RNA toxin-antitoxin system from Bacillus thuringiensis promotes plasmid retention during spore development
title A Type III protein-RNA toxin-antitoxin system from Bacillus thuringiensis promotes plasmid retention during spore development
title_full A Type III protein-RNA toxin-antitoxin system from Bacillus thuringiensis promotes plasmid retention during spore development
title_fullStr A Type III protein-RNA toxin-antitoxin system from Bacillus thuringiensis promotes plasmid retention during spore development
title_full_unstemmed A Type III protein-RNA toxin-antitoxin system from Bacillus thuringiensis promotes plasmid retention during spore development
title_short A Type III protein-RNA toxin-antitoxin system from Bacillus thuringiensis promotes plasmid retention during spore development
title_sort type iii protein-rna toxin-antitoxin system from bacillus thuringiensis promotes plasmid retention during spore development
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4615649/
https://www.ncbi.nlm.nih.gov/pubmed/26274022
http://dx.doi.org/10.1080/15476286.2015.1073438
work_keys_str_mv AT shortfrancescal atypeiiiproteinrnatoxinantitoxinsystemfrombacillusthuringiensispromotesplasmidretentionduringsporedevelopment
AT monsonritae atypeiiiproteinrnatoxinantitoxinsystemfrombacillusthuringiensispromotesplasmidretentionduringsporedevelopment
AT salmondgeorgepc atypeiiiproteinrnatoxinantitoxinsystemfrombacillusthuringiensispromotesplasmidretentionduringsporedevelopment
AT shortfrancescal typeiiiproteinrnatoxinantitoxinsystemfrombacillusthuringiensispromotesplasmidretentionduringsporedevelopment
AT monsonritae typeiiiproteinrnatoxinantitoxinsystemfrombacillusthuringiensispromotesplasmidretentionduringsporedevelopment
AT salmondgeorgepc typeiiiproteinrnatoxinantitoxinsystemfrombacillusthuringiensispromotesplasmidretentionduringsporedevelopment