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Toward the identification of a type I toxin-antitoxin system in the plasmid DNA of dairy Lactobacillus rhamnosus

Plasmids carry genes that give bacteria beneficial traits and allow them to survive in competitive environments. In many cases, they also harbor toxin-antitoxin (TA) systems necessary for plasmid maintenance. TA systems are generally characterized by a stable “toxin”, a protein or peptide capable of...

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Autores principales: Folli, Claudia, Levante, Alessia, Percudani, Riccardo, Amidani, Davide, Bottazzi, Stefania, Ferrari, Alberto, Rivetti, Claudio, Neviani, Erasmo, Lazzi, Camilla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608710/
https://www.ncbi.nlm.nih.gov/pubmed/28935987
http://dx.doi.org/10.1038/s41598-017-12218-5
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author Folli, Claudia
Levante, Alessia
Percudani, Riccardo
Amidani, Davide
Bottazzi, Stefania
Ferrari, Alberto
Rivetti, Claudio
Neviani, Erasmo
Lazzi, Camilla
author_facet Folli, Claudia
Levante, Alessia
Percudani, Riccardo
Amidani, Davide
Bottazzi, Stefania
Ferrari, Alberto
Rivetti, Claudio
Neviani, Erasmo
Lazzi, Camilla
author_sort Folli, Claudia
collection PubMed
description Plasmids carry genes that give bacteria beneficial traits and allow them to survive in competitive environments. In many cases, they also harbor toxin-antitoxin (TA) systems necessary for plasmid maintenance. TA systems are generally characterized by a stable “toxin”, a protein or peptide capable of killing the cell upon plasmid loss and by an unstable “antitoxin”, a protein or a non-coding RNA that inhibits toxin activity. Here we report data toward the identification of a RNA-regulated TA system in the plasmid DNA of L. rhamnosus isolated from cheese. The proposed TA system comprises two convergently transcribed RNAs: a toxin RNA encoding a 29 amino acid peptide named Lpt and an antitoxin non-coding RNA. Both toxin and antitoxin RNAs resulted upregulated under conditions mimicking cheese ripening. The toxicity of the Lpt peptide was demonstrated in E. coli by cloning the Lpt ORF under the control of an inducible promoter. Bioinformatics screening of the bacterial nucleotide database, shows that regions homologous to the Lpt TA locus are widely distributed in the Lactobacillus genus, particularly within the L. casei group, suggesting a relevant role of TA systems in plasmid maintenance of cheese microbiota.
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spelling pubmed-56087102017-10-04 Toward the identification of a type I toxin-antitoxin system in the plasmid DNA of dairy Lactobacillus rhamnosus Folli, Claudia Levante, Alessia Percudani, Riccardo Amidani, Davide Bottazzi, Stefania Ferrari, Alberto Rivetti, Claudio Neviani, Erasmo Lazzi, Camilla Sci Rep Article Plasmids carry genes that give bacteria beneficial traits and allow them to survive in competitive environments. In many cases, they also harbor toxin-antitoxin (TA) systems necessary for plasmid maintenance. TA systems are generally characterized by a stable “toxin”, a protein or peptide capable of killing the cell upon plasmid loss and by an unstable “antitoxin”, a protein or a non-coding RNA that inhibits toxin activity. Here we report data toward the identification of a RNA-regulated TA system in the plasmid DNA of L. rhamnosus isolated from cheese. The proposed TA system comprises two convergently transcribed RNAs: a toxin RNA encoding a 29 amino acid peptide named Lpt and an antitoxin non-coding RNA. Both toxin and antitoxin RNAs resulted upregulated under conditions mimicking cheese ripening. The toxicity of the Lpt peptide was demonstrated in E. coli by cloning the Lpt ORF under the control of an inducible promoter. Bioinformatics screening of the bacterial nucleotide database, shows that regions homologous to the Lpt TA locus are widely distributed in the Lactobacillus genus, particularly within the L. casei group, suggesting a relevant role of TA systems in plasmid maintenance of cheese microbiota. Nature Publishing Group UK 2017-09-21 /pmc/articles/PMC5608710/ /pubmed/28935987 http://dx.doi.org/10.1038/s41598-017-12218-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Folli, Claudia
Levante, Alessia
Percudani, Riccardo
Amidani, Davide
Bottazzi, Stefania
Ferrari, Alberto
Rivetti, Claudio
Neviani, Erasmo
Lazzi, Camilla
Toward the identification of a type I toxin-antitoxin system in the plasmid DNA of dairy Lactobacillus rhamnosus
title Toward the identification of a type I toxin-antitoxin system in the plasmid DNA of dairy Lactobacillus rhamnosus
title_full Toward the identification of a type I toxin-antitoxin system in the plasmid DNA of dairy Lactobacillus rhamnosus
title_fullStr Toward the identification of a type I toxin-antitoxin system in the plasmid DNA of dairy Lactobacillus rhamnosus
title_full_unstemmed Toward the identification of a type I toxin-antitoxin system in the plasmid DNA of dairy Lactobacillus rhamnosus
title_short Toward the identification of a type I toxin-antitoxin system in the plasmid DNA of dairy Lactobacillus rhamnosus
title_sort toward the identification of a type i toxin-antitoxin system in the plasmid dna of dairy lactobacillus rhamnosus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608710/
https://www.ncbi.nlm.nih.gov/pubmed/28935987
http://dx.doi.org/10.1038/s41598-017-12218-5
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