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Identification and first characterization of DinJ-YafQ toxin-antitoxin systems in Lactobacillus species of biotechnological interest

DinJ-YafQ is a type II TA system comprising the ribosome-dependent RNase YafQ toxin and the DinJ antitoxin protein. Although the module has been extensively characterized in Escherichia coli, little information is available for homologous systems in lactic acid bacteria. In this study, we employed b...

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Autores principales: Ferrari, Alberto, Maggi, Stefano, Montanini, Barbara, Levante, Alessia, Lazzi, Camilla, Yamaguchi, Yoshihiro, Rivetti, Claudio, Folli, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529426/
https://www.ncbi.nlm.nih.gov/pubmed/31114007
http://dx.doi.org/10.1038/s41598-019-44094-6
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author Ferrari, Alberto
Maggi, Stefano
Montanini, Barbara
Levante, Alessia
Lazzi, Camilla
Yamaguchi, Yoshihiro
Rivetti, Claudio
Folli, Claudia
author_facet Ferrari, Alberto
Maggi, Stefano
Montanini, Barbara
Levante, Alessia
Lazzi, Camilla
Yamaguchi, Yoshihiro
Rivetti, Claudio
Folli, Claudia
author_sort Ferrari, Alberto
collection PubMed
description DinJ-YafQ is a type II TA system comprising the ribosome-dependent RNase YafQ toxin and the DinJ antitoxin protein. Although the module has been extensively characterized in Escherichia coli, little information is available for homologous systems in lactic acid bacteria. In this study, we employed bioinformatics tools to identify DinJ-YafQ systems in Lactobacillus casei, Lactobacillus paracasei and Lactobacillus rhamnosus species, commonly used in biotechnological processes. Among a total of nineteen systems found, two TA modules from Lactobacillus paracasei and two modules from Lactobacillus rhamnosus wild strains were isolated and their activity was verified by growth assays in Escherichia coli either in liquid and solid media. The RNase activity of the YafQ toxins was verified in vivo by probing mRNA dynamics and metabolism with single-cell Thioflavin T fluorescence. Our findings demonstrate that, albeit DinJ-YafQ TA systems are widely distributed in lactic acid bacteria, only few are fully functional, while others have lost toxicity even though they maintain high sequence identity with wild type YafQ and a likely functional antitoxin protein.
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spelling pubmed-65294262019-05-30 Identification and first characterization of DinJ-YafQ toxin-antitoxin systems in Lactobacillus species of biotechnological interest Ferrari, Alberto Maggi, Stefano Montanini, Barbara Levante, Alessia Lazzi, Camilla Yamaguchi, Yoshihiro Rivetti, Claudio Folli, Claudia Sci Rep Article DinJ-YafQ is a type II TA system comprising the ribosome-dependent RNase YafQ toxin and the DinJ antitoxin protein. Although the module has been extensively characterized in Escherichia coli, little information is available for homologous systems in lactic acid bacteria. In this study, we employed bioinformatics tools to identify DinJ-YafQ systems in Lactobacillus casei, Lactobacillus paracasei and Lactobacillus rhamnosus species, commonly used in biotechnological processes. Among a total of nineteen systems found, two TA modules from Lactobacillus paracasei and two modules from Lactobacillus rhamnosus wild strains were isolated and their activity was verified by growth assays in Escherichia coli either in liquid and solid media. The RNase activity of the YafQ toxins was verified in vivo by probing mRNA dynamics and metabolism with single-cell Thioflavin T fluorescence. Our findings demonstrate that, albeit DinJ-YafQ TA systems are widely distributed in lactic acid bacteria, only few are fully functional, while others have lost toxicity even though they maintain high sequence identity with wild type YafQ and a likely functional antitoxin protein. Nature Publishing Group UK 2019-05-21 /pmc/articles/PMC6529426/ /pubmed/31114007 http://dx.doi.org/10.1038/s41598-019-44094-6 Text en © The Author(s) 2019 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
Ferrari, Alberto
Maggi, Stefano
Montanini, Barbara
Levante, Alessia
Lazzi, Camilla
Yamaguchi, Yoshihiro
Rivetti, Claudio
Folli, Claudia
Identification and first characterization of DinJ-YafQ toxin-antitoxin systems in Lactobacillus species of biotechnological interest
title Identification and first characterization of DinJ-YafQ toxin-antitoxin systems in Lactobacillus species of biotechnological interest
title_full Identification and first characterization of DinJ-YafQ toxin-antitoxin systems in Lactobacillus species of biotechnological interest
title_fullStr Identification and first characterization of DinJ-YafQ toxin-antitoxin systems in Lactobacillus species of biotechnological interest
title_full_unstemmed Identification and first characterization of DinJ-YafQ toxin-antitoxin systems in Lactobacillus species of biotechnological interest
title_short Identification and first characterization of DinJ-YafQ toxin-antitoxin systems in Lactobacillus species of biotechnological interest
title_sort identification and first characterization of dinj-yafq toxin-antitoxin systems in lactobacillus species of biotechnological interest
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529426/
https://www.ncbi.nlm.nih.gov/pubmed/31114007
http://dx.doi.org/10.1038/s41598-019-44094-6
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