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Type II and type IV toxin–antitoxin systems show different evolutionary patterns in the global Klebsiella pneumoniae population

The Klebsiella pneumoniae species complex includes important opportunistic pathogens which have become public health priorities linked to major hospital outbreaks and the recent emergence of multidrug-resistant hypervirulent strains. Bacterial virulence and the spread of multidrug resistance have pr...

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Autores principales: Horesh, Gal, Fino, Cinzia, Harms, Alexander, Dorman, Matthew J, Parts, Leopold, Gerdes, Kenn, Heinz, Eva, Thomson, Nicholas R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7192599/
https://www.ncbi.nlm.nih.gov/pubmed/32232417
http://dx.doi.org/10.1093/nar/gkaa198
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author Horesh, Gal
Fino, Cinzia
Harms, Alexander
Dorman, Matthew J
Parts, Leopold
Gerdes, Kenn
Heinz, Eva
Thomson, Nicholas R
author_facet Horesh, Gal
Fino, Cinzia
Harms, Alexander
Dorman, Matthew J
Parts, Leopold
Gerdes, Kenn
Heinz, Eva
Thomson, Nicholas R
author_sort Horesh, Gal
collection PubMed
description The Klebsiella pneumoniae species complex includes important opportunistic pathogens which have become public health priorities linked to major hospital outbreaks and the recent emergence of multidrug-resistant hypervirulent strains. Bacterial virulence and the spread of multidrug resistance have previously been linked to toxin–antitoxin (TA) systems. TA systems encode a toxin that disrupts essential cellular processes, and a cognate antitoxin which counteracts this activity. Whilst associated with the maintenance of plasmids, they also act in bacterial immunity and antibiotic tolerance. However, the evolutionary dynamics and distribution of TA systems in clinical pathogens are not well understood. Here, we present a comprehensive survey and description of the diversity of TA systems in 259 clinically relevant genomes of K. pneumoniae. We show that TA systems are highly prevalent with a median of 20 loci per strain. Importantly, these toxins differ substantially in their distribution patterns and in their range of cognate antitoxins. Classification along these properties suggests different roles of TA systems and highlights the association and co-evolution of toxins and antitoxins.
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spelling pubmed-71925992020-05-06 Type II and type IV toxin–antitoxin systems show different evolutionary patterns in the global Klebsiella pneumoniae population Horesh, Gal Fino, Cinzia Harms, Alexander Dorman, Matthew J Parts, Leopold Gerdes, Kenn Heinz, Eva Thomson, Nicholas R Nucleic Acids Res Genomics The Klebsiella pneumoniae species complex includes important opportunistic pathogens which have become public health priorities linked to major hospital outbreaks and the recent emergence of multidrug-resistant hypervirulent strains. Bacterial virulence and the spread of multidrug resistance have previously been linked to toxin–antitoxin (TA) systems. TA systems encode a toxin that disrupts essential cellular processes, and a cognate antitoxin which counteracts this activity. Whilst associated with the maintenance of plasmids, they also act in bacterial immunity and antibiotic tolerance. However, the evolutionary dynamics and distribution of TA systems in clinical pathogens are not well understood. Here, we present a comprehensive survey and description of the diversity of TA systems in 259 clinically relevant genomes of K. pneumoniae. We show that TA systems are highly prevalent with a median of 20 loci per strain. Importantly, these toxins differ substantially in their distribution patterns and in their range of cognate antitoxins. Classification along these properties suggests different roles of TA systems and highlights the association and co-evolution of toxins and antitoxins. Oxford University Press 2020-05-07 2020-03-31 /pmc/articles/PMC7192599/ /pubmed/32232417 http://dx.doi.org/10.1093/nar/gkaa198 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genomics
Horesh, Gal
Fino, Cinzia
Harms, Alexander
Dorman, Matthew J
Parts, Leopold
Gerdes, Kenn
Heinz, Eva
Thomson, Nicholas R
Type II and type IV toxin–antitoxin systems show different evolutionary patterns in the global Klebsiella pneumoniae population
title Type II and type IV toxin–antitoxin systems show different evolutionary patterns in the global Klebsiella pneumoniae population
title_full Type II and type IV toxin–antitoxin systems show different evolutionary patterns in the global Klebsiella pneumoniae population
title_fullStr Type II and type IV toxin–antitoxin systems show different evolutionary patterns in the global Klebsiella pneumoniae population
title_full_unstemmed Type II and type IV toxin–antitoxin systems show different evolutionary patterns in the global Klebsiella pneumoniae population
title_short Type II and type IV toxin–antitoxin systems show different evolutionary patterns in the global Klebsiella pneumoniae population
title_sort type ii and type iv toxin–antitoxin systems show different evolutionary patterns in the global klebsiella pneumoniae population
topic Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7192599/
https://www.ncbi.nlm.nih.gov/pubmed/32232417
http://dx.doi.org/10.1093/nar/gkaa198
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