Mobilization of pdif modules in Acinetobacter: A novel mechanism for antibiotic resistance gene shuffling?

Abstract XerCD‐ dif site‐specific recombination is a well characterized system, found in most bacteria and archaea. Its role is resolution of chromosomal dimers that arise from homologous recombination. Xer‐mediated recombination is also used by several plasmids for multimer resolution to enhance st...

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Published in:Molecular Microbiology
Main Authors: Balalovski, Phillip, Grainge, Ian
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2020
Subjects:
Online Access:http://dx.doi.org/10.1111/mmi.14563
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spelling crwiley:10.1111/mmi.14563 2024-06-23T07:56:09+00:00 Mobilization of pdif modules in Acinetobacter: A novel mechanism for antibiotic resistance gene shuffling? Balalovski, Phillip Grainge, Ian 2020 http://dx.doi.org/10.1111/mmi.14563 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fmmi.14563 https://onlinelibrary.wiley.com/doi/pdf/10.1111/mmi.14563 https://onlinelibrary.wiley.com/doi/full-xml/10.1111/mmi.14563 en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor Molecular Microbiology volume 114, issue 5, page 699-709 ISSN 0950-382X 1365-2958 journal-article 2020 crwiley https://doi.org/10.1111/mmi.14563 2024-06-06T04:21:39Z Abstract XerCD‐ dif site‐specific recombination is a well characterized system, found in most bacteria and archaea. Its role is resolution of chromosomal dimers that arise from homologous recombination. Xer‐mediated recombination is also used by several plasmids for multimer resolution to enhance stability and by some phage for integration into the chromosome. In the past decade, it has been hypothesized that an alternate and novel function exists for this system in the dissemination of genetic elements, notably antibiotic resistance genes, in Acinetobacter species. Currently the mechanism underlying this apparent genetic mobility is unknown. Multidrug resistant Acinetobacter baumannii is an increasingly problematic pathogen that can cause recurring infections. Sequencing of numerous plasmids from clinical isolates of A. baumannii revealed the presence of possible mobile modules: genes were found flanked by pairs of Xer recombination sites, called plasmid‐ dif (p dif ) sites. These modules have been identified in multiple otherwise unrelated plasmids and in different genetic contexts suggesting they are mobile elements. In most cases, the pairs of sites flanking a gene (or genes) are in inverted repeat, but there can be multiple modules per plasmid providing pairs of recombination sites that can be used for inversion or fusion/deletion reactions; as many as 16 p dif sites have been seen in a single plasmid. Similar modules including genes for surviving environmental toxins have also been found in strains of Acinetobacter Iwoffi isolated from permafrost cores; this suggests that these mobile modules are an ancient adaptation and not a novel response to antibiotic pressure. These modules bear all the hallmarks of mobile genetic elements, yet, their movement has never been directly observed to date. This review gives an overview of the current state of this novel research field. Article in Journal/Newspaper permafrost Wiley Online Library Molecular Microbiology 114 5 699 709
institution Open Polar
collection Wiley Online Library
op_collection_id crwiley
language English
description Abstract XerCD‐ dif site‐specific recombination is a well characterized system, found in most bacteria and archaea. Its role is resolution of chromosomal dimers that arise from homologous recombination. Xer‐mediated recombination is also used by several plasmids for multimer resolution to enhance stability and by some phage for integration into the chromosome. In the past decade, it has been hypothesized that an alternate and novel function exists for this system in the dissemination of genetic elements, notably antibiotic resistance genes, in Acinetobacter species. Currently the mechanism underlying this apparent genetic mobility is unknown. Multidrug resistant Acinetobacter baumannii is an increasingly problematic pathogen that can cause recurring infections. Sequencing of numerous plasmids from clinical isolates of A. baumannii revealed the presence of possible mobile modules: genes were found flanked by pairs of Xer recombination sites, called plasmid‐ dif (p dif ) sites. These modules have been identified in multiple otherwise unrelated plasmids and in different genetic contexts suggesting they are mobile elements. In most cases, the pairs of sites flanking a gene (or genes) are in inverted repeat, but there can be multiple modules per plasmid providing pairs of recombination sites that can be used for inversion or fusion/deletion reactions; as many as 16 p dif sites have been seen in a single plasmid. Similar modules including genes for surviving environmental toxins have also been found in strains of Acinetobacter Iwoffi isolated from permafrost cores; this suggests that these mobile modules are an ancient adaptation and not a novel response to antibiotic pressure. These modules bear all the hallmarks of mobile genetic elements, yet, their movement has never been directly observed to date. This review gives an overview of the current state of this novel research field.
format Article in Journal/Newspaper
author Balalovski, Phillip
Grainge, Ian
spellingShingle Balalovski, Phillip
Grainge, Ian
Mobilization of pdif modules in Acinetobacter: A novel mechanism for antibiotic resistance gene shuffling?
author_facet Balalovski, Phillip
Grainge, Ian
author_sort Balalovski, Phillip
title Mobilization of pdif modules in Acinetobacter: A novel mechanism for antibiotic resistance gene shuffling?
title_short Mobilization of pdif modules in Acinetobacter: A novel mechanism for antibiotic resistance gene shuffling?
title_full Mobilization of pdif modules in Acinetobacter: A novel mechanism for antibiotic resistance gene shuffling?
title_fullStr Mobilization of pdif modules in Acinetobacter: A novel mechanism for antibiotic resistance gene shuffling?
title_full_unstemmed Mobilization of pdif modules in Acinetobacter: A novel mechanism for antibiotic resistance gene shuffling?
title_sort mobilization of pdif modules in acinetobacter: a novel mechanism for antibiotic resistance gene shuffling?
publisher Wiley
publishDate 2020
url http://dx.doi.org/10.1111/mmi.14563
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fmmi.14563
https://onlinelibrary.wiley.com/doi/pdf/10.1111/mmi.14563
https://onlinelibrary.wiley.com/doi/full-xml/10.1111/mmi.14563
genre permafrost
genre_facet permafrost
op_source Molecular Microbiology
volume 114, issue 5, page 699-709
ISSN 0950-382X 1365-2958
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op_doi https://doi.org/10.1111/mmi.14563
container_title Molecular Microbiology
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container_issue 5
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