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Comment on “the IS6 family, a clinically important group of insertion sequences including IS26” by Varani and co-authors

The insertion sequence IS26 has long been known to play a major role in the recruitment of antibiotic resistance genes into the mobile resistance gene pool of Gram-negative bacteria and IS26 also plays a major role in their subsequent broad dissemination. Related IS, IS431/257 and IS1216 are importa...

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Autor principal: Hall, Ruth M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722046/
https://www.ncbi.nlm.nih.gov/pubmed/34980247
http://dx.doi.org/10.1186/s13100-021-00257-9
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author Hall, Ruth M.
author_facet Hall, Ruth M.
author_sort Hall, Ruth M.
collection PubMed
description The insertion sequence IS26 has long been known to play a major role in the recruitment of antibiotic resistance genes into the mobile resistance gene pool of Gram-negative bacteria and IS26 also plays a major role in their subsequent broad dissemination. Related IS, IS431/257 and IS1216 are important in the same roles in Gram positive bacteria. However, until recently the properties of IS26 movement that could potentially explain this ability had not been explored. A much needed insight has come from our recent demonstration that IS26 uses a novel targeted mechanism that is conservative. The targeted conservative mechanism is much more efficient than the known replicative mechanism, which is now more accurately called copy-in. A recent review “The IS6 family, a clinically important group of insertion sequences including IS26” by Varani, He, Siguier, Ross and Chandler published in Mobile DNA has substantially misrepresented the recent studies on the targeted conservative mechanism and at the same time incorrectly implied that any mechanism established for IS26 can be assumed to apply to a range of IS that are at best very distantly related. A few of the most important issues are examined in this comment. Readers are advised to consult the original literature to check facts before drawing firm conclusions.
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spelling pubmed-87220462022-01-06 Comment on “the IS6 family, a clinically important group of insertion sequences including IS26” by Varani and co-authors Hall, Ruth M. Mob DNA Letter to the Editor The insertion sequence IS26 has long been known to play a major role in the recruitment of antibiotic resistance genes into the mobile resistance gene pool of Gram-negative bacteria and IS26 also plays a major role in their subsequent broad dissemination. Related IS, IS431/257 and IS1216 are important in the same roles in Gram positive bacteria. However, until recently the properties of IS26 movement that could potentially explain this ability had not been explored. A much needed insight has come from our recent demonstration that IS26 uses a novel targeted mechanism that is conservative. The targeted conservative mechanism is much more efficient than the known replicative mechanism, which is now more accurately called copy-in. A recent review “The IS6 family, a clinically important group of insertion sequences including IS26” by Varani, He, Siguier, Ross and Chandler published in Mobile DNA has substantially misrepresented the recent studies on the targeted conservative mechanism and at the same time incorrectly implied that any mechanism established for IS26 can be assumed to apply to a range of IS that are at best very distantly related. A few of the most important issues are examined in this comment. Readers are advised to consult the original literature to check facts before drawing firm conclusions. BioMed Central 2022-01-03 /pmc/articles/PMC8722046/ /pubmed/34980247 http://dx.doi.org/10.1186/s13100-021-00257-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Letter to the Editor
Hall, Ruth M.
Comment on “the IS6 family, a clinically important group of insertion sequences including IS26” by Varani and co-authors
title Comment on “the IS6 family, a clinically important group of insertion sequences including IS26” by Varani and co-authors
title_full Comment on “the IS6 family, a clinically important group of insertion sequences including IS26” by Varani and co-authors
title_fullStr Comment on “the IS6 family, a clinically important group of insertion sequences including IS26” by Varani and co-authors
title_full_unstemmed Comment on “the IS6 family, a clinically important group of insertion sequences including IS26” by Varani and co-authors
title_short Comment on “the IS6 family, a clinically important group of insertion sequences including IS26” by Varani and co-authors
title_sort comment on “the is6 family, a clinically important group of insertion sequences including is26” by varani and co-authors
topic Letter to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722046/
https://www.ncbi.nlm.nih.gov/pubmed/34980247
http://dx.doi.org/10.1186/s13100-021-00257-9
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