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The expression of aminoglycoside resistance genes in integron cassettes is not controlled by riboswitches
Regulation of gene expression is a key factor influencing the success of antimicrobial resistance determinants. A variety of determinants conferring resistance against aminoglycosides (Ag) are commonly found in clinically relevant bacteria, but whether their expression is regulated or not is controv...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410878/ https://www.ncbi.nlm.nih.gov/pubmed/35947699 http://dx.doi.org/10.1093/nar/gkac662 |
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author | Hipólito, Alberto García-Pastor, Lucía Blanco, Paula Trigo da Roza, Filipa Kieffer, Nicolas Vergara, Ester Jové, Thomas Álvarez, Julio Escudero, José Antonio |
author_facet | Hipólito, Alberto García-Pastor, Lucía Blanco, Paula Trigo da Roza, Filipa Kieffer, Nicolas Vergara, Ester Jové, Thomas Álvarez, Julio Escudero, José Antonio |
author_sort | Hipólito, Alberto |
collection | PubMed |
description | Regulation of gene expression is a key factor influencing the success of antimicrobial resistance determinants. A variety of determinants conferring resistance against aminoglycosides (Ag) are commonly found in clinically relevant bacteria, but whether their expression is regulated or not is controversial. The expression of several Ag resistance genes has been reported to be controlled by a riboswitch mechanism encoded in a conserved sequence. Yet this sequence corresponds to the integration site of an integron, a genetic platform that recruits genes of different functions, making the presence of such a riboswitch counterintuitive. We provide, for the first time, experimental evidence against the existence of such Ag-sensing riboswitch. We first tried to reproduce the induction of the well characterized aacA5 gene using its native genetic environment, but were unsuccessful. We then broadened our approach and analyzed the inducibility of all AgR genes encoded in integrons against a variety of antibiotics. We could not observe biologically relevant induction rates for any gene in the presence of several aminoglycosides. Instead, unrelated antibiotics produced mild but consistently higher increases in expression, that were the result of pleiotropic effects. Our findings rule out the riboswitch control of aminoglycoside resistance genes in integrons. |
format | Online Article Text |
id | pubmed-9410878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-94108782022-08-26 The expression of aminoglycoside resistance genes in integron cassettes is not controlled by riboswitches Hipólito, Alberto García-Pastor, Lucía Blanco, Paula Trigo da Roza, Filipa Kieffer, Nicolas Vergara, Ester Jové, Thomas Álvarez, Julio Escudero, José Antonio Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Regulation of gene expression is a key factor influencing the success of antimicrobial resistance determinants. A variety of determinants conferring resistance against aminoglycosides (Ag) are commonly found in clinically relevant bacteria, but whether their expression is regulated or not is controversial. The expression of several Ag resistance genes has been reported to be controlled by a riboswitch mechanism encoded in a conserved sequence. Yet this sequence corresponds to the integration site of an integron, a genetic platform that recruits genes of different functions, making the presence of such a riboswitch counterintuitive. We provide, for the first time, experimental evidence against the existence of such Ag-sensing riboswitch. We first tried to reproduce the induction of the well characterized aacA5 gene using its native genetic environment, but were unsuccessful. We then broadened our approach and analyzed the inducibility of all AgR genes encoded in integrons against a variety of antibiotics. We could not observe biologically relevant induction rates for any gene in the presence of several aminoglycosides. Instead, unrelated antibiotics produced mild but consistently higher increases in expression, that were the result of pleiotropic effects. Our findings rule out the riboswitch control of aminoglycoside resistance genes in integrons. Oxford University Press 2022-08-10 /pmc/articles/PMC9410878/ /pubmed/35947699 http://dx.doi.org/10.1093/nar/gkac662 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Gene regulation, Chromatin and Epigenetics Hipólito, Alberto García-Pastor, Lucía Blanco, Paula Trigo da Roza, Filipa Kieffer, Nicolas Vergara, Ester Jové, Thomas Álvarez, Julio Escudero, José Antonio The expression of aminoglycoside resistance genes in integron cassettes is not controlled by riboswitches |
title | The expression of aminoglycoside resistance genes in integron cassettes is not controlled by riboswitches |
title_full | The expression of aminoglycoside resistance genes in integron cassettes is not controlled by riboswitches |
title_fullStr | The expression of aminoglycoside resistance genes in integron cassettes is not controlled by riboswitches |
title_full_unstemmed | The expression of aminoglycoside resistance genes in integron cassettes is not controlled by riboswitches |
title_short | The expression of aminoglycoside resistance genes in integron cassettes is not controlled by riboswitches |
title_sort | expression of aminoglycoside resistance genes in integron cassettes is not controlled by riboswitches |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410878/ https://www.ncbi.nlm.nih.gov/pubmed/35947699 http://dx.doi.org/10.1093/nar/gkac662 |
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