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Evolved resistance to colistin and its loss due to genetic reversion in Pseudomonas aeruginosa

The increased reliance on colistin for treating multidrug-resistant Gram-negative bacterial infections has resulted in the emergence of colistin-resistant Pseudomonas aeruginosa. We attempted to identify genetic contributors to colistin resistance in vitro evolved isogenic colistin-resistant and -su...

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Autores principales: Lee, Ji-Young, Park, Young Kyoung, Chung, Eun Seon, Na, In Young, Ko, Kwan Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4858706/
https://www.ncbi.nlm.nih.gov/pubmed/27150578
http://dx.doi.org/10.1038/srep25543
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author Lee, Ji-Young
Park, Young Kyoung
Chung, Eun Seon
Na, In Young
Ko, Kwan Soo
author_facet Lee, Ji-Young
Park, Young Kyoung
Chung, Eun Seon
Na, In Young
Ko, Kwan Soo
author_sort Lee, Ji-Young
collection PubMed
description The increased reliance on colistin for treating multidrug-resistant Gram-negative bacterial infections has resulted in the emergence of colistin-resistant Pseudomonas aeruginosa. We attempted to identify genetic contributors to colistin resistance in vitro evolved isogenic colistin-resistant and -susceptible strains of two P. aeruginosa lineages (P5 and P155). Their evolutionary paths to acquisition and loss of colistin resistance were also tracked. Comparative genomic analysis revealed 13 and five colistin resistance determinants in the P5 and P155 lineages, respectively. Lipid A in colistin-resistant mutants was modified through the addition of 4-amino-L-arabinose; this modification was absent in colistin-susceptible revertant strains. Many amino acid substitutions that emerged during the acquisition of colistin resistance were reversed in colistin-susceptible revertants. We demonstrated that evolved colistin resistance in P. aeruginosa was mediated by a complicated regulatory network that likely emerges through diverse genetic alterations. Colistin-resistant P. aeruginosa became susceptible to the colistin upon its withdrawal because of genetic reversion. The mechanisms through which P. aeruginosa acquires and loses colistin resistance have implications on the treatment options that can be applied against P. aeruginosa infections, with respect to improving bactericidal efficacy and preventing further resistance to antibiotics.
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spelling pubmed-48587062016-05-19 Evolved resistance to colistin and its loss due to genetic reversion in Pseudomonas aeruginosa Lee, Ji-Young Park, Young Kyoung Chung, Eun Seon Na, In Young Ko, Kwan Soo Sci Rep Article The increased reliance on colistin for treating multidrug-resistant Gram-negative bacterial infections has resulted in the emergence of colistin-resistant Pseudomonas aeruginosa. We attempted to identify genetic contributors to colistin resistance in vitro evolved isogenic colistin-resistant and -susceptible strains of two P. aeruginosa lineages (P5 and P155). Their evolutionary paths to acquisition and loss of colistin resistance were also tracked. Comparative genomic analysis revealed 13 and five colistin resistance determinants in the P5 and P155 lineages, respectively. Lipid A in colistin-resistant mutants was modified through the addition of 4-amino-L-arabinose; this modification was absent in colistin-susceptible revertant strains. Many amino acid substitutions that emerged during the acquisition of colistin resistance were reversed in colistin-susceptible revertants. We demonstrated that evolved colistin resistance in P. aeruginosa was mediated by a complicated regulatory network that likely emerges through diverse genetic alterations. Colistin-resistant P. aeruginosa became susceptible to the colistin upon its withdrawal because of genetic reversion. The mechanisms through which P. aeruginosa acquires and loses colistin resistance have implications on the treatment options that can be applied against P. aeruginosa infections, with respect to improving bactericidal efficacy and preventing further resistance to antibiotics. Nature Publishing Group 2016-05-06 /pmc/articles/PMC4858706/ /pubmed/27150578 http://dx.doi.org/10.1038/srep25543 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Lee, Ji-Young
Park, Young Kyoung
Chung, Eun Seon
Na, In Young
Ko, Kwan Soo
Evolved resistance to colistin and its loss due to genetic reversion in Pseudomonas aeruginosa
title Evolved resistance to colistin and its loss due to genetic reversion in Pseudomonas aeruginosa
title_full Evolved resistance to colistin and its loss due to genetic reversion in Pseudomonas aeruginosa
title_fullStr Evolved resistance to colistin and its loss due to genetic reversion in Pseudomonas aeruginosa
title_full_unstemmed Evolved resistance to colistin and its loss due to genetic reversion in Pseudomonas aeruginosa
title_short Evolved resistance to colistin and its loss due to genetic reversion in Pseudomonas aeruginosa
title_sort evolved resistance to colistin and its loss due to genetic reversion in pseudomonas aeruginosa
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4858706/
https://www.ncbi.nlm.nih.gov/pubmed/27150578
http://dx.doi.org/10.1038/srep25543
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