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Small Klebsiella pneumoniae Plasmids: Neglected Contributors to Antibiotic Resistance
Klebsiella pneumoniae is the causative agent of community- and, more commonly, hospital-acquired infections. Infections caused by this bacterium have recently become more dangerous due to the acquisition of multiresistance to antibiotics and the rise of hypervirulent variants. Plasmids usually carry...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764390/ https://www.ncbi.nlm.nih.gov/pubmed/31616398 http://dx.doi.org/10.3389/fmicb.2019.02182 |
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author | Ramirez, Maria S. Iriarte, Andrés Reyes-Lamothe, Rodrigo Sherratt, David J. Tolmasky, Marcelo E. |
author_facet | Ramirez, Maria S. Iriarte, Andrés Reyes-Lamothe, Rodrigo Sherratt, David J. Tolmasky, Marcelo E. |
author_sort | Ramirez, Maria S. |
collection | PubMed |
description | Klebsiella pneumoniae is the causative agent of community- and, more commonly, hospital-acquired infections. Infections caused by this bacterium have recently become more dangerous due to the acquisition of multiresistance to antibiotics and the rise of hypervirulent variants. Plasmids usually carry genes coding for resistance to antibiotics or virulence factors, and the recent sequence of complete K. pneumoniae genomes showed that most strains harbor many of them. Unlike large plasmids, small, usually high copy number plasmids, did not attract much attention. However, these plasmids may include genes coding for specialized functions, such as antibiotic resistance, that can be expressed at high levels due to gene dosage effect. These genes may be part of mobile elements that not only facilitate their dissemination but also participate in plasmid evolution. Furthermore, high copy number plasmids may also play a role in evolution by allowing coexistence of mutated and non-mutated versions of a gene, which helps to circumvent the constraints imposed by trade-offs after certain genes mutate. Most K. pneumoniae plasmids 25-kb or smaller replicate by the ColE1-type mechanism and many of them are mobilizable. The transposon Tn1331 and derivatives were found in a high percentage of these plasmids. Another transposon that was found in representatives of this group is the bla(KPC)-containing Tn4401. Common resistance determinants found in these plasmids were aac(6′)-Ib and genes coding for β-lactamases including carbapenemases. |
format | Online Article Text |
id | pubmed-6764390 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67643902019-10-15 Small Klebsiella pneumoniae Plasmids: Neglected Contributors to Antibiotic Resistance Ramirez, Maria S. Iriarte, Andrés Reyes-Lamothe, Rodrigo Sherratt, David J. Tolmasky, Marcelo E. Front Microbiol Microbiology Klebsiella pneumoniae is the causative agent of community- and, more commonly, hospital-acquired infections. Infections caused by this bacterium have recently become more dangerous due to the acquisition of multiresistance to antibiotics and the rise of hypervirulent variants. Plasmids usually carry genes coding for resistance to antibiotics or virulence factors, and the recent sequence of complete K. pneumoniae genomes showed that most strains harbor many of them. Unlike large plasmids, small, usually high copy number plasmids, did not attract much attention. However, these plasmids may include genes coding for specialized functions, such as antibiotic resistance, that can be expressed at high levels due to gene dosage effect. These genes may be part of mobile elements that not only facilitate their dissemination but also participate in plasmid evolution. Furthermore, high copy number plasmids may also play a role in evolution by allowing coexistence of mutated and non-mutated versions of a gene, which helps to circumvent the constraints imposed by trade-offs after certain genes mutate. Most K. pneumoniae plasmids 25-kb or smaller replicate by the ColE1-type mechanism and many of them are mobilizable. The transposon Tn1331 and derivatives were found in a high percentage of these plasmids. Another transposon that was found in representatives of this group is the bla(KPC)-containing Tn4401. Common resistance determinants found in these plasmids were aac(6′)-Ib and genes coding for β-lactamases including carbapenemases. Frontiers Media S.A. 2019-09-20 /pmc/articles/PMC6764390/ /pubmed/31616398 http://dx.doi.org/10.3389/fmicb.2019.02182 Text en Copyright © 2019 Ramirez, Iriarte, Reyes-Lamothe, Sherratt and Tolmasky. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Ramirez, Maria S. Iriarte, Andrés Reyes-Lamothe, Rodrigo Sherratt, David J. Tolmasky, Marcelo E. Small Klebsiella pneumoniae Plasmids: Neglected Contributors to Antibiotic Resistance |
title | Small Klebsiella pneumoniae Plasmids: Neglected Contributors to Antibiotic Resistance |
title_full | Small Klebsiella pneumoniae Plasmids: Neglected Contributors to Antibiotic Resistance |
title_fullStr | Small Klebsiella pneumoniae Plasmids: Neglected Contributors to Antibiotic Resistance |
title_full_unstemmed | Small Klebsiella pneumoniae Plasmids: Neglected Contributors to Antibiotic Resistance |
title_short | Small Klebsiella pneumoniae Plasmids: Neglected Contributors to Antibiotic Resistance |
title_sort | small klebsiella pneumoniae plasmids: neglected contributors to antibiotic resistance |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764390/ https://www.ncbi.nlm.nih.gov/pubmed/31616398 http://dx.doi.org/10.3389/fmicb.2019.02182 |
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