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Characterization of Pseudomonas aeruginosa with discrepant carbapenem susceptibility profile

Pseudomonas aeruginosa is the most common nosocomial pathogen, notorious for its multidrug resistance and causes life threatening infections. Carbapenems were considered as the last resort of drugs for the treatment of multi drug resistant P. aeruginosa infections. The emergence of resistance to car...

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Autores principales: Pragasam, Agila K., Raghanivedha, M., Anandan, Shalini, Veeraraghavan, Balaji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4765188/
https://www.ncbi.nlm.nih.gov/pubmed/26911874
http://dx.doi.org/10.1186/s12941-016-0127-3
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author Pragasam, Agila K.
Raghanivedha, M.
Anandan, Shalini
Veeraraghavan, Balaji
author_facet Pragasam, Agila K.
Raghanivedha, M.
Anandan, Shalini
Veeraraghavan, Balaji
author_sort Pragasam, Agila K.
collection PubMed
description Pseudomonas aeruginosa is the most common nosocomial pathogen, notorious for its multidrug resistance and causes life threatening infections. Carbapenems were considered as the last resort of drugs for the treatment of multi drug resistant P. aeruginosa infections. The emergence of resistance to carbapenems limits its use for treatment. Unlike other organisms, in P. aeruginosa intrinsic/chromosomal mediated resistance mechanisms plays a major role for carbapenem resistance rather than the carbapenemases. Carbapenemase producing organisms becomes resistant to both imipenem and meropenem. However, in our clinical settings, we have observed rare carbapenem resistant phenotypes such as imipenem resistant but meropenem susceptible (IRMS) and meropenem resistant but imipenem susceptible (MRIS) phenotypes. Thus we have chosen these rare phenotypes to look for the respective resistance mechanisms by phenotypic and molecular methods. From this study we found that, IRMS is primarily due to the mutations across various regions in the loops of oprD gene and MRIS is due to the over expression of mexAB efflux pumps. This study results confirms that, this rare phenotypes are due to the intrinsic/chromosomal mediated mechanisms, which occurred due to the antibiotic selection pressure. This study also provided data concerning alterations in outer membrane permeability which is often associated with the increased levels of antibiotic efflux. Consequently, this study provided the prevalence of the various resistance mechanisms that have deployed by the organism to resist antibiotics through different phenotypes.
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spelling pubmed-47651882016-02-25 Characterization of Pseudomonas aeruginosa with discrepant carbapenem susceptibility profile Pragasam, Agila K. Raghanivedha, M. Anandan, Shalini Veeraraghavan, Balaji Ann Clin Microbiol Antimicrob Short Report Pseudomonas aeruginosa is the most common nosocomial pathogen, notorious for its multidrug resistance and causes life threatening infections. Carbapenems were considered as the last resort of drugs for the treatment of multi drug resistant P. aeruginosa infections. The emergence of resistance to carbapenems limits its use for treatment. Unlike other organisms, in P. aeruginosa intrinsic/chromosomal mediated resistance mechanisms plays a major role for carbapenem resistance rather than the carbapenemases. Carbapenemase producing organisms becomes resistant to both imipenem and meropenem. However, in our clinical settings, we have observed rare carbapenem resistant phenotypes such as imipenem resistant but meropenem susceptible (IRMS) and meropenem resistant but imipenem susceptible (MRIS) phenotypes. Thus we have chosen these rare phenotypes to look for the respective resistance mechanisms by phenotypic and molecular methods. From this study we found that, IRMS is primarily due to the mutations across various regions in the loops of oprD gene and MRIS is due to the over expression of mexAB efflux pumps. This study results confirms that, this rare phenotypes are due to the intrinsic/chromosomal mediated mechanisms, which occurred due to the antibiotic selection pressure. This study also provided data concerning alterations in outer membrane permeability which is often associated with the increased levels of antibiotic efflux. Consequently, this study provided the prevalence of the various resistance mechanisms that have deployed by the organism to resist antibiotics through different phenotypes. BioMed Central 2016-02-24 /pmc/articles/PMC4765188/ /pubmed/26911874 http://dx.doi.org/10.1186/s12941-016-0127-3 Text en © Pragasam et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Pragasam, Agila K.
Raghanivedha, M.
Anandan, Shalini
Veeraraghavan, Balaji
Characterization of Pseudomonas aeruginosa with discrepant carbapenem susceptibility profile
title Characterization of Pseudomonas aeruginosa with discrepant carbapenem susceptibility profile
title_full Characterization of Pseudomonas aeruginosa with discrepant carbapenem susceptibility profile
title_fullStr Characterization of Pseudomonas aeruginosa with discrepant carbapenem susceptibility profile
title_full_unstemmed Characterization of Pseudomonas aeruginosa with discrepant carbapenem susceptibility profile
title_short Characterization of Pseudomonas aeruginosa with discrepant carbapenem susceptibility profile
title_sort characterization of pseudomonas aeruginosa with discrepant carbapenem susceptibility profile
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4765188/
https://www.ncbi.nlm.nih.gov/pubmed/26911874
http://dx.doi.org/10.1186/s12941-016-0127-3
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