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Modulation of Bacterial Multidrug Resistance Efflux Pumps of the Major Facilitator Superfamily

Bacterial infections pose a serious public health concern, especially when an infectious disease has a multidrug resistant causative agent. Such multidrug resistant bacteria can compromise the clinical utility of major chemotherapeutic antimicrobial agents. Drug and multidrug resistant bacteria harb...

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Detalles Bibliográficos
Autores principales: Kumar, Sanath, Mukherjee, Mun Mun, Varela, Manuel F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4347946/
https://www.ncbi.nlm.nih.gov/pubmed/25750934
http://dx.doi.org/10.1155/2013/204141
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author Kumar, Sanath
Mukherjee, Mun Mun
Varela, Manuel F.
author_facet Kumar, Sanath
Mukherjee, Mun Mun
Varela, Manuel F.
author_sort Kumar, Sanath
collection PubMed
description Bacterial infections pose a serious public health concern, especially when an infectious disease has a multidrug resistant causative agent. Such multidrug resistant bacteria can compromise the clinical utility of major chemotherapeutic antimicrobial agents. Drug and multidrug resistant bacteria harbor several distinct molecular mechanisms for resistance. Bacterial antimicrobial agent efflux pumps represent a major mechanism of clinical resistance. The major facilitator superfamily (MFS) is one of the largest groups of solute transporters to date and includes a significant number of bacterial drug and multidrug efflux pumps. We review recent work on the modulation of multidrug efflux pumps, paying special attention to those transporters belonging primarily to the MFS.
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spelling pubmed-43479462015-03-04 Modulation of Bacterial Multidrug Resistance Efflux Pumps of the Major Facilitator Superfamily Kumar, Sanath Mukherjee, Mun Mun Varela, Manuel F. Int J Bacteriol Review Article Bacterial infections pose a serious public health concern, especially when an infectious disease has a multidrug resistant causative agent. Such multidrug resistant bacteria can compromise the clinical utility of major chemotherapeutic antimicrobial agents. Drug and multidrug resistant bacteria harbor several distinct molecular mechanisms for resistance. Bacterial antimicrobial agent efflux pumps represent a major mechanism of clinical resistance. The major facilitator superfamily (MFS) is one of the largest groups of solute transporters to date and includes a significant number of bacterial drug and multidrug efflux pumps. We review recent work on the modulation of multidrug efflux pumps, paying special attention to those transporters belonging primarily to the MFS. Hindawi Publishing Corporation 2013 2013-12-05 /pmc/articles/PMC4347946/ /pubmed/25750934 http://dx.doi.org/10.1155/2013/204141 Text en Copyright © 2013 Sanath Kumar et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Kumar, Sanath
Mukherjee, Mun Mun
Varela, Manuel F.
Modulation of Bacterial Multidrug Resistance Efflux Pumps of the Major Facilitator Superfamily
title Modulation of Bacterial Multidrug Resistance Efflux Pumps of the Major Facilitator Superfamily
title_full Modulation of Bacterial Multidrug Resistance Efflux Pumps of the Major Facilitator Superfamily
title_fullStr Modulation of Bacterial Multidrug Resistance Efflux Pumps of the Major Facilitator Superfamily
title_full_unstemmed Modulation of Bacterial Multidrug Resistance Efflux Pumps of the Major Facilitator Superfamily
title_short Modulation of Bacterial Multidrug Resistance Efflux Pumps of the Major Facilitator Superfamily
title_sort modulation of bacterial multidrug resistance efflux pumps of the major facilitator superfamily
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4347946/
https://www.ncbi.nlm.nih.gov/pubmed/25750934
http://dx.doi.org/10.1155/2013/204141
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