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Whole Cell Screen for Inhibitors of pH Homeostasis in Mycobacterium tuberculosis
Bacterial pathogens like Mycobacterium tuberculosis (Mtb) encounter acidic microenvironments in the host and must maintain their acid-base homeostasis to survive. A genetic screen identified two Mtb strains that cannot control intrabacterial pH (pH(IB)) in an acidic environment; infection with eithe...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728290/ https://www.ncbi.nlm.nih.gov/pubmed/23935911 http://dx.doi.org/10.1371/journal.pone.0068942 |
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author | Darby, Crystal M. Ingólfsson, Helgi I. Jiang, Xiuju Shen, Chun Sun, Mingna Zhao, Nan Burns, Kristin Liu, Gang Ehrt, Sabine Warren, J. David Anderson, Olaf S. Brickner, Steven J. Nathan, Carl |
author_facet | Darby, Crystal M. Ingólfsson, Helgi I. Jiang, Xiuju Shen, Chun Sun, Mingna Zhao, Nan Burns, Kristin Liu, Gang Ehrt, Sabine Warren, J. David Anderson, Olaf S. Brickner, Steven J. Nathan, Carl |
author_sort | Darby, Crystal M. |
collection | PubMed |
description | Bacterial pathogens like Mycobacterium tuberculosis (Mtb) encounter acidic microenvironments in the host and must maintain their acid-base homeostasis to survive. A genetic screen identified two Mtb strains that cannot control intrabacterial pH (pH(IB)) in an acidic environment; infection with either strain led to severe attenuation in mice. To search for additional proteins that Mtb requires to survive at low pH, we introduced a whole-cell screen for compounds that disrupt pH(IB), along with counter-screens that identify ionophores and membrane perturbors. Application of these methods to a natural product library identified four compounds of interest, one of which may inhibit novel pathway(s). This approach yields compounds that may lead to the identification of pathways that allow Mtb to survive in acidic environments, a setting in which Mtb is resistant to most of the drugs currently used to treat tuberculosis. |
format | Online Article Text |
id | pubmed-3728290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37282902013-08-09 Whole Cell Screen for Inhibitors of pH Homeostasis in Mycobacterium tuberculosis Darby, Crystal M. Ingólfsson, Helgi I. Jiang, Xiuju Shen, Chun Sun, Mingna Zhao, Nan Burns, Kristin Liu, Gang Ehrt, Sabine Warren, J. David Anderson, Olaf S. Brickner, Steven J. Nathan, Carl PLoS One Research Article Bacterial pathogens like Mycobacterium tuberculosis (Mtb) encounter acidic microenvironments in the host and must maintain their acid-base homeostasis to survive. A genetic screen identified two Mtb strains that cannot control intrabacterial pH (pH(IB)) in an acidic environment; infection with either strain led to severe attenuation in mice. To search for additional proteins that Mtb requires to survive at low pH, we introduced a whole-cell screen for compounds that disrupt pH(IB), along with counter-screens that identify ionophores and membrane perturbors. Application of these methods to a natural product library identified four compounds of interest, one of which may inhibit novel pathway(s). This approach yields compounds that may lead to the identification of pathways that allow Mtb to survive in acidic environments, a setting in which Mtb is resistant to most of the drugs currently used to treat tuberculosis. Public Library of Science 2013-07-30 /pmc/articles/PMC3728290/ /pubmed/23935911 http://dx.doi.org/10.1371/journal.pone.0068942 Text en © 2013 Darby et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Darby, Crystal M. Ingólfsson, Helgi I. Jiang, Xiuju Shen, Chun Sun, Mingna Zhao, Nan Burns, Kristin Liu, Gang Ehrt, Sabine Warren, J. David Anderson, Olaf S. Brickner, Steven J. Nathan, Carl Whole Cell Screen for Inhibitors of pH Homeostasis in Mycobacterium tuberculosis |
title | Whole Cell Screen for Inhibitors of pH Homeostasis in Mycobacterium tuberculosis
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title_full | Whole Cell Screen for Inhibitors of pH Homeostasis in Mycobacterium tuberculosis
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title_fullStr | Whole Cell Screen for Inhibitors of pH Homeostasis in Mycobacterium tuberculosis
|
title_full_unstemmed | Whole Cell Screen for Inhibitors of pH Homeostasis in Mycobacterium tuberculosis
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title_short | Whole Cell Screen for Inhibitors of pH Homeostasis in Mycobacterium tuberculosis
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title_sort | whole cell screen for inhibitors of ph homeostasis in mycobacterium tuberculosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728290/ https://www.ncbi.nlm.nih.gov/pubmed/23935911 http://dx.doi.org/10.1371/journal.pone.0068942 |
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