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A Novel Antioxidant Gene from Mycobacterium tuberculosis

Among the major antimicrobial products of macrophages are reactive intermediates of the oxidation of nitrogen (RNI) and the reduction of oxygen (ROI). Selection of recombinants in acidified nitrite led to the cloning of a novel gene, noxR1, from a pathogenic clinical isolate of Mycobacterium tubercu...

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Detalles Bibliográficos
Autores principales: Ehrt, Sabine, Shiloh, Michael U., Ruan, Jia, Choi, Michael, Gunzburg, Stuart, Nathan, Carl, Xie, Qiao-wen, Riley, Lee W.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2199150/
https://www.ncbi.nlm.nih.gov/pubmed/9382887
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author Ehrt, Sabine
Shiloh, Michael U.
Ruan, Jia
Choi, Michael
Gunzburg, Stuart
Nathan, Carl
Xie, Qiao-wen
Riley, Lee W.
author_facet Ehrt, Sabine
Shiloh, Michael U.
Ruan, Jia
Choi, Michael
Gunzburg, Stuart
Nathan, Carl
Xie, Qiao-wen
Riley, Lee W.
author_sort Ehrt, Sabine
collection PubMed
description Among the major antimicrobial products of macrophages are reactive intermediates of the oxidation of nitrogen (RNI) and the reduction of oxygen (ROI). Selection of recombinants in acidified nitrite led to the cloning of a novel gene, noxR1, from a pathogenic clinical isolate of Mycobacterium tuberculosis. Expression of noxR1 conferred upon Escherichia coli and Mycobacterium smegmatis enhanced ability to resist RNI and ROI, whether the bacteria were exposed to exogenous compounds in medium or to endogenous products in macrophages. These studies provide the first identification of an RNI resistance mechanism in mycobacteria, point to a new mechanism for resistance to ROI, and raise the possibility that inhibition of the noxR1 pathway might enhance the ability of macrophages to control tuberculosis.
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spelling pubmed-21991502008-04-16 A Novel Antioxidant Gene from Mycobacterium tuberculosis Ehrt, Sabine Shiloh, Michael U. Ruan, Jia Choi, Michael Gunzburg, Stuart Nathan, Carl Xie, Qiao-wen Riley, Lee W. J Exp Med Article Among the major antimicrobial products of macrophages are reactive intermediates of the oxidation of nitrogen (RNI) and the reduction of oxygen (ROI). Selection of recombinants in acidified nitrite led to the cloning of a novel gene, noxR1, from a pathogenic clinical isolate of Mycobacterium tuberculosis. Expression of noxR1 conferred upon Escherichia coli and Mycobacterium smegmatis enhanced ability to resist RNI and ROI, whether the bacteria were exposed to exogenous compounds in medium or to endogenous products in macrophages. These studies provide the first identification of an RNI resistance mechanism in mycobacteria, point to a new mechanism for resistance to ROI, and raise the possibility that inhibition of the noxR1 pathway might enhance the ability of macrophages to control tuberculosis. The Rockefeller University Press 1997-12-01 /pmc/articles/PMC2199150/ /pubmed/9382887 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Ehrt, Sabine
Shiloh, Michael U.
Ruan, Jia
Choi, Michael
Gunzburg, Stuart
Nathan, Carl
Xie, Qiao-wen
Riley, Lee W.
A Novel Antioxidant Gene from Mycobacterium tuberculosis
title A Novel Antioxidant Gene from Mycobacterium tuberculosis
title_full A Novel Antioxidant Gene from Mycobacterium tuberculosis
title_fullStr A Novel Antioxidant Gene from Mycobacterium tuberculosis
title_full_unstemmed A Novel Antioxidant Gene from Mycobacterium tuberculosis
title_short A Novel Antioxidant Gene from Mycobacterium tuberculosis
title_sort novel antioxidant gene from mycobacterium tuberculosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2199150/
https://www.ncbi.nlm.nih.gov/pubmed/9382887
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