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Novel gene similar to nitrite reductase (NO forming) plays potentially important role in the latency of tuberculosis
The development of the latent phenotype of Mycobacterium tuberculosis (Mtb) in the human lungs is the major hurdle to eradicate Tuberculosis. We recently reported that exposure to nitrite (10 mM) for six days under in vitro aerobic conditions completely transforms the bacilli into a viable but non-c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494734/ https://www.ncbi.nlm.nih.gov/pubmed/34615967 http://dx.doi.org/10.1038/s41598-021-99346-1 |
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author | Agrawal, Sonia Gample, Suwarna Yeware, Amar Sarkar, Dhiman |
author_facet | Agrawal, Sonia Gample, Suwarna Yeware, Amar Sarkar, Dhiman |
author_sort | Agrawal, Sonia |
collection | PubMed |
description | The development of the latent phenotype of Mycobacterium tuberculosis (Mtb) in the human lungs is the major hurdle to eradicate Tuberculosis. We recently reported that exposure to nitrite (10 mM) for six days under in vitro aerobic conditions completely transforms the bacilli into a viable but non-cultivable phenotype. Herein, we show that nitrite (beyond 5 mM) treated Mtb produces nitric oxide (NO) within the cell in a dose-dependent manner. Our search for the conserved sequence of NO synthesizing enzyme in the bacterial system identified MRA2164 and MRA0854 genes, of which the former was found to be significantly up regulated after nitrite exposure. In addition, the purified recombinant MRA2164 protein shows significant nitrite dependent NO synthesizing activity. The knockdown of the MRA2164 gene at mRNA level expression resulted in a significantly reduced NO level compared to the wild type bacilli with a simultaneous return of its replicative capability. Therefore, this study first time reports that nitrite induces dormancy in Mtb cells through induced expression of the MRA2164 gene and productions of NO as a mechanism for maintaining non-replicative stage in Mtb. This observation could help to control the Tuberculosis disease, especially the latent phenotype of the bacilli. |
format | Online Article Text |
id | pubmed-8494734 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84947342021-10-07 Novel gene similar to nitrite reductase (NO forming) plays potentially important role in the latency of tuberculosis Agrawal, Sonia Gample, Suwarna Yeware, Amar Sarkar, Dhiman Sci Rep Article The development of the latent phenotype of Mycobacterium tuberculosis (Mtb) in the human lungs is the major hurdle to eradicate Tuberculosis. We recently reported that exposure to nitrite (10 mM) for six days under in vitro aerobic conditions completely transforms the bacilli into a viable but non-cultivable phenotype. Herein, we show that nitrite (beyond 5 mM) treated Mtb produces nitric oxide (NO) within the cell in a dose-dependent manner. Our search for the conserved sequence of NO synthesizing enzyme in the bacterial system identified MRA2164 and MRA0854 genes, of which the former was found to be significantly up regulated after nitrite exposure. In addition, the purified recombinant MRA2164 protein shows significant nitrite dependent NO synthesizing activity. The knockdown of the MRA2164 gene at mRNA level expression resulted in a significantly reduced NO level compared to the wild type bacilli with a simultaneous return of its replicative capability. Therefore, this study first time reports that nitrite induces dormancy in Mtb cells through induced expression of the MRA2164 gene and productions of NO as a mechanism for maintaining non-replicative stage in Mtb. This observation could help to control the Tuberculosis disease, especially the latent phenotype of the bacilli. Nature Publishing Group UK 2021-10-06 /pmc/articles/PMC8494734/ /pubmed/34615967 http://dx.doi.org/10.1038/s41598-021-99346-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Agrawal, Sonia Gample, Suwarna Yeware, Amar Sarkar, Dhiman Novel gene similar to nitrite reductase (NO forming) plays potentially important role in the latency of tuberculosis |
title | Novel gene similar to nitrite reductase (NO forming) plays potentially important role in the latency of tuberculosis |
title_full | Novel gene similar to nitrite reductase (NO forming) plays potentially important role in the latency of tuberculosis |
title_fullStr | Novel gene similar to nitrite reductase (NO forming) plays potentially important role in the latency of tuberculosis |
title_full_unstemmed | Novel gene similar to nitrite reductase (NO forming) plays potentially important role in the latency of tuberculosis |
title_short | Novel gene similar to nitrite reductase (NO forming) plays potentially important role in the latency of tuberculosis |
title_sort | novel gene similar to nitrite reductase (no forming) plays potentially important role in the latency of tuberculosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494734/ https://www.ncbi.nlm.nih.gov/pubmed/34615967 http://dx.doi.org/10.1038/s41598-021-99346-1 |
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