期刊名称：Proceedings of the National Academy of Sciences
印刷版ISSN：0027-8424
电子版ISSN：1091-6490
出版年度：2018
卷号：115
期号：7
页码：1599-1604
DOI：10.1073/pnas.1721545115
语种：English
出版社：The National Academy of Sciences of the United States of America
摘要：Worldwide control of the tuberculosis (TB) epidemic has not been achieved, and the latest statistics show that the TB problem might be more endemic than previously thought. Although drugs and a TB vaccine are available, TB eradication faces the challenges of increasing occurrences of multidrug-resistant and extensively drug-resistant Mycobacterium tuberculosis ( Mtb ) strains. To forestall this trend, the development of drugs targeting novel pathways is actively pursued. Recently, enzymes of the electron transport chain (ETC) have been determined to be the targets of potent antimycobacterial drugs such as bedaquiline. We focused on the three NADH dehydrogenases (Ndh, NdhA, and Nuo) of the Mtb ETC with the purpose of defining their role and essentiality in Mtb . Each NADH dehydrogenase was deleted in both virulent and BSL2-approved Mtb strains, from which the double knockouts Δ ndh Δ nuoAN and Δ ndhA Δ nuoAN were constructed. The Δ ndh Δ ndhA double knockout could not be obtained, suggesting that at least one type II NADH dehydrogenase is required for Mtb growth. Δ ndh and Δ ndh Δ nuoAN showed growth defects in vitro and in vivo, susceptibility to oxidative stress, and redox alterations, while the phenotypes of Δ ndhA, Δ nuoAN , and Δ ndhA Δ nuoAN were similar to the parental strain. Interestingly, although Δ nuoAN had no phenotype in vivo, Δ ndh Δ nuoAN was the most severely attenuated strain in mice, suggesting a key role for Nuo in vivo when Ndh is absent. We conclude that Ndh is the main NADH dehydrogenase of Mtb and that compounds that could target both Ndh and Nuo would be good candidates for TB drug development.
