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A Novel Small-Molecule Inhibitor of the Mycobacterium tuberculosis Demethylmenaquinone Methyltransferase MenG Is Bactericidal to Both Growing and Nutritionally Deprived Persister Cells

Active tuberculosis (TB) and latent Mycobacterium tuberculosis infection both require lengthy treatments to achieve durable cures. This problem has partly been attributable to the existence of nonreplicating M. tuberculosis “persisters” that are difficult to kill using conventional anti-TB treatment...

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Autores principales: Sukheja, Paridhi, Kumar, Pradeep, Mittal, Nisha, Li, Shao-Gang, Singleton, Eric, Russo, Riccardo, Perryman, Alexander L., Shrestha, Riju, Awasthi, Divya, Husain, Seema, Soteropoulos, Patricia, Brukh, Roman, Connell, Nancy, Freundlich, Joel S., Alland, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312080/
https://www.ncbi.nlm.nih.gov/pubmed/28196957
http://dx.doi.org/10.1128/mBio.02022-16
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author Sukheja, Paridhi
Kumar, Pradeep
Mittal, Nisha
Li, Shao-Gang
Singleton, Eric
Russo, Riccardo
Perryman, Alexander L.
Shrestha, Riju
Awasthi, Divya
Husain, Seema
Soteropoulos, Patricia
Brukh, Roman
Connell, Nancy
Freundlich, Joel S.
Alland, David
author_facet Sukheja, Paridhi
Kumar, Pradeep
Mittal, Nisha
Li, Shao-Gang
Singleton, Eric
Russo, Riccardo
Perryman, Alexander L.
Shrestha, Riju
Awasthi, Divya
Husain, Seema
Soteropoulos, Patricia
Brukh, Roman
Connell, Nancy
Freundlich, Joel S.
Alland, David
author_sort Sukheja, Paridhi
collection PubMed
description Active tuberculosis (TB) and latent Mycobacterium tuberculosis infection both require lengthy treatments to achieve durable cures. This problem has partly been attributable to the existence of nonreplicating M. tuberculosis “persisters” that are difficult to kill using conventional anti-TB treatments. Compounds that target the respiratory pathway have the potential to kill both replicating and persistent M. tuberculosis and shorten TB treatment, as this pathway is essential in both metabolic states. We developed a novel respiratory pathway-specific whole-cell screen to identify new respiration inhibitors. This screen identified the biphenyl amide GSK1733953A (DG70) as a likely respiration inhibitor. DG70 inhibited both clinical drug-susceptible and drug-resistant M. tuberculosis strains. Whole-genome sequencing of DG70-resistant colonies identified mutations in menG (rv0558), which is responsible for the final step in menaquinone biosynthesis and required for respiration. Overexpression of menG from wild-type and DG70-resistant isolates increased the DG70 MIC by 4× and 8× to 30×, respectively. Radiolabeling and high-resolution mass spectrometry studies confirmed that DG70 inhibited the final step in menaquinone biosynthesis. DG70 also inhibited oxygen utilization and ATP biosynthesis, which was reversed by external menaquinone supplementation. DG70 was bactericidal in actively replicating cultures and in a nutritionally deprived persistence model. DG70 was synergistic with the first-line TB drugs isoniazid, rifampin, and the respiratory inhibitor bedaquiline. The combination of DG70 and isoniazid completely sterilized cultures in the persistence model by day 10. These results suggest that MenG is a good therapeutic target and that compounds targeting MenG along with standard TB therapy have the potential to shorten TB treatment duration.
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spelling pubmed-53120802017-02-21 A Novel Small-Molecule Inhibitor of the Mycobacterium tuberculosis Demethylmenaquinone Methyltransferase MenG Is Bactericidal to Both Growing and Nutritionally Deprived Persister Cells Sukheja, Paridhi Kumar, Pradeep Mittal, Nisha Li, Shao-Gang Singleton, Eric Russo, Riccardo Perryman, Alexander L. Shrestha, Riju Awasthi, Divya Husain, Seema Soteropoulos, Patricia Brukh, Roman Connell, Nancy Freundlich, Joel S. Alland, David mBio Research Article Active tuberculosis (TB) and latent Mycobacterium tuberculosis infection both require lengthy treatments to achieve durable cures. This problem has partly been attributable to the existence of nonreplicating M. tuberculosis “persisters” that are difficult to kill using conventional anti-TB treatments. Compounds that target the respiratory pathway have the potential to kill both replicating and persistent M. tuberculosis and shorten TB treatment, as this pathway is essential in both metabolic states. We developed a novel respiratory pathway-specific whole-cell screen to identify new respiration inhibitors. This screen identified the biphenyl amide GSK1733953A (DG70) as a likely respiration inhibitor. DG70 inhibited both clinical drug-susceptible and drug-resistant M. tuberculosis strains. Whole-genome sequencing of DG70-resistant colonies identified mutations in menG (rv0558), which is responsible for the final step in menaquinone biosynthesis and required for respiration. Overexpression of menG from wild-type and DG70-resistant isolates increased the DG70 MIC by 4× and 8× to 30×, respectively. Radiolabeling and high-resolution mass spectrometry studies confirmed that DG70 inhibited the final step in menaquinone biosynthesis. DG70 also inhibited oxygen utilization and ATP biosynthesis, which was reversed by external menaquinone supplementation. DG70 was bactericidal in actively replicating cultures and in a nutritionally deprived persistence model. DG70 was synergistic with the first-line TB drugs isoniazid, rifampin, and the respiratory inhibitor bedaquiline. The combination of DG70 and isoniazid completely sterilized cultures in the persistence model by day 10. These results suggest that MenG is a good therapeutic target and that compounds targeting MenG along with standard TB therapy have the potential to shorten TB treatment duration. American Society for Microbiology 2017-02-14 /pmc/articles/PMC5312080/ /pubmed/28196957 http://dx.doi.org/10.1128/mBio.02022-16 Text en Copyright © 2017 Sukheja et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Sukheja, Paridhi
Kumar, Pradeep
Mittal, Nisha
Li, Shao-Gang
Singleton, Eric
Russo, Riccardo
Perryman, Alexander L.
Shrestha, Riju
Awasthi, Divya
Husain, Seema
Soteropoulos, Patricia
Brukh, Roman
Connell, Nancy
Freundlich, Joel S.
Alland, David
A Novel Small-Molecule Inhibitor of the Mycobacterium tuberculosis Demethylmenaquinone Methyltransferase MenG Is Bactericidal to Both Growing and Nutritionally Deprived Persister Cells
title A Novel Small-Molecule Inhibitor of the Mycobacterium tuberculosis Demethylmenaquinone Methyltransferase MenG Is Bactericidal to Both Growing and Nutritionally Deprived Persister Cells
title_full A Novel Small-Molecule Inhibitor of the Mycobacterium tuberculosis Demethylmenaquinone Methyltransferase MenG Is Bactericidal to Both Growing and Nutritionally Deprived Persister Cells
title_fullStr A Novel Small-Molecule Inhibitor of the Mycobacterium tuberculosis Demethylmenaquinone Methyltransferase MenG Is Bactericidal to Both Growing and Nutritionally Deprived Persister Cells
title_full_unstemmed A Novel Small-Molecule Inhibitor of the Mycobacterium tuberculosis Demethylmenaquinone Methyltransferase MenG Is Bactericidal to Both Growing and Nutritionally Deprived Persister Cells
title_short A Novel Small-Molecule Inhibitor of the Mycobacterium tuberculosis Demethylmenaquinone Methyltransferase MenG Is Bactericidal to Both Growing and Nutritionally Deprived Persister Cells
title_sort novel small-molecule inhibitor of the mycobacterium tuberculosis demethylmenaquinone methyltransferase meng is bactericidal to both growing and nutritionally deprived persister cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312080/
https://www.ncbi.nlm.nih.gov/pubmed/28196957
http://dx.doi.org/10.1128/mBio.02022-16
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