Literature DB >> 27672155

Inhibiting Mycobacterium tuberculosis within and without.

Stewart T Cole1.   

Abstract

Tuberculosis remains a scourge of global health with shrinking treatment options due to the spread of drug-resistant strains of Mycobacterium tuberculosis Intensive efforts have been made in the past 15 years to find leads for drug development so that better, more potent drugs inhibiting new targets could be produced and thus shorten treatment duration. Initial attempts focused on repurposing drugs that had been developed for other therapeutic areas but these agents did not meet their goals in clinical trials. Attempts to find new lead compounds employing target-based screens were unsuccessful as the leads were inactive against M. tuberculosis Greater success was achieved using phenotypic screening against live tubercle bacilli and this gave rise to the drugs bedaquiline, pretomanid and delamanid, currently in phase III trials. Subsequent phenotypic screens also uncovered new leads and targets but several of these targets proved to be promiscuous and inhibited by a variety of seemingly unrelated pharmacophores. This setback sparked an interest in alternative screening approaches that mimic the disease state more accurately. Foremost among these were cell-based screens, often involving macrophages, as these should reflect the bacterium's niche in the host more faithfully. A major advantage of this approach is its ability to uncover functions that are central to infection but not necessarily required for growth in vitro For instance, inhibition of virulence functions mediated by the ESX-1 secretion system severely attenuates intracellular M. tuberculosis, preventing intercellular spread and ultimately limiting tissue damage. Cell-based screens have highlighted the druggability of energy production via the electron transport chain and cholesterol metabolism. Here, I review the scientific progress and the pipeline, but warn against over-optimism due to the lack of industrial commitment for tuberculosis drug development and other socio-economic factors.This article is part of the themed issue 'The new bacteriology'.
© 2016 The Author(s).

Entities:  

Keywords:  antibiotics; drug discovery; drug resistance; phagocytes; tuberculosis

Mesh:

Substances:

Year:  2016        PMID: 27672155      PMCID: PMC5052748          DOI: 10.1098/rstb.2015.0506

Source DB:  PubMed          Journal:  Philos Trans R Soc Lond B Biol Sci        ISSN: 0962-8436            Impact factor:   6.237


  75 in total

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Review 2.  Target-based drug discovery: is something wrong?

Authors:  Frank Sams-Dodd
Journal:  Drug Discov Today       Date:  2005-01-15       Impact factor: 7.851

3.  Mycobacterium tuberculosis Differentially Activates cGAS- and Inflammasome-Dependent Intracellular Immune Responses through ESX-1.

Authors:  Ruth Wassermann; Muhammet F Gulen; Claudia Sala; Sonia Garcia Perin; Ye Lou; Jan Rybniker; Jonathan L Schmid-Burgk; Tobias Schmidt; Veit Hornung; Stewart T Cole; Andrea Ablasser
Journal:  Cell Host Microbe       Date:  2015-06-02       Impact factor: 21.023

Review 4.  Advances in the development of new tuberculosis drugs and treatment regimens.

Authors:  Alimuddin Zumla; Payam Nahid; Stewart T Cole
Journal:  Nat Rev Drug Discov       Date:  2013-05       Impact factor: 84.694

Review 5.  Why are membrane targets discovered by phenotypic screens and genome sequencing in Mycobacterium tuberculosis?

Authors:  Robert C Goldman
Journal:  Tuberculosis (Edinb)       Date:  2013-09-18       Impact factor: 3.131

Review 6.  Who will develop new antibacterial agents?

Authors:  Stewart T Cole
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2014-05-12       Impact factor: 6.237

Review 7.  High-content screening in infectious diseases.

Authors:  Priscille Brodin; Thierry Christophe
Journal:  Curr Opin Chem Biol       Date:  2011-06-20       Impact factor: 8.822

8.  The Type I IFN response to infection with Mycobacterium tuberculosis requires ESX-1-mediated secretion and contributes to pathogenesis.

Authors:  Sarah A Stanley; James E Johndrow; Paolo Manzanillo; Jeffery S Cox
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9.  Antiinfectives targeting enzymes and the proton motive force.

Authors:  Xinxin Feng; Wei Zhu; Lici A Schurig-Briccio; Steffen Lindert; Carolyn Shoen; Reese Hitchings; Jikun Li; Yang Wang; Noman Baig; Tianhui Zhou; Boo Kyung Kim; Dean C Crick; Michael Cynamon; J Andrew McCammon; Robert B Gennis; Eric Oldfield
Journal:  Proc Natl Acad Sci U S A       Date:  2015-12-07       Impact factor: 11.205

10.  Inhibition of mycolic acid transport across the Mycobacterium tuberculosis plasma membrane.

Authors:  Anna E Grzegorzewicz; Ha Pham; Vijay A K B Gundi; Michael S Scherman; Elton J North; Tamara Hess; Victoria Jones; Veronica Gruppo; Sarah E M Born; Jana Korduláková; Sivagami Sundaram Chavadi; Christophe Morisseau; Anne J Lenaerts; Richard E Lee; Michael R McNeil; Mary Jackson
Journal:  Nat Chem Biol       Date:  2012-02-19       Impact factor: 15.040

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  21 in total

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Authors:  Anthony M Cadena; Sarah M Fortune; JoAnne L Flynn
Journal:  Nat Rev Immunol       Date:  2017-07-24       Impact factor: 53.106

2.  Biochemical Investigation of Rv3404c from Mycobacterium tuberculosis.

Authors:  Murray M Dunsirn; James B Thoden; Michel Gilbert; Hazel M Holden
Journal:  Biochemistry       Date:  2017-07-14       Impact factor: 3.162

3.  The new bacteriology.

Authors:  Pascale Cossart; David Holden; Stephen Busby
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2016-11-05       Impact factor: 6.237

4.  Structural Variability of EspG Chaperones from Mycobacterial ESX-1, ESX-3, and ESX-5 Type VII Secretion Systems.

Authors:  Anne T Tuukkanen; Diana Freire; Sum Chan; Mark A Arbing; Robert W Reed; Timothy J Evans; Grasilda Zenkeviciutė; Jennifer Kim; Sara Kahng; Michael R Sawaya; Catherine T Chaton; Matthias Wilmanns; David Eisenberg; Annabel H A Parret; Konstantin V Korotkov
Journal:  J Mol Biol       Date:  2018-11-10       Impact factor: 5.469

5.  GSK2556286 Is a Novel Antitubercular Drug Candidate Effective In Vivo with the Potential To Shorten Tuberculosis Treatment.

Authors:  Eric L Nuermberger; Maria Santos Martínez-Martínez; Olalla Sanz; Beatriz Urones; Jorge Esquivias; Heena Soni; Rokeya Tasneen; Sandeep Tyagi; Si-Yang Li; Paul J Converse; Helena I Boshoff; Gregory T Robertson; Gurdyal S Besra; Katherine A Abrahams; Anna M Upton; Khisimuzi Mdluli; Gary W Boyle; Sam Turner; Nader Fotouhi; Nicholas C Cammack; Juan Miguel Siles; Marta Alonso; Jaime Escribano; Joel Lelievre; Joaquin Rullas-Trincado; Esther Pérez-Herrán; Robert H Bates; Gareth Maher-Edwards; David Barros; Lluís Ballell; Elena Jiménez
Journal:  Antimicrob Agents Chemother       Date:  2022-05-24       Impact factor: 5.938

6.  In Silico Screen and Structural Analysis Identifies Bacterial Kinase Inhibitors which Act with β-Lactams To Inhibit Mycobacterial Growth.

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Journal:  Mol Pharm       Date:  2018-10-18       Impact factor: 4.939

7.  The structure of glucose-1-phosphate thymidylyltransferase from Mycobacterium tuberculosis reveals the location of an essential magnesium ion in the RmlA-type enzymes.

Authors:  Haley A Brown; James B Thoden; Peter A Tipton; Hazel M Holden
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8.  Ex vivo expansion of alveolar macrophages with Mycobacterium tuberculosis from the resected lungs of patients with pulmonary tuberculosis.

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Journal:  PLoS One       Date:  2018-02-05       Impact factor: 3.240

9.  Acute Modulation of Mycobacterial Cell Envelope Biogenesis by Front-Line Tuberculosis Drugs.

Authors:  Frances P Rodriguez-Rivera; Xiaoxue Zhou; Julie A Theriot; Carolyn R Bertozzi
Journal:  Angew Chem Int Ed Engl       Date:  2018-04-14       Impact factor: 15.336

10.  Structure of a Wbl protein and implications for NO sensing by M. tuberculosis.

Authors:  Bassam K Kudhair; Andrea M Hounslow; Matthew D Rolfe; Jason C Crack; Debbie M Hunt; Roger S Buxton; Laura J Smith; Nick E Le Brun; Michael P Williamson; Jeffrey Green
Journal:  Nat Commun       Date:  2017-12-22       Impact factor: 14.919

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