Literature DB >> 29458544

Antimicrobial activity against Mycobacterium tuberculosis under in vitro lipid-rich dormancy conditions.

Diana Angelica Aguilar-Ayala1,2, Margo Cnockaert1, Peter Vandamme1, Juan Carlos Palomino1, Anandi Martin1,3, Jorge Gonzalez-Y-Merchand2.   

Abstract

Although tuberculosis treatment is dependent on drug-susceptibility testing (DST) and molecular drug-resistance detection, treatment failure and relapse remain a challenge. This could be partially due to the emergence of antibiotic-tolerant dormant mycobacteria, where host lipids have been shown to play an important role. This study evaluated the susceptibility of Mycobacterium tuberculosis to two antibiotic combinations - rifampicin, moxifloxacin, amikacin and metronidazole (RIF-MXF-AMK-MTZ), and rifampicin, moxifloxacin, amikacin and pretomanid (RIF-MXF-AMK-PA) - in a lipid-rich dormancy model. Although their effectiveness in in vitro cultures with dextrose as a carbon source has been proved, we observed that none of the antibiotic mixtures were bactericidal in the presence of lipids. The presence of lipids may confer tolerance to M. tuberculosis against the mixture of antibiotics tested and such tolerance could be even higher during the dormant stages. The implementation of lipids in DST on clinical isolates could potentially lead to a better treatment strategy.

Entities:  

Keywords:  dormancy model; dormant mycobacteria; drug susceptibility testing; drug-tolerant mycobacteria; lipids as carbon source; treatment failures and relapses

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Year:  2018        PMID: 29458544     DOI: 10.1099/jmm.0.000681

Source DB:  PubMed          Journal:  J Med Microbiol        ISSN: 0022-2615            Impact factor:   2.472


  3 in total

Review 1.  Potential anti-TB investigational compounds and drugs with repurposing potential in TB therapy: a conspectus.

Authors:  Adetomiwa A Adeniji; Kirsten E Knoll; Du Toit Loots
Journal:  Appl Microbiol Biotechnol       Date:  2020-05-05       Impact factor: 4.813

2.  Chemical-genetic interaction mapping links carbon metabolism and cell wall structure to tuberculosis drug efficacy.

Authors:  Eun-Ik Koh; Peter O Oluoch; Nadine Ruecker; Megan K Proulx; Vijay Soni; Kenan C Murphy; Kadamba Papavinasasundaram; Charlotte J Reames; Carolina Trujillo; Anisha Zaveri; Matthew D Zimmerman; Roshanak Aslebagh; Richard E Baker; Scott A Shaffer; Kristine M Guinn; Michael Fitzgerald; Véronique Dartois; Sabine Ehrt; Deborah T Hung; Thomas R Ioerger; Eric J Rubin; Kyu Y Rhee; Dirk Schnappinger; Christopher M Sassetti
Journal:  Proc Natl Acad Sci U S A       Date:  2022-04-05       Impact factor: 12.779

3.  Optimization and Lead Selection of Benzothiazole Amide Analogs Toward a Novel Antimycobacterial Agent.

Authors:  Mary A De Groote; Thale C Jarvis; Christina Wong; James Graham; Teresa Hoang; Casey L Young; Wendy Ribble; Joshua Day; Wei Li; Mary Jackson; Mercedes Gonzalez-Juarrero; Xicheng Sun; Urs A Ochsner
Journal:  Front Microbiol       Date:  2018-09-20       Impact factor: 5.640

  3 in total

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