Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/148764
Title: Telacebec (Q203)-containing intermittent oral regimens sterilized mice infected with Mycobacterium ulcerans after only 16 doses
Authors: Chauffour, Aurélie
Robert, Jérôme
Veziris, Nicolas
Aubry, Alexandra
Pethe, Kevin
Jarlier, Vincent
Keywords: Science::Medicine
Issue Date: 2020
Source: Chauffour, A., Robert, J., Veziris, N., Aubry, A., Pethe, K. & Jarlier, V. (2020). Telacebec (Q203)-containing intermittent oral regimens sterilized mice infected with Mycobacterium ulcerans after only 16 doses. PLoS Neglected Tropical Diseases, 14(8). https://dx.doi.org/10.1371/journal.pntd.0007857
Journal: PLoS Neglected Tropical Diseases 
Abstract: Buruli ulcer (BU), caused by Mycobacterium ulcerans, is currently treated with a daily combination of rifampin and either injectable streptomycin or oral clarithromycin. An intermittent oral regimen would facilitate treatment supervision. We first evaluated the bactericidal activity of newer antimicrobials against M. ulcerans using a BU animal model. The imidazopyridine amine telacebec (Q203) exhibited high bactericidal activity whereas tedizolid (an oxazolidinone closely related to linezolid), selamectin and ivermectin (two avermectine compounds) and the benzothiazinone PBTZ169 were not active. Consequently, telacebec was evaluated for its bactericidal and sterilizing activities in combined intermittent regimens. Telacebec given twice a week in combination with a long-half-life compound, either rifapentine or bedaquiline, sterilized mouse footpads in 8 weeks, i.e. after a total of only 16 doses, and prevented relapse during a period of 20 weeks after the end of treatment. These results are very promising for future intermittent oral regimens which would greatly simplify BU treatment in the field.
URI: https://hdl.handle.net/10356/148764
ISSN: 1935-2727
DOI: 10.1371/journal.pntd.0007857
Schools: Lee Kong Chian School of Medicine (LKCMedicine) 
School of Biological Sciences 
Rights: © 2020 Chauffour et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:LKCMedicine Journal Articles

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