A Screening of the MMV Pandemic Response Box Reveals Epetraborole as A New Potent Inhibitor against Mycobacterium abscessus

被引:21
|
作者
Kim, Taeho [1 ]
Hanh, Bui-Thi-Bich [1 ]
Heo, Boeun [2 ]
Quang, Nguyenthanh [2 ]
Park, Yujin [2 ]
Shin, Jihyeon [2 ]
Jeon, Seunghyeon [3 ]
Park, June-Woo [4 ,5 ]
Samby, Kirandeep [6 ]
Jang, Jichan [2 ]
机构
[1] Gyeongsang Natl Univ, Res Inst Life Sci, Div Appl Life Sci, BK21 Four Program, Jinju 52828, South Korea
[2] Gyeongsang Natl Univ, Res Inst Life Sci, Dept Bio & Med Big Data, Div Life Sci,BK21 Four Program,Mol Mech Antibiot, Jinju 52828, South Korea
[3] Gyeongsang Natl Univ, Div Life Sci, Jinju 52828, South Korea
[4] Korea Inst Toxicol, Dept Environm Toxicol & Chem, Jinju 52843, South Korea
[5] Korea Univ Sci & Technol UST, Human & Environm Toxicol Program, Daejeon 34113, South Korea
[6] Med Malaria Venture MMV, 20 Route Pre Bois, CH-1215 Geneva, Switzerland
基金
新加坡国家研究基金会;
关键词
Mycobacterium abscessus; epetraborole; benzoxaboroles; drug discovery; antibiotics; DRUG EFFICACY; ZEBRAFISH; TUBERCULOSIS; MODEL;
D O I
10.3390/ijms22115936
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mycobacterium abscessus is the one of the most feared bacterial respiratory pathogens in the world. Unfortunately, there are many problems with the current M. abscessus therapies available. These problems include misdiagnoses, high drug resistance, poor long-term treatment outcomes, and high costs. Until now, there have only been a few new compounds or drug formulations which are active against M. abscessus, and these are present in preclinical and clinical development only. With that in mind, new and more powerful anti-M. abscessus medicines need to be discovered and developed. In this study, we conducted an in vitro-dual screen against M. abscessus rough (R) and smooth (S) variants using a Pandemic Response Box and identified epetraborole as a new effective candidate for M. abscessus therapy. For further validation, epetraborole showed significant activity against the growth of the M. abscessus wild-type strain, three subspecies, drug-resistant strains and clinical isolates in vitro, while also inhibiting the growth of M. abscessus that reside in macrophages without cytotoxicity. Furthermore, the in vivo efficacy of epetraborole in the zebrafish infection model was greater than that of tigecycline. Thus, we concluded that epetraborole is a potential anti-M. abscessus candidate in the M. abscessus drug search.
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页数:14
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