An anti-mycobacterial conjugated oligoelectrolyte effective against Mycobacterium abscessus

被引:2
|
作者
Zhang, Kaixi [1 ,9 ]
Limwongyut, Jakkarin [1 ,2 ]
Moreland, Alex S. [2 ]
Wei, Samuel Chan Jun [1 ]
Min, Tania Jim Jia [1 ]
Sun, Yan [3 ]
Shin, Sung Jae [4 ]
Kim, Su-Young [5 ]
Jhun, Byung Woo [5 ]
Pethe, Kevin [3 ,6 ,7 ]
Bazan, Guillermo C. [1 ,2 ,6 ,8 ]
机构
[1] Natl Univ Singapore, Dept Chem, 4 Sci Dr 2, Singapore 117543, Singapore
[2] Univ Calif Santa Barbara, Ctr Polymers & Organ Solids, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
[3] Nanyang Technol Univ, Lee Kong Chian Sch Med, 59 Nanyang Dr, Singapore 636921, Singapore
[4] Yonsei Univ, Coll Med, Grad Sch Med Sci, Dept Microbiol,Brain Korea Project 21, Seoul 03722, South Korea
[5] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Div Pulm & Crit Care Med,Dept Med, Seoul 06351, South Korea
[6] Singapore Ctr Environm Life Sci Engn SCELSE, 60 Nanyang Dr, Singapore 639798, Singapore
[7] Natl Ctr Infect Dis NCID, 16 Jalan Tan Tock Seng, Singapore 308442, Singapore
[8] Natl Univ Singapore, Inst Funct Intelligent Mat I FIM, Singapore 117544, Singapore
[9] Singapore MIT Alliance Res & Technol Ctr, Antimicrobial Resistance Interdisciplinary Res Grp, Singapore 138602, Singapore
基金
新加坡国家研究基金会;
关键词
MYCOLIC ACID TRANSPORT; NONTUBERCULOUS MYCOBACTERIA; INFECTIONS; DISEASE; ONTARIO;
D O I
10.1126/scitranslmed.adi7558
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Infections caused by nontuberculous mycobacteria have increased more than 50% in the past two decades and more than doubled in the elderly population. Mycobacterium abscessus (Mab), one of the most prevalent of these rapidly growing species, is intrinsically resistant to numerous antibiotics. Current standard-of-care treatments are not satisfactory, with high failure rate and notable adverse effects. We report here a potent anti-Mab compound from the flexible molecular framework afforded by conjugated oligoelectrolytes (COEs). A screen of structurally diverse, noncytotoxic COEs identified a lead compound, COE-PNH2, which was bactericidal against replicating, nonreplicating persisters and intracellular Mab.COE-PNH2 had low propensity for resistance development, with a frequency of resistance below 1.25 x 10(-9) and showed no detectable resistance upon serial passaging. Mechanism of action studies were in line with COE-PNH2 affecting the physical and functional integrity of the bacterial envelope and disrupting the mycomembrane and associated essential bioenergetic pathways. Moreover, COE-PNH2 was well-tolerated and efficacious in a mouse model of Mab lung infection. This study highlights desirable in vitro and in vivo potency and safety index of this COE structure, which represents a promising anti-mycobacterial to tackle an unmet medical need.
引用
收藏
页数:12
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