Sudapyridine (WX-081) antibacterial activity against Mycobacterium avium, Mycobacterium abscessus, and Mycobacterium chelonae in vitro and in vivo

被引:1
|
作者
Zheng, Luyao [1 ]
Wang, Hong [1 ]
Qi, Xueting [1 ]
Zhang, Weiyan [1 ]
Wang, Bin [1 ]
Fu, Lei [1 ]
Chen, Xi [1 ]
Chen, Xiaoyou [2 ,3 ]
Lu, Yu [1 ]
机构
[1] Capital Med Univ, Beijing TB & Thorac Tumor Res Inst, Beijing Key Lab Drug Resistance TB Res, Dept Pharmacol,Beijing Chest Hosp, Beijing, Peoples R China
[2] Capital Med Univ, Beijing Chest Hosp, Beijing TB & Thorac Tumor Res Inst, TB Dept, Beijing, Peoples R China
[3] Capital Med Univ, Beijing Ditan Hosp, Infect Dis Dept, Beijing, Peoples R China
关键词
non-tuberculous mycobacteria (NTM); sudapyridine (WX-081); J774A.1; macrophages; BALB/c mice; BEDAQUILINE;
D O I
10.1128/msphere.00518-23
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Sudapyridine (WX-081) is a structural analog of bedaquiline (BDQ), which shows anti-tuberculosis and non-tuberculous mycobacteria (NTM) activities but, unlike BDQ, did not prolong QT interval in animal model studies. This study evaluated the antibacterial activity of this novel compound against Mycobacterium avium, Mycobacterium abscessus, and Mycobacterium chelonae in vitro and in vivo. The minimum inhibitory concentration (MIC) of WX-081 against three kinds of non-tuberculous mycobacteria (NTM) clinical strains was determined using microplate-based alamarBlue assay (MABA), and the antibacterial activity of WX-081 against NTM in J774A.1 cells and mice was evaluated. MIC ranges of WX-081 against clinical strains of M. avium and M. abscessus were 0.05-0.94 mu g/mL, 0.88-7.22 mu g/mL (M. abscessus subsp. abscessus), and 0.22-8.67 mu g/mL (M. abscessus subsp. massiliense), respectively, which were slightly higher than those of BDQ. For M. avium, M. abscessus, and M. chelonae, WX-081 can reduce the intracellular bacterial load by 0.13-1.18, 0.18-1.50, and 0.17-1.03 log10 colony forming units (CFU)/mL, respectively, in a concentration-dependent manner. WX-081 has bactericidal activity against three NTM species in mice. WX-081 exhibited anti-NTM activity to the same extent as BDQ both in vivo and in vitro. WX-081 is a promising clinical candidate and should be studied further in clinical trials.
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页数:10
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