Antimicrobial Effect of Oxazolidinones and Its Synergistic Effect with Bedaquiline Against Mycobacterium abscessus Complex

被引:3
|
作者
Gao, Tianhui [1 ]
Yao, Cong [1 ]
Shang, Yuanyuan [1 ]
Su, Renchun [1 ]
Zhang, Xuxia [1 ]
Ren, Weicong [1 ]
Li, Shanshan [1 ]
Shu, Wei [2 ]
Pang, Yu [1 ,3 ]
Li, Qi [2 ,3 ]
机构
[1] Capital Med Univ, Beijing Chest Hosp, Beijing TB & Thorac Tumor Inst, Dept Bacteriol & Immunol,Beijing Key Lab Drug Resi, Beijing, Peoples R China
[2] Capital Med Univ, Beijing Chest Hosp, Beijing TB & Thorac Tumor Inst, Clin Ctr TB Control, Beijing, Peoples R China
[3] Capital Med Univ, Beijing Chest Hosp, 97 Machang, Beijing 101149, Peoples R China
来源
关键词
bedaquiline; tedizolid; oxazolidinones; susceptibility testing; Mycobacterium abscessus complex; delpazolid; IN-VITRO SUSCEPTIBILITY; NONTUBERCULOUS MYCOBACTERIA; PULMONARY-DISEASE;
D O I
10.2147/IDR.S395750
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Purpose: Unsatisfactory efficacies of currently recommended anti-Mycobacterium abscessus complex (MABC) treatment regimens have led to development of novel drugs to combat MABC infections. In this study, we evaluated in vitro antimicrobial activities of bedaquiline (BDQ) and four oxazolidinones against MABC isolates.Methods: The resazurin microplate assay was performed to determine minimum inhibitory concentrations (MICs) of BDQ and four oxazolidinones, including tedizolid (TZD), sutezolid (SZD), delpazolid (DZD), and linezolid (LZD), against 65 MABC isolates. A checkerboard method was used to investigate efficacies of various antimicrobial drug combinations.Results: BDQ MICs for MABC isolates ranged from <0.031 to 1 mu g/mL, while MIC50 and MIC90 values were 0.125 mu g/mL and 0.25 mu g/mL, respectively. TZD MIC50 and MIC90 values for MABC isolates were 1 mu g/mL and 4 mu g/mL, respectively, which were fourfold lower than corresponding LZD values (P < 0.001). DZD MIC90 values for MABC isolates was 8 mu g/mL, which were 0.5-fold lower than corresponding LZD values (P < 0.01). MICs of BDQ, SZD, and LZD for M. abscessus subspecies massiliense isolates were significantly lower than corresponding MICs for M. abscessus subspecies abscessus isolates (P < 0.05). Notably, use of oxazolidinones (DZD, SZD, LZD, or TZD) with BDQ against MABC isolates led to reduction of the oxazolidinone median MIC range from 4 to 0.125 mu g/mL to 1-0.031 mu g/mL. Conclusion: These results demonstrated excellent BDQ inhibitory activity against MABC isolates. TZD exhibited stronger antimicrobial efficacy against MABC isolates as compared to efficacies of DZD, SZD, and LZD. Importantly, MICs of oxazolidinones were markedly decreased when they were combined with BDQ, thus suggesting that combinations of BDQ and oxazolidinones may be effective treatments for MABC infections.
引用
收藏
页码:279 / 287
页数:9
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