Activities of Biapenem against Mycobacterium tuberculosis in Macrophages and Mice

被引:0
|
作者
GUO Zhen Yong [1 ]
ZHAO Wei Jie [1 ]
ZHENG Mei Qin [1 ]
LIU Shuo [1 ]
YAN Chen Xia [1 ]
LI Peng [1 ]
XU Shao Fa [1 ]
机构
[1] Beijing Chest Hospital affiliated with the Capital Medical University/Beijing Tuberculosis and Thoracic Tumor Institute
关键词
Biapenem; Clavulanate; Multidrug resistant; Extensive drug-resistant; Mycobacterium tuberculosis; Activity; Macrophage; Synergy;
D O I
暂无
中图分类号
R52 [结核病];
学科分类号
1002 ; 100201 ;
摘要
Objective To assess the activities of biapenem against multidrug-resistant and extensively drug-resistant Mycobacterium tuberculosis. Methods Biapenem/clavulanate(BP/CL) was evaluated for in vitro activity against Mycobacterium tuberculosis(Mtb) multidrug-resistant(MDR) isolates, extensively drug-resistant(XDR) isolates, and the H37 RV strain. BP/CL activity against the H37 Rv strain was assessed in liquid cultures, in macrophages, and in mice. Results BP/CL exhibited activity against MDR and XDR Mtb isolates in liquid cultures. BP/CL treatment significantly reduced the number of colony forming units(CFU) of Mtb within macrophages compared with control untreated infected macrophages. Notably, BP/CL synergized in pairwise combinations with protionamide, aminosalicylate, and capreomycin to achieve a fractional inhibitory concentration for each pairing of 0.375 in vitro. In a mouse tuberculosis infection model, the efficacy of a cocktail of levofloxacin + pyrazinamide + protionamide + aminosalicylate against Mtb increased when the cocktail was combined with BP/CL, achieving efficacy similar to that of the positive control treatment(isoniazid + rifampin + pyrazinamide) after 2 months of treatment. Conclusion BP/CL may provide a new option to clinically treat MDR tuberculosis.
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页码:235 / 241
页数:7
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