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中国防痨杂志 ›› 2022, Vol. 44 ›› Issue (3): 234-238.doi: 10.19982/j.issn.1000-6621.20210465

• 论著 • 上一篇    下一篇

GSK656和阿米卡星对脓肿分枝杆菌的体外联合药物敏感性研究

陈磊1, 郭海萍2, 逄宇2, 刘光福1, 潘兆宝1, 韩守华1, 程娟1, 李姗姗2()   

  1. 1潍坊市第二人民医院检验科,潍坊 261041
    2首都医科大学附属北京胸科医院/北京市结核病胸部肿瘤研究所细菌免疫学实验室/耐药结核病研究北京市重点实验室,北京 101149
  • 收稿日期:2021-08-10 出版日期:2022-03-10 发布日期:2022-03-08
  • 通信作者: 李姗姗 E-mail:lss9011@126.com
  • 基金资助:
    北京市医院管理中心“登峰”人才培养计划(DFL20191601);北京市医院管理中心“扬帆”专业建设(ZYLX202122)

In vitro synergistic activities of GSK656 with amikacin against Mycobacterium abscessus

CHEN Lei1, GUO Hai-ping2, PANG Yu2, LIU Guang-fu1, PAN Zhao-bao1, HAN Shou-hua1, CHENG Juan1, LI Shan-shan2()   

  1. 1Department of Laboratory Medicine, the Second People’s Hospital of Weifang, Shandong Province, Weifang 261041, China
    2National Clinical Laboratory on Tuberculosis, Beijing Key Laboratory on Drug-Resistant Tuberculosis Research/Beijing Chest Hospital, Capital Medical University/Bacterial Immunology Laboratory, Beijing Tuberculosis and Thoracic Tumor Institute, Beijing 101149, China
  • Received:2021-08-10 Online:2022-03-10 Published:2022-03-08
  • Contact: LI Shan-shan E-mail:lss9011@126.com
  • Supported by:
    Beijing Hospitals Authority’ Ascent Plan(DFL20191601);Beijing Hospitals Authority Clinical Medicine Development of Special Funding(ZYLX202122)

摘要:

目的: 评价3-氨甲基-4-卤代苯并噁唑类化合物GSK656与阿米卡星联合用药对脓肿分枝杆菌分离株的体外抑菌作用。 方法: 收集首都医科大学附属北京胸科医院菌株库保存的30株脓肿分枝杆菌,采用微孔阿尔玛蓝检测法(MABA法)测定GSK656和阿米卡星对脓肿分枝杆菌的体外最低抑菌浓度(MIC)。采用棋盘稀释法进行联合药物敏感性试验,通过分级抑菌浓度指数判断联合抑菌的效果。 结果: GSK656对脓肿分枝杆菌的MIC为0.063~4.000mg/L;阿米卡星对脓肿分枝杆菌的MIC为4.000~16.000mg/L。GSK656对脓肿分枝杆菌分离株的MIC50和MIC90分别为0.250mg/L和2.000mg/L,阿米卡星对脓肿分枝杆菌分离株的MIC50和MIC90分别为8.000mg/L和16.000mg/L。GSK656与阿米卡星联合使用时,5株(16.7%)脓肿分枝杆菌分离株表现为协同作用,1株(3.3%)分离株表现为拮抗作用,其他分离株(80.0%,24/30)表现为无关作用。 结论: GSK656与阿米卡星的体外联合用药对脓肿分枝杆菌表现出良好的抑菌效果,可为临床用药提供一定参考价值。

关键词: GSK656, 抗菌药, 分枝杆菌,非典型性, 药物评价

Abstract:

Objective: To investigate the in vitro synergistic effect of GSK656, a novel member of 3-aminomethyl 4-halogen benzoxaboroles, with aminoglycoside-amikacin against Mycobacterium abscessus. Methods: Thirty clinical M.abscessus isolates were collected from the Biobank of Beijing Chest Hospital affiliated to Capital Medical University. Minimum inhibitory concentration (MIC) were determined using microdilution MABA assay. The checkerboard titration method was used to explore the in vitro synergistic effect between GSK656 and amikacin against M.abscessus isolates. Fractional inhibitory concentration index was calculated to determine the combined effects of these two compounds. Results: GSK656 and amikacin showed potent antibacterial activities against M.abscessus. The MIC of M.abscessus ranged from 0.063 to 4.000 mg/L for GSK656, the MIC50 and MIC90 of which were 0.250 and 2.000 mg/L, respectively. The MIC ranged from 4.000 to 16.000 mg/L for amikacin, the MIC50 and MIC90 of which were 8.000 and 16.000 mg/L, respectively. For GSK656-amikacin combination, only 1 strain (3.3%) had antagonistic effect. Synergy for GSK656-amikacin combination was observed in 5 isolates (16.7%); antagonism was observed in one isolate (3.3%); while the remaining isolates (80.0%) showed indifference. Conclusion: GSK656 and amikacin holds potent antibacterial activity against M.abscessus, which provids important clinical benefit for treatment of. M.abscessus infections.

Key words: GSK656, Antimicrobial agent, Mycobacteria,atypical, Drug evaluation

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