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对萘啶酸和四环素联合治疗鲍曼不动杆菌和大肠杆菌临床分离株协同作用的机制研究。

Mechanistic insights into synergy between nalidixic acid and tetracycline against clinical isolates of Acinetobacter baumannii and Escherichia coli.

机构信息

Department of Biotechnology, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand, India.

Department of Microbiology, Government Medical College and Hospital Chandigarh, Chandigarh, Punjab, India.

出版信息

Commun Biol. 2021 May 10;4(1):542. doi: 10.1038/s42003-021-02074-5.

Abstract

The increasing prevalence of antimicrobial resistance has become a global health problem. Acinetobacter baumannii is an important nosocomial pathogen due to its capacity to persist in the hospital environment. It has a high mortality rate and few treatment options. Antibiotic combinations can help to fight multi-drug resistant (MDR) bacterial infections, but they are rarely used in the clinics and mostly unexplored. The interaction between bacteriostatic and bactericidal antibiotics are mostly reported as antagonism based on the results obtained in the susceptible model laboratory strain Escherichia coli. However, in the present study, we report a synergistic interaction between nalidixic acid and tetracycline against clinical multi-drug resistant A. baumannii and E. coli. Here we provide mechanistic insight into this dichotomy. The synergistic combination was studied by checkerboard assay and time-kill curve analysis. We also elucidate the mechanism behind this synergy using several techniques such as fluorescence spectroscopy, flow cytometry, fluorescence microscopy, morphometric analysis, and real-time polymerase chain reaction. Nalidixic acid and tetracycline combination displayed synergy against most of the MDR clinical isolates of A. baumannii and E. coli but not against susceptible isolates. Finally, we demonstrate that this combination is also effective in vivo in an A. baumannii/Caenorhabditis elegans infection model (p < 0.001).

摘要

抗菌药物耐药性的不断增加已成为全球卫生问题。鲍曼不动杆菌因其能够在医院环境中持续存在而成为一种重要的医院获得性病原体。它的死亡率很高,治疗选择很少。抗生素联合使用可以帮助对抗多重耐药(MDR)细菌感染,但在临床上很少使用,而且大多未被探索。基于在敏感模式实验室菌株大肠杆菌中获得的结果,抑菌和杀菌抗生素之间的相互作用大多被报道为拮抗作用。然而,在本研究中,我们报告了萘啶酸和四环素对临床多重耐药鲍曼不动杆菌和大肠杆菌的协同作用。在这里,我们提供了对此二分法的机制见解。通过棋盘试验和时间杀伤曲线分析研究协同组合。我们还使用荧光光谱、流式细胞术、荧光显微镜、形态计量分析和实时聚合酶链反应等几种技术阐明了这种协同作用背后的机制。萘啶酸和四环素联合使用对大多数 MDR 临床分离株的鲍曼不动杆菌和大肠杆菌显示出协同作用,但对敏感分离株没有。最后,我们证明这种组合在鲍曼不动杆菌/秀丽隐杆线虫感染模型中也具有体内疗效(p < 0.001)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fef/8110569/b8c67b98045b/42003_2021_2074_Fig1_HTML.jpg

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