Zimenkov Danila
Center for Precision Genome Editing and Genetic Technologies for Biomedicine, Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.
Antibiotics (Basel). 2022 Dec 4;11(12):1756. doi: 10.3390/antibiotics11121756.
Non-tuberculous mycobacteria are widely distributed in environments and are capable of infecting humans, particularly those with a compromised immune system. The most prevalent species that cause nontuberculous mycobacterial lung diseases are slow-growing bacteria from the complex (MAC), mainly or . The key treatment of MAC infections includes macrolides, ethambutol, and rifampicin; however, the therapy outcomes are unsatisfactory. Phenotypic drug susceptibility testing is a conditional recommendation prior to treatment, and critical concentrations for clarithromycin, amikacin, moxifloxacin, and linezolid have been established. In this review, data from studies on the determination of MIC of clinical isolates using the broth microdilution method were summarized. A significant variation in the MIC distributions from different studies was found. The main reasons could impact the findings: insufficient reproducibility of the phenotypic testing and variation in species lineages identified in different laboratories, which could have various intrinsic susceptibility to drugs. For most of the drugs analyzed, the MICs are too high, which could undermine the treatment efficiency. Further improvement of treatment outcomes demands the validation of microbiological resistance criteria together with the identification of molecular mechanisms of resistance.
非结核分枝杆菌广泛分布于环境中,能够感染人类,尤其是免疫系统受损的人群。引起非结核分枝杆菌肺病的最常见菌种是来自鸟分枝杆菌复合群(MAC)的生长缓慢的细菌,主要是鸟分枝杆菌或胞内分枝杆菌。MAC感染的关键治疗药物包括大环内酯类、乙胺丁醇和利福平;然而,治疗效果并不理想。表型药敏试验是治疗前的一项有条件推荐,并且已经确定了克拉霉素、阿米卡星、莫西沙星和利奈唑胺的临界浓度。在本综述中,总结了使用肉汤微量稀释法测定临床分离株最低抑菌浓度(MIC)的研究数据。发现不同研究的MIC分布存在显著差异。主要原因可能影响研究结果:表型检测的可重复性不足以及不同实验室鉴定的菌种谱系存在差异,这可能导致对药物的固有敏感性各不相同。对于大多数分析的药物,MIC过高,这可能会削弱治疗效果。进一步改善治疗效果需要验证微生物耐药标准并确定耐药的分子机制。