在诺氟沙星的压力下,可以扰乱保守的进化轨迹,通过迫使分枝杆菌走上替代性进化路径来防止耐药性进化。

IF 8.3 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
ACS Applied Materials & Interfaces Pub Date : 2024-08-09 Epub Date: 2024-07-03 DOI:10.1021/acsinfecdis.3c00605
Akanksha, Sarika Mehra
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引用次数: 0

摘要

抗生素耐药性是一个紧迫的健康问题,细菌耐药性的出现超过了新型候选药物的发现。虽然许多研究利用适应性实验室进化(ALE)来了解耐药性的决定因素,但药物剂量对进化轨迹的影响仍未得到充分研究。在这项研究中,我们对暴露于不同浓度诺氟沙星的分枝杆菌采用了适应性实验室进化(ALE)方法,使用循环恒定和逐步增加的药物剂量来研究它们对所选耐药机制的影响。在所有进化种群中都发现了外排泵调节器 LfrR 的突变,而与药物特征和种群瓶颈无关,这表明基于外排的耐药机制是一致的。这种突变出现在进化轨迹的早期,单独出现时会产生低水平的抗药性,其他突变的连续积累会导致抗药性的进一步增强。值得注意的是,药物靶点突变与临床分离物中观察到的突变类似,只出现在最低抑菌浓度(MIC)大于 4 倍的阈值之上。lfrR、MSMEG_1959 和 MSMEG_5045 这三个基因突变的组合在多个品系中保持不变,导致了高水平的耐药性,并先于药物靶标突变的出现。有趣的是,在由缺乏 lfrA 外排泵(lfrR 调控因子的主要靶标)的亲本菌株进化而来的种群中,没有选择 lfrR 基因突变。此外,源自ΔlfrA菌株的进化轨迹在某些品系中显示出早期停滞,而在那些进化的品系中,尽管有所延迟,但没有出现靶基因突变。因此,阻断或抑制外排泵的表达可阻止或延迟药物靶基因突变的固定,从而可能限制可达到的最大抗药性水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Conserved Evolutionary Trajectory Can Be Perturbed to Prevent Resistance Evolution under Norfloxacin Pressure by Forcing <i>Mycobacterium smegmatis</i> on Alternate Evolutionary Paths.

Conserved Evolutionary Trajectory Can Be Perturbed to Prevent Resistance Evolution under Norfloxacin Pressure by Forcing Mycobacterium smegmatis on Alternate Evolutionary Paths.

Antibiotic resistance is a pressing health issue, with the emergence of resistance in bacteria outcompeting the discovery of novel drug candidates. While many studies have used Adaptive Laboratory Evolution (ALE) to understand the determinants of resistance, the influence of the drug dosing profile on the evolutionary trajectory remains understudied. In this study, we employed ALE on Mycobacterium smegmatis exposed to various concentrations of Norfloxacin using both cyclic constant and stepwise increasing drug dosages to examine their impact on the resistance mechanisms selected. Mutations in an efflux pump regulator, LfrR, were found in all of the evolved populations irrespective of the drug profile and population bottleneck, indicating a conserved efflux-based resistance mechanism. This mutation appeared early in the evolutionary trajectory, providing low-level resistance when present alone, with a further increase in resistance resulting from successive accumulation of other mutations. Notably, drug target mutations, similar to those observed in clinical isolates, were only seen above a threshold of greater than 4× the minimum inhibitory concentration (MIC). A combination of three mutations in the genes, lfrR, MSMEG_1959, and MSMEG_5045, was conserved across multiple lineages, leading to high-level resistance and preceding the appearance of drug target mutations. Interestingly, in populations evolved from parental strains lacking the lfrA efflux pump, the primary target of the lfrR regulator, no lfrR gene mutations are selected. Furthermore, evolutional trajectories originating from the ΔlfrA strain displayed early arrest in some lineages and the absence of target gene mutations in those that evolved, albeit delayed. Thus, blocking or inhibiting the expression of efflux pumps can arrest or delay the fixation of drug target mutations, potentially limiting the maximum attainable resistance levels.

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来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
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