海洋分枝杆菌贝达喹啉耐药相关新突变的鉴定

Long Wang, Yufan Xu, Zhe Wang
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引用次数: 1

摘要

由于非结核分枝杆菌(NTM)引起的感染在全球范围内迅速增加,需要开发新的抗生素并发现耐药机制。本研究旨在了解NTM模型种海洋分枝杆菌(m.m arinum)对贝达喹啉的耐药机制。用不同浓度的BDQ对海洋分枝杆菌M菌株进行突变体选择。经过三轮进化,分离出58个bdq抗性突变体并进行WGS。结果经PCR和Sanger测序证实。我们在这些突变体中发现了7个基因突变。最高耐药性(6 - 10倍MIC)与Mtb中BDQ的主要生化靶点AtpB突变有关。许多突变和插入定位到MMAR_1007基因(46/58),该基因编码MmpR (Rv0678)在Mtb中的同源物。超过93%的突变体(54/58)在MMAR_4049中包含一个单一突变(G563A),该突变编码整体膜蛋白YrbE3A-1。基于靶标和基于外排的作用都有助于海洋分枝杆菌的BDQ耐药。我们的发现可能有助于开发新的有效的抗ntm(基于bdq)药物方案和检测bdq耐药海洋分枝杆菌的诊断方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of Novel Mutations Associated with Bedaquiline Resistance in Mycobacterium Marinum
Because infections caused by nontuberculous mycobacteria (NTM) are rapidly increasing globally, a need exists for developing novel antibiotics and discovering the mechanism of resistance. This research was aimed at understanding the mechanism of bedaquiline resistance in the model NTM species Mycobacterium marinum (M. marinum). The Mycobacterium marinum M strain was subjected to mutant selection with different concentrations of BDQ. After three rounds of evolution, 58 BDQ-resistant mutants were isolated and subjected to WGS. The results were confirmed through PCR and Sanger sequencing. We identified seven genetic mutations among these mutants. The highest drug resistance (6–10× MIC) was associated with a mutation in AtpB, the primary biochemical target of BDQ in Mtb. Numerous mutations and insertions mapped to the gene MMAR_1007(46/58), which encodes the homolog of Rv0678 (MmpR) in Mtb. More than 93% of mutants (54/58) contained a single mutation (G563A) in MMAR_4049, which encodes the integral membrane protein YrbE3A-1. Both target-based and efflux-based actions contribute to BDQ resistance in M. marinum. Our findings may aid in developing novel potent anti-NTM (BDQ-based) drug regimens and diagnostic assays for the detection of BDQ-resistant M. marinum.
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