Molecular and Experimental Mycobacteriology, Research Center Borstel, Borstel, Germany.
German Center for Infection Research, Partner site Hamburg-Lübeck-Borstel-Riems, Borstel, Germany.
Nat Commun. 2022 Aug 30;13(1):5105. doi: 10.1038/s41467-022-32455-1.
Transmission-driven multi-/extensively drug resistant (M/XDR) tuberculosis (TB) is the largest single contributor to human mortality due to antimicrobial resistance. A few major clades of the Mycobacterium tuberculosis complex belonging to lineage 2, responsible for high prevalence of MDR-TB in Eurasia, show outstanding transnational distributions. Here, we determined factors underlying the emergence and epidemic spread of the W148 clade by genome sequencing and Bayesian demogenetic analyses of 720 isolates from 23 countries. We dated a common ancestor around 1963 and identified two successive epidemic expansions in the late 1980s and late 1990s, coinciding with major socio-economic changes in the post-Soviet Era. These population expansions favored accumulation of resistance mutations to up to 11 anti-TB drugs, with MDR evolving toward additional resistances to fluoroquinolones and second-line injectable drugs within 20 years on average. Timescaled haplotypic density analysis revealed that widespread acquisition of compensatory mutations was associated with transmission success of XDR strains. Virtually all W148 strains harbored a hypervirulence-associated ppe38 gene locus, and incipient recurrent emergence of prpR mutation-mediated drug tolerance was detected. The outstanding genetic arsenal of this geographically widespread M/XDR strain clade represents a "perfect storm" that jeopardizes the successful introduction of new anti-M/XDR-TB antibiotic regimens.
传播驱动的多药耐药/广泛耐药(M/XDR)结核病(TB)是导致抗微生物药物耐药导致人类死亡的最大单一因素。分枝杆菌复合群的少数几个主要分支属于 2 谱系,负责欧亚大陆 MDR-TB 的高流行率,表现出突出的跨国分布。在这里,我们通过对来自 23 个国家的 720 个分离株的基因组测序和贝叶斯遗传分析,确定了 W148 分支出现和流行传播的基础因素。我们确定了一个共同祖先大约在 1963 年,发现了两次连续的流行扩张,分别发生在 20 世纪 80 年代末和 90 年代末,这与后苏联时代的重大社会经济变化相吻合。这些种群扩张有利于积累多达 11 种抗结核病药物的耐药突变,MDR 平均在 20 年内进一步发展为对氟喹诺酮类和二线注射类药物的耐药性。时间密度分析表明,广泛获得补偿性突变与 XDR 菌株的传播成功有关。实际上,所有的 W148 菌株都携带有一个与高毒力相关的 ppe38 基因座,并且检测到了 prpR 突变介导的药物耐受性的初始反复出现。这种地理上广泛分布的 M/XDR 菌株分支具有出色的遗传武器库,这代表了一场“完美风暴”,威胁着新的抗 M/XDR-TB 抗生素方案的成功引入。