摩尔多瓦结核分枝杆菌的系统地理学和传播:一项前瞻性基因组分析。

IF 10.5 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL PLoS Medicine Pub Date : 2022-02-22 eCollection Date: 2022-02-01 DOI:10.1371/journal.pmed.1003933
Chongguang Yang, Benjamin Sobkowiak, Vijay Naidu, Alexandru Codreanu, Nelly Ciobanu, Kenneth S Gunasekera, Melanie H Chitwood, Sofia Alexandru, Stela Bivol, Marcus Russi, Joshua Havumaki, Patrick Cudahy, Heather Fosburgh, Christopher J Allender, Heather Centner, David M Engelthaler, Nicolas A Menzies, Joshua L Warren, Valeriu Crudu, Caroline Colijn, Ted Cohen
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引用次数: 12

摘要

背景:在前苏联国家,耐多药结核病(MDR-TB)的发病率仍然非常高,在这些国家,超过20%的新病例和超过50%的既往治疗病例对利福平和异烟肼有耐药性。耐药菌株的传播,而不是通过对药物敏感结核病的治疗不足而选择的耐药性,是这些国家耐多药结核病事件的主要驱动因素。方法和发现:我们对摩尔多瓦共和国2018年和2019年诊断的所有培养阳性结核病病例进行了前瞻性基因组分析。我们使用系统发育方法来识别假定的传播集群;对空间和人口统计学数据进行分析,以进一步描述结核分枝杆菌的本地传播。在2236名参与者中,779人(36%)患有耐多药结核病,其中386人(50%)以前从未接受过结核病治疗。此外,92%的耐多药结核分枝杆菌菌株属于假定的传播集群。系统发育重建确定了3个大的分支,它们几乎一致地由耐多药结核病组成:其中2个分支属于北京谱系,1个属于乌拉尔谱系,每个分支都有额外的独特的分支特异性二线耐药性突变和地理分布。集群内成对病例之间的空间和时间接近性与更大的基因组相似性相关。我们的研究只持续了2年,与结核病的自然史相比,持续时间相对较短,因此,推断传播全面程度的能力有限。结论:摩尔多瓦耐多药结核病的流行与多种结核分枝杆菌菌株的本地传播有关,包括具有不同地理分布和耐药性特征的高耐药性结核分枝杆菌的不同分支。这项研究证明了全面的基因组监测在了解结核分枝杆菌传播方面的作用,并强调了干预措施中断高耐药性结核分枝杆菌的传播的紧迫性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Phylogeography and transmission of M. tuberculosis in Moldova: A prospective genomic analysis.

Background: The incidence of multidrug-resistant tuberculosis (MDR-TB) remains critically high in countries of the former Soviet Union, where >20% of new cases and >50% of previously treated cases have resistance to rifampin and isoniazid. Transmission of resistant strains, as opposed to resistance selected through inadequate treatment of drug-susceptible tuberculosis (TB), is the main driver of incident MDR-TB in these countries.

Methods and findings: We conducted a prospective, genomic analysis of all culture-positive TB cases diagnosed in 2018 and 2019 in the Republic of Moldova. We used phylogenetic methods to identify putative transmission clusters; spatial and demographic data were analyzed to further describe local transmission of Mycobacterium tuberculosis. Of 2,236 participants, 779 (36%) had MDR-TB, of whom 386 (50%) had never been treated previously for TB. Moreover, 92% of multidrug-resistant M. tuberculosis strains belonged to putative transmission clusters. Phylogenetic reconstruction identified 3 large clades that were comprised nearly uniformly of MDR-TB: 2 of these clades were of Beijing lineage, and 1 of Ural lineage, and each had additional distinct clade-specific second-line drug resistance mutations and geographic distributions. Spatial and temporal proximity between pairs of cases within a cluster was associated with greater genomic similarity. Our study lasted for only 2 years, a relatively short duration compared with the natural history of TB, and, thus, the ability to infer the full extent of transmission is limited.

Conclusions: The MDR-TB epidemic in Moldova is associated with the local transmission of multiple M. tuberculosis strains, including distinct clades of highly drug-resistant M. tuberculosis with varying geographic distributions and drug resistance profiles. This study demonstrates the role of comprehensive genomic surveillance for understanding the transmission of M. tuberculosis and highlights the urgency of interventions to interrupt transmission of highly drug-resistant M. tuberculosis.

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来源期刊
PLoS Medicine
PLoS Medicine 医学-医学:内科
CiteScore
21.60
自引率
0.60%
发文量
227
审稿时长
3 months
期刊介绍: PLOS Medicine aims to be a leading platform for research and analysis on the global health challenges faced by humanity. The journal covers a wide range of topics, including biomedicine, the environment, society, and politics, that affect the well-being of individuals worldwide. It particularly highlights studies that contribute to clinical practice, health policy, or our understanding of disease mechanisms, with the ultimate goal of improving health outcomes in diverse settings. Unwavering in its commitment to ethical standards, PLOS Medicine ensures integrity in medical publishing. This includes actively managing and transparently disclosing any conflicts of interest during the reporting, peer review, and publication processes. The journal promotes transparency by providing visibility into the review and publication procedures. It also encourages data sharing and the reuse of published work. Author rights are upheld, allowing them to retain copyright. Furthermore, PLOS Medicine strongly supports Open Access publishing, making research articles freely available to all without restrictions, facilitating widespread dissemination of knowledge. The journal does not endorse drug or medical device advertising and refrains from exclusive sales of reprints to avoid conflicts of interest.
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