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支持属于罕见原始北京基因型的广泛耐药结核分枝杆菌克隆扩张的基因组证据。

Genomic evidence supporting the clonal expansion of extensively drug-resistant tuberculosis bacteria belonging to a rare protoBeijing genotype.

机构信息

Office for Research and Development, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

Drug Resistant Tuberculosis Research Fund, Siriraj Foundation, Bangkok, Thailand.

出版信息

Emerg Microbes Infect. 2020 Dec;9(1):2632-2641. doi: 10.1080/22221751.2020.1852891.

Abstract

Tuberculosis disease (TB), caused by , is a major public health issue in Thailand. The high prevalence of modern Beijing (Lineage 2.2.1) strains has been associated with multi- and extensively drug-resistant infections (MDR-, XDR-TB), complicating disease control. The impact of rarer proto-Beijing (L2.1) strains is less clear. In our study of thirty-seven L2.1 clinical isolates spanning thirteen years, we found a high prevalence of XDR-TB cases (32.4%). With ≤ 12 pairwise SNP distances, 43.2% of L2.1 patients belong to MDR-TB or XDR-TB transmission clusters suggesting a high level of clonal expansion across four Thai provinces. All XDR-TB (100%) were likely due to transmission rather than inadequate treatment. We found a 47 mutation signature and a partial deletion of the gene in the circulating XDR-TB cluster, which can be used for surveillance of this rare and resilient strain-type that is causing increasing health burden. We also detected three novel deletion positions, a deletion of 1285 bp within (Rv3230c) large deletions in the and gene which may play a role in the virulence, pathogenesis or evolution of the L2.1 strain-type.

摘要

结核病(TB)是由 引起的,是泰国的一个主要公共卫生问题。现代北京家族(Lineage 2.2.1)菌株的高流行率与耐多药和广泛耐药感染(MDR-,XDR-TB)有关,使疾病控制复杂化。较少见的原始北京家族(L2.1)菌株的影响不太清楚。在对跨越 13 年的 37 株 L2.1 临床分离株的研究中,我们发现 XDR-TB 病例的高患病率(32.4%)。在 SNP 距离≤12 的情况下,43.2%的 L2.1 患者属于 MDR-TB 或 XDR-TB 传播群,表明在四个泰国省份存在高水平的克隆扩张。所有 XDR-TB(100%)都可能是由于传播而不是治疗不当引起的。我们在循环 XDR-TB 群中发现了 47 个突变特征和 基因的部分缺失,这可用于监测这种罕见且有弹性的菌株型,该菌株型正在造成越来越大的健康负担。我们还检测到三个新的缺失位置,即在 基因内缺失 1285bp(Rv3230c)和 基因中的大缺失,这可能在 L2.1 菌株型的毒力,发病机理或进化中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f40/7738298/6601fbea0900/TEMI_A_1852891_F0001_OC.jpg

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