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采用常规和全基因组测序方法对越南河内流行的结核分枝杆菌进行基因分型。

Genotyping of Mycobacterium tuberculosis spreading in Hanoi, Vietnam using conventional and whole genome sequencing methods.

机构信息

Faculty of Pharmaceutical Sciences, Hokkaido University of Science, Hokkaido, Japan.

Department of Pathophysiology and Host Defense, The Research Institute of Tuberculosis JATA, Tokyo, Japan.

出版信息

Infect Genet Evol. 2020 Mar;78:104107. doi: 10.1016/j.meegid.2019.104107. Epub 2019 Nov 6.

Abstract

Hanoi is the capital of Vietnam, one of the 30 countries with a high tuberculosis (TB) burden. Fundamental data on the molecular epidemiology of the disease is required for future TB management. To identify lineages and genotypes of Mycobacterium tuberculosis (Mtb), conventional genotyping data from clinical isolates of the Hanoi area was compared with whole genome sequencing (WGS) analysis from 332 of 470 samples. It was obtained from lineage-specific single nucleotide variants (SNVs), large sequence polymorphisms, spoligotyping, and variable number of tandem repeats (VNTR) analysis using mycobacterial interspersed repetitive unit (MIRU) and Japan anti-tuberculosis association (JATA) locus sets. This information was directly compared with results obtained from WGS. Mini-satellite repeat unit variants were identified using BLAST search against concatenated short read sequences, the RepUnitTyping tool. WGS analysis revealed that the Mtb strains tested are diverse and classified into lineage (L) 1, 2 and 4 (24.7, 57.2 and 18.1% respectively). The majority of the L2 strains were further divided into ancient and modern Beijing genotypes, and most of the L1 group were EAI4_VNM strains. Although conventional PCR-based genotyping results were mostly consistent with information obtained through WGS analysis, in-depth analysis identified aberrant deletions and spacers that may cause discordance. JATA-VNTR sets, including hypervariable loci, separated large Beijing genotypic clusters generated by MIRU15 into smaller groups. The distribution of repeat unit variants observed within 33 VNTR loci showed clear variation depending on the three lineages. WGS-based pairwise-SNV differences within VNTR-defined genotypic clusters were greater in L1 than in L2 and L4 (P = .001). Direct comparisons between results of PCR-based genotyping and in silico analysis of WGS data would bridge a gap between classical and modern technologies during this transition period, and provide further information on Mtb genotypes in specific geographical areas.

摘要

河内是越南的首都,也是结核病(TB)负担 30 个国家之一。为了未来的结核病管理,需要了解该疾病的分子流行病学的基本数据。为了确定分枝杆菌(Mtb)的谱系和基因型,将来自河内地区临床分离株的传统基因分型数据与 470 个样本中的 332 个样本的全基因组测序(WGS)分析进行了比较。通过谱系特异性单核苷酸变异(SNV)、大片段序列多态性、 spoligotyping 以及使用分枝杆菌插入重复单元(MIRU)和日本结核协会(JATA)基因座组的可变数串联重复(VNTR)分析,从全基因组序列中获得了这些数据。直接将这些信息与 WGS 分析结果进行比较。使用 RepUnitTyping 工具,通过对串联短读序列的 BLAST 搜索,识别了微型卫星重复单元变异。WGS 分析表明,测试的 Mtb 菌株多样,分为谱系(L)1、2 和 4(分别为 24.7%、57.2%和 18.1%)。大多数 L2 菌株进一步分为古老和现代北京基因型,大多数 L1 组是 EAI4_VNM 菌株。虽然基于 PCR 的传统基因分型结果与 WGS 分析结果大多一致,但深入分析发现了可能导致不一致的异常缺失和间隔物。JATA-VNTR 组包括高变区,将 MIRU15 产生的大北京基因型簇分为更小的簇。在 33 个 VNTR 基因座内观察到的重复单元变异的分布因三个谱系而异而有明显差异。在 L1 中,VNTR 定义的基因簇内的 SNP 差异比在 L2 和 L4 中更大(P=0.001)。基于 PCR 的基因分型结果与 WGS 数据的计算机分析之间的直接比较将在这一过渡时期缩小经典技术和现代技术之间的差距,并为特定地理区域的 Mtb 基因型提供更多信息。

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