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全基因组测序表明,澳大利亚新南威尔士州已鉴定的结核分枝杆菌聚类中传播有限。

Whole Genome Sequencing Demonstrates Limited Transmission within Identified Mycobacterium tuberculosis Clusters in New South Wales, Australia.

机构信息

Marie Bashir Institute for Infectious Diseases and Biosecurity, The University of Sydney, Sydney, Australia.

Centre for Infectious Diseases and Microbiology-Public Health, Westmead Hospital, Sydney, Australia.

出版信息

PLoS One. 2016 Oct 13;11(10):e0163612. doi: 10.1371/journal.pone.0163612. eCollection 2016.

Abstract

Australia has a low tuberculosis incidence rate with most cases occurring among recent immigrants. Given suboptimal cluster resolution achieved with 24-locus mycobacterium interspersed repetitive unit (MIRU-24) genotyping, the added value of whole genome sequencing was explored. MIRU-24 profiles of all Mycobacterium tuberculosis culture-confirmed tuberculosis cases diagnosed between 2009 and 2013 in New South Wales (NSW), Australia, were examined and clusters identified. The relatedness of cases within the largest MIRU-24 clusters was assessed using whole genome sequencing and phylogenetic analyses. Of 1841 culture-confirmed TB cases, 91.9% (1692/1841) had complete demographic and genotyping data. East-African Indian (474; 28.0%) and Beijing (470; 27.8%) lineage strains predominated. The overall rate of MIRU-24 clustering was 20.1% (340/1692) and was highest among Beijing lineage strains (35.7%; 168/470). One Beijing and three East-African Indian (EAI) clonal complexes were responsible for the majority of observed clusters. Whole genome sequencing of the 4 largest clusters (30 isolates) demonstrated diverse single nucleotide polymorphisms (SNPs) within identified clusters. All sequenced EAI strains and 70% of Beijing lineage strains clustered by MIRU-24 typing demonstrated distinct SNP profiles. The superior resolution provided by whole genome sequencing demonstrated limited M. tuberculosis transmission within NSW, even within identified MIRU-24 clusters. Routine whole genome sequencing could provide valuable public health guidance in low burden settings.

摘要

澳大利亚的结核病发病率较低,大多数病例发生在最近移民中。鉴于 24 个基因座分枝杆菌散布重复单位(MIRU-24)基因分型的聚类分辨率不理想,探索了全基因组测序的增值作用。对 2009 年至 2013 年间在澳大利亚新南威尔士州(NSW)诊断的所有分枝杆菌培养确诊结核病病例的 MIRU-24 图谱进行了检查并确定了聚类。使用全基因组测序和系统发育分析评估了最大 MIRU-24 聚类中病例之间的相关性。在 1841 例培养确诊的结核病病例中,91.9%(1692/1841)具有完整的人口统计学和基因分型数据。东非印度裔(474;28.0%)和北京(470;27.8%)谱系菌株占主导地位。MIRU-24 聚类的总体率为 20.1%(340/1692),在北京谱系菌株中最高(35.7%;168/470)。一个北京和三个东非印度裔(EAI)克隆复合体负责大多数观察到的聚类。对 4 个最大聚类(30 个分离株)的全基因组测序显示,在鉴定的聚类中存在多种单核苷酸多态性(SNP)。所有测序的 EAI 菌株和 70%的北京谱系菌株通过 MIRU-24 分型聚类表现出明显的 SNP 谱。全基因组测序提供的更高分辨率表明,即使在鉴定的 MIRU-24 聚类中,新南威尔士州的结核分枝杆菌传播也有限。在低负担环境中,常规全基因组测序可以提供有价值的公共卫生指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2713/5063377/5400b891dc71/pone.0163612.g002.jpg

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