Gautam Sanjay S, Mac Aogáin Micheál, Cooley Louise A, Haug Greg, Fyfe Janet A, Globan Maria, O'Toole Ronan F
School of Medicine, University of Tasmania, Hobart, Tasmania, Australia.
Department of Clinical Microbiology, Trinity College Dublin, Dublin, Ireland.
PLoS One. 2018 Feb 21;13(2):e0192351. doi: 10.1371/journal.pone.0192351. eCollection 2018.
The origin and spread of tuberculosis (TB) in Tasmania and the types of strains of Mycobacterium tuberculosis complex (MTBC) present in the population are largely unknown.
The aim of this study was to perform the first genomic analysis of MTBC isolates from Tasmania to better understand the epidemiology of TB in the state.
Whole-genome sequencing was performed on cultured isolates of MTBC collected from 2014-2016. Single-locus variant analysis was applied to determine the phylogeny of the isolates and the presence of drug-resistance mutations. The genomic data were then cross-referenced against public health surveillance records on each of the cases.
We determined that 83.3% of TB cases in Tasmania from 2014-2016 occurred in non-Australian born individuals. Two possible TB clusters were identified based on single locus variant analysis, one from November-December 2014 (n = 2), with the second from May-August 2015 (n = 4). We report here the first known isolate of multi-drug resistant (MDR) M. tuberculosis in Tasmania from 2016 for which we established its drug resistance mutations and potential overseas origin. In addition, we characterised a case of M. bovis TB in a Tasmanian-born person who presented in 2014, approximately 40 years after the last confirmed case in the state's bovids.
TB in Tasmania is predominantly of overseas origin with genotypically-unique drug-susceptible isolates of M. tuberculosis. However, the state also exhibits features of TB that are observed in other jurisdictions, namely, the clustering of cases, and drug resistance. Early detection of TB and contact tracing, particularly of overseas-born cases, coordinated with rapid laboratory drug-susceptibility testing and molecular typing, will be essential for Tasmania to reach the World Health Organisation's TB eradication goals for low-incidence settings.
塔斯马尼亚州结核病(TB)的起源与传播以及人群中存在的结核分枝杆菌复合群(MTBC)菌株类型在很大程度上尚不清楚。
本研究旨在对来自塔斯马尼亚州的MTBC分离株进行首次基因组分析,以更好地了解该州结核病的流行病学情况。
对2014 - 2016年收集的MTBC培养分离株进行全基因组测序。应用单基因座变异分析来确定分离株的系统发育以及耐药突变的存在情况。然后将基因组数据与每个病例的公共卫生监测记录进行交叉比对。
我们确定2014 - 2016年塔斯马尼亚州83.3%的结核病病例发生在非澳大利亚出生的个体中。基于单基因座变异分析确定了两个可能的结核病聚集群,一个来自2014年11月至12月(n = 2),另一个来自2015年5月至8月(n = 4)。我们在此报告2016年塔斯马尼亚州首例已知的耐多药(MDR)结核分枝杆菌分离株,我们确定了其耐药突变及可能的海外来源。此外,我们对一名2014年出生在塔斯马尼亚州的牛型结核分枝杆菌结核病病例进行了特征描述,该病例出现时间距离该州牛群中最后一例确诊病例约40年。
塔斯马尼亚州的结核病主要源于海外,存在基因型独特的结核分枝杆菌药物敏感分离株。然而,该州也呈现出在其他地区观察到的结核病特征,即病例聚集和耐药性。对于塔斯马尼亚州实现世界卫生组织针对低发病率地区的结核病根除目标而言,早期发现结核病并进行接触者追踪,尤其是对海外出生病例,再配合快速的实验室药敏试验和分子分型,将至关重要。