Luo Tao, Yang Chongguang, Pang Yu, Zhao Yanlin, Mei Jian, Gao Qian
Key Laboratory of Medical Molecular Virology of Ministries of Education and Health, Institutes of Biomedical Sciences and Institute of Medical Microbiology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Chinese Center for Disease Control and Prevention, and Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing, China.
PLoS One. 2014 Feb 25;9(2):e89726. doi: 10.1371/journal.pone.0089726. eCollection 2014.
Molecular typing based on variable-number tandem repeats (VNTR) analysis is a promising tool for identifying transmission of Mycobacterium tuberculosis. However, the currently proposed 15- and 24-locus VNTR sets (VNTR-15/24) only have limited resolution and contain too many loci for large-scale typing in high burden countries. To develop an optimal typing scheme in China, we evaluated the resolution and robustness of 25 VNTR loci, using population-based collections of 1362 clinical isolates from six provinces across the country. The resolution of most loci showed considerable variations among regions. By calculating the average resolution of all possible combinations of 20 robust loci, we identified an optimal locus set with a minimum of 9 loci (VNTR-9) that could achieve comparable resolution of the standard VNTR-15. The VNTR-9 had consistently high resolutions in all six regions, and it was highly concordant with VNTR-15 for defining both clustered and unique genotypes. Furthermore, VNTR-9 was phylogenetically informative for classifying lineages/sublineages of M. tuberculosis. Three hypervariable loci (HV-3), VNTR 3232, VNTR 3820 and VNTR 4120, were proved important for further differentiating unrelated clustered strains based on VNTR-9. We propose the optimized VNTR-9 as first-line method and the HV-3 as second-line method for molecular typing of M. tuberculosis in China and surrounding countries. The development of hierarchical VNTR typing methods that can achieve high resolution with a small number of loci could be suitable for molecular epidemiology study in other high burden countries.
基于可变数目串联重复序列(VNTR)分析的分子分型是鉴定结核分枝杆菌传播的一种很有前景的工具。然而,目前提出的15位点和24位点VNTR组合(VNTR - 15/24)分辨率有限,对于高负担国家的大规模分型而言,所含位点过多。为在中国开发一种最佳分型方案,我们使用来自全国六个省份的1362株临床分离株的基于人群的样本集,评估了25个VNTR位点的分辨率和稳健性。大多数位点的分辨率在不同地区间存在显著差异。通过计算20个稳健位点的所有可能组合的平均分辨率,我们确定了一个最少包含9个位点的最佳位点组合(VNTR - 9),其可实现与标准VNTR - 15相当的分辨率。VNTR - 9在所有六个地区的分辨率一直很高,并且在定义聚集型和独特基因型方面与VNTR - 15高度一致。此外,VNTR - 9在对结核分枝杆菌的谱系/亚谱系进行分类时具有系统发育信息。三个高变位点(HV - 3),即VNTR 3232、VNTR 3820和VNTR 4120,被证明对于基于VNTR - 9进一步区分不相关的聚集菌株很重要。我们建议将优化后的VNTR - 9作为中国及周边国家结核分枝杆菌分子分型的一线方法,将HV - 3作为二线方法。开发能够通过少量位点实现高分辨率的分层VNTR分型方法可能适用于其他高负担国家的分子流行病学研究。