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[Estimation of molecular clock of based on whole genome sequencing data].

作者信息

Tao B L, Wang Y T, Li Z Q, Wu J Z, Wang J M

机构信息

Department of Epidemiology, Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing 211166, China.

Department of Epidemiology, Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing 211166, China Department of Epidemiology, Gusu School, Nanjing Medical University, Nanjing 211166, China.

出版信息

Zhonghua Liu Xing Bing Xue Za Zhi. 2022 Sep 10;43(9):1462-1468. doi: 10.3760/cma.j.cn112338-20220408-00272.

DOI:10.3760/cma.j.cn112338-20220408-00272
PMID:36117355
Abstract

To analyze the genomic mutation of () isolated in endogenous activation period and estimate the molecular clock based on the whole genome sequencing data. Literatures of the whole genome research of endogenous reactivated tuberculosis were retrieved, and the corresponding whole genome sequencing data were downloaded. We extracted the single nucleotide polymorphisms (SNPs) and strain isolation time of initial treatment and relapse of tuberculosis cases, explored the relationship between the different SNPs and interval between initial treatment and relapse by Poisson regression model, calculated the molecular clock, and estimated the mutation rate. When the generation time of was 18 hours, the mutation rate in 0-2 years, i.e. short-term endogenous activation, was 6.47×10 (95%: 5.59×10-7.44×10), which was significantly higher than that in 2-14 years in long term endogenous activation (3.27×10, 95%: 2.88×10-3.69×10). The mutation rates of 0-, 1-, 2-, 3-, 5- and 7-14 years were 7.10×10, 6.06×10, 4.24×10, 5.34×10, 2.59×10 and 1.26×10 respectively. In the period of endogenous reactivation, the mutation rate of decreases with the interval time between initial treatment and relapse, which verifies the clinically observed phenomenon that the relapse often occurs within two years after the initial treatment of tuberculosis.

摘要

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