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使用近似贝叶斯计算从基因型数据估计结核病传播参数。

Using approximate Bayesian computation to estimate tuberculosis transmission parameters from genotype data.

作者信息

Tanaka Mark M, Francis Andrew R, Luciani Fabio, Sisson S A

机构信息

School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, Australia.

出版信息

Genetics. 2006 Jul;173(3):1511-20. doi: 10.1534/genetics.106.055574. Epub 2006 Apr 19.

Abstract

Tuberculosis can be studied at the population level by genotyping strains of Mycobacterium tuberculosis isolated from patients. We use an approximate Bayesian computational method in combination with a stochastic model of tuberculosis transmission and mutation of a molecular marker to estimate the net transmission rate, the doubling time, and the reproductive value of the pathogen. This method is applied to a published data set from San Francisco of tuberculosis genotypes based on the marker IS6110. The mutation rate of this marker has previously been studied, and we use those estimates to form a prior distribution of mutation rates in the inference procedure. The posterior point estimates of the key parameters of interest for these data are as follows: net transmission rate, 0.69/year [95% credibility interval (C.I.) 0.38, 1.08]; doubling time, 1.08 years (95% C.I. 0.64, 1.82); and reproductive value 3.4 (95% C.I. 1.4, 79.7). These figures suggest a rapidly spreading epidemic, consistent with observations of the resurgence of tuberculosis in the United States in the 1980s and 1990s.

摘要

可通过对从患者中分离出的结核分枝杆菌菌株进行基因分型,在人群层面研究结核病。我们使用一种近似贝叶斯计算方法,结合结核病传播和分子标记突变的随机模型,来估计病原体的净传播率、倍增时间和繁殖值。该方法应用于基于标记IS6110的旧金山已发表的结核病基因型数据集。此前已对该标记的突变率进行了研究,我们在推理过程中使用这些估计值来形成突变率的先验分布。这些数据的关键参数的后验点估计如下:净传播率,0.69/年[95%可信区间(C.I.)0.38,1.08];倍增时间,1.08年(95% C.I. 0.64,1.82);繁殖值3.4(95% C.I. 1.4,79.7)。这些数据表明疫情正在迅速蔓延,这与20世纪80年代和90年代美国结核病卷土重来的观察结果一致。

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