Bayesian Reconstruction of Disease Outbreaks by Combining Epidemiologic and Genomic Data

被引:162
作者
Jombart, Thibaut [1 ]
Cori, Anne [1 ]
Didelot, Xavier [1 ]
Cauchemez, Simon [1 ]
Fraser, Christophe [1 ]
Ferguson, Neil [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Sch Publ Hlth, Dept Infect Dis, MRC Ctr Outbreak Anal & Modelling, London, England
基金
英国医学研究理事会; 比尔及梅琳达.盖茨基金会;
关键词
SARS CORONAVIRUS; REAL-TIME; FOLLOW-UP; TRANSMISSION; DYNAMICS; FOOT; TREES;
D O I
10.1371/journal.pcbi.1003457
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Recent years have seen progress in the development of statistically rigorous frameworks to infer outbreak transmission trees ("who infected whom") from epidemiological and genetic data. Making use of pathogen genome sequences in such analyses remains a challenge, however, with a variety of heuristic approaches having been explored to date. We introduce a statistical method exploiting both pathogen sequences and collection dates to unravel the dynamics of densely sampled outbreaks. Our approach identifies likely transmission events and infers dates of infections, unobserved cases and separate introductions of the disease. It also proves useful for inferring numbers of secondary infections and identifying heterogeneous infectivity and super-spreaders. After testing our approach using simulations, we illustrate the method with the analysis of the beginning of the 2003 Singaporean outbreak of Severe Acute Respiratory Syndrome (SARS), providing new insights into the early stage of this epidemic. Our approach is the first tool for disease outbreak reconstruction from genetic data widely available as free software, the R package outbreaker. It is applicable to various densely sampled epidemics, and improves previous approaches by detecting unobserved and imported cases, as well as allowing multiple introductions of the pathogen. Because of its generality, we believe this method will become a tool of choice for the analysis of densely sampled disease outbreaks, and will form a rigorous framework for subsequent methodological developments.
引用
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页数:14
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