Pomeroy Laura W, Bjørnstad Ottar N, Holmes Edward C
Center for Infectious Disease Dynamics, Department of Biology, The Pennsylvania State University, 501 ASI Building, University Park, PA 16802, USA.
J Mol Evol. 2008 Feb;66(2):98-106. doi: 10.1007/s00239-007-9040-x. Epub 2008 Jan 24.
Paramyxoviruses are responsible for considerable disease burden in human and wildlife populations: measles and mumps continue to affect the health of children worldwide, while canine distemper virus causes serious morbidity and mortality in a wide range of mammalian species. Although these viruses have been studied extensively at both the epidemiological and the phylogenetic scales, little has been done to integrate these two types of data. Using a Bayesian coalescent approach, we infer the evolutionary and epidemiological dynamics of measles, mumps and canine distemper viruses. Our analysis yielded data on viral substitution rates, the time to common ancestry, and elements of their demographic history. Estimates of rates of evolutionary change were similar to those observed in other RNA viruses, ranging from 6.585 to 11.350 x 10(-4 )nucleotide substitutions per site, per year. Strikingly, the mean Time to the Most Recent Common Ancestor (TMRCA) was both similar and very recent among the viruses studied, ranging from only 58 to 91 years (1908 to 1943). Worldwide, the paramyxoviruses studied here have maintained a relatively constant level of genetic diversity. However, detailed heterchronous samples illustrate more complex dynamics in some epidemic populations, and the relatively low levels of genetic diversity (population size) in all three viruses is likely to reflect the population bottlenecks that follow recurrent outbreaks.
麻疹和腮腺炎持续影响着全球儿童的健康,而犬瘟热病毒在多种哺乳动物物种中导致严重的发病和死亡。尽管这些病毒在流行病学和系统发育尺度上都得到了广泛研究,但将这两类数据整合起来的工作却做得很少。我们采用贝叶斯合并方法,推断麻疹、腮腺炎和犬瘟热病毒的进化和流行病学动态。我们的分析得出了关于病毒替代率、共同祖先时间以及它们种群历史要素的数据。进化变化率的估计值与在其他RNA病毒中观察到的相似,范围为每年每个位点6.585至11.350×10⁻⁴个核苷酸替代。引人注目的是,在所研究的病毒中,最近共同祖先的平均时间(TMRCA)既相似又非常近,仅为58至91年(1908年至1943年)。在全球范围内,这里研究的副黏病毒保持了相对恒定的遗传多样性水平。然而,详细的异步样本说明了一些流行种群中更复杂的动态,并且所有三种病毒相对较低的遗传多样性水平(种群大小)可能反映了反复爆发后出现的种群瓶颈。