Rest Joshua S, Mindell David P
Department of Ecology & Evolutionary Biology and Museum of Zoology, University of Michigan, 1109 Geddes Avenue, Ann Arbor, MI 48109-1079, USA.
Infect Genet Evol. 2003 Sep;3(3):219-25. doi: 10.1016/j.meegid.2003.08.001.
The sudden appearance and potential lethality of severe acute respiratory syndrome associated coronavirus (SARS-CoV) in humans has focused attention on understanding its origins. Here, we assess phylogenetic relationships for the SARS-CoV lineage as well as the history of host-species shifts for SARS-CoV and other coronaviruses. We used a Bayesian phylogenetic inference approach with sliding window analyses of three SARS-CoV proteins: RNA dependent RNA polymerase (RDRP), nucleocapsid (N) and spike (S). Conservation of RDRP allowed us to use a set of Arteriviridae taxa to root the Coronaviridae phylogeny. We found strong evidence for a recombination breakpoint within SARS-CoV RDRP, based on different, well supported trees for a 5' fragment (supporting SARS-CoV as sister to a clade including all other coronaviruses) and a 3' fragment (supporting SARS-CoV as sister to group three avian coronaviruses). These different topologies are statistically significant: the optimal 5' tree could be rejected for the 3' region, and the optimal 3' tree could be rejected for the 5' region. We did not find statistical evidence for recombination in analyses of N and S, as there is little signal to differentiate among alternative trees. Comparison of phylogenetic trees for 11 known host-species and 36 coronaviruses, representing coronavirus groups 1-3 and SARS-CoV, based on N showed statistical incongruence indicating multiple host-species shifts for coronaviruses. Inference of host-species associations is highly sensitive to sampling and must be considered cautiously. However, current sampling suggests host-species shifts between mouse and rat, chicken and turkey, mammals and manx shearwater, and humans and other mammals. The sister relationship between avian coronaviruses and the 3' RDRP fragment of SARS-CoV suggests an additional host-species shift. Demonstration of recombination in the SARS-CoV lineage indicates its potential for rapid unpredictable change, a potentially important challenge for public health management and for drug and vaccine development.
严重急性呼吸综合征相关冠状病毒(SARS-CoV)在人类中的突然出现及其潜在致死性,已使人们将注意力集中在了解其起源上。在此,我们评估了SARS-CoV谱系的系统发育关系,以及SARS-CoV和其他冠状病毒宿主物种转移的历史。我们采用贝叶斯系统发育推断方法,对三种SARS-CoV蛋白进行滑动窗口分析:RNA依赖性RNA聚合酶(RDRP)、核衣壳蛋白(N)和刺突蛋白(S)。RDRP的保守性使我们能够使用一组动脉炎病毒分类群来确定冠状病毒科系统发育树的根。基于5'片段(支持SARS-CoV作为包括所有其他冠状病毒的一个进化枝的姐妹)和3'片段(支持SARS-CoV作为第三组禽冠状病毒的姐妹)的不同且得到有力支持的树,我们发现SARS-CoV的RDRP内存在重组断点的有力证据。这些不同的拓扑结构具有统计学意义:最优的5'树在3'区域被拒绝,最优的3'树在5'区域被拒绝。在对N和S的分析中,我们没有发现重组的统计学证据,因为几乎没有信号能区分不同的树。基于N对代表冠状病毒1-3组和SARS-CoV的11种已知宿主物种和36种冠状病毒的系统发育树进行比较,显示出统计学上的不一致,表明冠状病毒发生了多次宿主物种转移。宿主物种关联的推断对抽样高度敏感,必须谨慎考虑。然而,目前的抽样表明宿主物种在小鼠和大鼠、鸡和火鸡、哺乳动物和马恩岛海鸥以及人类和其他哺乳动物之间发生了转移。禽冠状病毒与SARS-CoV的3'RDRP片段之间的姐妹关系表明存在额外的宿主物种转移。SARS-CoV谱系中重组的证明表明其具有快速不可预测变化的潜力,这对公共卫生管理以及药物和疫苗开发来说是一个潜在的重要挑战。