Mosaic structure of human coronavirus NL63, one thousand years of evolution

被引:136
作者
Pyrc, Krzysztof
Dijkman, Ronald
Deng, Lea
Jebbink, Maarten F.
Ross, Howard A.
Berkhout, Ben
Van der Hoek, Lia
机构
[1] Univ Amsterdam, Lab Expt Virol, Dept Med Microbiol, Ctr Infect & Immun Amsterdam,Acad Med Ctr, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Auckland, Sch Biol Sci, Auckland 1, New Zealand
[3] Univ Auckland, Bioinformat Inst, Auckland 1, New Zealand
关键词
coronavirus; HCoV-NL63; recombination; evolution; molecular clock;
D O I
10.1016/j.jmb.2006.09.074
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Before the SARS outbreak only two human coronaviruses (HCoV) were known: HCoV-OC43 and HCoV-229E. With the discovery of SARS-CoV in 2003, a third family member was identified. Soon thereafter, we described the fourth human coronavirus (HCoV-NL63), a virus that has spread worldwide and is associated with croup in children. We report here the complete genome sequence of two HCoV-NL63 clinical isolates, designated Amsterdam 57 and Amsterdam 496. The genomes are 27,538 and 27,550 nucleotides long, respectively, and share the same genome organization. We identified two variable regions, one within the la and one within the S gene, whereas the 1b and N genes were most conserved. Phylogenetic analysis revealed that HCoV-NL63 genomes have a mosaic structure with multiple recombination sites. Additionally, employing three different algorithms, we assessed the evolutionary rate for the S gene of group 1b coronaviruses to be similar to 3 x 10(-4) substitutions per site per year. Using this evolutionary rate we determined that HCoV-NL63 diverged in the 11th century from. its closest relative HCoV-229E. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:964 / 973
页数:10
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