Chang G J, Cropp B C, Kinney R M, Trent D W, Gubler D J
Division of Vector-Borne Infectious Diseases, Centers for Disease Control and Prevention, Fort Collins, Colorado 80522, USA.
J Virol. 1995 Sep;69(9):5773-80. doi: 10.1128/JVI.69.9.5773-5780.1995.
The evolution of yellow fever virus over 67 years was investigated by comparing the nucleotide sequences of the envelope (E) protein genes of 20 viruses isolated in Africa, the Caribbean, and South America. Uniformly weighted parsimony algorithm analysis defined two major evolutionary yellow fever virus lineages designated E genotypes I and II. E genotype I contained viruses isolated from East and Central Africa. E genotype II viruses were divided into two sublineages: IIA viruses from West Africa and IIB viruses from America, except for a 1979 virus isolated from Trinidad (TRINID79A). Unique signature patterns were identified at 111 nucleotide and 12 amino acid positions within the yellow fever virus E gene by signature pattern analysis. Yellow fever viruses from East and Central Africa contained unique signatures at 60 nucleotide and five amino acid positions, those from West Africa contained unique signatures at 25 nucleotide and two amino acid positions, and viruses from America contained such signatures at 30 nucleotide and five amino acid positions in the E gene. The dissemination of yellow fever viruses from Africa to the Americas is supported by the close genetic relatedness of genotype IIA and IIB viruses and genetic evidence of a possible second introduction of yellow fever virus from West Africa, as illustrated by the TRINID79A virus isolate. The E protein genes of American IIB yellow fever viruses had higher frequencies of amino acid substitutions than did genes of yellow fever viruses of genotypes I and IIA on the basis of comparisons with a consensus amino acid sequence for the yellow fever E gene. The great variation in the E proteins of American yellow fever virus probably results from positive selection imposed by virus interaction with different species of mosquitoes or nonhuman primates in the Americas.
通过比较在非洲、加勒比地区和南美洲分离出的20种病毒的包膜(E)蛋白基因的核苷酸序列,对黄热病病毒67年的进化情况进行了研究。采用均匀加权简约算法分析确定了两个主要的进化黄热病病毒谱系,分别命名为E基因型I和II。E基因型I包含从东非和中非分离出的病毒。E基因型II病毒分为两个亚谱系:来自西非的IIA病毒和来自美洲的IIB病毒,但1979年从特立尼达分离出的病毒(TRINID79A)除外。通过特征模式分析,在黄热病病毒E基因内的111个核苷酸和12个氨基酸位置鉴定出独特的特征模式。来自东非和中非的黄热病病毒在60个核苷酸和5个氨基酸位置含有独特特征,来自西非的病毒在25个核苷酸和2个氨基酸位置含有独特特征,而来自美洲的病毒在E基因的30个核苷酸和5个氨基酸位置含有此类特征。基因型IIA和IIB病毒的密切遗传相关性以及TRINID79A病毒分离株所表明的黄热病病毒可能从西非第二次传入的遗传证据,支持了黄热病病毒从非洲传播到美洲的观点。与黄热病E基因的共有氨基酸序列相比,美洲IIB黄热病病毒的E蛋白基因氨基酸替换频率高于基因型I和IIA的黄热病病毒基因。美洲黄热病病毒E蛋白的巨大变异可能是由于病毒与美洲不同种类的蚊子或非人类灵长类动物相互作用所施加的正选择导致的。