Brown B A, Oberste M S, Alexander J P, Kennett M L, Pallansch M A
Division of Viral Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Public Health Service, U.S. Department of Health and Human Services, Atlanta, Georgia 30333, USA.
J Virol. 1999 Dec;73(12):9969-75. doi: 10.1128/JVI.73.12.9969-9975.1999.
Enterovirus 71 (EV71) (genus Enterovirus, family Picornaviridae), a common cause of hand, foot, and mouth disease (HFMD), may also cause severe neurological diseases, such as encephalitis and poliomyelitis-like paralysis. To examine the genetic diversity and rate of evolution of EV71, we have determined and analyzed complete VP1 sequences (891 nucleotides) for 113 EV71 strains isolated in the United States and five other countries from 1970 to 1998. Nucleotide sequence comparisons demonstrated three distinct EV71 genotypes, designated A, B, and C. The genetic variation within genotypes (12% or fewer nucleotide differences) was less than the variation between genotypes (16.5 to 19.7%). Strains of all three genotypes were at least 94% identical to one another in deduced amino acid sequence. The EV71 prototype strain, BrCr-CA-70, isolated in California in 1970, is the sole member of genotype A. Strains isolated in the United States and Australia during the period from 1972 to 1988, a 1994 Colombian isolate, and isolates from a large HFMD outbreak in Malaysia in 1997 are all members of genotype B. Although strains of genotype B continue to circulate in other parts of the world, none have been isolated in the United States since 1988. Genotype C contains strains isolated in 1985 or later in the United States, Canada, Australia, and the Republic of China. The annual rate of evolution within both the B and C genotypes was estimated to be approximately 1.35 x 10(-2) substitutions per nucleotide and is similar to the rate observed for poliovirus. The results indicate that EV71 is a genetically diverse, rapidly evolving virus. Its worldwide circulation and potential to cause severe disease underscore the need for additional surveillance and improved methods to identify EV71 in human disease.
肠道病毒71型(EV71)(肠道病毒属,小核糖核酸病毒科)是手足口病(HFMD)的常见病因,也可能引发严重的神经系统疾病,如脑炎和脊髓灰质炎样麻痹。为了研究EV71的遗传多样性和进化速率,我们测定并分析了1970年至1998年期间在美国和其他五个国家分离出的113株EV71毒株的完整VP1序列(891个核苷酸)。核苷酸序列比较显示有三种不同的EV71基因型,分别命名为A、B和C。基因型内的遗传变异(核苷酸差异为12%或更少)小于基因型间的变异(16.5%至19.7%)。所有三种基因型的毒株在推导的氨基酸序列上彼此至少有94%的同一性。1970年在加利福尼亚分离出的EV71原型毒株BrCr-CA-70是基因型A的唯一成员。1972年至1988年期间在美国和澳大利亚分离出的毒株、1994年哥伦比亚的一株分离株以及1997年马来西亚一次手足口病大暴发中的分离株均为基因型B的成员。虽然基因型B的毒株仍在世界其他地区传播,但自1988年以来在美国未再分离出此类毒株。基因型C包含1985年或之后在美国、加拿大、澳大利亚和中国分离出的毒株。B和C基因型内的年进化速率估计约为每核苷酸1.35×10⁻²个替换,与脊髓灰质炎病毒的进化速率相似。结果表明,EV71是一种遗传多样、快速进化的病毒。其在全球的传播以及引发严重疾病的可能性突出了加强监测以及改进在人类疾病中鉴定EV71方法的必要性。