Oberste M Steven, Maher Kaija, Michele Suzanne M, Belliot Gaël, Uddin Moyez, Pallansch Mark A
Respiratory and Enteric Viruses Branch, Division of Viral and Rickettsial Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, 1600 Clifton Road NE, Mailstop G-17, Atlanta, GA 30333, USA.
Institute of Public Health, Dhaka, Bangladesh.
J Gen Virol. 2005 Feb;86(Pt 2):445-451. doi: 10.1099/vir.0.80475-0.
Molecular methods have enabled the rapid identification of new enterovirus (EV) serotypes that would have been untypable using existing neutralizing antisera. Nineteen strains of four new EV types termed EV76 (11 isolates), EV89 (two isolates), EV90 (four isolates) and EV91 (two isolates), isolated from clinical specimens from patients in France (one isolate) and Bangladesh (18 isolates), are described. Nucleotide sequences encoding the VP1 capsid protein (882-888 nt) are less than 65 % identical to the homologous sequences of the recognized human EV serotypes, but within each group the sequences are more than 78 % identical. The deduced amino acid sequences of the complete capsid (P1) region are more than 94 % identical within type but less than 76 % identical to those of the recognized serotypes. For both VP1 and P1, the 19 isolates are monophyletic by type with respect to all other EV serotypes. Using the proposed molecular typing scheme, these data support their identification as four new types within the species Human enterovirus A (HEV-A). In almost all cases, the VP1 sequences were more similar to those of some simian EVs than to the human EVs. Partial 3D sequences of all 19 isolates also clustered within HEV-A; they were monophyletic as a group, but not by type, suggesting that recombination has occurred among viruses of these four types. Partial 3D sequences were more closely related to those of simian EVs than to human viruses in HEV-A. These results suggest that the four new types may represent a new subgroup within HEV-A, in addition to the existing human and simian subgroups.
分子方法已能够快速鉴定出新的肠道病毒(EV)血清型,而使用现有的中和抗血清则无法对其进行分型。本文描述了从法国(1株)和孟加拉国(18株)患者的临床标本中分离出的4种新型肠道病毒的19个毒株,分别命名为EV76(11株)、EV89(2株)、EV90(4株)和EV91(2株)。编码VP1衣壳蛋白(882 - 888 nt)的核苷酸序列与已确认的人类肠道病毒血清型的同源序列的同一性低于65%,但在每组内序列同一性超过78%。完整衣壳(P1)区域的推导氨基酸序列在型内同一性超过94%,但与已确认血清型的同一性低于76%。对于VP1和P1,这19个分离株相对于所有其他肠道病毒血清型在型上是单系的。使用提议的分子分型方案,这些数据支持将它们鉴定为人肠道病毒A(HEV - A)种内的4种新类型。在几乎所有情况下,VP1序列与一些猿猴肠道病毒的序列比与人类肠道病毒的序列更相似。所有19个分离株的部分3D序列也聚类在HEV - A内;它们作为一个群体是单系的,但不是按型单系,这表明这四种类型的病毒之间发生了重组。部分3D序列与猿猴肠道病毒的序列比与HEV - A中的人类病毒的序列关系更密切。这些结果表明,除了现有的人类和猿猴亚组外,这四种新类型可能代表HEV - A内的一个新亚组。