Chumakov Institute of Poliomyelitis and Viral Encephalitides, Moscow, Russia.
Institute of Virology, University of Bonn Medical Centre, Bonn, Germany.
J Gen Virol. 2012 Nov;93(Pt 11):2357-2362. doi: 10.1099/vir.0.043216-0. Epub 2012 Aug 15.
The full coding sequences of two novel human enterovirus (HEV)-C serotypes 105 and 116, sampled in the Republic of the Congo in 2010 and in Russia in 2011, were identified in this study. Enterovirus (EV)-105 was closest to EV-104 in the 5' NTR and to EV-109 in the coding genome region. It had the same unconventional 5' NTR as EV-104 and EV-109. The non-cytopathogenic EV-116 was phylogenetically close to coxsackievirus (CV)-A1, CV-A19 and CV-A22, which also cannot be propagated in routinely used cell cultures. There were signs of recombination within this subgroup of HEV-C; however, recombination with conventional HEV-C was restricted, implying partial reproductive isolation. As there is also evidence of different permissive replication systems and distinct genetic properties of these subgroups, they may represent subspecies of the HEV-C species or different stages of speciation.
本研究鉴定了两株新的人类肠道病毒(HEV)-C 血清型 105 和 116 的全长编码序列,它们分别于 2010 年在刚果共和国和 2011 年在俄罗斯被采集。肠道病毒(EV)-105 在 5' NTR 区与 EV-104 最为接近,在编码基因组区域与 EV-109 最为接近。它与 EV-104 和 EV-109 具有相同的非常规 5' NTR。无细胞病变性的 EV-116 在系统发育上与柯萨奇病毒(CV)-A1、CV-A19 和 CV-A22 最为接近,这些病毒也不能在常规使用的细胞培养物中繁殖。在这个 HEV-C 亚群中存在重组的迹象;然而,与常规 HEV-C 的重组受到限制,暗示存在部分生殖隔离。由于这些亚群还存在不同的许可复制系统和不同的遗传特性的证据,它们可能代表 HEV-C 种的亚种或种形成的不同阶段。