Sanchez A, Trappier S G, Mahy B W, Peters C J, Nichol S T
Division of Viral and Ricketsial Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.
Proc Natl Acad Sci U S A. 1996 Apr 16;93(8):3602-7. doi: 10.1073/pnas.93.8.3602.
In late 1994 and early 1995, Ebola (EBO) virus dramatically reemerged in Africa, causing human disease in the Ivory Coast and Zaire. Analysis of the entire glycoprotein genes of these viruses and those of other EBO virus subtypes has shown that the virion glycoprotein (130 kDa) is encoded in two reading frames, which are linked by transcriptional editing. This editing results in the addition of an extra nontemplated adenosine within a run of seven adenosines near the middle of the coding region. The primary gene product is a smaller (50-70 kDa), nonstructural, secreted glycoprotein, which is produced in large amounts and has an unknown function. Phylogenetic analysis indicates that EBO virus subtypes are genetically diverse and that the recent Ivory Coast isolate represents a new (fourth) subtype of EBO virus. In contrast, the EBO virus isolate from the 1995 outbreak in Kikwit, Zaire, is virtually identical to the virus that caused a similar epidemic in Yambuku, Zaire, almost 20 years earlier. This genetic stability may indicate that EBO viruses have coevolved with their natural reservoirs and do not change appreciably in the wild.
1994年末和1995年初,埃博拉(EBO)病毒在非洲显著再现,在象牙海岸和扎伊尔引发了人类疾病。对这些病毒以及其他埃博拉病毒亚型的完整糖蛋白基因进行分析后发现,病毒粒子糖蛋白(130 kDa)由两个阅读框编码,这两个阅读框通过转录编辑相连。这种编辑导致在编码区中部附近的七个腺苷序列中额外添加了一个非模板化腺苷。主要基因产物是一种较小的(50 - 70 kDa)非结构分泌糖蛋白,其大量产生且功能未知。系统发育分析表明,埃博拉病毒亚型在基因上具有多样性,最近在象牙海岸分离出的毒株代表了一种新的(第四种)埃博拉病毒亚型。相比之下,1995年在扎伊尔基奎特爆发疫情中分离出的埃博拉病毒毒株,与近20年前在扎伊尔扬布库引发类似疫情的病毒几乎完全相同。这种基因稳定性可能表明埃博拉病毒与其天然宿主共同进化,在自然环境中不会发生明显变化。