Lee E, Stocks C, Lobigs P, Hislop A, Straub J, Marshall I, Weir R, Dalgarno L
Division of Biochemistry and Molecular Biology, Faculty of Science, The Australian National University, Canberra.
Virology. 1997 Jan 20;227(2):509-14. doi: 10.1006/viro.1996.8343.
Barmah Forest virus (BFV) is an atypical alphavirus [Dalgarno, L., Short, N. J., Hardy, C. M., Bell, J. R., Strauss, J. H., and Marshall, I. D. (1984). Virology 133, 416-426] and has been classified as the sole known member of a seventh alphavirus serocomplex. The complete nucleotide sequence of BFV genomic RNA is 11,488 nucleotides in length excluding the poly(A) tail. Two long open reading frames in the RNA encode a nonstructural polyprotein of 2411 amino acids and a structural polyprotein of 1239 amino acids, respectively. The BFV envelope protein E2 is unique among sequenced alphaviruses in having no N-linked glycosylation sites; E1 carries two glycosylation sites. From amino acid sequence comparisons with sequenced alphaviruses BFV is most closely related to Ross River and Semliki Forest viruses. Sequence homology between BFV and other alphaviruses is relatively uniform along the length of the nonstructural and structural polyproteins, providing no evidence that BFV has arisen from recombination between ancestral alphaviruses in the coding region of the genome. The BFV 3' noncoding region of 445 nucleotides has unusual features. There are two unrelated sequence blocks of 48 nucleotides (sequence I) and 47 nucleotides (sequence II) both of which are repeated once. Sequence I is closely related to a repeat in the 3' noncoding region of Ross River and Getah viruses; sequence II is unrelated to repeat blocks in other sequenced alphaviruses. Thus, recombination between ancestral viruses may have played a role in the evolution of the BFV 3' noncoding region.
巴马森林病毒(BFV)是一种非典型甲病毒[达尔加诺,L.,肖特,N. J.,哈迪,C. M.,贝尔,J. R.,施特劳斯,J. H.,以及马歇尔,I. D.(1984年)。《病毒学》133卷,第416 - 426页],已被归类为第七个甲病毒血清复合群的唯一已知成员。BFV基因组RNA的完整核苷酸序列长度为11488个核苷酸,不包括聚腺苷酸尾。RNA中的两个长开放阅读框分别编码一个由2411个氨基酸组成的非结构多蛋白和一个由1239个氨基酸组成的结构多蛋白。BFV包膜蛋白E2在已测序的甲病毒中独一无二,没有N - 连接糖基化位点;E1带有两个糖基化位点。通过与已测序甲病毒的氨基酸序列比较,BFV与罗斯河病毒和塞姆利基森林病毒关系最为密切。BFV与其他甲病毒之间的序列同源性在非结构和结构多蛋白的长度上相对一致,没有证据表明BFV是由基因组编码区域中祖先甲病毒之间的重组产生的。BFV的445个核苷酸的3'非编码区具有不寻常的特征。有两个不相关的序列块,分别为48个核苷酸(序列I)和47个核苷酸(序列II),两者都重复了一次。序列I与罗斯河病毒和盖塔病毒3'非编码区的一个重复序列密切相关;序列II与其他已测序甲病毒中的重复块无关。因此,祖先病毒之间的重组可能在BFV 3'非编码区的进化中发挥了作用。