Kohl Alain, Lowen Anice C, Léonard Vincent H J, Elliott Richard M
Division of Virology, Institute of Biomedical and Life Sciences, University of Glasgow, Glasgow G11 5JR, Scotland, UK.
J Gen Virol. 2006 Jan;87(Pt 1):177-187. doi: 10.1099/vir.0.81227-0.
The genome of Bunyamwera virus (BUN; family Bunyaviridae, genus Orthobunyavirus) comprises three segments of negative-sense, single-stranded RNA. The RNA segments are encapsidated by the viral nucleocapsid (N) protein and form panhandle-like structures through interaction of complementary sequences at their 5' and 3' termini. Transcription and replication of a BUN genome analogue (minireplicon), comprising the viral non-coding sequences flanking a reporter gene, requires just the viral RNA polymerase (L protein) and N protein. Here, sequences of Bunyamwera serogroup M segment RNAs were compared and conserved elements within nt 20-33 of the 3' and 5' non-coding regions that can affect packaging of minireplicons into virions were identified. RNA-folding models suggest that a conserved sequence within nt 20-33 of the 5' end of the genome segments maintains conserved structural features necessary for efficient transcription. Competitive packaging experiments using M, L and S segment-derived minireplicons that encode different reporter genes showed variable packaging efficiencies of the three segments. Packaging of a particular segment appeared to be independent of the presence of other segments and, for the S segment, packaging efficiency was unaffected by the inclusion of viral coding sequences in the minireplicon.
布尼亚姆韦拉病毒(BUN;布尼亚病毒科正布尼亚病毒属)的基因组由三个负义单链RNA片段组成。这些RNA片段被病毒核衣壳(N)蛋白包裹,并通过其5'和3'末端互补序列的相互作用形成类似锅柄的结构。包含报告基因两侧病毒非编码序列的布尼亚姆韦拉病毒基因组类似物(微型复制子)的转录和复制仅需要病毒RNA聚合酶(L蛋白)和N蛋白。在此,对布尼亚姆韦拉血清群M片段RNA的序列进行了比较,并鉴定了3'和5'非编码区nt 20 - 33内可影响微型复制子包装入病毒粒子的保守元件。RNA折叠模型表明,基因组片段5'端nt 20 - 33内的保守序列维持了有效转录所需的保守结构特征。使用编码不同报告基因的M、L和S片段衍生微型复制子进行的竞争性包装实验显示,这三个片段的包装效率各不相同。特定片段的包装似乎独立于其他片段的存在,并且对于S片段,微型复制子中包含病毒编码序列对其包装效率没有影响。