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致倦库蚊浓核病毒的基因组结构与表达策略,一种具有双义组织的蚊虫浓核病毒

Structure and expression strategy of the genome of Culex pipiens densovirus, a mosquito densovirus with an ambisense organization.

作者信息

Baquerizo-Audiot Elizabeth, Abd-Alla Adly, Jousset Françoise-Xavière, Cousserans François, Tijssen Peter, Bergoin Max

机构信息

Laboratoire de Pathologie Comparée, Université Montpellier II, Montpellier, France.

出版信息

J Virol. 2009 Jul;83(13):6863-73. doi: 10.1128/JVI.00524-09. Epub 2009 Apr 22.

Abstract

The genome of all densoviruses (DNVs) so far isolated from mosquitoes or mosquito cell lines consists of a 4-kb single-stranded DNA molecule with a monosense organization (genus Brevidensovirus, subfamily Densovirinae). We previously reported the isolation of a Culex pipiens DNV (CpDNV) that differs significantly from brevidensoviruses by (i) having a approximately 6-kb genome, (ii) lacking sequence homology, and (iii) lacking antigenic cross-reactivity with Brevidensovirus capsid polypeptides. We report here the sequence organization and transcription map of this virus. The cloned genome of CpDNV is 5,759 nucleotides (nt) long, and it possesses an inverted terminal repeat (ITR) of 285 nt and an ambisense organization of its genes. The nonstructural (NS) proteins NS-1, NS-2, and NS-3 are located in the 5' half of one strand and are organized into five open reading frames (ORFs) due to the split of both NS-1 and NS-2 into two ORFs. The ORF encoding capsid polypeptides is located in the 5' half of the complementary strand. The expression of NS proteins is controlled by two promoters, P7 and P17, driving the transcription of a 2.4-kb mRNA encoding NS-3 and of a 1.8-kb mRNA encoding NS-1 and NS-2, respectively. The two NS mRNAs species are spliced off a 53-nt sequence. Capsid proteins are translated from an unspliced 2.3-kb mRNA driven by the P88 promoter. CpDNV thus appears as a new type of mosquito DNV, and based on the overall organization and expression modalities of its genome, it may represent the prototype of a new genus of DNV.

摘要

迄今为止,从蚊子或蚊子细胞系中分离出的所有浓核病毒(DNV)的基因组均由一个4 kb的单链DNA分子组成,具有单义组织(短浓核病毒属,浓核病毒亚科)。我们之前报道了一种致倦库蚊DNV(CpDNV)的分离,它与短浓核病毒有显著差异,表现为:(i)基因组约为6 kb;(ii)缺乏序列同源性;(iii)与短浓核病毒衣壳多肽缺乏抗原交叉反应性。我们在此报告该病毒的序列组织和转录图谱。CpDNV的克隆基因组长度为5759个核苷酸(nt),具有285 nt的反向末端重复序列(ITR),其基因呈双向性组织。非结构(NS)蛋白NS - 1、NS - 2和NS - 3位于一条链的5'端一半,由于NS - 1和NS - 2均被分割为两个开放阅读框(ORF),它们被组织成五个ORF。编码衣壳多肽的ORF位于互补链的5'端一半。NS蛋白的表达由两个启动子P7和P17控制,分别驱动转录一个编码NS - 3的2.4 kb mRNA和一个编码NS - 1和NS - 2的1.8 kb mRNA。这两种NS mRNA物种是从一个53 nt的序列剪接而来的。衣壳蛋白由P88启动子驱动的未剪接的2.3 kb mRNA翻译而来。因此,CpDNV似乎是一种新型的蚊子DNV,基于其基因组的整体组织和表达模式,它可能代表了浓核病毒一个新属的原型。

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