Le Goff Christian, Lamien Charles Euloge, Fakhfakh Emna, Chadeyras Amélie, Aba-Adulugba Elexpeter, Libeau Geneviève, Tuppurainen Eeva, Wallace David B, Adam Tajelser, Silber Roland, Gulyaz Velý, Madani Hafsa, Caufour Philippe, Hammami Salah, Diallo Adama, Albina Emmanuel
CIRAD, UMR Contrôle des Maladies, F-34398 Montpellier, France.
Animal Production Unit, FAO/IAEA Agriculture and Biotechnology Laboratory, IAEA Laboratories Seibersdorf, International Atomic Energy Agency, Wagramer Strasse 5, PO Box 100, A-1400 Vienna, Austria.
J Gen Virol. 2009 Aug;90(Pt 8):1967-1977. doi: 10.1099/vir.0.010686-0. Epub 2009 Apr 1.
The genus Capripoxvirus within the family Poxviridae comprises three closely related viruses, namely goat pox, sheep pox and lumpy skin disease viruses. This nomenclature is based on the animal species from which the virus was first isolated, respectively, goat, sheep and cattle. Since capripoxviruses are serologically identical, their specific identification relies exclusively on the use of molecular tools. We describe here the suitability of the G-protein-coupled chemokine receptor (GPCR) gene for use in host-range grouping of capripoxviruses. The analysis of 58 capripoxviruses showed three tight genetic clusters consisting of goat pox, sheep pox and lumpy skin disease viruses. However, a few discrepancies exist with the classical virus-host origin nomenclature: a virus isolated from sheep is grouped in the goat poxvirus clade and vice versa. Intra-group diversity was further observed for the goat pox and lumpy skin disease virus isolates. Despite the presence of nine vaccine strains, no genetic determinants of virulence were identified on the GPCR gene. For sheep poxviruses, the addition or deletion of 21 nucleic acids (7 aa) was consistently observed in the 5' terminal part of the gene. Specific signatures for each cluster were also identified. Prediction of the capripoxvirus GPCR topology, and its comparison with other known mammalian GPCRs and viral homologues, revealed not only a classical GPCR profile in the last three-quarters of the protein but also unique features such as a longer N-terminal end with a proximal hydrophobic alpha-helix and a shorter serine-rich C-tail.
痘病毒科的山羊痘病毒属包含三种密切相关的病毒,即山羊痘病毒、绵羊痘病毒和结节性皮炎病毒。这种命名法是基于最初分离出病毒的动物物种,分别是山羊、绵羊和牛。由于山羊痘病毒在血清学上是相同的,它们的特异性鉴定完全依赖于分子工具的使用。我们在此描述了G蛋白偶联趋化因子受体(GPCR)基因在山羊痘病毒宿主范围分组中的适用性。对58种山羊痘病毒的分析显示,存在由山羊痘病毒、绵羊痘病毒和结节性皮炎病毒组成的三个紧密遗传簇。然而,与传统的病毒-宿主起源命名法存在一些差异:从绵羊分离出的一种病毒被归为山羊痘病毒进化枝,反之亦然。在山羊痘病毒和结节性皮炎病毒分离株中还观察到了组内多样性。尽管存在九种疫苗株,但在GPCR基因上未鉴定出毒力的遗传决定因素。对于绵羊痘病毒,在基因的5'末端部分始终观察到21个核酸(7个氨基酸)的添加或缺失。还确定了每个簇的特异性特征。对山羊痘病毒GPCR拓扑结构的预测,以及将其与其他已知的哺乳动物GPCR和病毒同源物进行比较,不仅揭示了该蛋白最后四分之三部分具有经典的GPCR特征,还发现了一些独特特征,如具有近端疏水α螺旋的较长N末端和较短的富含丝氨酸的C末端。