Division of Virology, ICAR-Indian Veterinary Research Institute, Mukteswar 263 138, Nainital, Uttarakhand, India.
Division of Virology, ICAR-Indian Veterinary Research Institute, Mukteswar 263 138, Nainital, Uttarakhand, India.
Infect Genet Evol. 2018 Mar;58:224-231. doi: 10.1016/j.meegid.2018.01.001. Epub 2018 Jan 4.
Sheeppox virus (SPPV) and goatpox virus (GTPV) are members of the genus Capripoxvirus (CaPV) of the family Poxviridae. CaPVs are responsible for important contagious diseases of small ruminants that are enzootic to the Indian sub-continent, Central and Northern Africa and the Middle East. In the present study, the sequence and phylogenetic analysis of the L1R gene of sixteen CaPV isolates (seven SPPV and nine GTPV) from India were performed along with 3D homology modeling of the L1R protein. L1R is a myristoylated protein responsible for virion assembly and being present on intracellular mature virion (IMV) surface, it is also a potent target for eliciting neutralizing antibodies. Sequence analysis of CaPV L1R gene revealed an ORF of 738bp with >99% and >96% identity within species and between species, respectively, at both nucleotide as well as amino acid levels. Phylogenetic analysis displayed distinct clusters of members of genus Capripoxvirus, as GTPV, SPPV and LSDV. L1R at the protein level showed various species-specific signature residues that may be useful for future grouping or genotyping of CaPV members. CaPV L1R was predicted to possess myristoylation motif GAAASIQTTVNTLNEKI and a potential N-glycosylation site at amino acid residue 50 (Asn). Despite of different host specificity in poxviruses, comparative sequence analysis of L1R proteins revealed highly conserved nature with presence of myristoylation motif (GXXXS) and six cysteine residues forming three disulfide bonds among all poxviruses. The conserved and immunogenic nature of the CaPV L1R gene may prove to be a potential candidate/target for developing molecular diagnostics including recombinant protein based assays and prophylactics for the control of CaPV diseases in tropical countries like India.
绵羊痘病毒(SPPV)和山羊痘病毒(GTPV)是痘病毒科痘病毒属的成员。CaPV 可引起小反刍动物的重要传染病,这些疾病在印度次大陆、中北非和中东地区流行。本研究对来自印度的 16 株 CaPV 分离株(7 株 SPPV 和 9 株 GTPV)的 L1R 基因序列和系统进化进行了分析,并对 L1R 蛋白进行了 3D 同源建模。L1R 是一种豆蔻酰化蛋白,负责病毒粒子的组装,并且存在于细胞内成熟病毒粒子(IMV)的表面,它也是引发中和抗体的有效靶标。CaPV L1R 基因的序列分析显示,其开放阅读框为 738bp,在种内和种间的核苷酸和氨基酸水平上,分别具有 >99%和 >96%的同源性。系统进化分析显示,痘病毒属的成员分为明显的簇,如 GTPV、SPPV 和 LSDV。在蛋白质水平上,L1R 具有各种种特异性的特征残基,可能有助于未来对 CaPV 成员进行分组或基因分型。CaPV L1R 预测具有豆蔻酰化基序 GAAASIQTTVNTLNEKI 和位于第 50 位氨基酸(天冬酰胺)的潜在 N-糖基化位点。尽管痘病毒在宿主特异性上有所不同,但 L1R 蛋白的比较序列分析显示,所有痘病毒都具有高度保守的性质,存在豆蔻酰化基序(GXXXS)和 6 个半胱氨酸残基,形成三个二硫键。CaPV L1R 的保守性和免疫原性可能成为开发分子诊断的潜在候选物/靶标,包括基于重组蛋白的检测方法和预防热带国家(如印度)的 CaPV 疾病的预防性疫苗。