First complete genome sequence of lumpy skin disease virus directly from a clinical sample in South India

被引:4
|
作者
Putty, Kalyani [1 ]
Rao, Pachineella Lakshmana [2 ,3 ]
Ganji, Vishweshwar Kumar [1 ]
Dutta, Devasmita [2 ]
Mondal, Subhajit [2 ]
Hegde, Nagendra R. [2 ]
Srivastava, Anand [2 ]
Subbiah, Madhuri [2 ]
机构
[1] PVNR Telangana Vet Univ, Dept Vet Biotechnol, Hyderabad 500030, Telangana, India
[2] Natl Inst Anim Biotechnol, Hyderabad 500032, Telangana, India
[3] Reg Ctr Biotechnol, Grad Studies, Faridabad 121001, India
关键词
Lumpy skin disease; Lumpy skin disease virus; Capripoxvirus; Complete genome sequence; Phylogenetic analyses; GREECE;
D O I
10.1007/s11262-023-01967-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Lumpy skin disease (LSD), a notifiable disease listed by the World Organization for Animal Health and a fast fast-moving transboundary viral disease infecting cattle and buffaloes, was reported in India in 2019 and has since rapidly spread across the country. This study reports the first complete genome sequence and analysis of a pathogenic LSD virus (LSDV) from India (LSDV/208/PVNRTVU/2020) obtained by direct sequencing of a suspected clinical sample using Illumina and Nanopore sequencing technologies. The complete genome sequence of LSDV/208/PVNRTVU/2020 is 150445 bp long, codes for 156 putative genes and carries identical 2254 bp inverted terminal repeats at either ends. The unique features reported in the LSDV isolates from the recent outbreaks in Asia, namely, the insertions of 12 nucleotides in the viral G-protein coupled receptor (GPCR) and 27 nucleotides leading to duplication of 9 aminoacids in the extracellular enveloped virus-specific (EEV) genes were also conserved in LSDV/208/PVNRTVU/2020. Phylogenetic analysis of the complete genome sequence of LSDV/208/PVNRTVU/2020 revealed its close relation with Kenyan strains and clustered away from vaccine strains. Further analysis showed evidence of strong purifying selection without any recombination events. The data presented in this study could be useful for designing effective strategies such as developing rapid diagnostics and vaccines to control LSD.
引用
收藏
页码:317 / 322
页数:6
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