LSDV126 gene based molecular assays for specific detection and characterization of emerging Lumpy Skin Disease virus

• Published in: Journal of virological methods 2023-02, Vol.312, p.114665-114665, Article 114665
• Main Authors: Nandi, Sukdeb, Mahajan, Sonalika, Mishra, Ragini, Nautiyal, Sushmita, Agrawal, Ravi Kant, Singh, Mithilesh, Biswas, Sanchay K., Chander, Vishal, Singh, Karam Pal, Sharma, Gaurav Kumar
• Format: Article
• Language: English
• Subjects: Animals; Capripoxvirus - genetics; Cattle; DNA; Lumpy Skin disease; Lumpy Skin Disease - diagnosis; Lumpy Skin Disease - prevention & control; Lumpy skin disease virus - genetics; POCT; Poxviridae Infections - prevention & control; PSR; Real time PCR; Vaccines, Attenuated - genetics
• ISSN: 0166-0934; 1879-0984
• DOI: 10.1016/j.jviromet.2022.114665

Lumpy skin disease (LSD) is a highly infectious and economically important viral disease, which is currently emerging in the Indian subcontinent. LSD is caused by Lumpy Skin Disease Virus (LSDV) under the genus Capripoxvirus and the family Poxviridae. Since its first incursion in India in the year 2019, the virus is rapidly disseminating through different means like direct contact, fomites and mainly by blood-feeding insects. As the disease has never been reported from India or neighbouring countries, there is a lack of planning and preparatory measures in terms of diagnostics and vaccines to control the disease. In the absence of any homologous vaccine, a live attenuated heterologous goat pox vaccine (Uttarkashi strain) is now being widely used in the country for the prevention of LSDV infection. Use of live attenuated goat pox virus vaccine necessitates the availability of an assay which could specifically detect and differentiate LSDV from goat pox virus. In this study, nucleotide sequences of LSDV126 gene encoding extracellular enveloped virus protein of circulating LSDV and goat pox virus were determined and analyzed. Deletion of 27 nt tandem repeats was observed in LSDV in comparison to goat pox and LSDV vaccine viruses. The deletion region was targeted for designing primers specific to LSDV, but not goat pox virus. A novel isothermal polymerase spiral reaction (PSR) was optimized as pen side diagnostic for prompt and sensitive detection of genomic DNA of LSDV. The assay was found to be highly sensitive and specific when compared to the real-time PCR. The assay was found to be specifically detecting only LSDV but not the goat pox virus. The limit of detection was identified as 9 × 10−6 ng of positive DNA. The assay will provide a point of care tool that will be a boon for the successful control of LSD in India. •LSDV126 gene of field strains of Lumpy skin disease virus was characterized and the tandom nucleotide sequence was utilized for development of molecular assays.•LSDV126 gene was shown to be better for defining the phylogenetic tree for the members of Capripox genus.•A rapid isothermal polymerase spiral reaction (PSR) was developed to detect and differentiate LSDV from Goat pox virus.