Detection of classical swine fever virus E2 gene in cattle serum samples from cattle herds of Meghalaya

• Published in: Virusdisease Vol. 29; no. 1; pp. 89 - 95
• Main Authors: Chakraborty, A. K., Karam, A., Mukherjee, P., Barkalita, L., Borah, P., Das, S., Sanjukta, R., Puro, K., Ghatak, S., Shakuntala, I., Sharma, I., Laha, R. G., Sen, A.
• Format: Journal Article
• Language: English
• Published: New Delhi Springer India 01.03.2018; Springer Nature B.V
• Subjects: 5' Untranslated Regions; Antigens; Biochemistry; Biomedical and Life Sciences; Cattle; Cell Biology; Disease; E2 gene; Enzyme-linked immunosorbent assay; Farms; Fever; Genomes; Hog cholera; Hogs; Life Sciences; Livestock; Microbiology; Original; Original Article; Phylogenetics; Phylogeny; Plasmids; Polymerase chain reaction; Protein Structure; Proteins; Reverse transcription; Software; Viruses; United States > US; India; 5′UTR; E2; RT-PCR; I-TASSER; CSFV
• ISSN: 2347-3584; 2347-3517
• DOI: 10.1007/s13337-018-0433-9

The present study focused on the detection and genetic characterisation of 5′ untranslated region (5′UTR) and E2 gene of classical swine fever virus (CSFV, family Flaviviridae , genus Pestivirus ) from bovine population of the northeastern region of India. A total of 134 cattle serum samples were collected from organised cattle farms and were screened for CSFV antigen with a commercial antigen capture enzyme linked immunosorbent assay (Ag-ELISA) and reverse transcription-polymerase chain reaction (RT-PCR). A total of 10 samples were positive for CSFV antigen by ELISA, while all of them were positive in PCR for 5′UTR region. Full length E2 region of CSFV were successfully amplified from two positive samples and used for subsequent phylogenetic analysis and determination of protein 3D structure which showed similarity with reported CSFV isolate from Assam of sub-genogroup 2.1, with minor variations in protein structure.