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Detection of BTV antibodies by <t>c-ELISA</t> in BTV-24-infected (red line) and uninfected control (green line) animals at different days post-inoculation (DPI). Serum samples with percent inhibition (PI) values ≥ 45% were considered positive. Data are presented as mean ± SE. Asterisk (*) indicates significant difference ( p < 0.05) between groups.
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Detection of BTV antibodies by c-ELISA in BTV-24-infected (red line) and uninfected control (green line) animals at different days post-inoculation (DPI). Serum samples with percent inhibition (PI) values ≥ 45% were considered positive. Data are presented as mean ± SE. Asterisk (*) indicates significant difference ( p < 0.05) between groups.

Journal: Frontiers in Cellular and Infection Microbiology

Article Title: Pathology and pathogenesis of bluetongue virus serotype 24 during experimental infection in native sheep

doi: 10.3389/fcimb.2026.1710415

Figure Lengend Snippet: Detection of BTV antibodies by c-ELISA in BTV-24-infected (red line) and uninfected control (green line) animals at different days post-inoculation (DPI). Serum samples with percent inhibition (PI) values ≥ 45% were considered positive. Data are presented as mean ± SE. Asterisk (*) indicates significant difference ( p < 0.05) between groups.

Article Snippet: Twelve indigenous nondescript adult sheep of either sex aged between 2 and 3 years of approximately 30–40 kg were procured from livestock farmers after screening and negative for BTV antibodies using a competitive-enzyme linked immunosorbent assay (c-ELISA) kit (Bluetongue virus antibody cELISA test kit, VMRD Inc., Pullman, WA, USA).

Techniques: Enzyme-linked Immunosorbent Assay, Infection, Control, Inhibition