
doi: 10.1093/bbb/zbac206
pmid: 36535645
ABSTRACTSmall ruminant lentiviruses (SRLV) infect sheep and goats resulting in significant economic losses. This study evaluated for the first time the predicted conformational structure of the SRLV-capsid-protein 25 (SRLV-p25) and analyzed the antigenicity of recombinant protein (SRLV-rp25) in mice by coupling to an immunostimulatory complexes based on glycyrrhizinic acid liposomes (GAL) and tested plasma from goats and sheep naturally infected. Analysis in silico and conformational structure of SRLV-p25 (genotype B-FESC-752) showed similar characteristics to other lentiviral capsids. The efficient expression of SRLV-rp25 was confirmed by Western blot. The humoral immune responses in mice showed an increased level of antibodies from day 21 to 35 of the SRLV-rp25-GAL and SRLV-rp25-ISCOM® groups and the cellular immune response showed no significant difference in IL-10 levels (P >.05), however, a significant difference (P <.001) was observed when comparing SRLV-rp25-GAL with SRLV-rp25 groups. Immunoreactivity toward SRLV-rp25 revealed 61% of positive samples from naturally infected goats and sheep.
Sheep, Goats, Lentivirus, Sheep Diseases, Ruminants, Glycyrrhizic Acid, Mice, Lentivirus Infections, Animals, Capsid Proteins, Phylogeny
Sheep, Goats, Lentivirus, Sheep Diseases, Ruminants, Glycyrrhizic Acid, Mice, Lentivirus Infections, Animals, Capsid Proteins, Phylogeny
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