Small ruminant lentivirus capsid protein (SRLV-p25) antigenic structural prediction and immunogenicity to recombinant SRLV-rp25-coupled to immunostimulatory complexes based on glycyrrhizinic acid

Author:

Castañeda-Montes María Azucena1,Cuevas-Romero Julieta Sandra2,Cerriteño-Sánchez José Luis2,de María Ávila-De la Vega Lucero1,García-Cambrón José Bryan2,Ramírez-Álvarez Hugo1ORCID

Affiliation:

1. Virology, Genetics, and Molecular Biology Laboratory. Faculty of Higher Education, Cuautitlán, Veterinary Medicine , Campus 4. National Autonomous University of Mexico. Km. 2.5 ctra. Cuautitlán-Teoloyucan, San Sebastián Xhala. Cuautitlán Izcalli Estado de México , México

2. Laboratorio de Virología, Centro Nacional de Investigación Disciplinaria en Salud Animal e Inocuidad (CENID-SAI), INIFAP , KM. 15.5 Carretera México-Toluca, Col. Palo Alto, Cuajimalpa, Ciudad de México , México

Abstract

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.

Funder

SEP

CONACYT

DGAPA, UNAM

Publisher

Oxford University Press (OUP)

Subject

Organic Chemistry,Molecular Biology,Applied Microbiology and Biotechnology,General Medicine,Biochemistry,Analytical Chemistry,Biotechnology

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