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Cloning, expression and characterization of potential immunogenic recombinant hemagglutinin-neuraminidase protein of Porcine rubulavirus.
Cuevas-Romero, Julieta Sandra; Rivera-Benítez, José Francisco; Hernández-Baumgarten, Eliseo; Hernández-Jaúregui, Pablo; Vega, Marco; Blomström, Anne-Lie; Berg, Mikael; Baule, Claudia.
Afiliación
  • Cuevas-Romero JS; Centro Nacional de Investigación Disciplinaria en Microbiología Animal, INIFAP, CP. 05110, Mexico City, Mexico; Division of Virology, Department of Biomedical Sciences and Veterinary Public Health, Swedish University of Agricultural Sciences, S-751 89, Uppsala, Sweden. Electronic address: cuevas.jul
  • Rivera-Benítez JF; Centro Nacional de Investigación Disciplinaria en Microbiología Animal, INIFAP, CP. 05110, Mexico City, Mexico.
  • Hernández-Baumgarten E; Facultad de Estudios Superiores Cuautitlán FES-C-UNAM, Edo. de México, Mexico.
  • Hernández-Jaúregui P; Private Researcher, Puebla, Mexico.
  • Vega M; Instituto Politécnico Nacional. Centro de Investigación y Estudios Avanzados, Mexico City, Mexico.
  • Blomström AL; Division of Virology, Department of Biomedical Sciences and Veterinary Public Health, Swedish University of Agricultural Sciences, S-751 89, Uppsala, Sweden.
  • Berg M; Division of Virology, Department of Biomedical Sciences and Veterinary Public Health, Swedish University of Agricultural Sciences, S-751 89, Uppsala, Sweden.
  • Baule C; Division of Virology, Department of Biomedical Sciences and Veterinary Public Health, Swedish University of Agricultural Sciences, S-751 89, Uppsala, Sweden.
Protein Expr Purif ; 128: 1-7, 2016 12.
Article en En | MEDLINE | ID: mdl-27496728
ABSTRACT
Blue eye disease caused by Porcine rubulavirus (PorPV) is an endemic viral infection of swine causing neurological and respiratory disease in piglets, and reproductive failure in sows and boars. The hemagglutinin-neuraminidase (HN) glycoprotein of PorPV is the most abundant component in the viral envelope and the main target of the immune response in infected animals. In this study, we expressed the HN-PorPV-recombinant (rHN-PorPV) protein in an Escherichia coli system and analyzed the immune responses in mice. The HN gene was cloned from the reference strain PorPV-La Piedad Michoacan Virus (GenBank accession number BK005918), into the pDual expression vector. The expressed protein was identified at a molecular weight of 61.7 kDa. Three-dimensional modeling showed that the main conformational and functional domains of the rHN-PorPV protein were preserved. The antigenicity of the expressed protein was confirmed by Western blot with a monoclonal antibody recognizing the HN, and by testing against serum samples from pigs experimentally infected with PorPV. The immunogenicity of the rHN-PorPV protein was tested by inoculation of BALB/c mice with AbISCO-100(®) as adjuvant. Analysis of the humoral immune responses in mice showed an increased level of specific antibodies 14 days after the first immunization, compared to the control group (P < 0.0005). The results show the ability of the rHN-PorPV protein to induce an antibody response in mice. Due to its immunogenic potential, the rHN-PorPV protein will be further evaluated in pig trials for its suitability for prevention and control of blue eye disease.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vacunas Virales / Expresión Génica / Proteína HN / Clonación Molecular / Rubulavirus / Inmunogenicidad Vacunal Límite: Animals Idioma: En Revista: Protein Expr Purif Asunto de la revista: BIOLOGIA MOLECULAR Año: 2016 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vacunas Virales / Expresión Génica / Proteína HN / Clonación Molecular / Rubulavirus / Inmunogenicidad Vacunal Límite: Animals Idioma: En Revista: Protein Expr Purif Asunto de la revista: BIOLOGIA MOLECULAR Año: 2016 Tipo del documento: Article