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Immunogenicity of a Recombinant Mycobacterium smegmatis Vaccine Expressing the Fusion Protein CMX in Cattle from Goiás State, Brazil

This study aimed to evaluate the immunogenicity of a recombinant Mycobacterium smegmatis vaccine expressing the CMX fusion protein composed of immunodominant epitopes Ag85C, MPT51 and HspX of Mycobacterium tuberculosis, which are important mycobacteria virulence factors. A group of Nelore heifers th...

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Autores principales: ALVES DA SILVA, Duanne, CAVALCANTI, Marcos Antônio Rocha, MUNIZ DE OLIVEIRA, Fábio, TRENTINI, Monalisa Martins, JUNQUEIRA-KIPNIS, Ana Paula, KIPNIS, André
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Veterinary Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143659/
https://www.ncbi.nlm.nih.gov/pubmed/24681608
http://dx.doi.org/10.1292/jvms.13-0338
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author ALVES DA SILVA, Duanne
CAVALCANTI, Marcos Antônio Rocha
MUNIZ DE OLIVEIRA, Fábio
TRENTINI, Monalisa Martins
JUNQUEIRA-KIPNIS, Ana Paula
KIPNIS, André
author_facet ALVES DA SILVA, Duanne
CAVALCANTI, Marcos Antônio Rocha
MUNIZ DE OLIVEIRA, Fábio
TRENTINI, Monalisa Martins
JUNQUEIRA-KIPNIS, Ana Paula
KIPNIS, André
author_sort ALVES DA SILVA, Duanne
collection PubMed
description This study aimed to evaluate the immunogenicity of a recombinant Mycobacterium smegmatis vaccine expressing the CMX fusion protein composed of immunodominant epitopes Ag85C, MPT51 and HspX of Mycobacterium tuberculosis, which are important mycobacteria virulence factors. A group of Nelore heifers that were 10 to 12 months of age and negative for the tuberculin skin test (TST) were immunized with four doses of the recombinant vaccine mc(2)-CMX (M. smegmatis-Ag85C-MPT51-HspX) during a period of one year. Before each immunization, blood was collected to obtain sera for antibody analysis. Serological analysis demonstrated that mc(2)-CMX was able to induce a humoral response with increased levels of specific IgG antibodies against CMX, despite minimum antibody levels being detected for individual Ag85C, MPT51 or HspX recombinant antigens. However, there was no significant increase in specific CD4(+) IFN-γ-positive T cells. Lymphadenomegaly was observed in superficial cervical lymph nodes adjacent to the site of vaccination among mc(2)-CMX-vaccinated bovines, and the histopathological analysis demonstrated follicular hyperplasia without inflammatory infiltrate or granuloma formation. Animals remained negative for the TST until the end of the experiments, showing no cross-reactivity with the recombinant vaccine and tuberculin proteins. We discuss the potential of mc(2)-CMX to induce an immune response in cattle.
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spelling pubmed-41436592014-08-26 Immunogenicity of a Recombinant Mycobacterium smegmatis Vaccine Expressing the Fusion Protein CMX in Cattle from Goiás State, Brazil ALVES DA SILVA, Duanne CAVALCANTI, Marcos Antônio Rocha MUNIZ DE OLIVEIRA, Fábio TRENTINI, Monalisa Martins JUNQUEIRA-KIPNIS, Ana Paula KIPNIS, André J Vet Med Sci Immunology This study aimed to evaluate the immunogenicity of a recombinant Mycobacterium smegmatis vaccine expressing the CMX fusion protein composed of immunodominant epitopes Ag85C, MPT51 and HspX of Mycobacterium tuberculosis, which are important mycobacteria virulence factors. A group of Nelore heifers that were 10 to 12 months of age and negative for the tuberculin skin test (TST) were immunized with four doses of the recombinant vaccine mc(2)-CMX (M. smegmatis-Ag85C-MPT51-HspX) during a period of one year. Before each immunization, blood was collected to obtain sera for antibody analysis. Serological analysis demonstrated that mc(2)-CMX was able to induce a humoral response with increased levels of specific IgG antibodies against CMX, despite minimum antibody levels being detected for individual Ag85C, MPT51 or HspX recombinant antigens. However, there was no significant increase in specific CD4(+) IFN-γ-positive T cells. Lymphadenomegaly was observed in superficial cervical lymph nodes adjacent to the site of vaccination among mc(2)-CMX-vaccinated bovines, and the histopathological analysis demonstrated follicular hyperplasia without inflammatory infiltrate or granuloma formation. Animals remained negative for the TST until the end of the experiments, showing no cross-reactivity with the recombinant vaccine and tuberculin proteins. We discuss the potential of mc(2)-CMX to induce an immune response in cattle. The Japanese Society of Veterinary Science 2014-03-31 2014-07 /pmc/articles/PMC4143659/ /pubmed/24681608 http://dx.doi.org/10.1292/jvms.13-0338 Text en ©2014 The Japanese Society of Veterinary Science http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Immunology
ALVES DA SILVA, Duanne
CAVALCANTI, Marcos Antônio Rocha
MUNIZ DE OLIVEIRA, Fábio
TRENTINI, Monalisa Martins
JUNQUEIRA-KIPNIS, Ana Paula
KIPNIS, André
Immunogenicity of a Recombinant Mycobacterium smegmatis Vaccine Expressing the Fusion Protein CMX in Cattle from Goiás State, Brazil
title Immunogenicity of a Recombinant Mycobacterium smegmatis Vaccine Expressing the Fusion Protein CMX in Cattle from Goiás State, Brazil
title_full Immunogenicity of a Recombinant Mycobacterium smegmatis Vaccine Expressing the Fusion Protein CMX in Cattle from Goiás State, Brazil
title_fullStr Immunogenicity of a Recombinant Mycobacterium smegmatis Vaccine Expressing the Fusion Protein CMX in Cattle from Goiás State, Brazil
title_full_unstemmed Immunogenicity of a Recombinant Mycobacterium smegmatis Vaccine Expressing the Fusion Protein CMX in Cattle from Goiás State, Brazil
title_short Immunogenicity of a Recombinant Mycobacterium smegmatis Vaccine Expressing the Fusion Protein CMX in Cattle from Goiás State, Brazil
title_sort immunogenicity of a recombinant mycobacterium smegmatis vaccine expressing the fusion protein cmx in cattle from goiás state, brazil
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143659/
https://www.ncbi.nlm.nih.gov/pubmed/24681608
http://dx.doi.org/10.1292/jvms.13-0338
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