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Immunogenicity and Protection against Mycobacterium caprae Challenge in Goats Vaccinated with BCG and Revaccinated after One Year

Vaccination has been proposed as a supplementary tool for the control of tuberculosis in livestock. The long-term immunogenicity elicited by bacillus Calmette–Guerin (BCG) and the efficacy of revaccination were investigated in thirty goat kids distributed into three groups: unvaccinated controls, BC...

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Autores principales: Arrieta-Villegas, Claudia, Vidal, Enric, Martín, Maite, Verdés, Judit, Moll, Xavier, Espada, Yvonne, Singh, Mahavir, Villarreal-Ramos, Bernardo, Domingo, Mariano, Pérez de Val, Bernat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770602/
https://www.ncbi.nlm.nih.gov/pubmed/33322064
http://dx.doi.org/10.3390/vaccines8040751
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author Arrieta-Villegas, Claudia
Vidal, Enric
Martín, Maite
Verdés, Judit
Moll, Xavier
Espada, Yvonne
Singh, Mahavir
Villarreal-Ramos, Bernardo
Domingo, Mariano
Pérez de Val, Bernat
author_facet Arrieta-Villegas, Claudia
Vidal, Enric
Martín, Maite
Verdés, Judit
Moll, Xavier
Espada, Yvonne
Singh, Mahavir
Villarreal-Ramos, Bernardo
Domingo, Mariano
Pérez de Val, Bernat
author_sort Arrieta-Villegas, Claudia
collection PubMed
description Vaccination has been proposed as a supplementary tool for the control of tuberculosis in livestock. The long-term immunogenicity elicited by bacillus Calmette–Guerin (BCG) and the efficacy of revaccination were investigated in thirty goat kids distributed into three groups: unvaccinated controls, BCG (vaccinated at week 0) and BCG-BCG (vaccinated at weeks 0 and 56). Sixty-four weeks after the first vaccination, all animals were challenged with Mycobacterium caprae and examined post-mortem (pathology and bacterial load) at week 73. Antigen-specific interferon-gamma (IFN-γ) release was measured throughout the experiment. At week 59, peripheral blood mononuclear cells were stained for CD4, CD45RO and IFN-γ to determine the presence of antigen-specific cells secreting IFN-γ. The BCG-BCG group showed reductions in rectal temperatures, M. caprae DNA load in pulmonary lymph nodes (LN), the volume of lesions in pulmonary LN, mineralization in lungs, and higher weight gains compared to unvaccinated controls. IFN-γ responses were undetectable from 32 weeks after primary vaccination until revaccination, when the BCG-BCG group showed detectable IFN-γ production and a greater percentage of antigen-specific CD4(+)CD45RO(+)IFNγ(+) and CD4(−)CD45RO(+)IFNγ(+) cells compared to the BCG and control groups, which may be an indicator of the mechanisms of protection. Thus, re-vaccination of goats with BCG appears to prolong protection against infection with M. caprae.
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spelling pubmed-77706022020-12-30 Immunogenicity and Protection against Mycobacterium caprae Challenge in Goats Vaccinated with BCG and Revaccinated after One Year Arrieta-Villegas, Claudia Vidal, Enric Martín, Maite Verdés, Judit Moll, Xavier Espada, Yvonne Singh, Mahavir Villarreal-Ramos, Bernardo Domingo, Mariano Pérez de Val, Bernat Vaccines (Basel) Article Vaccination has been proposed as a supplementary tool for the control of tuberculosis in livestock. The long-term immunogenicity elicited by bacillus Calmette–Guerin (BCG) and the efficacy of revaccination were investigated in thirty goat kids distributed into three groups: unvaccinated controls, BCG (vaccinated at week 0) and BCG-BCG (vaccinated at weeks 0 and 56). Sixty-four weeks after the first vaccination, all animals were challenged with Mycobacterium caprae and examined post-mortem (pathology and bacterial load) at week 73. Antigen-specific interferon-gamma (IFN-γ) release was measured throughout the experiment. At week 59, peripheral blood mononuclear cells were stained for CD4, CD45RO and IFN-γ to determine the presence of antigen-specific cells secreting IFN-γ. The BCG-BCG group showed reductions in rectal temperatures, M. caprae DNA load in pulmonary lymph nodes (LN), the volume of lesions in pulmonary LN, mineralization in lungs, and higher weight gains compared to unvaccinated controls. IFN-γ responses were undetectable from 32 weeks after primary vaccination until revaccination, when the BCG-BCG group showed detectable IFN-γ production and a greater percentage of antigen-specific CD4(+)CD45RO(+)IFNγ(+) and CD4(−)CD45RO(+)IFNγ(+) cells compared to the BCG and control groups, which may be an indicator of the mechanisms of protection. Thus, re-vaccination of goats with BCG appears to prolong protection against infection with M. caprae. MDPI 2020-12-10 /pmc/articles/PMC7770602/ /pubmed/33322064 http://dx.doi.org/10.3390/vaccines8040751 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Arrieta-Villegas, Claudia
Vidal, Enric
Martín, Maite
Verdés, Judit
Moll, Xavier
Espada, Yvonne
Singh, Mahavir
Villarreal-Ramos, Bernardo
Domingo, Mariano
Pérez de Val, Bernat
Immunogenicity and Protection against Mycobacterium caprae Challenge in Goats Vaccinated with BCG and Revaccinated after One Year
title Immunogenicity and Protection against Mycobacterium caprae Challenge in Goats Vaccinated with BCG and Revaccinated after One Year
title_full Immunogenicity and Protection against Mycobacterium caprae Challenge in Goats Vaccinated with BCG and Revaccinated after One Year
title_fullStr Immunogenicity and Protection against Mycobacterium caprae Challenge in Goats Vaccinated with BCG and Revaccinated after One Year
title_full_unstemmed Immunogenicity and Protection against Mycobacterium caprae Challenge in Goats Vaccinated with BCG and Revaccinated after One Year
title_short Immunogenicity and Protection against Mycobacterium caprae Challenge in Goats Vaccinated with BCG and Revaccinated after One Year
title_sort immunogenicity and protection against mycobacterium caprae challenge in goats vaccinated with bcg and revaccinated after one year
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770602/
https://www.ncbi.nlm.nih.gov/pubmed/33322064
http://dx.doi.org/10.3390/vaccines8040751
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