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Protective efficacy by various doses of a new brucellosis vaccine candidate based on Salmonella strains expressing Brucella abortus BSCP31, Omp3b and superoxide dismutase against brucellosis in murine model

Brucella species are important etiological agents of zoonotic diseases. Attenuated Salmonella strains expressing Brucella abortus BCSP31, Omp3b and superoxide dismutase proteins were tested as vaccine candidates in this study. In order to determine the optimal dose for intraperitoneal (IP) inoculati...

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Autores principales: Kim, Won Kyong, Moon, Ja Young, Cho, Jeong Sang, Hur, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5808651/
https://www.ncbi.nlm.nih.gov/pubmed/28873944
http://dx.doi.org/10.1093/femspd/ftx094
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author Kim, Won Kyong
Moon, Ja Young
Cho, Jeong Sang
Hur, Jin
author_facet Kim, Won Kyong
Moon, Ja Young
Cho, Jeong Sang
Hur, Jin
author_sort Kim, Won Kyong
collection PubMed
description Brucella species are important etiological agents of zoonotic diseases. Attenuated Salmonella strains expressing Brucella abortus BCSP31, Omp3b and superoxide dismutase proteins were tested as vaccine candidates in this study. In order to determine the optimal dose for intraperitoneal (IP) inoculation required to obtain effective protection against brucellosis, mice were immunized with various doses of a mixture of the three vaccine strains. Fifty BALB/c mice were divided into five equal groups (groups A–E). Group A mice were intraperitoneally inoculated with 100 μL of sterile phosphate-buffered saline. Group B, C, D and E mice were intraperitoneally immunized with approximately 1.2 × 10(5) colony-forming units (CFU) mL(−1) of Salmonella containing pMMP65 in 100 μL and with 1.2 × 10(4) CFU mL(−1), 1.2 × 10(5) CFU mL(−1) and 1.2 × 10(6) CFU mL(−1) of the mixture of the three strains in 100 μL, respectively. Serum IgG, tumor necrosis factor alpha and interferon gamma concentrations were significantly higher in group E than in groups A–D. Following challenge with B. abortus 544, the challenge strain was not detected in the spleen of any mouse from group E. Thus, IP immunization with 1.2 × 10(6) CFU mL(−1) of the mixture of the three vaccine strains induced immune responses and provided effective protection against brucellosis in mice.
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spelling pubmed-58086512018-02-15 Protective efficacy by various doses of a new brucellosis vaccine candidate based on Salmonella strains expressing Brucella abortus BSCP31, Omp3b and superoxide dismutase against brucellosis in murine model Kim, Won Kyong Moon, Ja Young Cho, Jeong Sang Hur, Jin Pathog Dis Research Article Brucella species are important etiological agents of zoonotic diseases. Attenuated Salmonella strains expressing Brucella abortus BCSP31, Omp3b and superoxide dismutase proteins were tested as vaccine candidates in this study. In order to determine the optimal dose for intraperitoneal (IP) inoculation required to obtain effective protection against brucellosis, mice were immunized with various doses of a mixture of the three vaccine strains. Fifty BALB/c mice were divided into five equal groups (groups A–E). Group A mice were intraperitoneally inoculated with 100 μL of sterile phosphate-buffered saline. Group B, C, D and E mice were intraperitoneally immunized with approximately 1.2 × 10(5) colony-forming units (CFU) mL(−1) of Salmonella containing pMMP65 in 100 μL and with 1.2 × 10(4) CFU mL(−1), 1.2 × 10(5) CFU mL(−1) and 1.2 × 10(6) CFU mL(−1) of the mixture of the three strains in 100 μL, respectively. Serum IgG, tumor necrosis factor alpha and interferon gamma concentrations were significantly higher in group E than in groups A–D. Following challenge with B. abortus 544, the challenge strain was not detected in the spleen of any mouse from group E. Thus, IP immunization with 1.2 × 10(6) CFU mL(−1) of the mixture of the three vaccine strains induced immune responses and provided effective protection against brucellosis in mice. Oxford University Press 2017-07-29 2017-10 /pmc/articles/PMC5808651/ /pubmed/28873944 http://dx.doi.org/10.1093/femspd/ftx094 Text en © FEMS 2017. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Kim, Won Kyong
Moon, Ja Young
Cho, Jeong Sang
Hur, Jin
Protective efficacy by various doses of a new brucellosis vaccine candidate based on Salmonella strains expressing Brucella abortus BSCP31, Omp3b and superoxide dismutase against brucellosis in murine model
title Protective efficacy by various doses of a new brucellosis vaccine candidate based on Salmonella strains expressing Brucella abortus BSCP31, Omp3b and superoxide dismutase against brucellosis in murine model
title_full Protective efficacy by various doses of a new brucellosis vaccine candidate based on Salmonella strains expressing Brucella abortus BSCP31, Omp3b and superoxide dismutase against brucellosis in murine model
title_fullStr Protective efficacy by various doses of a new brucellosis vaccine candidate based on Salmonella strains expressing Brucella abortus BSCP31, Omp3b and superoxide dismutase against brucellosis in murine model
title_full_unstemmed Protective efficacy by various doses of a new brucellosis vaccine candidate based on Salmonella strains expressing Brucella abortus BSCP31, Omp3b and superoxide dismutase against brucellosis in murine model
title_short Protective efficacy by various doses of a new brucellosis vaccine candidate based on Salmonella strains expressing Brucella abortus BSCP31, Omp3b and superoxide dismutase against brucellosis in murine model
title_sort protective efficacy by various doses of a new brucellosis vaccine candidate based on salmonella strains expressing brucella abortus bscp31, omp3b and superoxide dismutase against brucellosis in murine model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5808651/
https://www.ncbi.nlm.nih.gov/pubmed/28873944
http://dx.doi.org/10.1093/femspd/ftx094
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