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The immune response and protective efficacy of a potential DNA vaccine against virulent Pasteurella multocida

BACKGROUND: Pasteurella multocida is the main cause of several infections of farm animals, and the immunity gained from commercial vaccines is for the short term only and needs to be routinely administered, so work on new vaccines against virulent P. multocida is crucial. RESULTS: In this study, the...

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Autores principales: Yassein, Ahmed A. M., Teleb, Ayaat A., Hassan, Gamal M., El Fiky, Zaki A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8167001/
https://www.ncbi.nlm.nih.gov/pubmed/34057640
http://dx.doi.org/10.1186/s43141-021-00180-9
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author Yassein, Ahmed A. M.
Teleb, Ayaat A.
Hassan, Gamal M.
El Fiky, Zaki A.
author_facet Yassein, Ahmed A. M.
Teleb, Ayaat A.
Hassan, Gamal M.
El Fiky, Zaki A.
author_sort Yassein, Ahmed A. M.
collection PubMed
description BACKGROUND: Pasteurella multocida is the main cause of several infections of farm animals, and the immunity gained from commercial vaccines is for the short term only and needs to be routinely administered, so work on new vaccines against virulent P. multocida is crucial. RESULTS: In this study, the OmpH gene was amplified from ten P. multocida strains, and the PCR products were sequenced and analyzed. The results of RFLP analysis of OmpH gene digested by MspI enzyme showed that all of ten strains examined possessed one restriction site and two fragments, 350 and 650 bp. The OmpH sequence of strain No. 10 was cloned into bacterial expression vector pUCP24, and the recombinant pUCP24-OmpH was expressed in E. coli DH5α. Serum samples obtained from the ELISA test from a group of vaccinated rats indicate that the antibodies were present at high titer in immunized rats and can be tested as a vaccine candidate with a challenge. CONCLUSIONS: In rats infected with the DNA vaccine and inactivated vaccine, a significant increase in serum antibody levels was observed. In addition, the DNA vaccine provided the vaccinated rats with partial protection; however, the protective efficacy was greater than that offered by the live attenuated vaccine. This successful recombinant vaccine is immunogenic and may potentially be used as a vaccine in the future.
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spelling pubmed-81670012021-06-17 The immune response and protective efficacy of a potential DNA vaccine against virulent Pasteurella multocida Yassein, Ahmed A. M. Teleb, Ayaat A. Hassan, Gamal M. El Fiky, Zaki A. J Genet Eng Biotechnol Research BACKGROUND: Pasteurella multocida is the main cause of several infections of farm animals, and the immunity gained from commercial vaccines is for the short term only and needs to be routinely administered, so work on new vaccines against virulent P. multocida is crucial. RESULTS: In this study, the OmpH gene was amplified from ten P. multocida strains, and the PCR products were sequenced and analyzed. The results of RFLP analysis of OmpH gene digested by MspI enzyme showed that all of ten strains examined possessed one restriction site and two fragments, 350 and 650 bp. The OmpH sequence of strain No. 10 was cloned into bacterial expression vector pUCP24, and the recombinant pUCP24-OmpH was expressed in E. coli DH5α. Serum samples obtained from the ELISA test from a group of vaccinated rats indicate that the antibodies were present at high titer in immunized rats and can be tested as a vaccine candidate with a challenge. CONCLUSIONS: In rats infected with the DNA vaccine and inactivated vaccine, a significant increase in serum antibody levels was observed. In addition, the DNA vaccine provided the vaccinated rats with partial protection; however, the protective efficacy was greater than that offered by the live attenuated vaccine. This successful recombinant vaccine is immunogenic and may potentially be used as a vaccine in the future. Springer Berlin Heidelberg 2021-05-31 /pmc/articles/PMC8167001/ /pubmed/34057640 http://dx.doi.org/10.1186/s43141-021-00180-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research
Yassein, Ahmed A. M.
Teleb, Ayaat A.
Hassan, Gamal M.
El Fiky, Zaki A.
The immune response and protective efficacy of a potential DNA vaccine against virulent Pasteurella multocida
title The immune response and protective efficacy of a potential DNA vaccine against virulent Pasteurella multocida
title_full The immune response and protective efficacy of a potential DNA vaccine against virulent Pasteurella multocida
title_fullStr The immune response and protective efficacy of a potential DNA vaccine against virulent Pasteurella multocida
title_full_unstemmed The immune response and protective efficacy of a potential DNA vaccine against virulent Pasteurella multocida
title_short The immune response and protective efficacy of a potential DNA vaccine against virulent Pasteurella multocida
title_sort immune response and protective efficacy of a potential dna vaccine against virulent pasteurella multocida
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8167001/
https://www.ncbi.nlm.nih.gov/pubmed/34057640
http://dx.doi.org/10.1186/s43141-021-00180-9
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