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Evaluation of Host-Pathogen Responses and Vaccine Efficacy in Mice
Published on: February 22, 2019
[Immunogenicity and protective efficacy of pertactin recombinants against Bordetella bronchiseptica challenge]
Zhanqin Zhao1, Chen Wang, Yun Xue
1Lab of Veterinary Microbiology, College of Animal Science and Technology, Henan University of Science and Techology, China. zhaozhanqin@126.com
Wei Sheng Wu Xue Bao = Acta Microbiologica Sinica
|November 25, 2010
Summary
Five pertactin recombinants showed varying immunogenicity and protective efficacy against Bordetella bronchiseptica challenge. The GST-PC recombinant demonstrated superior survival rates in mice compared to GST-PN, suggesting potential for new bordetellosis vaccines.
Area of Science:
- Immunology
- Microbiology
- Vaccine Development
Background:
- Bordetella bronchiseptica (Bb) causes significant respiratory disease in various animal species.
- Pertactin (PRN) is a key virulence factor of B. pertussis and B. bronchiseptica.
- Developing effective subunit vaccines against bordetellosis is crucial for animal health.
Purpose of the Study:
- To evaluate the immunogenicity and protective efficacy of five pertactin recombinants against Bordetella bronchiseptica challenge.
- To compare the survival rates of mice immunized with different pertactin fragments.
- To assess the potential of these recombinants as components of novel subunit vaccines.
Main Methods:
- Cloning and expression of five pertactin gene fragments (PRN, PN, PC, 2PR I, 2PR II) in E. coli.
- Purification and characterization of recombinant proteins (GST-PRN, GST-PN, GST-PC, GST-2PR I, GST-2PR II).
- Immunization of mice with purified recombinant proteins and subsequent challenge with virulent Bb.
Main Results:
- All five recombinant proteins elicited PRN-specific IgG antibody responses in mice.
- Mice immunized with GST-PC showed better survival rates against Bb challenge compared to those immunized with GST-PN.
- GST-2PR II and GST-2PR I also demonstrated significant protective efficacy, with varying survival rates observed across different challenge models.
Conclusions:
- The five pertactin recombinants exhibit differential immunogenicity and protective capabilities against Bb.
- GST-PC appears to be a promising candidate for developing subunit vaccines against bordetellosis.
- These findings support the development of safe and effective pertactin-based vaccines for preventing bordetellosis.

