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Two novel cross‑protective antigens for bovine Pasteurella multocida
Huihui Du1, Chenlu Wu2, Chunming Li2
1The State Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing 400716, P.R. China.
Molecular Medicine Reports
|August 10, 2017
Summary
Researchers identified novel cross-protective antigens from Pasteurella multocida outer membrane proteins (OMPs). These findings pave the way for developing effective vaccines against bovine respiratory diseases caused by P. multocida serotypes A and B.
Area of Science:
- Veterinary Immunology
- Bacteriology
- Vaccine Development
Background:
- Pasteurella multocida causes significant economic losses in cattle production due to various diseases.
- Developing effective vaccines against P. multocida is crucial for protecting cattle health and the agricultural economy.
Purpose of the Study:
- To identify cross-protective outer membrane proteins (OMPs) of Pasteurella multocida serotypes A, B, and F for vaccine development.
- To screen and validate candidate antigens using immunoproteomics and bioinformatics.
Main Methods:
- Immunoproteomics approach to analyze OMPs from P. multocida serotypes A, B, and F.
- Linear trap quadrupole mass spectrometry and bioinformatics for candidate antigen screening.
- Cloning, expression, ELISA, and immunoblotting to analyze antigen reactogenicity.
- Infective animal models to determine vaccine efficacy and cross-protective potential.
Main Results:
- Identified three candidate proteins: rPmCQ2_2g0128, rPmCQ2_1g0327, and rPmCQ2_1g0020.
- rPmCQ2_2g0128 showed protective rates of 40%, 30%, and 20% against serotypes A, B, and F, respectively.
- rPmCQ2_1g0327 demonstrated protective rates of 50%, 40%, and 0% against serotypes A, B, and F, respectively.
- rPmCQ2_1g0020 provided 0%, 40%, and 30% protection against serotypes A, B, and F, respectively.
Conclusions:
- The proteins rPmCQ2_2g0128 and rPmCQ2_1g0327 show potential as vaccine candidates against bovine P. multocida serotypes A and B.
- This study is the first to identify cross-protective antigens by extracting OMPs from bovine P. multocida.

