Cloning, Expression and Antigenicity of <i>Omp H</i> Gene of <i>Pasteurella multocida</i>

CHEN Cui-teng; CHENG Long-fei; LIU Rong-chang; WAN Chun-he; FU Guang-hua; CHEN Zhen; ZHU Chun-hua; HUANG Yu

doi:10.19303/j.issn.1008-0384.2018.05.001

Volume 33 Issue 5

Mar. 2019

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Article Navigation > Fujian Journal of Agricultural Sciences > 2018 > 33(5): 451-455

CHEN Cui-teng, CHENG Long-fei, LIU Rong-chang, WAN Chun-he, FU Guang-hua, CHEN Zhen, ZHU Chun-hua, HUANG Yu. Cloning, Expression and Antigenicity of Omp H Gene of Pasteurella multocida[J]. Fujian Journal of Agricultural Sciences, 2018, 33(5): 451-455. doi: 10.19303/j.issn.1008-0384.2018.05.001

Citation:

CHEN Cui-teng, CHENG Long-fei, LIU Rong-chang, WAN Chun-he, FU Guang-hua, CHEN Zhen, ZHU Chun-hua, HUANG Yu. Cloning, Expression and Antigenicity of Omp H Gene of Pasteurella multocida[J]. Fujian Journal of Agricultural Sciences, 2018, 33(5): 451-455. doi: 10.19303/j.issn.1008-0384.2018.05.001

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Cloning, Expression and Antigenicity of Omp H Gene of Pasteurella multocida

doi: 10.19303/j.issn.1008-0384.2018.05.001

Institute of Animal Husbandry and Veterinary Medicine, Fujian Academy of Agricultural Science/Fujian Key Laboratory of Poultry Disease Prevention and Control/Fujian Livestock and Poultry Disease Prevention and Control Technology Major Research and Development Platform, Fuzhou, Fujian 350013, China

Received Date: 2017-06-12
Rev Recd Date: 2018-04-01
Publish Date: 2018-05-01

Abstract

Abstract

The immunological activity of the outer membrane protein H (Omp H) of Pasteurella multocida (Pm) was identified. Based on the published data on P. multocida strain X-73 (U50907.1), two pairs of primers were used to amplify the Omp H of P. multocida strain CVCC 44801 by PCR.The amplified fragment was determined to be 1 348 bp (ORF at 1 056 bp). The sequence alignment on Omp H of Pm70, C44-1, P52, XJ121, X-73 and P-1059 with those registered in GenBank showed a nucleotide homology between 80.2% and 98.4% and an amino acid homology between 79.6% and 98.5%. The recombinant plasmid pET-Omp H was constructed and transformed into BL21. The expressed protein was about 56 ku, which was close to the expected molecular weight. The western blot also confirmed its immunological activity. The results would provide the information for the establishment of a viable serological detection method and an applicable Omp vaccine against P. multocida.
- Pasteurella multocida,
- Omp H gene,
- prokaryotic expression

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References(12)

References

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