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Vet Microbiol. 2017 Jun;205:14-21. doi: 10.1016/j.vetmic.2017.04.026. Epub 2017 Apr 29.

B cell cross-epitope of Propionibacterium acnes and Actinobacillus pleuropneumonia selected by phage display library can efficiently protect from Actinobacillus pleuropneumonia infection.

Author information

1
College of Veterinary Medicine, Jinlin University, Changchun, Jilin, 130062, People's Republic of China.
2
Section of Paediatrics, Imperial College London, St. Mary's Campus, London W2 1 PG, United Kingdom.
3
Department of Respiratory Medicine, The Second Hospital of Jilin University, Changchun, Jilin, 130062, People's Republic of China.
4
College of Veterinary Medicine, Jinlin University, Changchun, Jilin, 130062, People's Republic of China. Electronic address: leiliancheng@163.com.

Abstract

Contagious porcine pleuropneumonia (CPP), caused by Actinobacillus pleuropneumoniae (APP), is a highly transmissible and fatal respiratory illness that causes tremendous economic losses for the pig breeding industry worldwide. Propionibacterium acnes (PA) has a strong cross-reaction with anti-APP1 and anti-APP5 serum and can efficiently prevent APP infection, which was fortuitously found in researching the differential gene between the different APP serotypes. There seems to be some natural cross-protection between PA and APP. To identify the common epitope, the phage display library of a PA whole genome was constructed, whose size is 105. The DNA sequence of the positive clone was determined after three rounds of biopanning, and ten common protein types were identified and the epitope was predicted by computer software. Six peptide epitopes were selected and synthesized for further analysis. Among these epitopes, Ba1, Bb5 and C1 could bind to anti-PA serum and anti-APP1 serum and vice versa. Furthermore, the IgG and IL-4 levels and CD4+/CD8+ T cell ratios in the Ba1, Bb5 and C1 groups were significantly higher than that in the control group, indicating that the epitopes could trigger an immune response, which was mainly humoral immunity. Moreover, Ba1 and Bb5 equally protected 80% of mice from a fatal dose of APP1 infection compared with the control group. Mice could resist APP1 and APP5 challenge after being treated with the combination of Ba1 and Bb5, with survival rates of 80% and 90%, respectively. These findings suggest that the PA epitope confers antigenicity and can heterologously resist to the APP infection. This finding provides a novel strategy for preventing APP infection.

KEYWORDS:

Actinobacillus pleuropneumonia; B cell epitope; Heterologous protection; Phage display library; Propionibacterium acnes

PMID:
28622855
DOI:
10.1016/j.vetmic.2017.04.026
[Indexed for MEDLINE]

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