Abstract
A neutralizing epitope fragment of ApxIIA toxin (ApxIIA#5) of the Korean Actinobacillus pleuropneumoniae serotype 2 strain was expressed and immobilized on the cell surface of Saccharomyces cerevisiae for efficient vaccine development. Expression of ApxIIA#5 was confirmed by Western blot analysis using cell-wall proteins, and the surface display of ApxIIA#5 was further visualized under confocal microscopy. Quantitative ELISA revealed that the recombinant ApxIIA#5 directed to the cell surface consisted of approximately 16% cell-wall proteins, estimated to be 35mg of ApxIIA#5 protein per liter of cultured cells. An immunoassay revealed that antigen-specific antibodies against ApxIIA#5 were present in the sera of mice fed recombinant ApxIIA#5-expressing yeast, but not in mice fed the wild-type nor the vector-only transformant. Moreover, the mice fed the recombinant epitope-expressing yeast were protected from injection of a lethal dose of A. pleuropneumoniae.
| Original language | English |
|---|---|
| Pages (from-to) | 1362-1367 |
| Number of pages | 6 |
| Journal | Bioscience, Biotechnology, and Biochemistry |
| Volume | 74 |
| Issue number | 7 |
| DOIs | |
| State | Published - 2010 |
Keywords
- Actinobacillus pleuropneumoniae
- APX toxin
- Oral vaccination
- Saccharomyces cerevisiae
- Surface display
Quacquarelli Symonds(QS) Subject Topics
- Engineering - Petroleum
- Chemistry
- Biological Sciences
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