Studies on Development and Antigen Expression of Biofilm Cells of Vibrio anguillarum for Oral Vaccination in Aquaculture

Background: Vibrio anguillarum is one of the major pathogen causing economic loss in the aquaculture industry. And, most of the microorganisms will use biofilm strategy for their survival in the host. Hence, less effectiveness of antibiotic and free cell (whole cell) vaccine may be observed in the a...

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Veröffentlicht in:Indian journal of animal research 2021-02 (OF)
Hauptverfasser: Ramesh, K. S., Poojary, Sathish Rama, Kumar, B.T. Naveen, Patil, Prakash, Abhiman, P. B., Shankar, K. M., Patel, Deepti Manjari
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Sprache:eng
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Zusammenfassung:Background: Vibrio anguillarum is one of the major pathogen causing economic loss in the aquaculture industry. And, most of the microorganisms will use biofilm strategy for their survival in the host. Hence, less effectiveness of antibiotic and free cell (whole cell) vaccine may be observed in the aquaculture practice. Therefore the developed vaccine should be the mirror image of pathogen molecule, in regard; the present study was carried out to standardize the nutrient requirement for optimum biofilm production and antigen expression of biofilm and free cells of Vibrio anguillarum. Also, to identify the deferentially expressed protein in the biofilm mode. Methods: Culture conditions were optimized for the maximum biofilm production of V. anguillarum on chitin flakes as a substrate in nutrient restricted conditions. Through proteomic approach such as SDS PAGE was conducted to know the protein profile of biofilm and free cells of V. anguillarum and further, nanoLC-MS/MS was used to identify the differentially expressed protein in the biofilm of V. anguillarum. Result: Maximum biofilm production was observed on the 3rd day on 0.1% TSB concentration supplemented with 0.3% chitin flakes and 2% NaCl. Significant changes in the antigen expression of biofilm of V. anguillarum were observed in SDS PAGE and it revealed that in the biofilm mode, three new novel proteins were expressed and about ten proteins repressed as compared to that of free cell counterpart.
ISSN:0367-6722
0976-0555
DOI:10.18805/ijar.B-3927