Variation in the molecular weight of Photobacterium damselae subsp. piscicida antigens when cultured under different conditions in vitro.
- Author:
Tae S JUNG
1
;
Kim D THOMPSON
;
Donatella VOLPATTI
;
Marco GALEOTTI
;
A ADAMS
Author Information
- Publication Type:Original Article ; Comparative Study
- Keywords: Dicentrarchus labrax; glucose-rich medium; iron depletion; Photobacterium damselae subsp. piscicida; tryptone soya broth
- MeSH: Animals; Antibodies, Bacterial/blood; Antigens, Bacterial/immunology/*metabolism; Bass/blood/*immunology; Blotting, Western/veterinary; Cell Count/methods; Culture Media; Enzyme-Linked Immunosorbent Assay/veterinary; Fish Diseases/immunology/*microbiology; Molecular Weight; Pasteurella Infections/immunology/microbiology/*veterinary; Photobacterium/*immunology
- From:Journal of Veterinary Science 2007;8(3):255-261
- CountryRepublic of Korea
- Language:English
- Abstract: The antigenicity of Photobacterium damselae (Ph. d.)subsp. piscicida, cultured in four different growth media[tryptone soya broth (TSB), glucose-rich medium (GRM),iron-depleted TSB (TSB+IR-), and iron-depleted GRM(GRM+IR-)] was compared by enzyme-linked immuno-sorbent assay (ELISA) and Western blot analysis usingsera obtained from sea bass (Dicentrarchus labrax) raisedagainst live or heat-killed Ph. d. subsp. piscicida. Theantigenic expression of Ph. d. subsp. piscicida was found todiffer depending on the culture medium used. A significantlyhigher antibody response was obtained with iron-depletedbacteria by ELISA compared with non-iron depletedbacteria obtained from the sera of sea bass raised againstlive Ph. d. subsp. piscicida. The sera from sea bass raisedagainst live bacteria showed a band at 22kDa in bacteriacultured in TSB+IR- or GRM+IR- when bacteria thathad been freshly isolated from fish were used for thescreening, while bands at 24 and 47kDa were observedwith bacteria cultured in TSB or GRM. When bacteriawere passaged several times on tryptic soya agar prior toculturing in the four different media, only bands at 24 and47kDa were recognized, regardless of the medium used toculture the bacteria. It would appear that the molecularweight of Ph. d. subsp. piscicida antigens change in thepresence of iron restriction, and sera from sea bassinfected with live bacteria are able to detect epitopes onthe antigens after this shift in molecular weight.
