Journal
JOURNAL OF MOLECULAR MICROBIOLOGY AND BIOTECHNOLOGY
Volume 13, Issue 1-3, Pages 55-64Publisher
KARGER
DOI: 10.1159/000103597
Keywords
bacterial cold water disease; oncorhynchus mykiss; ribosomal protein L10; vaccine
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The psychrophilic bacterium Flavobacterium psychrophilum is a rapidly emerging, virulent pathogen of a variety of commercially important finfish species, including salmonids. No vaccines against F. psychrophilum are currently available, partly due to its recalcitrant growth in vitro. Consequently, we explored the possibility of constructing recombinant vaccines in Escherichia coli as a prophylactic biotechnological strategy to counter F. psychrophilum infections. An immunoreactive clone from a F. psychrophilum expression library was found to express a similar to 16 kDa protein antigen. A proteomics approach was taken to identify the ORF encoding the similar to 16 kDa protein. Tryptic fragments of the similar to 16 kDa protein were analyzed by MALDI-TOF mass spectrometry and compared to theoretical (in silico) tryptic fragments of translated ORFs predicted within the cloned DNA. The target protein was identified as a 166 amino acid protein (named 7-166) with homology to rplJ which encodes bacterial ribosomal protein L10. When highly expressed in E. coli as an N-terminal fusion protein, this chimera reacted with convalescent rainbow trout serum. When adjuvanted and administered intra-peritoneally to immature rainbow trout a high level of protection (82% RPS) was afforded against virulent F. psychrophilum challenge; thus establishing F. psychrophilum rplJ homologue 7-166 as a promising vaccine candidate for RTFS. Copyright (c) 2007 S. Karger AG, Basel.
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