BACTERIAL PROBLEMS ASSOCIATED WITH SCALLOP PECTEN-MAXIMUS LARVAL CULTURE

Citation
Jl. Nicolas et al., BACTERIAL PROBLEMS ASSOCIATED WITH SCALLOP PECTEN-MAXIMUS LARVAL CULTURE, Diseases of aquatic organisms, 27(1), 1996, pp. 67-76
Citations number
20
Categorie Soggetti
Veterinary Sciences","Marine & Freshwater Biology
ISSN journal
01775103
Volume
27
Issue
1
Year of publication
1996
Pages
67 - 76
Database
ISI
SICI code
0177-5103(1996)27:1<67:BPAWSP>2.0.ZU;2-X
Abstract
Scallop Pecten maximus larvae have been cultured at the Argenton and T induff (Brittany, France) hatcheries with antibiotic treatment (chlora mphenicol at 8 ppm) for 15 yr. Without treatment, outbreak of disease has normally occurred between Day 12 and Day 19 or sometimes earlier. A bacteriological study of larvae reared with and without antibiotic w as performed over a 4 yr period. Among the collected strains, 2 cluste rs (C and F) of vibrios were present at high densities only in larvae cultured without treatment. One cluster (C) was routinely isolated ove r the 4 yr of study, while the other (F) was collected only in the thi rd year. Their virulence with respect to scallop larvae and their lack of infectivity with respect to oyster larvae were demonstrated in an exposure experiment. The vibrio F strain tended to lose its virulence after 5 subcultures, whereas the vibrio C strain retained the ability to kill scallop larvae in experimental infections. Three other vibrios isolated in moribund oyster larvae caused mortality in oyster larvae but not in scallop larvae. Different methods were used to determine th e taxonomic position of these virulent bacteria. The phenotypic traits of bacterial isolates were determined with the Biolog GN microplate, the API 20E system and the reference method. Patterns of cytoplasmic p roteins were identified by electrophoresis in SDS-PAGE. These differen t methods consistently confirmed the existence of 2 vibrio species pat hogenic to scallop larvae. Affiliation of cluster F with Vibrio splend idus was assessed by Biolog tests and by analysis of 16S rRNA sequence s. One pathogenic bacteria of oyster larvae was also very close to thi s second cluster, whereas the 2 others from moribund oyster larvae and cluster C may constitute 2 different species.