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Comparative analysis of Vibrio splendidus-related strains isolated during Crassostrea gigas mortality events

Published online by Cambridge University Press:  15 September 2002

Frédérique Le Roux
Affiliation:
Laboratoire de Génétique et Pathologie, Ifremer, 17390 La Tremblade, France
Mélanie Gay
Affiliation:
Laboratoire de Génétique et Pathologie, Ifremer, 17390 La Tremblade, France
Christophe Lambert
Affiliation:
Laboratoire des Sciences de l'Environnement marin (LEMAR), Institut Universitaire Européen de la Mer (IUEM), Université de Bretagne Occidentale (UBO), Place Copernic, technopole Brest-Iroise, 29280, Plouzané, France
Magali Waechter
Affiliation:
Écloserie Grainocéan, 14 cours Dechézeaux, 17410 Saint, Martin de Ré, France
Saravanne Poubalanne
Affiliation:
Laboratoire de Génétique et Pathologie, Ifremer, 17390 La Tremblade, France
Bruno Chollet
Affiliation:
Laboratoire de Génétique et Pathologie, Ifremer, 17390 La Tremblade, France
Jean-Louis Nicolas
Affiliation:
Laboratoire de Physiologie des Invertébrés marins, Ifremer, 29280, Plouzané, France
Franck Berthe
Affiliation:
Laboratoire de Génétique et Pathologie, Ifremer, 17390 La Tremblade, France
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Abstract

French mollusc production is based mainly on the Pacific cupped oyster, Crassostrea gigas. Since 1991, annual mass mortality of juveniles has been reported during summer months. These recurring episodes concern professionals who fear that like Portugese oyster, C. angulata, C. gigas could in turn disappear following one of these epizooties. Previously, bacteriological analysis of moribund oyster juveniles yielded an isolate of a Vibrio splendidus biovar II strain, named TNEMF6. This isolate was demonstrated to be pathogenic to Crassostrea gigas spat by experimental challenge. To study the association between summer oyster mortality and presence of TNEMF6 cluster strains, Vibrionaceae fauna were isolated from infected spat along the French Atlantic coast between 1997-1998. Strains related to V. splendidus biovar II were selected. Comparison with TNEMF6 was performed by classical biochemical tests and polymerase chain reaction – restriction fragment length polymorphism (PCR-RFLP) of SSU rDNA, rpoD, and gyrB genes. Genomic similarities were confirmed by DNA/DNA hybridization. Only one strain out of 14, TNNIII7, was found to be closely related to the pathogenic bacteria. Neither the phenotypic nor the genotypic markers used in this study were able to distinguish pathogenic from non-pathogenic strains of the widespread V. splendidus. However, future genetic comparisons of TNEMF6 and TNNIII7 is likely to reveal genes involved in pathogenicity.

Type
Research Article
Copyright
© Elsevier, IRD, Inra, Ifremer, Cemagref, CNRS, 2002

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