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TWENTY-FIFTH ANNUAL EASTERN FISH HEALTH WORKSHOP


MARCH 10-13, 2000



 

Depuration Of Aeromonas Salmonicida By The Freshwater Bivalve Amblema plicata To Prevent The Bacterium’s Transmission To Arctic Char (Salvelinus alpinus)

 

 

 

Clifford E. Starliper

 

USGS,  Leetown Science Center, National Fish Health Research Laboratory, 1700 Leetown Road, Kearneysville,  WV 25430

 

 

 

Freshwater bivalves are very susceptible to environmental and biological factors that impact their existence. Factors such as dams, construction, siltation and most recently the unwanted introduction of zebra mussels (Dreissena polymorpha) have resulted in greater than 70% of the animals native to North America to become listed as threatened, endangered or of special concern. In 1995, the U.S. Fish and Wildlife Service, with other partners, initiated conservation efforts; one was a relocation program whereby animals would be collected and propagated at facilities, including fish hatcheries, free of their natural threats with the ultimate goal of reintroduction. With relocation, questions arose regarding the potential to introduce fish pathogens with the mussels. According to standard protocol, prior to relocation mussels must undergo a 30-day quarantine to ensure zebra mussels are not inadvertently spread. The study presented here was done to determine if quarantine in pathogen-free water would also provide for the mussels to depurate fish bacterial pathogens they might harbor. There are no bacterial pathogens known to cause disease to both mussels and fish, therefore, a model system was developed for study utilizing the bivalve Amblema plicata, the salmonid fish Arctic char (Salvelinus alpinus) and Aeromonas salmonicida. An artificial epizootic was established by injecting (i.p.) two groups of Arctic char (60 fish each) with 2.26 X 102 cfu and 2.26 X 100 cfu, respectively, of viable A. salmonicida per fish. These fish were placed in a tank with non-injected char, which became infected via cohabitation. The injected fish died and after the non-injected fish began to die, 120 A. plicata were placed in the tank. When the A. plicata had become carriers of, and potential vectors for A. salmonicida, the animals were transferred to four tanks and pathogen-free Arctic char were added after 1, 5, 15 and 30 day quarantine periods. Transmission of A. salmonicida from the mussels to the “clean” char was then monitored. Infectivity and transmission to fish and mussels was determined by bacteriological culture. It was found that a quarantine period in pathogen-free water is effective to prevent transmission of A. salmonicida, but effectiveness depends on the length of quarantine.

 

      



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