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United States Department of Agriculture

Agricultural Research Service

Research Project: DEVELOPMENT OF APPROACHES TO PREVENT AND AMELIORATE DISEASES OF CATFISH

Location: Warmwater Aquaculture Research Unit

Title: Laboratory mass culture of the freshwater oligochaete Dero digitata

Authors
item Mischke, C -
item Griffin, M -

Submitted to: North American Journal of Aquaculture
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: May 24, 2010
Publication Date: February 2, 2011
Citation: Mischke, C.C., Griffin, M.J. 2011. Laboratory mass culture of the freshwater oligochaete Dero digitata. North American Journal of Aquaculture. 73:13-16.

Interpretive Summary: The development of laboratory mass culture of D. digitata was described and this culture method allows for further research on myxozoan life cycles and oligochaete control.

Technical Abstract: Proliferative gill disease (PGD) in channel catfish Ictalurus punctatus is caused by the myxozoan parasite Henneguya ictaluri, which uses the freshwater oligochaete Dero digitata as an alternate host. Controlled studies on the transmission of PGD require sustainable D. digitata mass cultures. We developed methods to grow and sustain large D. digitata populations and compared population growth in aerated versus nonaerated containers. White paper towels (2-3cm) squares were placed into six 10.7-L dish pans into which 4 L of autoclaved pond water from commercial channel catfish ponds were then added along with 0.1 of fish food. Each of the six dish pans was initially stocked with 100 D. digitata and maintained at 22-25º C; three pans received aeration, and three did not. All worms were counted and returned to their respective pans once each week for 5 weeks. To compensate for evaporative loss, autoclaved pond water was added to the pans weekly, and pond water and paper towels were completely changed after 4 weeks. Over 5 weeks, the mean number of worms per pan increased significantly more in the nonaerated pans than in the aerated pans. We have maintained D. digitata mass cultures in our laboratory for over a year, starting with two pans containing 100 worms each. Through routine exchanges of pond water and paper towel squares, these populations have expanded to 16 pans, each supporting 3,000 – 6,000 worms. We have removed thousands of worms periodically to give to other researcher or for research in our laboratory. Using methods described here, researchers can maintain D. digitata mass cultures and predict population numbers, that will be available at given times for studies on myxozoan life cycles and oligochaete control.

Last Modified: 4/16/2014