Document Type

Article

Department/Program

Virginia Institute of Marine Science

Publication Date

2016

Journal

Aquaculture

Volume

450

First Page

199

Last Page

205

Abstract

Cytochalasin B (CB) has been used to induce tetraploidy in oysters since the practice began in 1993. However, CB is toxic and presents health risks to hatchery workers who administer the treatment. 6-dimethylaminopurine (6-DMAP) is also an effective cytokinetic inhibitor, and does not carry the health risks of CB. We examined the relative effectiveness of 6-DMAP vs CB for producing tetraploids in the Eastern oyster (Crassostrea virginica). Survival and yield of tetraploids varied widely among the 15 experiments. Larvae resulting from 6-DMAP treatment had higher survival in 11 of the 14 trials on day two and day six/seven. For yield of tetraploids, 10 of 13 6-DMAP treatments had higher proportions of tetraploids on day two and at the second sampling -day six, seven, ornine-7 of 10 had higher proportions of tetraploids. Tetraploid spat were obtained from the majority of surviving cultures. Based on these results, 6-DMAP can effectively replace CB for inducing polyploidy in C. virginica, and probably other Crassostrea spp., due to the success of the treatment, the ease of application, and the reduction in health risk to hatchery workers. This study set the precedent for the use of 6-DMAP on C. virginica and established a new procedure for inducing tetraploids using triploid eggs. It might be possible to refine the treatment to further optimize yield of tetraploids. Statement of relevance: In this manuscript we report a novel method of inducing tetraploid Crassostrea virginica from triploid eggs using 6-dimethylaminopurine. We compare the efficiency of cytochalasin B and 6-dimethylaminopurine for tetraploid induction. We also report the expected fecundity of triploid C. virginica females. The method of tetraploidy induction we report here will likely be useful for inducing tetraploidy in other Crassostrea spp. (C) 2015 Elsevier B.V. All rights reserved.

DOI

10.1016/j.aquaculture.2015.07.034

Keywords

Triploid Pacific Oysters; Polar Body-I; Gigas Thunberg; Genetic Consequences; Fertilized-Eggs; Polyploid Fish; Oocytes; Performance; Inhibition; Activation

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