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W.J. Slierendrecht

Publications -  12
Citations -  504

W.J. Slierendrecht is an academic researcher. The author has contributed to research in topics: Rainbow trout & Feed conversion ratio. The author has an hindex of 6, co-authored 12 publications receiving 480 citations.

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Genetic variation for growth rate, feed conversion efficiency, and disease resistance exists within a farmed population of rainbow trout

TL;DR: It is demonstrated that additive genetic (co)variation for growth rate, feed conversion efficiency, and VHS resistance does exist within the farmed population of rainbow trout, and indicates that selective breeding for these traits can be successful.
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Selective breeding provides an approach to increase resistance of rainbow trout (Onchorhynchus mykiss) to the diseases, enteric redmouth disease, rainbow trout fry syndrome, and viral haemorrhagic septicaemia

TL;DR: The additive genetic variation detected for resistance demonstrates that selectively breeding trout for resistance to ERM, RTFS, and VHS will be successful, providing a complementary approach to control these diseases.
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Experimental infection of rainbow trout Oncorhynchus mykiss with viral haemorrhagic septicaemia virus isolates from European marine and farmed fishes.

TL;DR: The susceptibility of rainbow trout Oncorhynchus mykiss to infection with various isolates of viral haemorrhagic septicaemia virus (VHSV) was examined, supporting the view that they originated from the marine environment.
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Immunocytochemical analysis of a monoclonal antibody specific for rainbow trout (Oncorhynchus mykiss) granulocytes and thrombocytes

TL;DR: A monoclonal antibody against rainbow trout peripheral blood leucocytes was selected for its lack of reactivity with rainbow trout immunoglobulin and revealed that the antibody reacted strongly with granulocytes and weakly with thrombocytes, and not with erythrocytes, lymphocytes, monocytes or macrophages.
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Rainbow trout offspring with different resistance to viral haemorrhagic septicaemia.

TL;DR: An attempt to associate the distribution of different MHC class II genotypes with low and high resistance gynogenetic offspring was performed, and a significantly different distribution of haplotypes in the low resistance offspring was observed, that could not be explained by a one- or two-locus model.