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Laboratory studies with some recent anticoccidials

Published online by Cambridge University Press:  06 April 2009

John F. Ryley and
Robert G. Wilson
John F. Ryley
Affiliation:
Imperial Chemical Industries Ltd., Pharmaceuticals Division, Alderley Park, Macclesfield, Cheshire, England
Robert G. Wilson
Affiliation:
Imperial Chemical Industries Ltd., Pharmaceuticals Division, Alderley Park, Macclesfield, Cheshire, England
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Extract

The activities of monensin, lasalocid and halofuginone against Eimeria tenella, E. brunetti and E. necatrix have been studied under laboratory conditions. Complete control of experimental infections in the chick, separable from toxicity, was not obtained with monensin, but was achieved with the other two compounds at levels of 150 and 6 ppm in the food respectively. All three compounds appear to inhibit coccidial development very early in the life-cycle, and to have a fairly rapid lethal effect, monensin and lasalocid more so than the febrifugine derivative. In vivo observations have been supplemented with in vitro studies. Some discussion of the difficulties of relating laboratory experiments to field performance is given.

Information

Type
Research Article
Information
Parasitology , Volume 70 , Issue 2 , April 1975, pp. 203 - 222
Copyright
Copyright © Cambridge University Press 1975

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References

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