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Laboratory evaluation of WBA 8119 as a rodenticide for use against warfarin-resistant and non-resistant rats and mice

Published online by Cambridge University Press:  15 May 2009

R. Redfern
Affiliation:
Sorex (London) Ltd, Research Department, Halebank Factory, Lower Road, Widnes, Cheshire
J. E. Gill
Affiliation:
Pest Infestation Control Laboratory, Ministry of Agriculture, Fisheries and Food, Hook Rise South, Tolworth, Surbiton, Surrey
M. R. Hadler
Affiliation:
Sorex (London) Ltd, Research Department, Halebank Factory, Lower Road, Widnes, Cheshire
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Summary

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Feeding tests were carried out in the laboratory to evaluate WBA 8119 as a potential new rodenticide against wild common rats (Rattus norvegicus), ship rats (R. rattus) and house mice (Mus musculus). The results obtained are compared with data previously obtained for difenacoum, another member of the same series of 4-hydroxycoumarin anticoagulants.

With warfarin-resistant and non-resistant common rats, complete kills were obtained using a concentration of 0·0005% for 2 days, or 0·001 % for 1 day: a 1-day test at 0·0005% killed 6 out of 10 and 17 out of 20 of the two types respectively. At 0·005% complete kills of resistant ship rats were obtained after 2 days exposure and of resistant house mice after 1 day, but at 0·002% for 2 days there was some survival. Non-resistant ship rats and house mice were all killed after 2 days feeding on 0·002% bait.

In 2-day palatability tests, R. norvegicus showed no significant aversion to the poison at 0·002% and 100% mortality was obtained. The poison was significantly unpalatable to R. rattus at 0·005% and to M. musculus at 0·005% and 0·002 %, although with the last species these concentrations gave complete kills.

It is concluded that WBA 8119 has greater activity than other known anticoagulants against the three commensal species examined. The laboratory results suggest that concentrations between 0·0005% and 0·002% would be suitable for field use against common rats, and between 0·002% and 0·005% for ship rats and house mice.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1976

References

REFERENCES

Drummond, D. C. & Wilson, B. J. (1968). Laboratory investigations of resistance to warfarm of Rattus norvegicus Berk. in Montgomeryshire and Shropshire. Annals of Applied Biology 61, 303.–12.Google ScholarPubMed
Greaves, J. H., Rennison, B. D. & Redfern, R. (1973). Warfarin resistance in the ship rat in Liverpool International Pest Control 15, 17.Google Scholar
Hadler, M. R., Redfern, R. & Rowe, F. P. (1975). Laboratory evaluation of difenacoum as a rodenticide Journal of Hygiene 74, 441–8.CrossRefGoogle ScholarPubMed
Hadler, M. R. & Shadbolt, R. S. (1975). Novel 4-hydroxycoumarm anticoagulants active against resistant rats Nature, London 253, 275–7.CrossRefGoogle ScholarPubMed
Rennison, B. D. & Hadler, M. R. (1975). Field trials of difenacoum against warfarin-resist ant infestations of Rattus norvegicus Journal of Hygiene 74, 449–55.CrossRefGoogle Scholar
Rowe, F. P. & Redfern, R. (1965). Toxicity tests on suspected warfarin-resistant house mice (Mus musculus L.) Journal of Hygiene 63, 417–25.CrossRefGoogle ScholarPubMed