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  4. An in Vitro Assay for Testing Mosquito Repellents Employing a Warm Body and Carbon Dioxide as a Behavioral Activator

An in Vitro Assay for Testing Mosquito Repellents Employing a Warm Body and Carbon Dioxide as a Behavioral Activator

Author(s)
Kroeber, Thomas  
Poste de physiologie comportementale  
Kessler, Sébastien  
Laboratoire de recherches fondamentales et appliquées en écologie chimique  
Frei, Jérôme
Bourquin, Martine  
Laboratoire d'écologie et évolution des parasites  
Guerin, Patrick  
Institut de biologie  
Date issued
2010
In
Journal of the American Mosquito Control Association
Vol
4
No
26
From page
381
To page
386
Subjects
in vitro repellent assay mosquito insect vector anopheles gambiae deet aedes-aegypti human-skin n n-diethyl-3-methylbenzamide deet anopheles-gambiae quantitation attraction culicidae responses bioassay efficacy
Abstract
We describe here an in vitro behavioral assay for testing mosquito repellents applied in a dose-based manner to a warm body (34 C) in test cages. The system was used to assess the sensitivity of 4-6-day-old Anopheles gambiae to the insect repellent diethyl methyl benzamide (deet). These tests were made in the absence and presence of additional carbon dioxide (CO(2)) applied as a pulse to activate mosquitoes in the cages. In the absence of the CO(2) pulse the mosquitoes hardly responded to the warm body. Increasing the CO(2) level in the cage by 1,000 parts per million caused a 25-fold increase in the number of landings by mosquitoes on the warm body in 2-min tests. This mosquito activation allowed the measurement of a significant reduction in the number of landings to bite on the warm body with increasing doses of deet (0.4 to 3.8 mu g/cm(2)). An asymptotic nonlinear model fitted to the repellency data in the presence of CO(2) allowed estimation of the effective dose of deet that reduced landings to bite by 50% (ED(50)) at 0.95 mu g/cm(2) (5 nmol/cm(2)) and the corresponding ED(95) at 4.12 mu g/cm(2) (21.5 nmol/cm(2)). This in vitro bioassay has the advantage of permitting a fast throughput of test products under standardized conditions and is suitable for screenings designed for the purpose of discovering lead products with as yet unknown human toxicological and dermatological profiles.
Publication type
journal article
Identifiers
https://libra.unine.ch/handle/20.500.14713/54226
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