Autor(es): Hellestad, Vanessa J; Witthuhn, Bruce A; Fallon, Ann M 

Resumo: DEET (N,N-diethyl-3-methylbenzamide) is the active ingredient used in many commonly used insect repellents, but its mode of action remains poorly understood. Efforts to identify properties that could lead to the development of more effective active ingredients have distinguished among DEETas repellent, deterrent, and insecticidal activities. We used an Aedes albopictus mosquito cell line to evaluate DEETas toxicological properties in the absence of sensory input mediated by the olfactory system. When cells were treated with DEET and labeled with [ super(35)S]methionine/cysteine, a single 25-kDa protein was induced, relative to other proteins, on SDSapolyacrylamide gels. The 25-kDa band from DEET-treated cells was enriched in peptides corresponding to glutathione S-transferase D10 and/or theta in the Aedes aegypti genome. Consistent with the increased expression of the labeled protein, DEET-treated cells had increased glutathione S-transferase activity, and the radiolabeled band bound to Sepharose 4B containing reduced glutathione. By analyzing partial tryptic digests, we established that DEET induces the homolog of A. aegypti glutathione S-transferase, class theta, corresponding to protein XP_001658009.1 in the NCBI database. This specific effect of DEET at the subcellular level suggests that DEET induces physiological responses that extend beyond recognition by the peripheral olfactory system.

Palavras-Chave: Genomes; Cysteine; Repellents; Cytology; Coenzymes; Pest control; Olfaction; Databases; Deterrents; DEET; Olfactory system; Glutathione transferase; Aedes aegypti; Aedes albopictus

Imprenta: Cell Biology and Toxicology, v. 27, n. 2, p. 149-157, 2011.

Descritores: Aedes aegypti - Cell ; Aedes aegypti - Protein synthesis ; Aedes aegypti - Proteins ; Aedes aegypti - Repellent

Data de publicação: 2011

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