Vector control is still the principal method to control dengue and chemical insecticides, especially the
pyrethroids such as permethrin are the forerunners of mosquito control agent. Intensive and extensive use
of pyrethroids often result in resistance, thereby hampering control efforts. The present study was
conducted to evaluate the susceptible status of Aedes aegypti, the primary vector of dengue against
permethrin. A nationwide mosquito sampling via ovitrapping was conducted in 12 dengue hotspots across 5
states in Peninsular Malaysia. Field collected Aedes eggs were hatched and reared until L3 larval and further
identified it species. Adult F0 Aedes aegypti were reared until F1 progeny and the female were used in
adult assay, performed according to World Health Organization (WHO) protocol as to determine the
resistance level. The laboratory strain maintained for more than 1000 generations that were susceptible to
permethrin served as the control strain. Evaluation of resistance ratio was assessed by comparing the
knockdown rate with laboratory susceptible strain. In this present study, 70% ofAe. aegypti population from
dengue hotspots was highly resistance to permethrin. The study clearly demonstrated that widespread of
permethrin resistant Ae. aegypti in Malaysian mosquito’s population, indicating the need of implementing
an efficient pyrethroid resistance management.
The mechanism of insecticide resistance is traditionally attributed to detoxification enzymes, target site alteration, decreased penetration of insecticides and behavioural resistance. Other form of mechanisms, such as the role of protein(s) in resistance is unknown. In the present study, the protein profiling of both IMR-PSS strain (permethrin-selected) and IMR-LS strain (laboratory-susceptible) 24 hours post exposure period to permethrin was carried out via 1D-gel electrophoresis and liquid chromatography mass spectrometry (LC-MS/ MS). The bands which appeared in the gel of 1D-electrophoresis revealed an abundance of proteins. The band pattern of both strains looked macroscopically alike and differed only in band intensity. However, LC-MS/MS analysis revealed that the IMR-PSS strain produced extra 388 peptides that were not found in the IMR-LS strain, indicating that IMR-PSS strain reacted differently from IMR-LS strain as a result of persistent exposure to permethrin. Since the complex banding patterns of 1D-gel electrophoresis were difficult to interpret the significance of the protein difference between IMR-PSS and IMR-LS strain, hence LC-MS/MS analysis is ideally suited for better protein resolution and thus will allow more in-depth comparison of the complex pattern. The findings here provide the first preliminary evidence that insecticide resistance in mosquito induces up regulation of proteins that may be protective to mosquitoes against insecticide and proteins could be another mechanism that contributes to development of resistance.