Species | Strain (Country of origin) | Resistance profile/additional information | Resistance mechanisms |
---|---|---|---|
Anopheles arabiensis | KGB (Zimbabwe) | Insecticide susceptible | N/A |
SENN (Sudan) | Mostly susceptible. Low-level resistance to permethrin | N/A [27] | |
SENN-DDT (Sudan) | Selected for resistance to DDT from SENN base colony. Also resistant to permethrin, deltamethrin and malathion [27, 28] | Elevated cytochrome P450, glutathione S-transferase (GST) and general esterase activity [27, 28] | |
Anopheles coluzzii | SILCa (Sierra Leone) | Resistant to pyrethroids and DDT | aNo data |
SUA (Liberia) | Insecticide susceptible | N/A | |
Anopheles gambiae | GAH (Ghana) | Resistant to pyrethroids, DDT, carbamates and organophosphates [29] | Monooxygenase and esterase mediated detoxification coupled with the L1014F kdr mutation are implicated in pyrethroid resistance. An assortment of L1014F kdr is also implacted in DDT resistance. Mutations of the Alanine296-glycine (Rdl) GABA receptor and acetylcholinesterase receptor (ace-1 R) are associated with dieldrin and bediocarb resistance respectively [29]. |
TONGSa (Cote d’Ivoire) | Resistant to pyrethroids, DDT, carbamates and organophosphates | aNo data | |
Anopheles quadriannulatus | SANGWE (Zimbabwe) | Insecticide susceptible. Anopheles quadriannulatus is zoophilic and not considered to be a vector species. | N/A |
Anopheles funestus | FANG (Angola) | Insecticide susceptible | N/A |
FUMOZ-R (Mozambique) | Resistant to pyrethroids and carbamates [30] | Overexpression of the cytochrome P450 CYP6P9 [30]. Thickened cuticles also contribute to adult insecticide-resistance [31]. |