Malaria is a disease of poverty inflicting a serious negative impact on health and socioeconomic development in the poorest countries of the world that cannot afford to succeed (
95). Presently we have minimized the global malaria burden considerably, by inducting the low-cost interventions like ITNs. Control of the vector mosquitoes has been an integral part of efforts to either eliminate or control the disease worldwide. In West Africa, where the main vectors are members of the
An. gambiae complex and the
An. funestus group, various attempts were made to control malaria, by use of insecticides, from the early 1930s until the 1960s. In West Africa, resistance to pyrethroids due to knockdown resistance (kdr) mutations in
An. gambiae populations has been reported in Côte d’Ivoire (
96,
97), Burkina Faso and Benin (
98) despite the absence of large-scale mosquito control in these countries. Resistance of
An. gambiae, the main malaria vector in West Africa, to pyrethroids poses a great challenge to the strategy of using insecticide-treated materials for malaria control. The number of available and effective pesticides for malaria vector control is also reported to be decreasing. Currently, only the pyrethroid class of insecticides is appropriate for ITNs impregnation and LLINs (
30). However, vectors developing resistance against pyrethroid is already a serious threat to sustain the continuous use of ITNs and IRS. Although 12 insecticides are currently recommended by the WHO for IRS, they belong only to four different chemical classes namely organochlorines, pyrethroids, carbamates, and organophosphates, and the cross-resistance among insecticides is often frequent.
The widespread use of the same insecticides in the agricultural sector has made the situation worse. Resistance may develop due to changes in the mosquito’s enzyme systems, resulting in more rapid detoxification or sequestration of the insecticide, or due to mutations in the target site preventing the insecticide-target site interaction (
99). Insecticides that can be used in malaria control are becoming increasingly limited. Introduction of inappropriate insecticides without a proper understanding of the prevailing resistance mechanisms may lead to enhanced vector resistance and vector control failure. Early detection and knowledge on the resistance status and the underlying mechanisms in vector mosquitoes are essential for effective long-term control of the vector.
It is obvious that the ongoing malaria vector control strategies heavily rely on the use of IRS and ITNs. The current success of these strategies in reducing the occurrence of malaria, contributed towards the optimism that elimination of this disease which is a major public health problem is a feasible objective. Substantial international efforts have been made for the last three years enabling access to approximately 289 million ITNs in sub-Saharan Africa, enough to cover 76% of the 765 million people at the risk of malaria. The number of countries that employed IRS as vector control strategy has increased from 31 in 2007 to 68 in 2009 (
56).
In Africa, LLINs and IRS are now being deployed in a large-scale more than ever before, which considerably exposes African vectors to enormous selection pressure for insecticide resistance. Unfortunately, since the introduction and commercialization of the pyrethroids in the 1970s and 1980s, little public investment has been observed in insecticides for public health purposes. Therefore, the majority of this selection pressure comes from the pyrethroid insecticides. These are the only class of insecticides currently applied to treated nets and most commonly used for IRS application (
56).
Therefore the widespread as well as indiscriminate usage of pyrethroid insecticide increases the risk of resistance. The situation may be accelerated by the reintroduction of DDT in several countries of Africa as cross-resistance between these classes of insecticides which can occur as a result of amino acid substitutions in the shared target sites. All major malaria vectors in Africa have developed resistance to these insecticides and the resistance alleles appear to be spreading at an exceptionally rapid rate (
16). Inheritable resistance traits develop by selective pressure exerted on a mosquito population. Fast-acting insecticides exert strong selection pressures, and the short generation time and prolific progeny characteristic of the mosquito lifecycle is well suited for quick development of resistance. Over 50 species of Anopheles are reported to be resistant to insecticides (
40).