Anopheles metabolic proteins in malaria transmission, prevention and control: a review
Anopheles metabolic proteins in malaria transmission, prevention and control: a review
AbstractThe increasing resistance to currently available insecticides in the malaria vector, Anopheles mosquitoes, hampers their use as an effective vector control strategy for the prevention of malaria transmission. Therefore, there is need for new insecticides and/or alternative vector control strategies, the development of which relies on the identification of possible targets in Anopheles. Some known and promising targets for the prevention or control of malaria transmission exist among Anopheles metabolic proteins. This review aims to elucidate the current and potential contribution of Anopheles metabolic proteins to malaria transmission and control. Highlighted are the roles of metabolic proteins as insecticide targets, in blood digestion and immune response as well as their contribution to insecticide resistance and Plasmodium parasite development. Furthermore, strategies by which these metabolic proteins can be utilized for vector control are described. Inhibitors of Anopheles metabolic proteins that are designed based on target specificity can yield insecticides with no significant toxicity to non-target species. These metabolic modulators combined with each other or with synergists, sterilants, and transmission-blocking agents in a single product, can yield potent malaria intervention strategies. These combinations can provide multiple means of controlling the vector. Also, they can help to slow down the development of insecticide resistance. Moreover, some metabolic proteins can be modulated for mosquito population replacement or suppression strategies, which will significantly help to curb malaria transmission.
- London School of Hygiene & Tropical Medicine United Kingdom
- Jena University Hospital Germany
- COVENANT UNIVERSITY
- Helmholtz Association of German Research Centres Germany
- Covenant University Nigeria
Insecticides, Plasmodium, Insecticide resistance, Mosquito Control, Infectious and parasitic diseases, RC109-216, Review, Mosquito Vectors, Vector control, Malaria, Acetylcholinesterase ; Mosquito Vectors/genetics [MeSH] ; Plasmodium/physiology [MeSH] ; Insecticide Resistance [MeSH] ; Insecticide ; Mosquito Control [MeSH] ; Mosquito Vectors/metabolism [MeSH] ; Anopheles/genetics [MeSH] ; Anopheles/drug effects [MeSH] ; Mosquito Vectors/parasitology [MeSH] ; ; Immune response ; Insecticides/pharmacology [MeSH] ; Anopheles/parasitology [MeSH] ; Insect Proteins/metabolism [MeSH] ; Malaria/transmission [MeSH] ; Humans [MeSH] ; Malaria/parasitology [MeSH] ; Insecticide resistance ; Animals [MeSH] ; Vector control ; Insect Proteins/genetics [MeSH] ; Malaria/prevention ; Mosquito Vectors/drug effects [MeSH] ; Anopheles/metabolism [MeSH] ; Review, Insecticide Resistance, Anopheles, Acetylcholinesterase, Animals, Humans, Insect Proteins, Immune response, Insecticide
Insecticides, Plasmodium, Insecticide resistance, Mosquito Control, Infectious and parasitic diseases, RC109-216, Review, Mosquito Vectors, Vector control, Malaria, Acetylcholinesterase ; Mosquito Vectors/genetics [MeSH] ; Plasmodium/physiology [MeSH] ; Insecticide Resistance [MeSH] ; Insecticide ; Mosquito Control [MeSH] ; Mosquito Vectors/metabolism [MeSH] ; Anopheles/genetics [MeSH] ; Anopheles/drug effects [MeSH] ; Mosquito Vectors/parasitology [MeSH] ; ; Immune response ; Insecticides/pharmacology [MeSH] ; Anopheles/parasitology [MeSH] ; Insect Proteins/metabolism [MeSH] ; Malaria/transmission [MeSH] ; Humans [MeSH] ; Malaria/parasitology [MeSH] ; Insecticide resistance ; Animals [MeSH] ; Vector control ; Insect Proteins/genetics [MeSH] ; Malaria/prevention ; Mosquito Vectors/drug effects [MeSH] ; Anopheles/metabolism [MeSH] ; Review, Insecticide Resistance, Anopheles, Acetylcholinesterase, Animals, Humans, Insect Proteins, Immune response, Insecticide
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