Author:
Mugenzi Leon M. J.,Akosah-Brempong Gabriel,Tchouakui Magellan,Menze Benjamin D.,Tekoh Theofelix A.,Tchoupo Micareme,Nkemngo Francis N.,Wondji Murielle J.,Nwaefuna Ekene K.,Osae Michael,Wondji Charles S.
Abstract
Abstract
Background
Aggravation of insecticide resistance in malaria vectors is threatening the efforts to control malaria by reducing the efficacy of insecticide-based interventions hence needs to be closely monitored. This study investigated the intensity of insecticide resistance of two major malaria vectors An. funestus sensu stricto (s.s.) and An. gambiae sensu lato (s.l.) collected in southern Ghana and assessed the bio-efficacy of several long-lasting insecticidal nets (LLINs) against these mosquito populations.
Methods
The insecticide susceptibility profiles of Anopheles funestus s.s. and Anopheles gambiae s.l. populations from Obuasi region (Atatam), southern Ghana were characterized and the bio-efficacy of some LLINs was assessed to determine the impact of insecticide resistance on the effectiveness of these tools. Furthermore, molecular markers associated with insecticide resistance in both species were characterized in the F0 and F1 populations using PCR and qPCR methods.
Results
Anopheles funestus s.s. was the predominant species and was resistant to pyrethroids, organochlorine and carbamate insecticides, but fully susceptible to organophosphates. An. gambiae s.l. was resistant to all four insecticide classes. High intensity of resistance to 5 × and 10 × the discriminating concentration (DC) of pyrethroids was observed in both species inducing a considerable loss of efficacy of long-lasting insecticidal nets (LLINs). Temporal expression analysis revealed a massive 12-fold increase in expression of the CYP6P4a cytochrome P450 gene in An. funestus s.s., initially from a fold change of 41 (2014) to 500 (2021). For both species, the expression of candidate genes did not vary according to discriminating doses. An. gambiae s.l. exhibited high frequencies of target-site resistance including Vgsc-1014F (90%) and Ace-1 (50%) while these mutations were absent in An. funestus s.s.
Conclusions
The multiple and high intensity of resistance observed in both malaria vectors highlights the need to implement resistance management strategies and the introduction of new insecticide chemistries.
Funder
Bill and Melinda Gates Foundation
Wellcome Trust
Publisher
Springer Science and Business Media LLC
Reference59 articles.
1. World Health Organization. World Malaria Report 2021. World Health Organization 2021. https://apps.who.int/iris/handle/10665/350147. License: CC BY-NC-SA 3.0 IGO.
2. World Health Organization. World malaria report 2020: 20 years of global progress and challenges. World Health Organization 2020. https://apps.who.int/iris/handle/10665/337660. License: CC BY-NC-SA 3.0 IGO.
3. World Health Organization. Global technical strategy for malaria 2016–2030. World Health Organization 2019. https://apps.who.int/iris/handle/10665/176712.
4. World Health Organization. Global Malaria Programme. Global plan for insecticide resistance management in malaria vectors. World Health Organization 2012. https://apps.who.int/iris/handle/10665/44846.
5. Knox TB, Juma EO, Ochomo EO, Pates Jamet H, Ndungo L, Chege P, et al. An online tool for mapping insecticide resistance in major Anopheles vectors of human malaria parasites and review of resistance status for the Afrotropical region. Parasit Vectors. 2014;7:1–14. https://doi.org/10.1186/1756-3305-7-76.