Spatio-temporal characterization of phenotypic resistance in malaria vector species

BMC Biol. 2024 May 20;22(1):117. doi: 10.1186/s12915-024-01915-z.

Abstract

Background: Malaria, a deadly disease caused by Plasmodium protozoa parasite and transmitted through bites of infected female Anopheles mosquitoes, remains a significant public health challenge in sub-Saharan Africa. Efforts to eliminate malaria have increasingly focused on vector control using insecticides. However, the emergence of insecticide resistance (IR) in malaria vectors pose a formidable obstacle, and the current IR mapping models remain static, relying on fixed coefficients. This study introduces a dynamic spatio-temporal approach to characterize phenotypic resistance in Anopheles gambiae complex and Anopheles arabiensis. We developed a cellular automata (CA) model and applied it to data collected from Ethiopia, Nigeria, Cameroon, Chad, and Burkina Faso. The data encompasses georeferenced records detailing IR levels in mosquito vector populations across various classes of insecticides. In characterizing the dynamic patterns of confirmed resistance, we identified key driving factors through correlation analysis, chi-square tests, and extensive literature review.

Results: The CA model demonstrated robustness in capturing the spatio-temporal dynamics of confirmed IR states in the vector populations. In our model, the key driving factors included insecticide usage, agricultural activities, human population density, Land Use and Land Cover (LULC) characteristics, and environmental variables.

Conclusions: The CA model developed offers a robust tool for countries that have limited data on confirmed IR in malaria vectors. The embrace of a dynamical modeling approach and accounting for evolving conditions and influences, contribute to deeper understanding of IR dynamics, and can inform effective strategies for malaria vector control, and prevention in regions facing this critical health challenge.

Keywords: Cellular automata; Insecticide resistance; Malaria vectors; Spatio-temporal modeling.

MeSH terms

  • Africa South of the Sahara
  • Animals
  • Anopheles* / genetics
  • Anopheles* / parasitology
  • Female
  • Insecticide Resistance* / genetics
  • Insecticides / pharmacology
  • Malaria* / transmission
  • Mosquito Vectors* / genetics
  • Mosquito Vectors* / parasitology
  • Mosquito Vectors* / physiology
  • Phenotype
  • Spatio-Temporal Analysis