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Spatial variation in the frequency of knockdown resistance genotypes in Florida Aedes aegypti populations.
Mundis, Stephanie J; Estep, Alden S; Waits, Christy M; Ryan, Sadie J.
Affiliation
  • Mundis SJ; Quantitative Disease Ecology and Conservation (QDEC) Lab, Department of Geography, University of Florida, Gainesville, FL, 32607, USA. s.mundis@ufl.edu.
  • Estep AS; Emerging Pathogens Institute, University of Florida, Gainesville, FL, 32608, USA. s.mundis@ufl.edu.
  • Waits CM; Navy Entomology Center of Excellence, R&D Department, Gainesville, FL, 32608, USA.
  • Ryan SJ; Navy Entomology Center of Excellence, R&D Department, Gainesville, FL, 32608, USA.
Parasit Vectors ; 13(1): 241, 2020 May 11.
Article in En | MEDLINE | ID: mdl-32393364
ABSTRACT

BACKGROUND:

The development of insecticide resistance in disease-vectoring mosquito species can lead to vector control failure and disease resurgence. However, insecticide applications remain an essential public health intervention. In Florida, insecticide resistance in Aedes aegypti, an anthropophilic mosquito species capable of transmitting dengue, chikungunya, and Zika virus, is a major concern. Understanding the location, scale, and driving factors of insecticide resistance can enhance the ability of vector control organizations to target populations effectively.

METHODS:

We used previously collected data on frequencies of mutations that confer resistance to commonly used pyrethroid insecticides in Ae. aegypti specimens from 62 sites distributed across 18 counties in Florida. To determine the scale of clustering for the most resistant variant, we used a Ripley's K function. We also used a spatial scanning statistic technique to identify locations of clusters where higher than expected frequencies of susceptible or resistant mosquitoes occurred. We then tested for associations between landscape, demographic, and insecticide-use factors using a beta regression modelling approach and evaluated the effect of spatial lag and spatial error terms on overall explanatory power of these models.

RESULTS:

The scale at which maximum clustering of the most resistant variant occurs is approximately 20 kilometers. We identified statistically significant clusters of genotypes associated with resistance in several coastal cities, although some of these clusters were near significant clusters of susceptible mosquitoes, indicating selection pressures vary at the local scale. Vegetation density, distance from roads, and pyrethroid-use by vector control districts were consistently significant predictors of knockdown resistance genotype frequency in the top-performing beta regression models, although pyrethroid use surprisingly had a negatively associated with resistance. The incorporation of spatial lags resulted in improvements to the fit and explanatory power of the models, indicating an underlying diffusion process likely explains some of the spatial patterns observed.

CONCLUSIONS:

The genetic mutations that confer resistance to pyrethroids in Ae. aegypti mosquitoes in Florida exhibit spatial autocorrelation and patterns that can be partially explained by landscape and insecticide-use factors. Further work at local scales should be able to identify the mechanisms by which these variables influence selection for alleles associated with resistance.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Insecticide Resistance / Aedes / Spatial Analysis / Insecticides / Mutation Type of study: Prognostic_studies Limits: Animals Country/Region as subject: America do norte Language: En Journal: Parasit Vectors Year: 2020 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Insecticide Resistance / Aedes / Spatial Analysis / Insecticides / Mutation Type of study: Prognostic_studies Limits: Animals Country/Region as subject: America do norte Language: En Journal: Parasit Vectors Year: 2020 Document type: Article Affiliation country: United States