The Anderson Lab

Investigating parasite genetic variation and evolution, with a focus on malaria and schistosome parasites

We think that the central obstacle to parasite control stems from parasite variation and evolution, including drug resistance, vaccine escape, immune evasion, and host shifts. Better understanding of the evolution of these biomedically important parasite traits can lead to more efficient control strategies.

Additionally, because selection tends to be strong, parasites infecting humans provide excellent systems for studying rapid evolution in recombining eukaryotes, and genetic variation offers useful tools for better understanding parasite transmission strategies.


Our Lab goals

The Anderson lab aims to bridge the gap between mainstream evolutionary biology and parasitology. We focus on malaria and schistosomes, the most important of the protozoan and helminth parasites infecting humans, which are also genetically and experimentally tractable. We utilize a population/quantitative genetics framework and both experimental and field-based research to explore the evolution, ecology and transmission of these parasites.

 

Our malaria research focuses on understanding the frequency of drug resistance evolution in Malaria parasites in red blood cells nature, as well as the genetic basis of drug resistance, and parasite fitness using parasite genetic crosses and bulk-segregrant analysis. This includes investigating the role of specific SNPs, compensatory mutations, and epistasis, and the impact of gene copy number variation on parasite phenotypes. We are also interested in deciphering the genetic structure of parasite populations and the composition of complex parasite infections containing multiple genotypes.

 

Our schistosome research pioneers the use of laboratory genetic crosses combined with linkage Schistosome worms, male and female paired together analysis, bulk-segregant analysis, and genome-wide association studies to map the genetic bases of drug resistance, snail host specificity, cercarial transmission, and chronobiology in this parasite. We are also interested in understanding the dynamics of natural populations of schistosomes: by using single miracidia larvae collected from infected patients in African and South American countries, we investigate schistosome epidemiology, population biology and genomic introgression between parasite species.