Authors

V Howick ¹; D Loesbanluechai¹; L Sollelis²; M Armstrong¹; I Menezes¹; A Cox¹; LB Tchongwe Divala²; A Lawson¹; S Pradhan¹; PC Ubiaru¹; A Pallikara¹; D Armstrong¹; G Parker²; C Lee⁴; RD Pearson⁴; BH Stokes³; L Ranford-Cartwright¹; M Marti³;  ¹ School of Biodiversity, One Health and Veterinary Medicine; College of Medical, Veterinary and Life Sciences, University of Glasgow, UK;  ² School of Infection and Immunity, College of Medical, Veterinary and Life Sciences, University of Glasgow, UK;  ³ Institute of Parasitology Zurich, VetSuisse and Medical Faculties, University of Zurich, UK;  ⁴ Genomic Surveillance Unit, Wellcome Sanger Institute, UK

Discussion

Transmission of Plasmodium falciparum through mosquitoes represents the most severe population bottleneck in the parasite’s life cycle, yet the genetic basis of parasite–vector compatibility remains poorly understood. Here, we show that mosquito species–specific transmissibility depends on allelic variation in multiple P. falciparum genes expressed during midgut invasion, in addition to the well-studied Pfs47. Using an allelic replacement strategy, we targeted highly geographically differentiated SNPs in P. falciparum that match regional variation in vector community composition. Transmissibility was compared across four mosquito species representing distinct geographic ranges (An. gambiae, An. stephensi, An. minimus, and An. albimanus). Two of the five tested polymorphisms showed increased oocyst and sporozoite burdens in sympatric parasite–vector combinations compared to allopatric ones. Both substitutions occurred in ookinete micronemal proteins, CTRP and WARP, within von Willebrand factor A domains, suggesting that regional allelic variation modulates Plasmodium–vector compatibility by altering midgut adhesion interactions. These findings reveal that vector compatibility is a polygenic trait shaped by molecular interactions across several loci. Understanding this complexity refines models of parasite adaptation and can inform the design of transmission-blocking interventions effective across diverse vector-parasite combinations.