ArticleMolecular biology and evolution2025
Genome Structural Variants Shape Adaptive Success of an Invasive Urban Malaria Vector Anopheles stephensi.
Article in Molecular biology and evolution, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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5 citing papers in PubMed.
- Structural variants are enriched in deleterious visible phenotypes inGenome research · 2026Article
- Genomic Signatures of Microgeographic Adaptation in Anopheles coluzzii Across Urban, Rural, and Forested Environments in Gabon.Molecular ecology · 2026Article
- Investigating genetic differentiation between brackish and fresh water collections of the arboviral vector Aedes aegypti.Parasites & vectors · 2026Article
- The origin, invasion history and resistance architecture ofbioRxiv : the preprint server for biology · 2025Article
- Physiological and Molecular Mechanisms of Lepidopteran Insects: Genomic Insights and Applications of Genome Editing for Future Research.International journal of molecular sciences · 2024Review
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Abstract
Global changes are associated with the emergence of several invasive species, although genetic determinants of their adaptive success remain poorly understood. To address this problem, we investigated the role genome structural variants (SVs) play in adaptations of Anopheles stephensi, a primary vector of urban malaria in South Asia and an invasive malaria vector in South Asian islands and Africa. Using whole genome sequencing data, we identified 2,988 duplications and 16,038 deletions of SVs in 115 mosquitoes from invasive island populations and four locations from mainland India, the species' ancestral range. The minor allele frequency of SVs and amino acid polymorphism suggests SVs are more deleterious than the amino acid variants. However, high-frequency SVs are enriched in genomic regions with signatures of selective sweeps, implying a putative adaptive role of some SVs. We revealed three novel candidate duplication mutations for recurrent evolution of resistance to diverse insecticides in An. stephensi populations. These mutations exhibit distinct population genetic signatures of recent adaptive evolution, suggesting different mechanisms of rapid adaptations involving hard and soft sweeps helping the species thwart chemical control strategies. We also identify candidate SVs for the larval tolerance to brackish water, which is likely an adaptation in island and coastal populations. Nearly all high-frequency SVs and the candidate adaptive variants in the island populations are derived from the mainland, suggesting a sizable contribution of existing variation to the success of the island populations. Our results highlight the important role of SVs in the evolutionary success of invasive malaria vector An. stephensi.
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