Complex genome evolution in Anopheles coluzzii associated with increased insecticide usage in Mali
In certain cases, a species may have access to important genetic variation present in a related species via adaptive introgression. These novel alleles may interact with their new genetic background, resulting in unexpected phenotypes. In this study, we describe a selective sweep on standing variati...
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Published in | Molecular ecology Vol. 24; no. 20; pp. 5145 - 5157 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Blackwell Scientific Publications
01.10.2015
Blackwell Publishing Ltd John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
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Summary: | In certain cases, a species may have access to important genetic variation present in a related species via adaptive introgression. These novel alleles may interact with their new genetic background, resulting in unexpected phenotypes. In this study, we describe a selective sweep on standing variation on the X chromosome in the mosquito Anopheles coluzzii, a principal malaria vector in West Africa. This event may have been influenced by the recent adaptive introgression of the insecticide resistance gene known as kdr from the sister species Anopheles gambiae. Individuals carrying both kdr and a nearly fixed X‐linked haplotype, encompassing at least four genes including the P450 gene CYP9K1 and the cuticular protein CPR125, have rapidly increased in relative frequency. In parallel, a reproductively isolated insecticide‐susceptible A. gambiae population (Bamako form) has been driven to local extinction, likely due to strong selection from increased insecticide‐treated bed net usage. |
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Bibliography: | http://dx.doi.org/10.1111/mec.13382 National Institute of Allergy and Infectious Diseases of the National Institutes of Health - No. R21AI117174; No. D43TW007390; No. R01AI078183; No. T32AI074550 istex:192543BE1485CA95234735AA56DE7DC50658791A NIH S10 Instrumentation - No. S10RR029668; No. S10RR027303 ArticleID:MEC13382 Table S1 Genome sequencing reads per sample. Table S2 Candidate nonsynonymous mutations. Table S3 Sequenome iPLEX primer design. Fig. S1 Estimating the size of the cyp-l haplotype. Data S1 Haplotype estimates from genotype data at the CYP9K1 region. Data S2 Bioassay data. Data S3 Copy number analysis using CNVnator (v0.3). ark:/67375/WNG-QC977QBW-L ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0962-1083 1365-294X |
DOI: | 10.1111/mec.13382 |