Signatures of Insecticide Selection in the Genome of Drosophila melanogaster.
Signatures of Insecticide Selection in the Genome of Drosophila melanogaster.
复制标题
在果蝇果蝇基因组中选择杀虫剂的特征。
DOI:
10.1534/g3.118.200537
复制
发表时间:
2018-11-06
期刊:
影响因子:
--
通讯作者:
Buchon N
中科院分区:
文献类型:
--
作者:
Duneau D;Sun H;Revah J;San Miguel K;Kunerth HD;Caldas IV;Messer PW;Scott JG;Buchon N
Resistance to insecticides has evolved in multiple insect species, leading to increased application rates and even control failures. Understanding the genetic basis of insecticide resistance is fundamental for mitigating its impact on crop production and disease control. We performed a GWAS approach with the Drosophila Genetic Reference Panel (DGRP) to identify the mutations involved in resistance to two widely used classes of insecticides: organophosphates (OPs, parathion) and pyrethroids (deltamethrin). Most variation in parathion resistance was associated with mutations in the target gene Ace, while most variation in deltamethrin resistance was associated with mutations in Cyp6a23, a gene encoding a detoxification enzyme never previously associated with resistance. A “nested GWAS” further revealed the contribution of other loci: Dscam1 and trpl were implicated in resistance to parathion, but only in lines lacking Wolbachia. Cyp6a17, the paralogous gene of Cyp6a23, and CG7627, an ATP-binding cassette transporter, were implicated in deltamethrin resistance. We observed signatures of recent selective sweeps at all of these resistance loci and confirmed that the soft sweep at Ace is indeed driven by the identified resistance mutations. Analysis of allele frequencies in additional population samples revealed that most resistance mutations are segregating across the globe, but that frequencies can vary substantially among populations. Altogether, our data reveal that the widely used OP and pyrethroid insecticides imposed a strong selection pressure on natural insect populations. However, it remains unclear why, in Drosophila, resistance evolved due to changes in the target site for OPs, but due to a detoxification enzyme for pyrethroids.
登录
查看更多内容
影响因子:
3.4
作者:
Menozzi P;Shi MA;Lougarre A;Tang ZH;Fournier D
通讯作者:
Fournier D
影响因子:
4.6
作者:
Denecke S;Fusetto R;Martelli F;Giang A;Battlay P;Fournier-Level A;O' Hair RA;Batterham P
通讯作者:
Batterham P
影响因子:
5.1
作者:
FOURNIER, D;MUTERO, A;BRIDE, JM
通讯作者:
BRIDE, JM
DOI:
10.1534/g3.116.031054
发表时间:
2016-08-09
期刊:
G3 (Bethesda, Md.)
影响因子:
--
作者:
Battlay P;Schmidt JM;Fournier-Level A;Robin C
通讯作者:
Robin C
影响因子:
16.8
作者:
Messer PW;Petrov DA
通讯作者:
Petrov DA