Genome-wide association studies unveil major genetic loci driving insecticide resistance in Anopheles funestus in four eco-geographical settings across Cameroon.

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY BMC Genomics Pub Date : 2024-12-18 DOI:10.1186/s12864-024-11148-7
Mahamat Gadji, Jonas A Kengne-Ouafo, Magellan Tchouakui, Murielle J Wondji, Leon M J Mugenzi, Jack Hearn, Onana Boyomo, Charles S Wondji
{"title":"Genome-wide association studies unveil major genetic loci driving insecticide resistance in Anopheles funestus in four eco-geographical settings across Cameroon.","authors":"Mahamat Gadji, Jonas A Kengne-Ouafo, Magellan Tchouakui, Murielle J Wondji, Leon M J Mugenzi, Jack Hearn, Onana Boyomo, Charles S Wondji","doi":"10.1186/s12864-024-11148-7","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Insecticide resistance is jeopardising malaria control efforts in Africa. Deciphering the evolutionary dynamics of mosquito populations country-wide is essential for designing effective and sustainable national and subnational tailored strategies to accelerate malaria elimination efforts. Here, we employed genome-wide association studies through pooled template sequencing to compare four eco-geographically different populations of the major vector, Anopheles funestus, across a South North transect in Cameroon, aiming to identify genomic signatures of adaptive responses to insecticides.</p><p><strong>Results: </strong>Our analysis revealed limited population structure within Northern and Central regions (F<sub>ST</sub><0.02), suggesting extensive gene flow, while populations from the Littoral/Coastal region exhibited more distinct genetic patterns (F<sub>ST</sub>>0.049). Greater genetic differentiation was observed at known resistance-associated loci, resistance-to-pyrethroids 1 (rp1) (2R chromosome) and CYP9 (X chromosome), with varying signatures of positive selection across populations. Allelic variation between variants underscores the pervasive impact of selection pressures, with rp1 variants more prevalent in Central and Northern populations (F<sub>ST</sub>>0.3), and the CYP9 associated variants more pronounced in the Littoral/Coastal region (F<sub>ST</sub> =0.29). Evidence of selective sweeps was supported by negative Tajima's D and reduced genetic diversity in all populations, particularly in Central (Elende) and Northern (Tibati) regions. Genomic variant analysis identified novel missense mutations and signatures of complex genomic alterations such as duplications, deletions, transposable element (TE) insertions, and chromosomal inversions, all associated with selective sweeps. A 4.3 kb TE insertion was fixed in all populations with Njombe Littoral/Coastal population, showing higher frequency of CYP9K1 (G454A), a known resistance allele and TE upstream compared to elsewhere.</p><p><strong>Conclusion: </strong>Our study uncovered regional variations in insecticide resistance candidate variants, emphasizing the need for a streamlined DNA-based diagnostic assay for genomic surveillance across Africa. These findings will contribute to the development of tailored resistance management strategies crucial for addressing the dynamic challenges of malaria control in Cameroon.</p>","PeriodicalId":9030,"journal":{"name":"BMC Genomics","volume":"25 1","pages":"1202"},"PeriodicalIF":3.7000,"publicationDate":"2024-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11654272/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Genomics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s12864-024-11148-7","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Insecticide resistance is jeopardising malaria control efforts in Africa. Deciphering the evolutionary dynamics of mosquito populations country-wide is essential for designing effective and sustainable national and subnational tailored strategies to accelerate malaria elimination efforts. Here, we employed genome-wide association studies through pooled template sequencing to compare four eco-geographically different populations of the major vector, Anopheles funestus, across a South North transect in Cameroon, aiming to identify genomic signatures of adaptive responses to insecticides.

Results: Our analysis revealed limited population structure within Northern and Central regions (FST<0.02), suggesting extensive gene flow, while populations from the Littoral/Coastal region exhibited more distinct genetic patterns (FST>0.049). Greater genetic differentiation was observed at known resistance-associated loci, resistance-to-pyrethroids 1 (rp1) (2R chromosome) and CYP9 (X chromosome), with varying signatures of positive selection across populations. Allelic variation between variants underscores the pervasive impact of selection pressures, with rp1 variants more prevalent in Central and Northern populations (FST>0.3), and the CYP9 associated variants more pronounced in the Littoral/Coastal region (FST =0.29). Evidence of selective sweeps was supported by negative Tajima's D and reduced genetic diversity in all populations, particularly in Central (Elende) and Northern (Tibati) regions. Genomic variant analysis identified novel missense mutations and signatures of complex genomic alterations such as duplications, deletions, transposable element (TE) insertions, and chromosomal inversions, all associated with selective sweeps. A 4.3 kb TE insertion was fixed in all populations with Njombe Littoral/Coastal population, showing higher frequency of CYP9K1 (G454A), a known resistance allele and TE upstream compared to elsewhere.

Conclusion: Our study uncovered regional variations in insecticide resistance candidate variants, emphasizing the need for a streamlined DNA-based diagnostic assay for genomic surveillance across Africa. These findings will contribute to the development of tailored resistance management strategies crucial for addressing the dynamic challenges of malaria control in Cameroon.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
全基因组关联研究揭示了在喀麦隆四个生态地理环境中驱动funestus按蚊杀虫剂抗性的主要遗传位点。
背景:杀虫剂耐药性正在危及非洲的疟疾控制工作。破译全国范围内蚊子种群的进化动态对于设计有效和可持续的国家和次国家定制战略以加快消除疟疾的努力至关重要。在这里,我们采用全基因组关联研究,通过汇集模板测序,比较了喀麦隆南北样带的主要媒介按蚊(Anopheles funestus)的四个生态地理不同种群,旨在确定对杀虫剂适应性反应的基因组特征。结果:我们的分析显示北部和中部地区的人口结构有限(FSTST>0.049)。在已知的抗性相关位点,对拟除虫菊酯抗性1 (rp1) (2R染色体)和CYP9 (X染色体)上观察到更大的遗传分化,在不同群体中具有不同的正选择特征。变异之间的等位基因变异强调了选择压力的普遍影响,rp1变异在中部和北部人群中更为普遍(FST =0.29),而CYP9相关变异在沿海/沿海地区更为明显(FST =0.29)。Tajima's D阴性和所有人群遗传多样性减少的证据支持了选择性清除,特别是在中部(Elende)和北部(Tibati)地区。基因组变异分析发现了新的错义突变和复杂基因组改变的特征,如重复、缺失、转座因子(TE)插入和染色体倒位,所有这些都与选择性扫描相关。在Njombe滨海/沿海人群的所有人群中,固定了4.3 kb的TE插入,与其他地方相比,CYP9K1 (G454A)(一种已知的抗性等位基因)和TE上游的频率更高。结论:我们的研究揭示了杀虫剂抗性候选变异的区域差异,强调需要一种简化的基于dna的诊断分析方法用于整个非洲的基因组监测。这些发现将有助于制定量身定制的耐药性管理战略,这对应对喀麦隆疟疾控制的动态挑战至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
期刊最新文献
Transcriptome analysis identifies key miRNAs involved in the regulation of rabbit intramuscular fat deposition. Comparative analysis of the transcriptome and methylome in distinct trophoblast populations at the time of embryo implantation in mares. An improved Agrobacterium-mediated transformation method for genome editing using CRISPR/Cas9 in elite indica rice (Oryza sativa L.). Assembling telomere-to-telomere genomes of Fusarium oxysporum f. sp. lactucae provides a roadmap for studying genome and phenotype evolution. Development and application of genome-derived SSR markers for genetic diversity analysis, molecular fingerprinting, and core collection construction in bougainvillea (Bougainvillea spp.).
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1