拷贝数变异是阿拉伯按蚊杀虫剂抗性基因主要选择性扫描的基础。

IF 9.8 1区 生物学 Q1 Agricultural and Biological Sciences
PLoS Biology Pub Date : 2024-12-05 eCollection Date: 2024-12-01 DOI:10.1371/journal.pbio.3002898
Eric R Lucas, Sanjay C Nagi, Bilali Kabula, Bernard Batengana, William Kisinza, Alexander Egyir-Yawson, John Essandoh, Sam Dadzie, Joseph Chabi, Arjen E Van't Hof, Emily J Rippon, Dimitra Pipini, Nicholas J Harding, Naomi A Dyer, Chris S Clarkson, Alistair Miles, David Weetman, Martin J Donnelly
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引用次数: 0

摘要

为了赶在蚊子对杀虫剂产生抗药性的演变之前,国家疟疾控制规划必须利用一系列杀虫剂,包括新旧杀虫剂,同时监测抗药性机制。室外叮咬疟疾媒介阿拉伯按蚊在疟疾传播方面日益受到关注,因为它显然对许多室内控制干预措施不太敏感,但对其耐药机制的了解仍然有限。此外,对非拟除虫菊酯类杀虫剂(如吡虫磷-甲基)的抗性一般知之甚少,而在全球对拟除虫菊酯类杀虫剂高度抗性的背景下,这种杀虫剂对有效控制至关重要。我们进行了一项全基因组关联研究,以确定对拟除虫菊酯溴氰菊酯(通常用于蚊帐)和PM(广泛用于室内喷洒)抗性的分子机制。来自坦桑尼亚2个地区的阿拉伯种。在这些人群中,正选择的基因组区域主要是由参与代谢抗性的基因家族中的拷贝数变异(CNVs)驱动的。我们发现了一个新的基因簇参与抗PM的证据,确定了与羧酸酯酶基因Coeae2g - Coeae6g的CNV相关的强选择性扫描。利用来自另一疟疾病媒的补充数据。coluzzii,在加纳,我们发现该位点的拷贝数与PM抗性显著相关。同样,对于溴氰菊酯,抗性与Cyp6aa / Cyp6p簇中的新型CNV等位基因(Cyp6aap_Dup33)密切相关。在这种代谢抗性的背景下,由杀虫剂靶点突变引起的抗性非常罕见或不存在。在坦桑尼亚,拟除虫菊酯靶位点Vgsc的突变频率非常低,但将这些样本与3an相结合。来自西非的阿拉伯人个体显示出惊人的进化多样性,在8个单倍型中发现了多达5个独立的Vgsc-995突变起源。因此,尽管在10多年前首次记录到Vgsc抗性突变,但坦桑尼亚安。Arabiensis一直保持在稳定的低频率。本研究结果为疟疾蚊对PM的耐药性监测提供了一种新的拷贝数标记,揭示了我国疟疾蚊对PM的复杂抗性格局。arabiensis。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Copy number variants underlie major selective sweeps in insecticide resistance genes in Anopheles arabiensis.

To keep ahead of the evolution of resistance to insecticides in mosquitoes, national malaria control programmes must make use of a range of insecticides, both old and new, while monitoring resistance mechanisms. The outdoor-biting malaria vector Anopheles arabiensis is of increasing concern for malaria transmission because it is apparently less susceptible to many indoor control interventions, yet knowledge of its mechanisms of resistance remains limited. Furthermore, comparatively little is known in general about resistance to non-pyrethroid insecticides such as pirimiphos-methyl (PM), which are crucial for effective control in the context of globally high resistance to pyrethroids. We performed a genome-wide association study to determine the molecular mechanisms of resistance to the pyrethroid deltamethrin (commonly used in bednets) and PM (widespread use for indoor spraying), in An. arabiensis from 2 regions in Tanzania. Genomic regions of positive selection in these populations were largely driven by copy number variants (CNVs) in gene families involved in metabolic resistance. We found evidence of a new gene cluster involved in resistance to PM, identifying a strong selective sweep tied to a CNV in the carboxylesterase genes Coeae2g - Coeae6g. Using complementary data from another malaria vector, An. coluzzii, in Ghana, we show that copy number at this locus is significantly associated with PM resistance. Similarly, for deltamethrin, resistance was strongly associated with a novel CNV allele in the Cyp6aa / Cyp6p cluster (Cyp6aap_Dup33). Against this background of metabolic resistance, resistance caused by mutations in the insecticide target sites was very rare or absent. Mutations in the pyrethroid target site Vgsc were at very low frequency in Tanzania, yet combining these samples with 3 An. arabiensis individuals from West Africa revealed a startling evolutionary diversity, with up to 5 independent origins of Vgsc-995 mutations found within just 8 haplotypes. Thus, despite having been first recorded over 10 years ago, Vgsc resistance mutations in Tanzanian An. arabiensis have remained at stable low frequencies. Overall, our results provide a new copy number marker for monitoring resistance to PM in malaria mosquitoes, and reveal the complex picture of resistance patterns in An. arabiensis.

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来源期刊
PLoS Biology
PLoS Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-BIOLOGY
CiteScore
15.40
自引率
2.00%
发文量
359
审稿时长
3-8 weeks
期刊介绍: PLOS Biology is the flagship journal of the Public Library of Science (PLOS) and focuses on publishing groundbreaking and relevant research in all areas of biological science. The journal features works at various scales, ranging from molecules to ecosystems, and also encourages interdisciplinary studies. PLOS Biology publishes articles that demonstrate exceptional significance, originality, and relevance, with a high standard of scientific rigor in methodology, reporting, and conclusions. The journal aims to advance science and serve the research community by transforming research communication to align with the research process. It offers evolving article types and policies that empower authors to share the complete story behind their scientific findings with a diverse global audience of researchers, educators, policymakers, patient advocacy groups, and the general public. PLOS Biology, along with other PLOS journals, is widely indexed by major services such as Crossref, Dimensions, DOAJ, Google Scholar, PubMed, PubMed Central, Scopus, and Web of Science. Additionally, PLOS Biology is indexed by various other services including AGRICOLA, Biological Abstracts, BIOSYS Previews, CABI CAB Abstracts, CABI Global Health, CAPES, CAS, CNKI, Embase, Journal Guide, MEDLINE, and Zoological Record, ensuring that the research content is easily accessible and discoverable by a wide range of audiences.
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