Lucas Eric R, Nagi Sanjay C, Kabula Bilali, Batengana Bernard, Kisinza William, Egyir-Yawson Alexander, Essandoh John, Dadzie Sam, Chabi Joseph, Van't Hof Arjen E, Rippon Emily J, Pipini Dimitra, Harding Nicholas J, Dyer Naomi A, Clarkson Chris S, Miles Alistair, Weetman David, Donnelly Martin J
Department of Vector Biology, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool L3 5QA, UK.
National Institute for Medical Research, Amani Research Centre, P.O. Box 81, Muheza, Tanzania.
bioRxiv. 2024 Mar 13:2024.03.11.583874. doi: 10.1101/2024.03.11.583874.
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. Knowledge of the mechanisms of resistance remains limited in , which in many parts of Africa is of increasing importance because it is apparently less susceptible to many indoor control interventions. 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 resistance to pyrethroids. We performed a genome-wide association study to determine the molecular mechanisms of resistance to deltamethrin (commonly used in bednets) and PM, in from two regions in Tanzania. Genomic regions of positive selection in these populations were largely driven by copy number variants (CNVs) in gene families involved in resistance to these two insecticides. We found evidence of a new gene cluster involved in resistance to PM, identifying a strong selective sweep tied to a CNV in the cluster of carboxylesterase genes. Using complementary data from 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 / cluster. Against this background of metabolic resistance, target site resistance was very rare or absent for both insecticides. Mutations in the pyrethroid target site were at very low frequency in Tanzania, yet combining these samples with three individuals from West Africa revealed a startling diversity of evolutionary origins of target site resistance, with up to 5 independent origins of -995 mutations found within just 8 haplotypes. Thus, despite having been first recorded over 10 years ago, resistance mutations in Tanzanian 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 .
为了在蚊子对杀虫剂的抗性演变方面保持领先,国家疟疾控制规划必须使用一系列新旧杀虫剂,同时监测抗性机制。在非洲许多地区,由于其对许多室内控制干预措施显然不太敏感,对抗性机制的了解仍然有限。此外,对于诸如甲基嘧啶磷(PM)等非拟除虫菊酯类杀虫剂的抗性,总体上了解较少,而这些杀虫剂对于在拟除虫菊酯抗性背景下的有效控制至关重要。我们进行了一项全基因组关联研究,以确定来自坦桑尼亚两个地区的按蚊对溴氰菊酯(常用于蚊帐)和PM的抗性分子机制。这些种群中的正向选择基因组区域在很大程度上由参与对这两种杀虫剂抗性的基因家族中的拷贝数变异(CNV)驱动。我们发现了一个参与对PM抗性的新基因簇的证据,确定了与羧酸酯酶基因簇中的一个CNV相关的强烈选择性清除。利用来自加纳按蚊的补充数据,我们表明该位点的拷贝数与对PM的抗性显著相关。同样,对于溴氰菊酯,抗性与酯酶/细胞色素P450基因簇中的一个新的CNV等位基因密切相关。在这种代谢抗性的背景下,两种杀虫剂的靶标位点抗性非常罕见或不存在。在坦桑尼亚,拟除虫菊酯靶标位点的突变频率非常低,但将这些样本与来自西非的三个冈比亚按蚊个体相结合,揭示了靶标位点抗性进化起源的惊人多样性,在仅8个单倍型中发现了多达5个独立的-995突变起源。因此,尽管坦桑尼亚按蚊的抗性突变在10多年前就首次被记录,但它们一直保持在稳定的低频率。总体而言,我们的结果为监测疟疾蚊子对PM的抗性提供了一个新的拷贝数标记,并揭示了按蚊抗性模式的复杂情况。