Wilding C S, Weetman D, Rippon E J, Steen K, Mawejje H D, Barsukov I, Donnelly M J
Department of Vector Biology, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool, L3 5QA, UK,
Mol Genet Genomics. 2015 Feb;290(1):201-15. doi: 10.1007/s00438-014-0910-9. Epub 2014 Sep 12.
Insecticide resistance is a major impediment to the control of vectors and pests of public health importance and is a strongly selected trait capable of rapid spread, sometimes even between closely related species. Elucidating the mechanisms generating insecticide resistance in mosquito vectors of disease, and understanding the spread of resistance within and between populations and species are vital for the development of robust resistance management strategies. Here, we studied the mechanisms of resistance in two sympatric members of the Anopheles gambiae species complex-the major vector of malaria in sub-Saharan Africa-to understand how resistance has developed and spread in eastern Uganda, a region with some of the highest levels of malaria. In eastern Uganda, where the mosquitoes Anopheles arabiensis and An. gambiae can be found sympatrically, low levels of hybrids (0.4 %) occur, offering a route for introgression of adaptively important variants between species. In independent microarray studies of insecticide resistance, Gste4, an insect-specific glutathione S-transferase, was among the most significantly up-regulated genes in both species. To test the hypothesis of interspecific introgression, we sequenced 2.3 kbp encompassing Gste4. Whilst this detailed sequencing ruled out introgression, we detected strong positive selection acting on Gste4. However, these sequences, followed by haplotype-specific qPCR, showed that the apparent up-regulation in An. arabiensis is a result of allelic variation across the microarray probe binding sites which artefactually elevates the gene expression signal. Thus, face-value acceptance of microarray data can be misleading and it is advisable to conduct a more detailed investigation of the causes and nature of such signal. The identification of positive selection acting on this locus led us to functionally express and characterise allelic variants of GSTE4. Although the in vitro data do not support a direct role for GSTE4 in metabolism, they do support a role for this enzyme in insecticide sequestration. Thus, the demonstration of a role for an up-regulated gene in metabolic resistance to insecticides should not be limited to simply whether it can metabolise insecticide; such a strict criterion would argue against the involvement of GSTE4 despite the weight of evidence to the contrary.
杀虫剂抗性是控制对公共卫生具有重要意义的病媒和害虫的主要障碍,是一种经过强烈选择的性状,能够迅速传播,有时甚至在亲缘关系密切的物种之间传播。阐明疾病蚊媒产生杀虫剂抗性的机制,以及了解抗性在种群内部和种群之间及物种之间的传播情况,对于制定强有力的抗性管理策略至关重要。在这里,我们研究了冈比亚按蚊复合种的两个同域成员(撒哈拉以南非洲疟疾的主要病媒)的抗性机制,以了解抗性在乌干达东部(疟疾发病率最高的地区之一)是如何发展和传播的。在乌干达东部,阿拉伯按蚊和冈比亚按蚊可以同域分布,杂交水平较低(0.4%),这为适应性重要变异在物种间的渗入提供了一条途径。在关于杀虫剂抗性的独立微阵列研究中,昆虫特异性谷胱甘肽S-转移酶Gste4是两个物种中上调最显著的基因之一。为了检验种间渗入的假设,我们对包含Gste4的2.3kbp进行了测序。虽然这种详细的测序排除了渗入,但我们检测到对Gste4有强烈的正选择作用。然而,这些序列以及单倍型特异性定量PCR显示,阿拉伯按蚊中明显的上调是微阵列探针结合位点等位基因变异的结果,这人为地提高了基因表达信号。因此,表面接受微阵列数据可能会产生误导,建议对这种信号的原因和性质进行更详细的调查。对该位点正选择作用的鉴定使我们对GSTE4的等位基因变异进行了功能表达和表征。虽然体外数据不支持GSTE4在代谢中起直接作用,但它们确实支持该酶在杀虫剂隔离中的作用。因此,证明一个上调基因在杀虫剂代谢抗性中的作用不应仅限于它是否能代谢杀虫剂;尽管有大量相反证据,但这样一个严格的标准会反对GSTE4的参与。