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用于监测主要疟疾传播媒介冈比亚按蚊代谢抗性的快速多重基因表达检测法。

Rapid multiplex gene expression assays for monitoring metabolic resistance in the major malaria vector Anopheles gambiae.

机构信息

Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology-Hellas, 70013, Heraklion, Greece.

Department of Epidemiology and Public Health, Swiss Tropical and Public Health Institute, Socinstrasse 57, P.O. Box, CH-4002, Basel, Switzerland.

出版信息

Parasit Vectors. 2019 Jan 6;12(1):9. doi: 10.1186/s13071-018-3253-2.

Abstract

BACKGROUND

Metabolic resistance of the major malaria vector Anopheles gambiae (s.l.) to insecticides is operationally significant, particularly in combination with target site resistance. However, detection of metabolic resistance is not trivial and relies on laborious bioassays, unspecific biochemical methods, or sophisticated and expensive molecular approaches using transcriptomics.

METHODS

Rapid one-step multiplex TaqMan-probe based RT-qPCR assays were developed and optimised to measure the expression levels of genes associated with metabolic insecticide resistance in An. gambiae (s.l.). Primers and probes were designed to target the mRNA of cytochrome P450-dependent monooxygenases CYP6P3, CYP6M2, CYP9K1, CYP6P4 and CYP6Z1, and the glutathione-S-transferase GSTE2. The novel assays were validated versus gold standard methods with a range of phenotyped mosquito specimens. The assays were also tested directly on lysates of RNAlater®-preserved mosquitoes without an RNA extraction step.

RESULTS

The novel assays are efficient (reaction efficiencies = 95-109%), sensitive (covering a > 10.0 Ct range with R values > 0.99), specific (TaqMan chemistry), reproducible (%CV = 4.46-12.07%), as well as readily expandable to capture additional loci as they evolve or to cover additional species. The assays were successfully validated in terms of expression levels against standard two-step singleplex qPCR assays (overall % difference = -17.6%, 95% CI = -38.7-3.43%) and microarrays, using laboratory strains and field-caught samples. The assays can also be applied directly on lysates of mosquito specimens, without RNA extraction or DNase treatment.

CONCLUSIONS

The novel multiplex assays for monitoring the levels of major detoxification genes and metabolic resistance in An. gambiae (s.l.) are simple to perform, robust and rapid. They may complement current diagnostic assays to provide evidence-based and operationally relevant information for insecticide resistance management.

摘要

背景

主要疟疾传播媒介冈比亚按蚊(s.l.)对杀虫剂的代谢抗性在操作上具有重要意义,特别是与靶标抗性结合时。然而,代谢抗性的检测并不简单,需要费力的生物测定、非特异性生化方法或使用转录组学的复杂和昂贵的分子方法。

方法

开发并优化了快速一步多重 TaqMan 探针实时 RT-qPCR 测定法,以测量与冈比亚按蚊(s.l.)代谢性杀虫剂抗性相关的基因表达水平。设计了引物和探针以靶向与细胞色素 P450 依赖性单加氧酶 CYP6P3、CYP6M2、CYP9K1、CYP6P4 和 CYP6Z1 以及谷胱甘肽 S-转移酶 GSTE2 的 mRNA。该新测定法通过一系列表型蚊标本与金标准方法进行了验证。该测定法还直接在 RNAlater®保存的蚊子的裂解物上进行了测试,而无需进行 RNA 提取步骤。

结果

该新测定法效率高(反应效率=95-109%)、灵敏(涵盖 > 10.0 Ct 范围,R 值> 0.99)、特异性(TaqMan 化学)、重现性(%CV = 4.46-12.07%),并且易于扩展,以捕获随着进化而出现的其他基因座或覆盖其他物种。该测定法在使用实验室菌株和田间捕获样本的情况下,通过标准两步单重 qPCR 测定法(总体差异百分比=-17.6%,95%置信区间=-38.7-3.43%)和微阵列成功验证了表达水平。该测定法还可以直接应用于蚊子标本的裂解物,而无需进行 RNA 提取或 DNase 处理。

结论

用于监测冈比亚按蚊(s.l.)主要解毒基因和代谢抗性水平的新型多重测定法简单、稳健且快速。它们可以补充当前的诊断测定法,为杀虫剂抗性管理提供基于证据和具有操作相关性的信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5ec/6322220/8caa1e5f5681/13071_2018_3253_Fig1_HTML.jpg

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