Institut de Parasitologie et de Pathologie Tropicale, Université de Strasbourg, EA 4438, 67000 Strasbourg, France.
Vet Parasitol. 2011 Dec 15;182(2-4):297-306. doi: 10.1016/j.vetpar.2011.05.052. Epub 2011 Jun 12.
The two sympatric sibling species Culicoides obsoletus (Meigen) and Culicoides scoticus Downes and Kettle (Diptera: Ceratopogonidae), are known to be competent vectors for bluetongue virus in the Palaearctic region. However, morphological identification of constituent species is only readily applicable to adult males and these two species distinguishing traits have overlapping character states. As their vector competence may differ in space and time, the correct identification and quantification of specimens of both species are essential for understanding bluetongue epidemiology. However, no molecular tools are available for high-throughput identification of the two species. We therefore developed a quantitative duplex real-time PCR assay to determine the relative abundance of each sibling species in a sample using TaqMan probes. For each species, standard curves were constructed from serial dilutions of purified plasmid DNA containing ITS1-5.8S-ITS2 (rDNA) in the range of 10(-1) to 10(-5)ng/μL. Standard curves were used to quantify samples of mixed C. obsoletus/C. scoticus specimens. Specificity was evaluated with 5156 specimens representing 62 species. Based on the DNA quantities detected according to the standard curves, a quadratic model developed on 1100 males and validated on 555 females was able to predict the relative abundance of each species simultaneously in a one-shot reaction (Pearson coefficient of 0.999). Our assay showed a requirement of two specimens or less for 95% of the predictions, making it highly applicable to field collections. Extensive use of this real-time PCR assay will provide a better understanding of geographical distribution, dynamics, and bionomics on a species level, which is essential for risk assessment. This approach is an important contribution to medical entomology for investigating the vector role of arthropod sibling species.
两个同域近缘种,即厩螫蝇(Culicoides obsoletus)(Meigen)和斯科特厩螫蝇(Culicoides scoticus)Downes and Kettle(双翅目:蠓科),已知是在古北区传播蓝舌病病毒的有效媒介。然而,组成种的形态鉴定仅适用于成年雄性,并且这两个种的鉴别特征具有重叠的特征状态。由于它们的媒介效能可能在空间和时间上有所不同,因此正确识别和量化这两个种的标本对于理解蓝舌病的流行病学至关重要。然而,目前还没有可用于高通量鉴定这两个种的分子工具。因此,我们开发了一种定量双重实时 PCR 测定法,使用 TaqMan 探针确定样品中每个近缘种的相对丰度。对于每个种,均从包含 ITS1-5.8S-ITS2(rDNA)的纯化质粒 DNA 的系列稀释液中构建标准曲线,范围为 10(-1) 到 10(-5)ng/μL。使用标准曲线来量化混合 C. obsoletus/C. scoticus 标本。通过 5156 个代表 62 个种的标本评估了特异性。基于根据标准曲线检测到的 DNA 量,在 1100 个雄性和 555 个雌性上开发的二次模型能够同时在一次反应中预测每个种的相对丰度(Pearson 系数为 0.999)。我们的测定法显示,对于 95%的预测,需要两个或更少的标本,这使其非常适用于野外采集。广泛使用这种实时 PCR 测定法将提供对物种水平的地理分布、动态和生物学的更好理解,这对于风险评估至关重要。这种方法是医学昆虫学的一个重要贡献,可用于研究节肢动物近缘种的媒介作用。