首页> 外文期刊>Journal of Medical Entomology >Development of Multiplexed Species Specific Polymerase Chain Reaction Assays for Identification of the Culex (Melanoconion) Species (Diptera: Culicidae) of the Southeastern United States Based on rDNA
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Development of Multiplexed Species Specific Polymerase Chain Reaction Assays for Identification of the Culex (Melanoconion) Species (Diptera: Culicidae) of the Southeastern United States Based on rDNA

机译:基于rDNA的美国东南部库蚊(线虫)物种(双翅目:Culicidae)鉴定的多种物种特异性聚合酶链反应分析方法的建立

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摘要

Adult female mosquitoes within the subgenus Culex (Melanoconion) Theobald (Diptera: Culicidae) are difficult to identify to species using external morphological features. We present two multiplexed polymerase chain reaction assays that quickly and accurately identify specimens from the southeastern United States based on sequence differences in the internal transcribed spacers of the ribosomal DNA gene array. One assay identifies all species that occur only in Florida, whereas the second assay identifies species that may occur in other southeastern states. These assays require small amounts of DNA, such as DNA from two sonicated legs, or an individual specimen. These assays also may be run as multiple singleplex reactions to determine the mosquito species composition of virus-positive mosquito pools. Reaction volumes may be as low as 10 mu l, which reduces assay cost.
机译:Culex(Melanoconion)Theobald(Diptera:Culicidae)亚属内的成年雌性蚊子很难通过外部形态学特征进行识别。我们提出了两个多重聚合酶链反应测定法,可基于核糖体DNA基因阵列内部转录间隔区的序列差异,快速,准确地从美国东南部鉴定标本。一种测定法鉴定仅在佛罗里达发生的所有物种,而第二种测定法鉴定可能在其他东南州发生的物种。这些测定需要少量的DNA,例如来自两个超声腿的DNA或单个样本。这些测定也可以作为多个单重反应进行,以确定病毒阳性蚊帐的蚊种组成。反应体积可以低至10μl,这降低了测定成本。

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