Cornel A J, Porter C H, Collins F H
Entomology Branch, Division of Parasitic Diseases, Centers for Disease Control and Prevention, Chamblee, GA 30341, USA.
J Med Entomol. 1996 Jan;33(1):109-16. doi: 10.1093/jmedent/33.1.109.
Species-specific differences in the nucleotide sequences of the 2nd internal transcribed spacer (ITS2) of nuclear ribosomal DNA (rDNA) were used to develop a diagnostic assay based on the polymerase chain reaction (PCR) that can distinguish 4 of the 5 cryptic sibling species in the common malaria mosquito, Anopheles quadrimaculatus Say, complex. The assay requires only a small amount of tissue from an individual mosquito and a mixture of 5 PCR primers. The plus strand universal primer is derived from a sequence in the 5.8S coding region that is identical in all members of the complex. The 4 minus strand primers were selected from species-unique sequences within the ITS2 region. PCR amplification produces a different sized fragment for each of the 4 species which can be visualized readily under ultraviolet light after electrophoresis through an ethidium bromide-containing agarose gel. The assay has been developed and tested only with An. quadrimaculatus complex specimens from Florida populations.
利用核糖体DNA(rDNA)的第二内部转录间隔区(ITS2)核苷酸序列中的物种特异性差异,开发了一种基于聚合酶链反应(PCR)的诊断检测方法,该方法可区分常见疟蚊四斑按蚊(Anopheles quadrimaculatus Say)复合组中5个隐存姐妹种中的4个。该检测方法仅需要来自单个蚊子的少量组织和5种PCR引物的混合物。正向通用引物源自5.8S编码区中的一个序列,该序列在复合组的所有成员中都是相同的。4种反向引物是从ITS2区域内的物种特异性序列中选择的。PCR扩增为4个物种中的每一个产生不同大小的片段,在通过含溴化乙锭的琼脂糖凝胶电泳后,可在紫外光下轻松观察到这些片段。该检测方法仅针对来自佛罗里达种群的四斑按蚊复合组标本进行了开发和测试。