Saccaggi D L, Krüger K, Pietersen G
Department of Zoology and Entomology, University of Pretoria, Pretoria 0002, South Africa.
Bull Entomol Res. 2008 Feb;98(1):27-33. doi: 10.1017/S000748530700538X. Epub 2007 Dec 13.
Molecular species identification is becoming more wide-spread in diagnostics and ecological studies, particularly with regard to insects for which morphological identification is difficult or time-consuming. In this study, we describe the development and application of a single-step multiplex PCR for the identification of three mealybug species (Hemiptera: Pseudococcidae) associated with grapevine in South Africa: Planococcus ficus (vine mealybug), Planococcus citri (citrus mealybug) and Pseudococcus longispinus (longtailed mealybug). Mealybugs are pests on many commercial crops, including grapevine, in which they transmit viral diseases. Morphological identification of mealybug species is usually time-consuming, requires a high level of taxonomic expertise and usually only adult females can be identified. The single-step multiplex PCR developed here, based on the mitochondrial cytochrome c oxidase subunit 1 (CO I) gene, is rapid, reliable, sensitive, accurate and simple. The entire identification protocol (including DNA extraction, PCR and electrophoresis) can be completed in approximately four hours. Successful DNA extraction from laboratory and unparasitized field-collected individuals stored in absolute ethanol was 97%. Specimens from which DNA could be extracted were always correctly identified (100% accuracy). The technique developed is simple enough to be implemented in any molecular laboratory. The principles described here can be extended to any organism for which rapid, reliable identification is needed.
分子物种鉴定在诊断和生态学研究中越来越普遍,特别是对于那些形态学鉴定困难或耗时的昆虫。在本研究中,我们描述了一种单步多重PCR的开发和应用,用于鉴定与南非葡萄藤相关的三种粉蚧物种(半翅目:粉蚧科):无花果粉蚧(葡萄粉蚧)、柑橘粉蚧和长尾粉蚧。粉蚧是许多商业作物(包括葡萄藤)上的害虫,它们在葡萄藤上传播病毒病。粉蚧物种的形态学鉴定通常很耗时,需要高水平的分类学专业知识,而且通常只能鉴定成年雌性。这里开发的基于线粒体细胞色素c氧化酶亚基1(CO I)基因的单步多重PCR快速、可靠、灵敏、准确且简单。整个鉴定方案(包括DNA提取、PCR和电泳)大约可以在四小时内完成。从保存在无水乙醇中的实验室个体和未被寄生的野外采集个体中成功提取DNA的比例为97%。能够提取DNA的标本总是能被正确鉴定(准确率100%)。所开发的技术足够简单,可以在任何分子实验室中实施。这里描述的原理可以扩展到任何需要快速、可靠鉴定的生物体。