Barr N B, Copeland R S, De Meyer M, Masiga D, Kibogo H G, Billah M K, Osir E, Wharton R A, McPheron B A
Department of Entomology, Pennsylvania State University, University Park, PA 16802, USA.
Bull Entomol Res. 2006 Oct;96(5):505-21.
The predominantly Afrotropical fruit fly genus Ceratitis contains many species of agricultural importance. Consequently, quarantine of Ceratitis species is a major concern for governmental regulatory agencies. Although diagnostic keys exist for identification of all described Ceratitis species, these tools are based on adult characters. Flies intercepted at ports of entry are usually immatures, and Ceratitis species cannot be diagnosed based on larval morphology. To facilitate identification of Ceratitis pests at ports of entry, this study explores the utility of DNA-based diagnostic tools for a select group of Ceratitis species and related tephritids, some of which infest agriculturally important crops in Africa. The application of the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method to analyse three mitochondrial genes (12S ribosomal RNA, 16S ribosomal RNA, and NADH-dehydrogenase subunit 6) is sufficient to diagnose 25 species and two species clusters. PCR analysis of the internal transcribed spacer region 1 (ITS-1) is able to distinguish three of the five species left unresolved by mitochondrial DNA analysis.
以非洲热带地区为主的果实蝇属果实蝇包含许多具有农业重要性的物种。因此,对果实蝇属物种进行检疫是政府监管机构的主要关注点。尽管存在用于鉴定所有已描述的果实蝇属物种的诊断检索表,但这些工具是基于成虫特征的。在入境口岸截获的果蝇通常是未成熟的,而且无法根据幼虫形态来诊断果实蝇属物种。为便于在入境口岸鉴定果实蝇属害虫,本研究探讨了基于DNA的诊断工具对一组选定的果实蝇属物种及相关实蝇科昆虫的实用性,其中一些实蝇科昆虫侵害非洲具有农业重要性的作物。应用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法分析三个线粒体基因(12S核糖体RNA、16S核糖体RNA和NADH脱氢酶亚基6)足以诊断25个物种和两个物种集群。对内部转录间隔区1(ITS-1)进行PCR分析能够区分线粒体DNA分析未解决的五个物种中的三个。