Southern Crop Protection and Food Research Centre, Agriculture and Agri-Food Canada, London, Ontario, Canada, N5V 4T3.
Mol Ecol. 2014 Aug;23(15):3912-24. doi: 10.1111/mec.12515. Epub 2013 Oct 22.
Evaluation of host-parasitoid associations can be tenuous using conventional methods. Molecular techniques are well placed to identify trophic links and resolve host-parasitoid associations. Establishment of the highly invasive brown marmorated stink bug, Halyomorpha halys (Hemiptera: Pentatomidae), outside Asia has prompted interest in the use of egg parasitoids (Hymenoptera: Scelionidae) as biological control agents. However, little is known regarding their host ranges. To address this, a DNA barcoding approach was taken wherein general PCR primers for Scelionidae and Pentatomidae were developed to amplify and sequence >500-bp products within the DNA barcoding region of the cytochrome oxidase I (COI) gene that would permit the identification of key players in this association. Amplification of DNA from Pentatomidae and Scelionidae was consistent across a broad range of taxa within these families, and permitted the detection of Scelionidae eggs within H. halys 1 h following oviposition. In laboratory assays, amplification and sequencing of DNA from empty, parasitized eggs was successful for both host (100% success) and parasitoid (50% success). When applied to field-collected, empty egg masses, the primers permitted host identification in 50-100% of the eggs analysed, and yielded species-level identifications. Parasitoid identification success ranged from 33 to 67% among field-collected eggs, with genus-level identification for most specimens. The inability to obtain species-level identities for these individuals is due to the lack of coverage of this taxonomic group in public DNA sequence databases; this situation is likely to improve as more species are sequenced and recorded in these databases. These primers were able to detect and identify both pentatomid host and scelionid parasitoid in a hyperparasitized egg mass, thereby clarifying trophic links otherwise unresolved by conventional methodology.
使用传统方法评估宿主-寄生蜂关系可能不太可靠。分子技术非常适合识别营养联系和解决宿主-寄生蜂关系。高度入侵的棕臭蝽(Halyomorpha halys)(半翅目:蝽科)在亚洲以外的地区建立起来后,人们对利用卵寄生蜂(膜翅目:长尾小蜂科)作为生物防治剂产生了兴趣。然而,对于它们的宿主范围知之甚少。为了解决这个问题,采用了 DNA 条形码方法,其中开发了针对长尾小蜂科和蝽科的通用 PCR 引物,以扩增和测序 DNA 条形码区的细胞色素氧化酶 I(COI)基因的>500-bp 产物,从而能够鉴定出这种关系中的关键参与者。在这些科内的广泛分类群中,对蝽科和长尾小蜂科的 DNA 进行扩增是一致的,并允许在 H. halys 产卵后 1 小时内检测到 Scelionidae 卵。在实验室试验中,成功地对空卵和寄生卵的 DNA 进行了扩增和测序,宿主(100%成功)和寄生蜂(50%成功)都成功了。将这些引物应用于野外采集的空卵块时,引物允许在分析的 50-100%的卵中鉴定出宿主,并获得种级别的鉴定。从野外采集的卵中获得的寄生蜂鉴定成功率为 33-67%,大多数标本的鉴定为属级。无法为这些个体获得种级别的身份是由于公共 DNA 序列数据库中缺乏对该分类群的覆盖;随着更多的物种被测序并记录在这些数据库中,这种情况可能会得到改善。这些引物能够在超寄生的卵块中检测和鉴定蝽科宿主和长尾小蜂科寄生蜂,从而澄清了常规方法无法解决的营养联系。