Work

Identification of insect-specific target genes for development of RNAi based control of the Eucalyptus gall pest Leptocybe invasaFisher & La Salle (Hymenoptera: Eulophidae)

Year: 2011

Type: article

Abstract: Eucalyptus is grown in around 3.9 Mha in India. Leptocybe invasa Fisher & La Salle (Hymenoptera: Eulophidae) has emerged as a serious pest in Eucalyptus causing considerable loss of quality planting materials besides loss in productivity and quality of timber. Current strategies for its control include selected deployment of Eucalyptus clones tolerant to the pest resulting in several productive Eucalyptus genetic resources, not being considered for plantation programmes, as in the case of the widely planted Eucalyptus clone, ITC 10, and ITC 271. The securely ensconced grub within the gall for a period of around 4 months post oviposition makes it refractory to pesticide applications. This feature, however, makes plant- incorporated protectants, via RNAi approaches a potential strategy for engineering resistance [ 1 – 3 ]. However, application of RNAi technology requires determination of sequence information of insect-specific genes so that off-target effects in plants as well as human beings are avoided. Grubs were collected from the galls of E. camaldulensis clones, APNP 1.1 and ITC 351, infested with L .invasa from the nursery of the Institute of Forest Genetics and Tree Breeding, Coimbatore, India. Genomic DNA was isolated from the grubs homogenized in liquid nitrogen using a modified CTAB protocol [ 4 ]. RNA was isolated from the grubs using Qiagen RNeasy plant mini kit, followed by cDNA synthesis using SmartScribe reverse transcriptase. Grubs were also directly used for PCR amplification circumventing DNA isolation. Furthermore, to enable multiple PCR analysis, a single grub was collected into 50 µl of sterile distilled water, vigorously vortexed for 2 min followed by brief denaturation at 95 C for 10 min and centrifugation at 10,000 rpm for 10 min. The supernatant was used for PCR analysis. The PCR mix consisted either 100 ng genomic DNA or 100 ng cDNA or a single grub or 2 µl of supernatant from denatured grub, in 1X PCR buffer, 0.8 mM dNTPs, 1 µM of each primer, 2.5 U Pfu polymerase (Fermentas). The PCR conditions used were initial denaturation at 94 C for 5 min, cycle denaturation at 94 C for 40s; annealing at 60 C for 40s; extension at 72 C for 2 min for 30 cycles, and a final extension of 72 C for 5 min. In case of grub PCR, initial denaturation was for 10 min at 95 C. The PCR products were resolved on a 1.0 % Agarose gel in 1X TAE. When multiple bands were obtained, the products were gel eluted and either directly sequenced or cloned into pGEMTeasy vector prior to sequencing. Sequencing was done using the ABI PRISM 3130 XL Genetic Analyzer using Big Dye Terminator version 3.1” Cycle sequencing kit through the commercial sequencing services available at Chromous Biotech India Pvt Ltd.

Source: BMC Proceedings

DOI: 10.1186/1753-6561-5-s7-p98