Abstract

BackgroundDNA extraction is a routine step in many insect molecular studies. A variety of methods have been used to isolate DNA molecules from insects, and many commercial kits are available. Extraction methods need to be evaluated for their efficiency, cost, and side effects such as DNA degradation during extraction.Methodology/Principal FindingsFrom individual western corn rootworm beetles, Diabrotica virgifera virgifera, DNA extractions by the SDS method, CTAB method, DNAzol® reagent, Puregene® solutions and DNeasy® column were compared in terms of DNA quantity and quality, cost of materials, and time consumed. Although all five methods resulted in acceptable DNA concentrations and absorbance ratios, the SDS and CTAB methods resulted in higher DNA yield (ng DNA vs. mg tissue) at much lower cost and less degradation as revealed on agarose gels. The DNeasy® kit was most time-efficient but was the costliest among the methods tested. The effects of ethanol volume, temperature and incubation time on precipitation of DNA were also investigated. The DNA samples obtained by the five methods were tested in PCR for six microsatellites located in various positions of the beetle's genome, and all samples showed successful amplifications.Conclusion/SignificanceThese evaluations provide a guide for choosing methods of DNA extraction from western corn rootworm beetles based on expected DNA yield and quality, extraction time, cost, and waste control. The extraction conditions for this mid-size insect were optimized. The DNA extracted by the five methods was suitable for further molecular applications such as PCR and sequencing by synthesis.

Highlights

  • DNA extraction is a routine step in many biological studies including molecular identification, phylogenetic inference, genetics, and genomics

  • The sodium dodecyl sulfate (SDS) and cetyltrimethyl ammonium bromide (CTAB) methods are commonly used for DNA extraction from diverse organisms [1]

  • The yield rates by the SDS and CTAB methods were significantly higher than those obtained by the DNAzolH Reagent, PuregeneH Kit, and DNeasyH Kit (Tukey’s, P,0.05)

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Summary

Introduction

DNA extraction is a routine step in many biological studies including molecular identification, phylogenetic inference, genetics, and genomics. DNA extraction is often used in medical examinations, clinical diagnostics, and forensic investigations. A variety of methods have been established to isolate DNA molecules from biological materials [1], and many DNA extraction kits are commercially available. DNA extraction is a routine step in many insect molecular studies. A variety of methods have been used to isolate DNA molecules from insects, and many commercial kits are available. Extraction methods need to be evaluated for their efficiency, cost, and side effects such as DNA degradation during extraction

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