Article ID Journal Published Year Pages File Type
6389450 Journal of Invertebrate Pathology 2014 4 Pages PDF
Abstract

•A PCR-based method for detection of the thuE gene was established.•Specific primers produced amplification in 13.3% (4/30) of the exotic strains.•Specific primers produced amplification in 3.7% (4/107) of the native isolates.•Positive strains by PCR were also β-exotoxin producers.•Type II β-exotoxin producing strains are not predicted by this methodology.

Some Bacillus thuringiensis strains secrete type I β-exotoxin, which is a non-specific insecticidal and thermostable adenine nucleoside oligosaccharide. Toxicity bioassays and HPLC are traditional methods for detecting β-exotoxin. With the aim of establish a first rapid approach for prediction of type I β-exotoxin production, two PCR-based methods were successfully evaluated in B. thuringiensis strains and native isolates. In order to validate a reliable technology, results obtained by this method were correlated with that obtained from Musca domestica bioassays.

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