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Arch Insect Biochem Physiol


Title:Development of a highly accurate and sensitive diagnostic tool for pyrethroid-resistant chimeric P450 CYP337B3 of Helicoverpa armigera using loop-mediated isothermal amplification
Author(s):Choi BH; Hur JH; Heckel DG; Kim J; Koh YH;
Address:"Department of Biomedical Gerontology, Hallym University Graduate School, Chuncheon, Korea. lsong Institute of Life Science, Hallym University, Anyang, Korea. Department of Entomology, Max Planck Institute for Chemical Ecology, Jena, Germany. Highland Agriculture Research Institute, NICS, RDA, Pyeongchang, Korea"
Journal Title:Arch Insect Biochem Physiol
Year:2018
Volume:20180915
Issue:3
Page Number:e21504 -
DOI: 10.1002/arch.21504
ISSN/ISBN:1520-6327 (Electronic) 0739-4462 (Linking)
Abstract:"Recent studies have shown that pyrethroid resistance in the cotton bollworm (CBW) Helicoverpa armigera is conferred by the generation of a chimeric CYP337B3 gene, which resulted from unequal crossing-over between the CYP337B1 and CYP337B2 genes. In this study, we developed a diagnostic protocol based on the loop-mediated isothermal amplification (LAMP) assay for the detection of chimeric CYP337B3. The CYP337B3 LAMP assay utilized six primers and generated strong fluorescence signals visible to the naked eye under normal or ultraviolet light. The primers were designed based on CYP337B3v1 (JQ995292), the major allele detected in Australia. The detection limit of this LAMP assay was 10 fg genomic DNA in a 25-microl reaction mixture. Compared with CYP337B2v1, the Korean CYP337B3v2 allele had two nucleotide mismatches within the amplifying regions of this LAMP assay; therefore, we confirmed that polymerase chain reaction-synthesized CYP337B3v2 was well amplified using this LAMP assay. In addition, we determined that the presence of CYP337B3 from H. armigera collected by pheromone traps from Korean fields could be confirmed using this LAMP assay. This assay could detect CYP337B3 even in heterozygotes, which is relevant because CYP337B3 is dominant, and heterozygotes are pyrethroid resistant. Therefore, the newly developed CYP337B3 LAMP assay could detect the presence of pyrethroid resistance in H. armigera that were captured by pheromone traps during the early season and provide information on whether pyrethroids could be used to control H. armigera"
Keywords:Animals Base Sequence Cytochrome P-450 Enzyme System/*genetics Heterozygote Insecticide Resistance/genetics *Insecticides Moths/enzymology/*genetics *Nucleic Acid Amplification Techniques Polymerase Chain Reaction *Pyrethrins Republic of Korea Zea mays Cy;
Notes:"MedlineChoi, Bo Hey Hur, Joon Haeng Heckel, David G Kim, Juil Koh, Young Ho eng 2018R1D1A3B0704086/National Research Foundation of Korea/ PJ011777/Cooperative Research Program for Agriculture Science & Technology Development/ Validation Study 2018/09/16 Arch Insect Biochem Physiol. 2018 Nov; 99(3):e21504. doi: 10.1002/arch.21504. Epub 2018 Sep 15"

 
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