基于线粒体COI基因的棉铃虫DNA条形码特征的开发

I. P. Shree, M. Muthuswami, N. Boopathi, K. Senguttuvan, S. Rajeswari
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引用次数: 0

摘要

背景:物种鉴定是一项高度专业化、耗时且严重依赖于主要存在于成年生活阶段的诊断特征的工作,这限制了识别,因为许多标本缺乏这些特征。方法:采用分子生物学方法,建立棉铃虫的分子标记。该研究于2021年至2022年在泰米尔纳德邦哥印拜陀泰米尔纳德邦农业大学农业昆虫学系和植物生物技术系进行。利用细胞色素c氧化酶亚基I基因的DNA序列,成功地建立了棉铃虫的DNA条形码特征。结果:利用MEGA X软件中的MUSCLE比对方法,通过系统发育树将序列分离为Clade 1(序列长度为264 bp)和Clade 2(序列长度为164 bp),并对每个分支的DNA进行了条形码标记。由于在棉铃虫早期阶段难以准确鉴定,因此利用这种分子特征对棉铃虫进行鉴定将更加简单、快速、准确和可靠。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of DNA Barcoding Signatures for Pink Bollworm in Cotton Ecosystem Based on the Mitochondrial COI Gene
Background: Species identification is a highly specialized, time-consuming and rely significantly on the diagnostic features that are present mostly in the adult life stages which constrains the recognition, as many specimens lack these characters. Methods: In this study, we used molecular strategy to develop markers for the identification of the pink bollworm in the cotton ecosystem. This research was conducted at the Department of Agricultural Entomology and Department of Plant Biotechnology, Tamil Nadu Agricultural University, Coimbatore, Tamil Nadu State, during 2021 and 2022. DNA sequences of the cytochrome c oxidase subunit I gene were used to successfully develop DNA barcoding signatures for pink bollworm. Result: Using the MUSCLE alignment method in MEGA X software and by the use of phylogenetic tree, the sequences were segregated into Clade 1 (had a sequence length of 264 bp) and Clade 2 (had a sequence length of 164 bp) and for each clade DNA barcoding signatures were developed. With such molecular identity would be simple, rapid, precise and more reliable to identify Pectinophora gossypiella, as it is difficult to accurately identify this bollworm during its early life stages.
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