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迈向鳞翅目特异性杆状病毒的分子鉴定与分类系统

Towards a molecular identification and classification system of lepidopteran-specific baculoviruses.

作者信息

Lange Martin, Wang Hualin, Zhihong Hu, Jehle Johannes A

机构信息

Laboratory for Biotechnological Crop Protection, Department of Phytopathology, Agricultural Service Center Palatinate, 67435 Neustadt an der Weinstrasse, Germany.

出版信息

Virology. 2004 Jul 20;325(1):36-47. doi: 10.1016/j.virol.2004.04.023.

Abstract

Virus genomics provides novel approaches for virus identification and classification. Based on the comparative analyses of sequenced lepidopteran-specific baculovirus genomes, degenerate oligonucleotides were developed that allow the specific amplification of several regions of the genome using polymerase chain reaction (PCR) followed by DNA sequencing. The DNA sequences within the coding regions of three highly conserved genes, namely polyhedrin/granulin (polh/gran), late expression factor 8 (lef-8), and late expression factor 9 (lef-9), were targeted for amplification. The oligonucleotides were tested on viral DNAs isolated from historical field samples, and amplification products were generated from 12 isolated nucleopolyhedrovirus (NPV) and 8 granulovirus (GV) DNAs. The PCR products were cloned or directly sequenced, and phylogenetic trees were inferred from individual and combined data sets of these three genes and compared to a phylogeny, which includes 22 baculoviruses using a combined data set of 30 core genes. This method allows a fast and reliable detection and identification of lepidopteran-specific NPVs and GVs. Furthermore, a strong correlation of the base composition of these three genome areas with that of the complete virus genome was observed and used to predict the base composition of uncharacterized baculovirus genomes. These analyses suggested that GVs have a significantly higher AT content than NPVs.

摘要

病毒基因组学为病毒鉴定和分类提供了新方法。基于对已测序的鳞翅目特异性杆状病毒基因组的比较分析,开发了简并寡核苷酸,可通过聚合酶链反应(PCR)对基因组的几个区域进行特异性扩增,随后进行DNA测序。三个高度保守基因,即多角体蛋白/颗粒蛋白(polh/gran)、晚期表达因子8(lef-8)和晚期表达因子9(lef-9)编码区域内的DNA序列被作为扩增目标。这些寡核苷酸在从历史田间样本中分离的病毒DNA上进行了测试,并从12种分离的核型多角体病毒(NPV)和8种颗粒体病毒(GV)DNA中产生了扩增产物。PCR产物被克隆或直接测序,并从这三个基因的单独和组合数据集中推断出系统发育树,并与一个系统发育进行比较,该系统发育包括使用30个核心基因的组合数据集的22种杆状病毒。该方法能够快速、可靠地检测和鉴定鳞翅目特异性NPV和GV。此外,观察到这三个基因组区域的碱基组成与完整病毒基因组的碱基组成有很强的相关性,并用于预测未表征杆状病毒基因组的碱基组成。这些分析表明,GV的AT含量明显高于NPV。

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