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通过逆转录聚合酶链反应(RT-PCR)对番木瓜乳汁中的番木瓜黑腐果病毒进行分子检测。

Molecular detection of Papaya meleira virus in the latex of Carica papaya by RT-PCR.

作者信息

Araújo Marília Mendes Melo de, Tavares Eder Torres, Silva Felipe Rodrigues da, Marinho Vera Lúcia de Almeida, Júnior Manoel Teixeira Souza

机构信息

Embrapa Genetic Resources & Biotechnology, Parque Estação Biológica, Final Avenida W5 Norte, CP 02372, Brasília, DF, CEP 70.770-900, Brazil.

出版信息

J Virol Methods. 2007 Dec;146(1-2):305-10. doi: 10.1016/j.jviromet.2007.07.022. Epub 2007 Sep 10.

DOI:10.1016/j.jviromet.2007.07.022
PMID:17826848
Abstract

A RT-PCR assay was developed for early and accurate detection of Papaya meleira virus (PMeV) in the latex from infected papayas. The meleira disease is characterized by an excessive exudation of more fluidic latex from fruits, leaves and stems. This latex oxidises and gives the fruit a "sticky" texture. In the field, disease symptoms are seen almost exclusively on fruit. However, infected plants can be a source of virus for dissemination by insects. Primers specific for PMeV were designed based on nucleotide sequences of the viral dsRNA obtained using a RT-RAPD approach. When tested for RT-PCR amplification, one of these primers (C05-3') amplified a 669-nucleotide fragment using dsRNA obtained from purified virus particles as a template. The translated sequence of this DNA fragment showed a certain degree of similarity to the amino acid sequence of RNA-dependent RNA polymerases from other dsRNA viruses. When used as the single primer in two RT-PCR kits available commercially, primer C05-3' also amplified the DNA fragment from papaya latex of infected, but not from healthy plants. The RT-PCR-based method developed in this study could simplify early plant disease diagnosis, assist in monitoring the dissemination of the pathogen within and between fields, and assist in guiding plant disease management.

摘要

已开发出一种逆转录聚合酶链反应(RT-PCR)检测方法,用于早期准确检测感染番木瓜的乳胶中的番木瓜梅雷拉病毒(PMeV)。梅雷拉病的特征是果实、叶片和茎中分泌出更多流动性乳胶。这种乳胶会氧化,使果实具有“粘性”质地。在田间,病害症状几乎只出现在果实上。然而,受感染的植物可能是病毒通过昆虫传播的来源。基于使用逆转录随机扩增多态性DNA(RT-RAPD)方法获得的病毒双链RNA(dsRNA)的核苷酸序列,设计了针对PMeV的引物。在进行RT-PCR扩增测试时,其中一个引物(C05-3')以从纯化病毒颗粒获得的dsRNA为模板,扩增出一个669个核苷酸的片段。该DNA片段的翻译序列与其他dsRNA病毒的RNA依赖RNA聚合酶的氨基酸序列显示出一定程度的相似性。当在两种市售的RT-PCR试剂盒中用作单一引物时,引物C05-3'也能从受感染番木瓜的乳胶中扩增出DNA片段,但不能从健康植物中扩增出。本研究开发的基于RT-PCR的方法可以简化早期植物病害诊断,有助于监测病原体在田间内和田间间的传播,并有助于指导植物病害管理。

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