Suppr超能文献

用于快速检测花生芽坏死病毒的多重TaqMan检测法的开发:美国的一种检疫性病原

Development of a Multiplex TaqMan Assay for Rapid Detection of Groundnut Bud Necrosis Virus: A Quarantine Pathogen in the USA.

作者信息

Deraniyagala Anushi Suwaneththiya, Roy Avijit, Tallury Shyam, Sudini Hari Kishan, Culbreath Albert K, Bag Sudeep

机构信息

Department of Plant Pathology, University of Georgia, Tifton, GA 31793, USA.

Molecular Plant Pathology Laboratory, Beltsville Agricultural Research Center (BARC), Unites States Department of Agriculture (USDA)-Agricultural Research Service (ARS), Beltsville, MD 20705, USA.

出版信息

Viruses. 2025 Apr 5;17(4):532. doi: 10.3390/v17040532.

Abstract

Groundnut bud necrosis orthotospovirus (GBNV), a tripartite single-stranded RNA virus, poses a significant threat to United States agriculture. GBNV is a quarantine pathogen, and its introduction could lead to severe damage to economically important crops, such as groundnuts, tomatoes, potatoes, peas, and soybeans. For the rapid and accurate detection of GBNV at points of entry, TaqMan reverse transcriptase-quantitative polymerase chain reaction (RT-qPCR) assays were developed and the results validated using conventional reverse transcriptase-polymerase chain reaction (RT-PCR) followed by Sanger sequencing. These assays target highly conserved regions of the nucleocapsid (NP) and movement (MP) proteins within the viral genome. Multiplex GBNV detection assays targeting the NP and MP genes, as well as an internal control plant gene, ACT11, showed efficiency rates between 90% and 100% and R values of 0.98 to 0.99, indicating high accuracy and precision. Moreover, there was no significant difference in sensitivity between multiplex and singleplex assays, ensuring reliable detection across various plant tissues. This rapid, sensitive, and specific diagnostic assay will provide a valuable tool at ports of entry to prevent the entry of GBNV into the United States.

摘要

花生芽坏死正番茄斑萎病毒(GBNV)是一种三分体单链RNA病毒,对美国农业构成重大威胁。GBNV是一种检疫性病原菌,其传入可能会对花生、番茄、马铃薯、豌豆和大豆等经济作物造成严重损害。为了在入境点快速准确地检测GBNV,开发了TaqMan逆转录定量聚合酶链反应(RT-qPCR)检测方法,并使用常规逆转录聚合酶链反应(RT-PCR)随后进行桑格测序对结果进行验证。这些检测方法针对病毒基因组内核衣壳(NP)蛋白和运动(MP)蛋白的高度保守区域。针对NP和MP基因以及内部对照植物基因ACT11的多重GBNV检测方法显示效率在90%至100%之间,R值为0.98至0.99,表明具有高准确性和精密度。此外,多重检测和单重检测之间的灵敏度没有显著差异,确保了在各种植物组织中的可靠检测。这种快速、灵敏且特异的诊断检测方法将为入境口岸提供一个有价值的工具,以防止GBNV进入美国。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a42/12031075/0cb9da2912d3/viruses-17-00532-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验