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一种用于同时检测和鉴定番茄斑驳花叶病毒和番茄褐色皱叶果实病毒的一步法逆转录实时荧光定量PCR检测方法的开发与验证

Development and Validation of a One-Step Reverse Transcription Real-Time PCR Assay for Simultaneous Detection and Identification of Tomato Mottle Mosaic Virus and Tomato Brown Rugose Fruit Virus.

作者信息

Tiberini Antonio, Manglli Ariana, Taglienti Anna, Vučurović Ana, Brodarič Jakob, Ferretti Luca, Luigi Marta, Gentili Andrea, Mehle Nataša

机构信息

CREA-Research Centre for Plant Protection and Certification, Via C.G. Bertero 22, 00156 Roma, Italy.

Department of Biotechnology and Systems Biology, National Institute of Biology, Večna pot 111, SI-1000 Ljubljana, Slovenia.

出版信息

Plants (Basel). 2022 Feb 11;11(4):489. doi: 10.3390/plants11040489.

Abstract

species represent a threat to solanaceous crops worldwide, due to their extreme stability and because they are seed borne. In particular, recent outbreaks of tomato brown rugose fruit virus in tomato and pepper crops led to the establishment of prompt control measures, and the need for reliable diagnosis was urged. Another member of the genus, tomato mottle mosaic virus, has recently gained attention due to reports in different continents and its common features with tomato brown rugose fruit virus. In this study, a new real-time RT-PCR detection system was developed for tomato brown rugose fruit virus and tomato mottle mosaic virus on tomato leaves and seeds using TaqMan chemistry. This test was designed to detect tomato mottle mosaic virus by amplifying the movement protein gene in a duplex assay with the tomato brown rugose fruit virus target on the CP-3'NTR region, which was previously validated as a single assay. The performance of this test was evaluated, displaying analytical sensitivity 10-10-fold dilution for seeds and leaves, respectively, and good analytical specificity, repeatability, and reproducibility. Using the newly developed and validated test, tomato brown rugose fruit virus detection was 100% concordant with previously performed analyses on 106 official samples collected in 2021 from different continents.

摘要

由于其极端稳定性且通过种子传播,该物种对全球茄科作物构成威胁。特别是,近期番茄和辣椒作物中番茄褐色皱纹果病毒的爆发促使迅速采取控制措施,并迫切需要可靠的诊断方法。该属的另一个成员番茄斑驳花叶病毒,由于在不同大陆的报道及其与番茄褐色皱纹果病毒的共同特征,最近受到关注。在本研究中,利用TaqMan化学方法开发了一种用于检测番茄叶片和种子上的番茄褐色皱纹果病毒和番茄斑驳花叶病毒的新型实时RT-PCR检测系统。该检测方法旨在通过在双链检测中扩增运动蛋白基因来检测番茄斑驳花叶病毒,同时以番茄褐色皱纹果病毒为靶标,扩增CP-3'NTR区域,该区域先前已作为单一检测方法得到验证。对该检测方法的性能进行了评估,结果显示其对种子和叶片的分析灵敏度分别为10-10倍稀释,且具有良好的分析特异性、重复性和再现性。使用新开发并经验证的检测方法,对2021年从不同大陆采集的106个官方样本进行检测,番茄褐色皱纹果病毒的检测结果与先前进行的分析100%一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3790/8878898/9c420459914a/plants-11-00489-g001.jpg

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