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通过基于多重PCR的扩增子测序对大量苹果和核果类果树病毒及类病毒进行高通量检测。

High-throughput detection of a large set of viruses and viroids of pome and stone fruit trees by multiplex PCR-based amplicon sequencing.

作者信息

Costa Larissa Carvalho, Atha Benjamin, Hu Xiaojun, Lamour Kurt, Yang Yu, O'Connell Mary, McFarland Clint, Foster Joseph A, Hurtado-Gonzales Oscar P

机构信息

Plant Germplasm Quarantine Program, Animal and Plant Health Inspection Service, United States Department of Agriculture, Beltsville, MD, United States.

Department of Entomology and Plant Pathology, University of Tennessee, Knoxville, TN, United States.

出版信息

Front Plant Sci. 2022 Dec 12;13:1072768. doi: 10.3389/fpls.2022.1072768. eCollection 2022.

DOI:10.3389/fpls.2022.1072768
PMID:36578329
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9791224/
Abstract

A comprehensive diagnostic method of known plant viruses and viroids is necessary to provide an accurate phytosanitary status of fruit trees. However, most widely used detection methods have a small limit on either the number of targeted viruses/viroids or the number of samples to be evaluated at a time, hampering the ability to rapidly scale up the test capacity. Here we report that by combining the power of high multiplexing PCR (499 primer pairs) of small amplicons (120-135bp), targeting 27 viruses and 7 viroids of fruit trees, followed by a single high-throughput sequencing (HTS) run, we accurately diagnosed the viruses and viroids on as many as 123 pome and stone fruit tree samples. We compared the accuracy, sensitivity, and reproducibility of this approach and contrast it with other detection methods including HTS of total RNA (RNA-Seq) and individual RT-qPCR for every fruit tree virus or viroid under the study. We argue that this robust and high-throughput cost-effective diagnostic tool will enhance the viral/viroid knowledge of fruit trees while increasing the capacity for large scale diagnostics. This approach can also be adopted for the detection of multiple viruses and viroids in other crops.

摘要

一种针对已知植物病毒和类病毒的综合诊断方法对于准确评估果树的植物检疫状况至关重要。然而,大多数广泛使用的检测方法在靶向病毒/类病毒的数量或一次评估的样本数量方面存在一定限制,这阻碍了快速扩大检测能力。在此,我们报告通过结合针对27种果树病毒和7种类病毒的小扩增子(120 - 135bp)的高多重PCR(499对引物)的强大功能,随后进行一次高通量测序(HTS),我们准确诊断了多达123个梨果和核果类果树样本上的病毒和类病毒。我们比较了这种方法的准确性、灵敏度和可重复性,并将其与其他检测方法进行对比,包括对研究中的每种果树病毒或类病毒进行总RNA的高通量测序(RNA-Seq)和单独的逆转录定量PCR。我们认为这种强大且高通量的经济高效诊断工具将增进对果树病毒/类病毒的了解,同时提高大规模诊断的能力。这种方法也可用于检测其他作物中的多种病毒和类病毒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5fd/9791224/c45b3cfac3d8/fpls-13-1072768-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5fd/9791224/1dc07b6ea945/fpls-13-1072768-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5fd/9791224/559afcd27203/fpls-13-1072768-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5fd/9791224/c45b3cfac3d8/fpls-13-1072768-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5fd/9791224/1dc07b6ea945/fpls-13-1072768-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5fd/9791224/559afcd27203/fpls-13-1072768-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5fd/9791224/c45b3cfac3d8/fpls-13-1072768-g003.jpg

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