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一种用于检测李痘病毒 I(PlVd-I)的反转录环介导等温扩增(RT-LAMP)检测方法。

A reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay for the detection of plum viroid I (PlVd-I).

机构信息

Citrus Research International, PO Box 2201, Matieland 7602, South Africa; Department of Genetics, Stellenbosch University, Private Bag X1, Matieland 7602, South Africa.

Citrus Research International, PO Box 2201, Matieland 7602, South Africa; Department of Genetics, Stellenbosch University, Private Bag X1, Matieland 7602, South Africa.

出版信息

J Virol Methods. 2022 Aug;306:114543. doi: 10.1016/j.jviromet.2022.114543. Epub 2022 May 14.

DOI:10.1016/j.jviromet.2022.114543
PMID:35580684
Abstract

Plum viroid I (PlVd-I) is found in marbling and corky flesh diseased plum trees in South Africa. In this study a reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay for the high-throughput detection of PlVd-I was developed. This assay can be performed on crude extracts and detection can either be a pH dependent colorimetric reaction or a real-time fluorescent signal reaction. The false discovery rate was shown to be low and no decrease in sensitivity was detected compared to RT-PCR. The RT-LAMP assay allows for the fast and cost-effective detection of PlVd-I that will curtail the distribution of infected plant material.

摘要

李痘病毒 I(PlVd-I)存在于南非患有大理石纹和木栓化果肉的李树中。本研究开发了一种用于 PlVd-I 高通量检测的逆转录环介导等温扩增(RT-LAMP)检测方法。该检测方法可在粗提物上进行,检测可以是依赖 pH 的比色反应,也可以是实时荧光信号反应。结果表明假阳性率较低,与 RT-PCR 相比,检测灵敏度没有降低。RT-LAMP 检测方法可快速、经济有效地检测 PlVd-I,从而遏制受感染植物材料的传播。

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