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一种用于快速准确检测腐烂茎线虫的实时重组酶聚合酶扩增检测方法。

A real-time recombinase polymerase amplification assay for fast and accurate detection of Ditylenchus destructor.

作者信息

Gao Bo, Ma Juan, Li Xiuhua, Wang Rongyan, Chen Shulong

机构信息

Plant Protection Institute of Hebei Academy of Agricultural and Forestry Sciences, IPM Center of Hebei Province, Key Laboratory of IPM on Crops in Northern Region of North China, Ministry of Agriculture and Rural Affairs, Baoding, 071000, China.

Plant Protection Institute of Hebei Academy of Agricultural and Forestry Sciences, IPM Center of Hebei Province, Key Laboratory of IPM on Crops in Northern Region of North China, Ministry of Agriculture and Rural Affairs, Baoding, 071000, China.

出版信息

Mol Cell Probes. 2022 Feb;61:101788. doi: 10.1016/j.mcp.2021.101788. Epub 2021 Dec 22.

Abstract

Ditylenchus destructor is a plant-parasitic nematode that seriously infests sweet potato crop in China. Thus, fast and accurate detection of D. destructor in soil and plant tissue samples is of great significance. In this study, a real-time recombinase polymerase amplification (RPA) assay was developed for the rapid and accurate detection of D. destructor in various samples. The RPA assay could be easily operated and detected as low as 1/500 individual J4 nematode DNA per reaction in 20 min at 39 °C with high specificity. The assay meets the requirements of rapid detection prior to port quarantine as well as on-site real-time detection and can be applied to detect the parasite in soil and plant samples. The modified gDNA extraction method for a single nematode established in this study significantly reduced the time of detection and improved the applicability of the real-time RPA assay for on-site detection in different environments. The real-time RPA assay to detect D. destructor will be useful for epidemiological investigations in the field as well as for quarantine processes in the sweet potato and potato trade.

摘要

腐烂茎线虫是一种植物寄生线虫,在中国严重危害甘薯作物。因此,快速准确地检测土壤和植物组织样本中的腐烂茎线虫具有重要意义。在本研究中,开发了一种实时重组酶聚合酶扩增(RPA)检测方法,用于快速准确地检测各种样本中的腐烂茎线虫。该RPA检测方法操作简便,在39℃下20分钟内每个反应能检测低至1/500条J4期线虫个体的DNA,且特异性高。该检测方法满足口岸检疫前快速检测以及现场实时检测的要求,可应用于检测土壤和植物样本中的寄生虫。本研究建立的针对单个线虫的改良基因组DNA提取方法显著缩短了检测时间,提高了实时RPA检测方法在不同环境下现场检测的适用性。检测腐烂茎线虫的实时RPA检测方法将有助于田间流行病学调查以及甘薯和马铃薯贸易中的检疫工作。

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