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Development of a Loop-Mediated Isothermal Amplification Method for the Rapid Detection of Phytopythium vexans
Brown root rot caused by Phytopythium vexans is a new destructive root disease on many plants such as Gingko, Citrus, kiwifruit, and ramie. The establishment of loop-mediated isothermal amplification (LAMP) technology for detecting P. vexans can help monitor and control brown root rot quickly, effic...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450588/ https://www.ncbi.nlm.nih.gov/pubmed/34552572 http://dx.doi.org/10.3389/fmicb.2021.720485 |
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author | Wang, Tuhong Ji, Haojun Yu, Yongting Wang, Xiaojie Cheng, Yi Li, Zhimin Chen, Jia Guo, Litao Xu, Jianping Gao, Chunsheng |
author_facet | Wang, Tuhong Ji, Haojun Yu, Yongting Wang, Xiaojie Cheng, Yi Li, Zhimin Chen, Jia Guo, Litao Xu, Jianping Gao, Chunsheng |
author_sort | Wang, Tuhong |
collection | PubMed |
description | Brown root rot caused by Phytopythium vexans is a new destructive root disease on many plants such as Gingko, Citrus, kiwifruit, and ramie. The establishment of loop-mediated isothermal amplification (LAMP) technology for detecting P. vexans can help monitor and control brown root rot quickly, efficiently, and accurately. LAMP technology is known for its simplicity, sensitivity, and speed; and it does not require any specialized equipment – a water bath or a thermoblock is sufficient for isothermal amplifications. LAMP products can be visualized by using hydroxy naphthol blue (HNB) dye or agarose gel electrophoresis. In this study, by searching and comparing the internal transcribed spacer (ITS) sequences of P. vexans and the related species in oomycete genera Pythium, Phytopythium, and Phytophthora, we designed specific primers targeting the ITS gene region of P. vexans. Using HNB dye, we established a LAMP technique for rapid detection of P. vexans by visible color change. In addition, we optimized the protocol to enhance both sensitivity and specificity for P. vexans detection. Under the optimized condition, our protocol based on LAMP technology could detect as low as 24 copies of the P. vexans genomic DNA, which is ∼100 times more sensitive than conventional PCR. This method can successfully detect P. vexans using cell suspensions from P. vexans – infected ramie root tissues. |
format | Online Article Text |
id | pubmed-8450588 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84505882021-09-21 Development of a Loop-Mediated Isothermal Amplification Method for the Rapid Detection of Phytopythium vexans Wang, Tuhong Ji, Haojun Yu, Yongting Wang, Xiaojie Cheng, Yi Li, Zhimin Chen, Jia Guo, Litao Xu, Jianping Gao, Chunsheng Front Microbiol Microbiology Brown root rot caused by Phytopythium vexans is a new destructive root disease on many plants such as Gingko, Citrus, kiwifruit, and ramie. The establishment of loop-mediated isothermal amplification (LAMP) technology for detecting P. vexans can help monitor and control brown root rot quickly, efficiently, and accurately. LAMP technology is known for its simplicity, sensitivity, and speed; and it does not require any specialized equipment – a water bath or a thermoblock is sufficient for isothermal amplifications. LAMP products can be visualized by using hydroxy naphthol blue (HNB) dye or agarose gel electrophoresis. In this study, by searching and comparing the internal transcribed spacer (ITS) sequences of P. vexans and the related species in oomycete genera Pythium, Phytopythium, and Phytophthora, we designed specific primers targeting the ITS gene region of P. vexans. Using HNB dye, we established a LAMP technique for rapid detection of P. vexans by visible color change. In addition, we optimized the protocol to enhance both sensitivity and specificity for P. vexans detection. Under the optimized condition, our protocol based on LAMP technology could detect as low as 24 copies of the P. vexans genomic DNA, which is ∼100 times more sensitive than conventional PCR. This method can successfully detect P. vexans using cell suspensions from P. vexans – infected ramie root tissues. Frontiers Media S.A. 2021-09-06 /pmc/articles/PMC8450588/ /pubmed/34552572 http://dx.doi.org/10.3389/fmicb.2021.720485 Text en Copyright © 2021 Wang, Ji, Yu, Wang, Cheng, Li, Chen, Guo, Xu and Gao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Wang, Tuhong Ji, Haojun Yu, Yongting Wang, Xiaojie Cheng, Yi Li, Zhimin Chen, Jia Guo, Litao Xu, Jianping Gao, Chunsheng Development of a Loop-Mediated Isothermal Amplification Method for the Rapid Detection of Phytopythium vexans |
title | Development of a Loop-Mediated Isothermal Amplification Method for the Rapid Detection of Phytopythium vexans |
title_full | Development of a Loop-Mediated Isothermal Amplification Method for the Rapid Detection of Phytopythium vexans |
title_fullStr | Development of a Loop-Mediated Isothermal Amplification Method for the Rapid Detection of Phytopythium vexans |
title_full_unstemmed | Development of a Loop-Mediated Isothermal Amplification Method for the Rapid Detection of Phytopythium vexans |
title_short | Development of a Loop-Mediated Isothermal Amplification Method for the Rapid Detection of Phytopythium vexans |
title_sort | development of a loop-mediated isothermal amplification method for the rapid detection of phytopythium vexans |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450588/ https://www.ncbi.nlm.nih.gov/pubmed/34552572 http://dx.doi.org/10.3389/fmicb.2021.720485 |
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