Cargando…
Rapid and Efficient Detection of 16SrI Group Areca Palm Yellow Leaf Phytoplasma in China by Loop-Mediated Isothermal Amplification
Areca palm yellow leaf (AYL) disease caused by the 16SrI group phytoplasma is a serious threat to the development of the Areca palm industry in China. The 16S rRNA gene sequence was utilized to establish a rapid and efficient detection system efficient for the 16SrI-B subgroup AYL phytoplasma in Chi...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society of Plant Pathology
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542027/ https://www.ncbi.nlm.nih.gov/pubmed/33082730 http://dx.doi.org/10.5423/PPJ.OA.06.2020.0094 |
_version_ | 1783591475722846208 |
---|---|
author | Yu, Shao-shuai Che, Hai-yan Wang, Sheng-jie Lin, Cai-li Lin, Ming-xing Song, Wei-wei Tang, Qing-hua Yan, Wei Qin, Wei-quan |
author_facet | Yu, Shao-shuai Che, Hai-yan Wang, Sheng-jie Lin, Cai-li Lin, Ming-xing Song, Wei-wei Tang, Qing-hua Yan, Wei Qin, Wei-quan |
author_sort | Yu, Shao-shuai |
collection | PubMed |
description | Areca palm yellow leaf (AYL) disease caused by the 16SrI group phytoplasma is a serious threat to the development of the Areca palm industry in China. The 16S rRNA gene sequence was utilized to establish a rapid and efficient detection system efficient for the 16SrI-B subgroup AYL phytoplasma in China by loop-mediated isothermal amplification (LAMP). The results showed that two sets of LAMP detection primers, 16SrDNA-2 and 16SrDNA-3, were efficient for 16SrIB subgroup AYL phytoplasma in China, with positive results appearing under reaction conditions of 64oC for 40 min. The lowest detection limit for the two LAMP detection assays was the same at 200 ag/μl, namely approximately 53 copies/μl of the target fragments. Phytoplasma was detected in all AYL disease samples from Baoting, Tunchang, and Wanning counties in Hainan province using the two sets of LAMP primers 16SrDNA-2 and 16SrDNA-3, whereas no phytoplasma was detected in the negative control. The LAMP method established in this study with comparatively high sensitivity and stability, provides reliable results that could be visually detected, making it suitable for application and research in rapid diagnosis of AYL disease, detection of seedlings with the pathogen and breeding of disease-resistant Areca palm varieties. |
format | Online Article Text |
id | pubmed-7542027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Korean Society of Plant Pathology |
record_format | MEDLINE/PubMed |
spelling | pubmed-75420272020-10-19 Rapid and Efficient Detection of 16SrI Group Areca Palm Yellow Leaf Phytoplasma in China by Loop-Mediated Isothermal Amplification Yu, Shao-shuai Che, Hai-yan Wang, Sheng-jie Lin, Cai-li Lin, Ming-xing Song, Wei-wei Tang, Qing-hua Yan, Wei Qin, Wei-quan Plant Pathol J Research Article Areca palm yellow leaf (AYL) disease caused by the 16SrI group phytoplasma is a serious threat to the development of the Areca palm industry in China. The 16S rRNA gene sequence was utilized to establish a rapid and efficient detection system efficient for the 16SrI-B subgroup AYL phytoplasma in China by loop-mediated isothermal amplification (LAMP). The results showed that two sets of LAMP detection primers, 16SrDNA-2 and 16SrDNA-3, were efficient for 16SrIB subgroup AYL phytoplasma in China, with positive results appearing under reaction conditions of 64oC for 40 min. The lowest detection limit for the two LAMP detection assays was the same at 200 ag/μl, namely approximately 53 copies/μl of the target fragments. Phytoplasma was detected in all AYL disease samples from Baoting, Tunchang, and Wanning counties in Hainan province using the two sets of LAMP primers 16SrDNA-2 and 16SrDNA-3, whereas no phytoplasma was detected in the negative control. The LAMP method established in this study with comparatively high sensitivity and stability, provides reliable results that could be visually detected, making it suitable for application and research in rapid diagnosis of AYL disease, detection of seedlings with the pathogen and breeding of disease-resistant Areca palm varieties. Korean Society of Plant Pathology 2020-10-01 2020-10-01 /pmc/articles/PMC7542027/ /pubmed/33082730 http://dx.doi.org/10.5423/PPJ.OA.06.2020.0094 Text en © The Korean Society of Plant Pathology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Yu, Shao-shuai Che, Hai-yan Wang, Sheng-jie Lin, Cai-li Lin, Ming-xing Song, Wei-wei Tang, Qing-hua Yan, Wei Qin, Wei-quan Rapid and Efficient Detection of 16SrI Group Areca Palm Yellow Leaf Phytoplasma in China by Loop-Mediated Isothermal Amplification |
title | Rapid and Efficient Detection of 16SrI Group Areca Palm Yellow Leaf Phytoplasma in China by Loop-Mediated Isothermal Amplification |
title_full | Rapid and Efficient Detection of 16SrI Group Areca Palm Yellow Leaf Phytoplasma in China by Loop-Mediated Isothermal Amplification |
title_fullStr | Rapid and Efficient Detection of 16SrI Group Areca Palm Yellow Leaf Phytoplasma in China by Loop-Mediated Isothermal Amplification |
title_full_unstemmed | Rapid and Efficient Detection of 16SrI Group Areca Palm Yellow Leaf Phytoplasma in China by Loop-Mediated Isothermal Amplification |
title_short | Rapid and Efficient Detection of 16SrI Group Areca Palm Yellow Leaf Phytoplasma in China by Loop-Mediated Isothermal Amplification |
title_sort | rapid and efficient detection of 16sri group areca palm yellow leaf phytoplasma in china by loop-mediated isothermal amplification |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542027/ https://www.ncbi.nlm.nih.gov/pubmed/33082730 http://dx.doi.org/10.5423/PPJ.OA.06.2020.0094 |
work_keys_str_mv | AT yushaoshuai rapidandefficientdetectionof16srigrouparecapalmyellowleafphytoplasmainchinabyloopmediatedisothermalamplification AT chehaiyan rapidandefficientdetectionof16srigrouparecapalmyellowleafphytoplasmainchinabyloopmediatedisothermalamplification AT wangshengjie rapidandefficientdetectionof16srigrouparecapalmyellowleafphytoplasmainchinabyloopmediatedisothermalamplification AT lincaili rapidandefficientdetectionof16srigrouparecapalmyellowleafphytoplasmainchinabyloopmediatedisothermalamplification AT linmingxing rapidandefficientdetectionof16srigrouparecapalmyellowleafphytoplasmainchinabyloopmediatedisothermalamplification AT songweiwei rapidandefficientdetectionof16srigrouparecapalmyellowleafphytoplasmainchinabyloopmediatedisothermalamplification AT tangqinghua rapidandefficientdetectionof16srigrouparecapalmyellowleafphytoplasmainchinabyloopmediatedisothermalamplification AT yanwei rapidandefficientdetectionof16srigrouparecapalmyellowleafphytoplasmainchinabyloopmediatedisothermalamplification AT qinweiquan rapidandefficientdetectionof16srigrouparecapalmyellowleafphytoplasmainchinabyloopmediatedisothermalamplification |