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针对与椰子致死黄化病相关植原体的通用、快速且可视化检测方法,靶向16S rRNA基因序列。

Universal, Rapid, and Visual Detection Methods for Phytoplasmas Associated with Coconut Lethal Yellowing Diseases Targeting 16S rRNA Gene Sequences.

作者信息

Yu Shao-Shuai, Pan Ying-Wen, Zhu Hui, Song Wei-Wei

机构信息

Coconut Research Institute, Chinese Academy of Tropical Agricultural Sciences, Wenchang 571339, Hainan Province, China.

Post-Entry Quarantine Station for Tropical Plant, Haikou Customs, Haikou 570311, Hainan Province, China.

出版信息

Plant Dis. 2023 Feb;107(2):276-280. doi: 10.1094/PDIS-05-22-0996-SC. Epub 2023 Feb 15.

Abstract

Coconut lethal yellowing (LY) diseases caused by phytoplasmas are devastating diseases for coconut cultivation and seriously threaten the coconut industry around world. The phytoplasmas associated with the LY diseases belonged to six 16Sr groups containing 16SrI, 16SrIV, 16SrXI, 16SrXIV, 16SrXXII, and 16SrXXXII with comparatively higher variable levels. Conserved regions of the 16S rRNA genes of LY phytoplasmas belonging to the six 16Sr groups were obtained in the study. Based on the conserved region sequences of 16S rRNA genes, two sets of LAMP primers, Co-4 and Co-6, were designed and screened, and the rapid and visual detection methods universal for different groups LY phytoplasmas were established. The entire detection reactions of the universal detection methods could be completed with only 30 to 40 min of constant temperature amplification at 64°C, and the detection results were judged by the color changes of the reaction systems, which are convenient and quick. For the six groups of phytoplasmas, the estimated minimum detection limit range of the universal detection primers Co-4 and Co-6 were identical: 4.8 × 10 to 4.8 × 10 copies per 200 μl. The universal detection methods for the LY phytoplasmas established in the study are of great significance for the rapid diagnosis and identification and the efficient monitoring and early warning as well as the port inspection and quarantine of the LY phytoplasmas and their related diseases.

摘要

由植原体引起的椰子致死黄化病是椰子种植的毁灭性病害,严重威胁着全球椰子产业。与致死黄化病相关的植原体属于六个16Sr组,包括16SrI、16SrIV、16SrXI、16SrXIV、16SrXXII和16SrXXXII,具有相对较高的变异水平。本研究获得了属于六个16Sr组的致死黄化植原体16S rRNA基因的保守区域。基于16S rRNA基因的保守区域序列,设计并筛选了两组LAMP引物Co-4和Co-6,建立了适用于不同组致死黄化植原体的快速可视化检测方法。通用检测方法的整个检测反应在64℃恒温扩增仅30至40分钟即可完成,检测结果通过反应体系颜色变化判断,方便快捷。对于六组植原体,通用检测引物Co-4和Co-6的估计最低检测限范围相同:每200μl为4.8×10至4.8×10拷贝。本研究建立的致死黄化植原体通用检测方法对于致死黄化植原体及其相关病害的快速诊断与鉴定、高效监测与预警以及口岸检验检疫具有重要意义。

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