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加勒比海地区掌状侵染植原体的高分辨率熔解曲线分析基因差异。

Differentiation of Palm-Infecting Phytoplasmas in the Caribbean Basin Using High Resolution Melt Curve Analysis of the Gene.

机构信息

University of Florida, Department of Entomology and Nematology - Fort Lauderdale Research and Education Center, Davie, FL 33314-7719.

出版信息

Plant Dis. 2022 Sep;106(9):2480-2489. doi: 10.1094/PDIS-02-22-0393-RE. Epub 2022 Aug 10.

Abstract

Palm lethal decline is a disease that is always fatal to infected palm hosts and is caused by three species of phytoplasma in the Caribbean basin: ' Phytoplasma palmae', '. P. aculeata', and '. P. hispanola'. Movement of these pathogens throughout the Caribbean has been documented since their discovery in Jamaica. Over time, means of confirming infections in palms have improved. Current protocols utilize quantitative PCR (qPCR) for rapid amplification and distinction of these phytoplasmas using TaqMan probes and high-resolution melt-curve analysis (HRMA) of the 16S rRNA gene. These assays either do not detect all three phytoplasmas (HRMA) or do not distinguish between the three (TaqMan). In this study, a new qPCR-HRMA assay is developed that amplifies and distinguishes all three phytoplasmas currently known to kill palms in the Caribbean. Efficiency for the primer set secA614_F/secA759_R was shown to be consistent for all species at each concentration and yielded distinct melting temperature ranges for amplicons of ' P. palmae' (73.3 to 73.4°C), '. P. aculeata' (72.9 to 73.0°C), and '. P. hispanola' (73.5 to 73.6°C). This assay is a useful new tool not only for diagnostics that will contribute to monitoring and management programs, but it will also aid in basic research by allowing rapid screening of large samples in the context of vector surveys or identification of reservoir hosts.

摘要

棕榈致死衰退病是一种对受感染的棕榈宿主总是致命的疾病,由加勒比盆地的三种植原体引起:“植原体棕榈”、“植原体aculeata”和“植原体hispanola”。自它们在牙买加被发现以来,这些病原体在加勒比地区的传播情况已有记录。随着时间的推移,确认棕榈树感染的方法得到了改进。目前的方案利用定量 PCR(qPCR)使用 TaqMan 探针和 16S rRNA 基因的高分辨率熔解曲线分析(HRMA)快速扩增和区分这些植原体。这些检测要么不能检测到所有三种植原体(HRMA),要么不能区分这三种植原体(TaqMan)。在这项研究中,开发了一种新的 qPCR-HRMA 检测方法,该方法可扩增和区分目前已知在加勒比地区杀死棕榈树的所有三种植原体。在每个浓度下,secA614_F/secA759_R 引物对的效率对所有物种都是一致的,并产生了“植原体棕榈”(73.3 至 73.4°C)、“植原体aculeata”(72.9 至 73.0°C)和“植原体hispanola”(73.5 至 73.6°C)扩增子的独特熔点范围。该检测方法不仅是一种用于诊断的有用新工具,有助于监测和管理计划,而且还将通过允许在载体调查或鉴定储主宿主的背景下快速筛选大量样本,为基础研究提供帮助。

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