Real-Time and Rapid Detection of Phytopythium vexans Using Loop-Mediated Isothermal Amplification Assay

被引:7
作者
Ghimire, Bhawana [1 ]
Avin, Farhat A. [1 ]
Waliullah, Sumyya [2 ]
Ali, Emran [3 ]
Baysal-Gurel, Fulya [1 ]
机构
[1] Tennessee State Univ, Coll Agr, Otis L Floyd Nursery Res Ctr, Dept Agr & Environm Sci, Mcminnville, TN 37110 USA
[2] Univ Georgia, Coll Agr & Environm Sci, Dept Plant Pathol, Tifton, GA USA
[3] Univ New Hampshire, Coll Life Sci & Agr, Dept Food & Agr, Durham, NH USA
关键词
filtration; multiple sequence alignment; ornamentals; trees; warm start colorimetric; zoospore; RECYCLED IRRIGATION WATER; PLANT-PATHOGENS; PHYTOPHTHORA; PYTHIUM; POPULATIONS; DIAGNOSIS; NURSERIES; PONDS; LAMP;
D O I
10.1094/PDIS-08-22-1944-RE
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Phytopythium vexans (de Bary) Abad, de Cock, Bala, Robideau, A. M. Lodhi & Levesque is an important waterborne and soil-inhabiting oomycete pathogen causing root and crown rot of various plants including certain woody ornamentals, fruit, and forest trees. Early and accurate detection of Phytopythium in the nursery production system is critical, as this pathogen is quickly transported to neighboring healthy plants through the irrigation system. Conventional methods for the detection of this pathogen are tedious, frequently inconclusive, and costly. Hence, a specific, sensitive, and rapid molecular diagnostic method is required to overcome the limitations of traditional identification. In the current study, loop-mediated isothermal amplification (LAMP) for DNA amplification was developed for the identification of P. vexans. It was evaluated using real-time and colorimetric assays. Several sets of LAMP primers were designed and screened, but PVLSU2 was found to be specific to P. vexans as it did not amplify other closely related oomycetes, fungi, and bacteria. Moreover, the developed assays were sensitive enough to amplify DNA up to 102 fg per reaction. The real-time LAMP assay was more sensitive than traditional PCR and culture-based methods to detect infected plant samples. In addition, both LAMP assays detected as few as 100 zoospores suspended in 100 ml water. These LAMP assays are anticipated to save time in P. vexans detection by disease diagnostic laboratories and research institutions and enable early preparedness in the event of disease outbreaks.
引用
收藏
页码:3394 / 3402
页数:9
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