Rapid detection of Heterobasidion annosum using a loop-mediated isothermal amplification assay

被引:1
|
作者
Hong-min, Zhou [1 ,2 ]
Jian, Yu [2 ]
Ying, Liu [2 ]
Yuan, Yuan [1 ]
Cui-ping, Wu [3 ]
Yu-cheng, Dai [1 ]
Jia-jia, Chen [2 ]
机构
[1] Beijing Forestry Univ, Inst Microbiol, Sch Ecol & Nat Conservat, Beijing, Peoples R China
[2] Jiangsu Vocat Coll Agr & Forestry, Coll Landscape Architecture, Zhenjiang, Peoples R China
[3] Nanjing Customs, Anim Plant & Food Inspect Ctr, Nanjing, Peoples R China
基金
中国国家自然科学基金;
关键词
Heterobasidion annosum; pathogens of Pinus; LAMP assay; molecular diagnosis; port quarantine; INTERSTERILITY GROUPS; PICEA-ABIES; ROOT-ROT; DECAY; DNA; PHYLOGEOGRAPHY; SEQUENCE; VIRUS; GENE; PCR;
D O I
10.3389/fcimb.2023.1134921
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Heterobasidion annosum is one of the most aggressive pathogens of Pinus forests in Europe, causing considerable economic losses. To detect H. annosum for disease diagnosis and control, we developed a loop-mediated isothermal amplification (LAMP) reaction with a primer set designed from the glyceraldehyde 3-phosphate dehydrogenase (GAPDH) DNA sequences of H. annosum. In our study, this LAMP assay was found to be capable of efficiently amplifying the target gene within 60 min at 63 degrees C. In specificity tests, H. annosum was positively detected, and other species were negative. The detection limit of this assay was found to be 100 pg center dot mu L-1, and the assay was also successfully tested for use with basidiospore suspensions and wood samples. This study provides a rapid method for diagnosing root and butt rot caused by H. annosum, which will be of use in port surveillance of logs imported from Europe.
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页数:10
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