A Duplex PCR Assay for Rapid Detection of Phytophthora nicotianae and Thielaviopsis basicola

被引:7
|
作者
Liu, Na [1 ]
Jiang, Shijun [2 ]
Feng, Songli [1 ]
Shang, Wenyan [1 ]
Xing, Guozhen [1 ]
Qiu, Rui [3 ]
Li, Chengjun [3 ]
Li, Shujun [3 ]
Zheng, Wenming [1 ]
机构
[1] Henan Agr Univ, Coll Life Sci, Zhengzhou 450002, Henan, Peoples R China
[2] Henan Agr Univ, Coll Plant Protect, Zhengzhou 450002, Henan, Peoples R China
[3] Henan Acad Agr Sci, Key Lab Green Preservat & Control Tobacco Dis & P, Tobacco Res Inst, Xuchang 461000, Peoples R China
来源
PLANT PATHOLOGY JOURNAL | 2019年 / 35卷 / 02期
关键词
duplex PCR; molecular detection; Phytophthora nicotianae; Thielaviopsis basicola; tobacco; POLYMERASE-CHAIN-REACTION; PARASITICA VAR NICOTIANAE; SENSITIVE DETECTION; SOIL; MARKERS; TOBACCO; GENE; PRIMERS; DNA;
D O I
10.5423/PPJ.OA.09.2018.0173
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
A duplex PCR method was developed for simultaneous detection and identification of tobacco root rot pathogens Phytophthora nicotianae and Thielaviopsis basicola. The specific primers for P. nicotianae were developed based on its internal transcribed spacer (ITS) regions of ribosomal gene, ras gene and hgd gene, while the specific primers for T. basicola were designed based on its ITS regions and beta-tubulin gene. The specificity of the primers was determined using isolates of P. nicotianae, T. basicola and control samples. The results showed that the target pathogens could be detected from diseased tobacco plants by a combination of the specific primers. The sensitivity limitation was 100 fg/mu l of pure genomic DNA of the pathogens. This new assay can be applied to screen out target pathogens rapidly and reliably in one PCR and will be an important tool for the identification and precise early prediction of these two destructive diseases of tobacco.
引用
收藏
页码:172 / 177
页数:6
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