Multiplex TaqMan qPCR Assay for Detection, Identification, and Quantification of Three Sclerotinia Species

被引:4
作者
Lee, Dong Jae [1 ]
Lee, Jin A. [1 ]
Chae, Dae-Han [2 ]
Jang, Hwi-Seo [2 ]
Choi, Young-Joon [1 ]
Kim, Dalsoo [2 ]
机构
[1] Kunsan Natl Univ, Dept Biol Sci, Gunsan, South Korea
[2] Moghu Res Ctr Ltd, Daejeon, South Korea
关键词
asp gene; phylogeny; TaqMan probe; sclerotia; white mold; PCR ASSAY; BOTRYTIS; INOCULUM; DISEASES;
D O I
10.1080/12298093.2022.2131999
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
White mold (or Sclerotinia stem rot), caused by Sclerotinia species, is a major air, soil, or seed-transmitted disease affecting numerous crops and wild plants. Microscopic or culture-based methods currently available for their detection and identification are time-consuming, laborious, and often erroneous. Therefore, we developed a multiplex quantitative PCR (qPCR) assay for the discrimination, detection, and quantification of DNA collected from each of the three economically relevant Sclerotinia species, namely, S. sclerotiorum, S. minor, and S. nivalis. TaqMan primer/probe combinations specific for each Sclerotinia species were designed based on the gene sequences encoding aspartyl protease. High specificity and sensitivity of each probe were confirmed for sclerotium and soil samples, as well as pure cultures, using simplex and multiplex qPCRs. This multiplex assay could be helpful in detecting and quantifying specific species of Sclerotinia, and therefore, may be valuable for disease diagnosis, forecasting, and management.
引用
收藏
页码:382 / 388
页数:7
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