Narae Kim, You Ri Choi, Mun Won Seo, Jeong Young Song and Hong Gi Kim*
Department of Applied Biology, Chungnam National University, Daejeon 34134, Korea
Correspondence to hgkim@cnu.ac.kr
Korean Journal of Mycology (Kor J Mycol) June, 2016, 44(2):103-107.
https://doi.org/10.4489/KJM.2016.44.2.103
Received: April 19, 2016; Revised: June 14, 2016; Accepted: June 23, 2016
Published: June, 2016.
© The Korean Society of Mycology
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
To establish a rapid and accurate detection of Phytophthora pinifolia, which is a quarantine pathogenic fungus in Korea, a species-specific primer was developed based on the ras-related protein (Ypt1) gene. Species-specific primer based on the DNA sequences of Ypt1 gene amplified 193 bp polymerase chain reaction (PCR) product for P. pinifolia. The primer pair yielded the predicted PCR product size exactly in testing with target pathogen DNAs, but not from the other 10 species of Phytophthora and 14 species of other phytopathogenic fungi. The primer pair also showed only the species-specific amplification curve on real-time PCR on target pathogen DNA. The detection sensitivity of real time PCR using species-specific primer pair was 10 to 100 times higher than conventional PCR, with 1 to 10 pg/μL.
Detection, Phytophthora pinifolia, Quarantine measure, Species-specific primers