Loop-Mediated Isothermal Amplification (LAMP)-Based Turn on Fluorescent Paper (ToFP) Device for Detecting Rosellinia necatrix

被引:6
作者
Lee, Se Hee [1 ]
Lee, Sang-Hee [2 ]
Won, Kyungho [3 ]
Kim, Myung-Su [4 ]
Ryu, Hojin [1 ]
Kim, Yang-Hoon [1 ]
Ahn, Ji-Young [1 ]
机构
[1] Chungbuk Natl Univ, Sch Biol Sci, 1 Chungdae Ro, Cheongju 28644, South Korea
[2] Chungbuk Natl Univ, HPBIO Adv Inst Technol, Ind Technol Res Pk E9,1 Chungdae Ro, Cheongju 28644, South Korea
[3] Rural Dev Adm, Natl Inst Hort & Herbal Sci, Pear Res Inst, Naju 58126, South Korea
[4] Rural Dev Adm, Natl Inst Hort & Herbal Sci, Apple Res Inst, Gunwi 54875, Gyeongsangbuk D, South Korea
基金
新加坡国家研究基金会;
关键词
Loop-Mediated Isothermal Amplification (LAMP); LAMP-Based Turn-on Fluorescent Paper (ToFP) Devices; Rosellinia necatrix; White Root Rot (WRR) Disease; Diagnosis; DNA; ASSAY; LAMP; PCR; QUANTIFICATION; TRICHODERMA; PROBE; SOIL;
D O I
10.1166/jbn.2020.2889
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
White root rot (WRR) disease caused by Rosellinia necatrix, a fungal pathogen, results in severe damage to various fruit trees, decreasing their marketability. Regular monitoring is a major process because the pathogen can remain in the soil around the host for a long time. Loop-mediated isothermal amplification (LAMP) is a highly sensitive and efficient amplification technology of nucleic acids (DNA or RNA) that can be performed at constant temperatures. Thus, it has been spotlighted as a useful tool for detecting several infectious agents. In the present study, LAMP-based Turn-on Fluorescent Paper (ToFP) devices were designed and applied to detect R. necatrix. LAMP conditions were optimized and found to be optimal at a reaction temperature (62 degrees C) and a reaction time (30 minutes). These reaction conditions were confirmed by applying them to infectious soil samples collected from the field. The limitation of detection was identified as 10 fg of genomic DNA under optimized LAMP conditions. These LAMP-based ToFP devices were generated with easily available stationery materials and the utility of these devices to analyze the LAMP results were confirmed through several experiments on a total of 14 field samples. The results showed that the developed LAMP-based detection system was very sensitive and had the advantages of rapid detection and high availability in the field.
引用
收藏
页码:166 / 178
页数:13
相关论文
共 26 条
[1]   Inhibition of DNA Polymerases Used in Q-PCR by Structurally Different Soil-Derived Humic Substances [J].
Albers, Christian Nyrop ;
Jensen, Anders ;
Baelum, Jacob ;
Jacobsen, Carsten Suhr .
GEOMICROBIOLOGY JOURNAL, 2013, 30 (08) :675-681
[2]  
Arakawa Masao, 2002, Mycoscience, V43, P21, DOI 10.1007/s102670200004
[3]   Development and application of loop-mediated isothermal amplification for detection of the F167Y mutation of carbendazim-resistant isolates in Fusarium graminearum [J].
Duan, Yabing ;
Zhang, Xiaoke ;
Ge, Changyan ;
Wang, Yong ;
Cao, Junhong ;
Jia, Xiaojing ;
Wang, Jianxin ;
Zhou, Mingguo .
SCIENTIFIC REPORTS, 2014, 4
[4]   Bait twig method for soil detection of Rosellinia necatrix, causal agent of white root rot of Japanese pear and apple, at an early stage of tree infection [J].
Eguchi, Naoki ;
Kondo, Ken-ichi ;
Yamagishi, Naho .
JOURNAL OF GENERAL PLANT PATHOLOGY, 2009, 75 (05) :325-330
[5]   EVALUATION OF TRICHODERMA AS A BIOCONTROL AGENT FOR ROSELLINIA-NECATRIX [J].
FREEMAN, S ;
SZTEJNBERG, A ;
CHET, I .
PLANT AND SOIL, 1986, 94 (02) :163-170
[6]   Genomic DNA Extraction from Cells by Electroporation on an Integrated Microfluidic Platform [J].
Geng, Tao ;
Bao, Ning ;
Sriranganathanw, Nammalwar ;
Li, Liwu ;
Lu, Chang .
ANALYTICAL CHEMISTRY, 2012, 84 (21) :9632-9639
[7]  
Gupta V. K., 1977, Indian Phytopathology, V30, P527
[8]   Development of LAMP and Real-Time PCR Methods for the Rapid Detection of Xylella fastidiosa for Quarantine and Field Applications [J].
Harper, S. J. ;
Ward, L. I. ;
Clover, G. R. G. .
PHYTOPATHOLOGY, 2010, 100 (12) :1282-1288
[9]   Development of a Paper-Based Analytical Device for Colorimetric Detection of Select Foodborne Pathogens [J].
Jokerst, Jana C. ;
Adkins, Jaclyn A. ;
Bisha, Bledar ;
Mentele, Mallory M. ;
Goodridge, Lawrence D. ;
Henry, Charles S. .
ANALYTICAL CHEMISTRY, 2012, 84 (06) :2900-2907
[10]   Development of a reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay for the detection of Sugarcane mosaic virus and Sorghum mosaic virus in sugarcane [J].
Keizerweerd, Amber T. ;
Chandra, Amaresh ;
Grisham, Michael P. .
JOURNAL OF VIROLOGICAL METHODS, 2015, 212 :23-29