Development of a Real-Time Fluorescence Loop-Mediated Isothermal Amplification Assay for Rapid and Quantitative Detection of Fusarium oxysporum f. sp cubense Tropical Race 4 In Soil

被引:39
作者
Zhang, Xin [1 ]
Zhang, He [1 ]
Pu, Jinji [1 ]
Qi, Yanxiang [1 ]
Yu, Qunfang [1 ]
Xie, Yixian [1 ]
Peng, Jun [1 ,2 ,3 ]
机构
[1] Chinese Acad Trop Agr Sci, Environm & Plant Protect Inst, Minist Agr, Key Lab Integrated Pest Management Trop Crops, Haikou, Peoples R China
[2] China Agr Univ, State Key Lab Agrobiotechnol, Beijing 100094, Peoples R China
[3] China Agr Univ, Minist Agr, Key Lab Plant Pathol, Beijing 100094, Peoples R China
关键词
SENSITIVE DETECTION; POTATO-TUBERS; PCR; WILT; TAIWAN; DNA; SOLANI; BANANA; LAMP; QUANTIFICATION;
D O I
10.1371/journal.pone.0082841
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Fusarium oxysporum f. sp. cubense (Foc), the causal agent of Fusarium wilt (Panama disease), is one of the most devastating diseases of banana (Musa spp.). The Foc tropical race 4 (TR4) is currently known as a major concern in global banana production. No effective resistance is known in Musa to Foc, and no effective measures for controlling Foc once banana plants have been infected in place. Early and accurate detection of Foc TR4 is essential to protect banana industry and guide banana planting. A real-time fluorescence loop-mediated isothermal amplification assay (RealAmp) was developed for the rapid and quantitative detection of Foc TR4 in soil. The detection limit of the RealAmp assay was approximately 0.4 pg/mu l plasmid DNA when mixed with extracted soil DNA or 10(3) spores/g of artificial infested soil, and no cross-reaction with other relative pathogens were observed. The RealAmp assay for quantifying genomic DNA of TR4 was confirmed by testing both artificially and naturally infested samples. Quantification of the soil-borne pathogen DNA of Foc TR4 in naturally infested samples was no significant difference compared to classic real-time PCR (P>0.05). Additionally, RealAmp assay was visual with an improved closed-tube visual detection system by adding SYBR Green I fluorescent dye to the inside of the lid prior to amplification, which avoided the inhibitory effects of the stain on DNA amplification and makes the assay more convenient in the field and could thus become a simple, rapid and effective technique that has potential as an alternative tool for the detection and monitoring of Foc TR4 in field, which would be a routine DNA-based testing service for the soilborne pathogen in South China.
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页数:10
相关论文
共 48 条
[1]   Use of a real-time LAMP isothermal assay for detecting 16SrII and XII phytoplasmas in fruit and weeds of the Ethiopian Rift Valley [J].
Bekele, B. ;
Hodgetts, J. ;
Tomlinson, J. ;
Boonham, N. ;
Nikolic, P. ;
Swarbrick, P. ;
Dickinson, M. .
PLANT PATHOLOGY, 2011, 60 (02) :345-355
[2]   Genetic variation among vegetative compatibility groups of Fusarium oxysporum f. sp. cubense analyzed by DNA fingerprinting [J].
Bentley, S ;
Pegg, KG ;
Moore, NY ;
Davis, RD ;
Buddenhagen, IW .
PHYTOPATHOLOGY, 1998, 88 (12) :1283-1293
[3]  
Bilodeau G, 2010, PHYTOPATHOLOGY S, V100, pS14
[4]   Quantifying potato pathogen DNA in soil [J].
Brierley, Jennie L. ;
Stewart, Jennifer A. ;
Lees, Alison K. .
APPLIED SOIL ECOLOGY, 2009, 41 (02) :234-238
[5]  
Buddenhagen I. W., 2009, ISHS ACTA HORTICULTU, V828, P193
[6]   Detection of Colletotrichum coccodes from soil and potato tubers by conventional and quantitative real-time PCR [J].
Cullen, DW ;
Lees, AK ;
Toth, IK ;
Duncan, JM .
PLANT PATHOLOGY, 2002, 51 (03) :281-292
[7]   Conventional PCR and real-time quantitative PCR detection of Helminthosporium solani in soil and on potato tubers [J].
Cullen, DW ;
Lees, AK ;
Toth, IK ;
Duncan, JM .
EUROPEAN JOURNAL OF PLANT PATHOLOGY, 2001, 107 (04) :387-398
[8]   A molecular diagnostic for tropical race 4 of the banana fusarium wilt pathogen [J].
Dita, M. A. ;
Waalwijk, C. ;
Buddenhagen, I. W. ;
Souza, M. T., Jr. ;
Kema, G. H. J. .
PLANT PATHOLOGY, 2010, 59 (02) :348-357
[9]   SYTO dyes and EvaGreen outperform SYBR Green in real-time PCR [J].
Eischeid A.C. .
BMC Research Notes, 4 (1)
[10]   Current status of the taxonomic position of Fusarium oxysporum formae specialis cubense within the Fusarium oxysporum complex [J].
Fourie, G. ;
Steenkamp, E. T. ;
Ploetz, R. C. ;
Gordon, T. R. ;
Viljoen, A. .
INFECTION GENETICS AND EVOLUTION, 2011, 11 (03) :533-542