A Novel LAMP Assay for the Detection of Phytophthora cinnamomi Utilizing a New Target Gene Identified From Genome Sequences

被引:39
作者
Dai, Tingting [1 ]
Yang, Xiao [2 ]
Hu, Tao [1 ]
Li, Zhongyan [1 ]
Xu, Yue [1 ]
Lu, Chenchen [3 ]
机构
[1] Nanjing Forestry Univ, Coinnovat Ctr Sustainable Forestry Southern China, Coll Forestry, Nanjing, Jiangsu, Peoples R China
[2] Virginia Tech, Hampton Rd Agr Res & Extens Ctr, Virginia Beach, VA USA
[3] Lianyungang Customs, Lianyungang, Peoples R China
基金
中国博士后科学基金;
关键词
disease diagnosis; hydroxynaphthol blue; oomycetes; Phytophthora root rot; Phytophthora dieback; plant destroyers; MEDIATED ISOTHERMAL AMPLIFICATION; RAPID DETECTION; PHYLOGENETIC ANALYSIS; WESTERN-AUSTRALIA; INFORMED DESIGN; ROOT-ROT; PCR; PATHOGEN; SITE; DNA;
D O I
10.1094/PDIS-04-19-0781-RE
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Phytophthora cinnamomi is an ecologically and agriculturally significant plant pathogen. Early and accurate detection of P. cinnamomi is paramount to disease prevention and management. In this study, a loop-mediated isothermal amplification (LAMP) assay utilizing a new target gene Pcinn100006 identified from genomic sequence data was developed and evaluated for the detection of P. cinnamomi. This Pcinn100006 LAMP assay was found highly specific to P. cinnamomi. All 10 tested isolates of P. cinnamomi yielded positive results, whereas 50 isolates belonging to 16 other Phytophthora species, Globisporangium ultimum, and 14 fungal species lacked detection. This assay was 10 times more sensitive (100 pg in a 25-mu l reaction mixture) than a conventional PCR assay (2 ng in a 50-mu l reaction mixture) for detecting the genomic DNA of P. cinnamomi. In addition, it detected P. cinnamomi from artificially inoculated leaves of Cedrus deodara. Moreover, detection rates of P. cinnamomi using environmental DNAs extracted from 13 naturally infested rhizosphere samples were 100% in the Pcinn100006 LAMP assay versus 46% in the conventional PCR assay. Considering its higher accuracy and shorter time span, this Pcinn100006 LAMP assay is a promising diagnostic tool to replace conventional PCR-based and culture-dependent assays for screening of P. cinnamomi in regions at risk of infection or contamination.
引用
收藏
页码:3101 / 3107
页数:7
相关论文
共 53 条
[21]   Loop-mediated isothermal amplification for detection of the tomato and potato late blight pathogen, Phytophthora infestans [J].
Hansen, Z. R. ;
Knaus, B. J. ;
Tabima, J. F. ;
Press, C. M. ;
Judelson, H. S. ;
Gruenwald, N. J. ;
Smart, Christine D. .
JOURNAL OF APPLIED MICROBIOLOGY, 2016, 120 (04) :1010-1020
[22]   Phytophthora cinnamomi [J].
Hardham, AR .
MOLECULAR PLANT PATHOLOGY, 2005, 6 (06) :589-604
[23]   Evaluation of Different PCR-Based Assays and LAMP Method for Rapid Detection of Phytophthora infestans by Targeting the Ypt1 Gene [J].
Khan, Mehran ;
Li, Benjin ;
Jiang, Yue ;
Weng, Qiyong ;
Chen, Qinghe .
FRONTIERS IN MICROBIOLOGY, 2017, 8
[24]   Rapid detection of Phytophthora cinnamomi using PCR with primers derived from the Lpv putative storage protein genes [J].
Kong, P ;
Hong, CX ;
Richardson, PA .
PLANT PATHOLOGY, 2003, 52 (06) :681-693
[25]   Phylogenetic analysis of Phytophthora species based on mitochondrial and nuclear DNA sequences [J].
Kroon, LPNM ;
Bakker, FT ;
van den Bosch, GBM ;
Bonants, PJM ;
Flier, WG .
FUNGAL GENETICS AND BIOLOGY, 2004, 41 (08) :766-782
[26]   Pathways to false-positive diagnoses using molecular genetic detection methods; Phytophthora cinnamomi a case study [J].
Kunadiya, Manisha ;
White, Diane ;
Dunstan, William A. ;
Hardy, Giles E. St. J. ;
Andjic, Vera ;
Burgess, Treena I. .
FEMS MICROBIOLOGY LETTERS, 2017, 364 (07)
[27]   A qPCR Assay for the Detection of Phytophthora cinnamomi Including an mRNA Protocol Designed to Establish Propagule Viability in Environmental Samples [J].
Kunadiya, Manisha B. ;
Dunstan, William D. ;
White, Diane ;
Hardy, Giles E. St J. ;
Grigg, Andrew H. ;
Burgess, Treena, I .
PLANT DISEASE, 2019, 103 (09) :2443-2450
[28]   Characterization of the Xanthomonas translucens Complex Using Draft Genomes, Comparative Genomics, Phylogenetic Analysis, and Diagnostic LAMP Assays [J].
Langlois, Paul A. ;
Snelling, Jacob ;
Hamilton, John P. ;
Bragard, Claude ;
Koebnik, Ralf ;
Verdier, Valerie ;
Triplett, Lindsay R. ;
Blom, Jochen ;
Tisserat, Ned A. ;
Leach, Jan E. .
PHYTOPATHOLOGY, 2017, 107 (05) :519-527
[29]   Touchdown nested multiplex PCR detection of Phytophthora cinnamomi and P. cambivora from French and English chestnut grove soils [J].
Langrell, Stephen R. H. ;
Morel, Olivier ;
Robin, Cecile .
FUNGAL BIOLOGY, 2011, 115 (07) :672-682
[30]   Development of a genome-informed loop-mediated isothermal amplification assay for rapid and specific detection of Xanthomonas euvesicatoria [J].
Larrea-Sarmiento, Adriana ;
Dhakal, Upasana ;
Boluk, Gamze ;
Fatdal, Lilly ;
Alvarez, Anne ;
Strayer-Scherer, Amanda ;
Paret, Mathews ;
Jones, Jeff ;
Jenkins, Daniel ;
Arif, Mohammad .
SCIENTIFIC REPORTS, 2018, 8