A new and sensitive co-operational polymerase chain reaction for rapid detection of Ralstonia solanacearum in water

被引:35
作者
Caruso, P [1 ]
Bertolini, E [1 ]
Cambra, M [1 ]
López, MM [1 ]
机构
[1] Inst Valenciano Invest Agrarias IVIA, Dept Prot & Vegetal & Biotecnol, Valencia 46113, Spain
关键词
bacterial wilt; brown rot; diagnosis; identification; 16S rRNA gene;
D O I
10.1016/S0167-7012(03)00161-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
dThree primers from 16S rRNA were successfully assayed simultaneously in one reaction for sensitive detection of Ralstonia solanacearum in watercourses. The protocol is a modification of the Co-operational polymerase chain reaction (Co-PCR), which allows the simultaneous and co-operational action of the primers. It specifically amplified R. solanacearum strains belonging to biovars 1, 2 and 4. No products were obtained from any of the 162 unidentified isolates from river water. The sensitivity of the assay was < 1 cfu/ml as determined by analysis of beat-treated water samples spiked with R. solanacearum, also containing indigenous microbiota up to 10(5) cfu/ml. The developed Co-PCR assay was more sensitive than other standard PCR assays in the analysis of 51 Spanish environmental water samples. Namely 31.3% of the samples were positive using the newly developed assay, whereas 13.7% or less positive samples were found with the other protocols. The Co-PCR improves the detection sensitivity of R. solanacearum and provides an important tool for its routine detection from environmental water samples and for epidemiological studies. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:257 / 272
页数:16
相关论文
共 60 条
[31]   Development of a highly sensitive nested-PCR procedure using a single closed tube for detection of Erwinia amylovora in asymptomatic plant material [J].
Llop, P ;
Bonaterra, A ;
Peñalver, J ;
López, MM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (05) :2071-2078
[32]  
LOPEZ MM, 2003, IN PRESS 3 INT BACT
[33]   Identification and sensitive endophytic detection of the fire blight pathogen Erwinia amylovora with 23S ribosomal DNA sequences and the polymerase chain reaction [J].
Maes, M ;
Garbeva, P ;
Crepel, C .
PLANT PATHOLOGY, 1996, 45 (06) :1139-1149
[34]  
Niepold F, 1997, MICROBIOL RES, V152, P345, DOI 10.1016/S0944-5013(97)80050-X
[35]   Simultaneous and co-operational amplification (Co-PCR): a new concept for detection of plant viruses [J].
Olmos, A ;
Bertolini, E ;
Cambra, M .
JOURNAL OF VIROLOGICAL METHODS, 2002, 106 (01) :51-59
[36]  
OLSON K, 1976, B OEPP, V6, P199
[37]  
Opina N, 1997, ASIA-PAC J MOL BIOL, V5, P19
[38]  
Palomo JL, 2000, 10 C SOC ESP FIT VAL, P120
[39]   Detection of Ralstonia solanacearum in potato tubers by polymerase chain reaction [J].
Pastrik, KH ;
Maiss, E .
JOURNAL OF PHYTOPATHOLOGY-PHYTOPATHOLOGISCHE ZEITSCHRIFT, 2000, 148 (11-12) :619-626
[40]  
Persson P., 1998, Bulletin OEPP, V28, P113, DOI 10.1111/j.1365-2338.1998.tb00713.x