Simultaneous detection of stone fruit tree viruses by one-step multiplex RT-PCR

被引:28
作者
Jarosova, J. [1 ]
Kundu, J. K. [1 ]
机构
[1] Crop Res Inst, Dept Virol, Prague 16106 6, Czech Republic
关键词
PPV; PDV; PNRSV; Detection; Multiplex RT-PCR; PLUM-POX-VIRUS; NECROTIC RINGSPOT VIRUS; CHAIN-REACTION METHOD; VIROIDS; ASSAY; RNA; HYBRIDIZATION; CITRUS; ALMOND; TIME;
D O I
10.1016/j.scienta.2010.02.011
中图分类号
S6 [园艺];
学科分类号
0902 ;
摘要
A protocol of multiplex RT-PCR in a one-tube system for the detection of the most common stone fruit trees viruses [e.g., plum pox virus (PPV), prune dwarf virus (PDV), and Prunus necrotic ringspot virus (PNRSV)l, including the internal control of NADH dehydrogenase subunit 5 (nad5) gene are described here. The method specificity was tested on more than 80 different samples with various isolates and strains of the viruses. It showed that the targeted viruses produced the expected amplicons, whereas all other related viruses produced only the nad5 internal control amplicon. The method sensitivity was evaluated by comparing it with Simplex RT-PCR with the same primers; no significant differences in detection limits were recorded. Furthermore, the competitiveness of the primers in the assay was tested by serial RNA dilutions of samples with mixed and single infections. The least competitive was the internal control nad5 gene primer pair; therefore, there is a reduced risk of false negatives as all the other primers tend to be more efficient in the given primer cocktail than in the primers for internal control. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:68 / 72
页数:5
相关论文
共 31 条
[1]   Single-step multiplex RT-PCR for simultaneous and colourimetric detection of six RNA viruses in olive trees [J].
Bertolini, E ;
Olmos, A ;
Martínez, MC ;
Gorris, MT ;
Cambra, M .
JOURNAL OF VIROLOGICAL METHODS, 2001, 96 (01) :33-41
[2]   Detection of Prunus necrotic ringspot virus in almond:: effect of sampling time on the efficiency of serological and biological indexing methodologies [J].
Bertozzi, T ;
Alberts, E ;
Sedgley, M .
AUSTRALIAN JOURNAL OF EXPERIMENTAL AGRICULTURE, 2002, 42 (02) :207-210
[3]  
Cambra M., 1994, Bulletin OEPP, V24, P569, DOI 10.1111/j.1365-2338.1994.tb01070.x
[4]   Comparison of monoclonal antibodies and polymerase chain reaction assays for the typing of isolates belonging to the D and M serotypes of plum pox potyvirus [J].
Candresse, T ;
Cambra, M ;
Dallot, S ;
Lanneau, M ;
Asensio, M ;
Gorris, MT ;
Revers, F ;
Macquaire, G ;
Olmos, A ;
Boscia, D ;
Quiot, JB ;
Dunez, J .
PHYTOPATHOLOGY, 1998, 88 (03) :198-204
[5]   CHARACTERISTICS OF MICROPLATE METHOD OF ENZYME-LINKED IMMUNOSORBENT ASSAY FOR DETECTION OF PLANT-VIRUSES [J].
CLARK, MF ;
ADAMS, AN .
JOURNAL OF GENERAL VIROLOGY, 1977, 34 (MAR) :475-483
[6]  
DITERLIZI B, 2000, OPTIONS MEDITERRAN B, V19, P151
[7]   Multiplex PCR: Optimization and application in diagnostic virology [J].
Elnifro, EM ;
Ashshi, AM ;
Cooper, RJ ;
Klapper, PE .
CLINICAL MICROBIOLOGY REVIEWS, 2000, 13 (04) :559-+
[8]  
Gentit P., 2006, Bulletin OEPP, V36, P251
[9]   Geographically and temporally distant natural recombinant isolates of Plum pox virus (PPV) are genetically very similar and form a unique PPV subgroup [J].
Glasa, M ;
Palkovics, L ;
Komínek, P ;
Kabonne, G ;
Pittnerová, S ;
Kúdela, O ;
Candresse, T ;
Subr, Z .
JOURNAL OF GENERAL VIROLOGY, 2004, 85 :2671-2681
[10]  
Grieco F, 1999, J PHYTOPATHOL, V147, P183, DOI 10.1111/j.1439-0434.1999.tb03826.x