Detection of petunia vein-clearing virus:: model for the detection of DNA viruses in plants with homologous endogenous pararetrovirus sequences

被引:20
作者
Harper, G
Richert-Pöggeler, KR
Hohn, T
Hull, R
机构
[1] John Innes Ctr Plant Sci Res, Dept Dis & Stress Biol, Norwich NR4 7UH, Norfolk, England
[2] Friedrich Miescher Inst, CH-4002 Basel, Switzerland
关键词
petunia vein-clearing virus; PVCV; Caulimoviridae; EPRV; ion-exchange chromatography;
D O I
10.1016/S0166-0934(02)00231-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A number of cases of plant virus sequence integration into host plant genome have been reported. In at least two cases, endogenous pararetrovirus sequences are correlated strongly with subsequent episomal virus infection and there is circumstantial evidence that this also occurs for Petunia vein-clearing virus (PVCV). The detection of viruses is a critical component of plant health and therefore, it is important to have diagnostic procedures that differentiate between the detection of encapsidated viral DNA and homologous sequences in the host genome. PCR-based detection methods targeted at PVCV DNA have been tested and particular attention was paid to design controls that would indicate the existence of host DNA in the reaction. The use of ion-exchange chromatography for the partial purification of plant viruses from other cellular components, including chromosomal DNA, is described. The methods tested for PVCV detection are used to illustrate general principles for the specific detection of virus infections in host plants that carry homologous virus sequences in their genomes. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:177 / 184
页数:8
相关论文
共 28 条
[1]   VARIATION IN BIOLOGICAL PROPERTIES OF CAULIFLOWER MOSAIC-VIRUS CLONES [J].
ALKAFF, N ;
COVEY, SN .
JOURNAL OF GENERAL VIROLOGY, 1994, 75 :3137-3145
[2]  
[Anonymous], PLANT MOL BIOL
[3]   Integration of multiple repeats of geminiviral DNA into the nuclear genome of tobacco during evolution [J].
Bejarano, ER ;
Khashoggi, A ;
Witty, M ;
Lichtenstein, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (02) :759-764
[4]   Fractionation of Corynebacterium pekinense AS 1.299 phage subtypes by anion-exchange chromatography [J].
Chen, GR ;
Xu, XH ;
Xie, JB ;
Deng, WH ;
Lu, WH ;
Chen, RM ;
Zhang, RZ ;
Li, L ;
Chen, TB ;
Lin, XY ;
Rao, PF .
JOURNAL OF VIROLOGICAL METHODS, 2001, 95 (1-2) :11-17
[5]   Effect of temperature on symptom expression and reliability of banana streak badnavirus detection in naturally infected plantain and banana (Musa spp.) [J].
Dahal, G ;
Hughes, JD ;
Thottappilly, G ;
Lockhart, BEL .
PLANT DISEASE, 1998, 82 (01) :16-21
[6]  
Gawel N.J., 1991, PLANT MOL BIOL REP, V9, P262, DOI DOI 10.1007/BF02672076
[7]   Genetic diversity among Banana streak virus isolates from Australia [J].
Geering, ADW ;
McMichael, LA ;
Dietzgen, RG ;
Thomas, JE .
PHYTOPATHOLOGY, 2000, 90 (08) :921-927
[8]  
GEERING ADW, 2001, P 2 INT S MOL CELL B, V10
[9]   Pittosporum tobira: A New Host for Tomato spotted wilt virus [J].
Gera, A. ;
Kritzman, A. ;
Cohen, J. .
PLANT DISEASE, 2000, 84 (04) :491-491
[10]   Detection of episomal banana streak badnavirus by IC-PCR [J].
Harper, G ;
Dahal, G ;
Thottappilly, G ;
Hull, R .
JOURNAL OF VIROLOGICAL METHODS, 1999, 79 (01) :1-8