Comparison of enzyme-linked immunosorbent assays and reverse transcription-polymerase chain reaction for the reliable detection of Australian grapevine viruses in two climates during three growing seasons

被引:18
作者
Constable, F. E. [1 ]
Connellan, J. [2 ]
Nicholas, P. [3 ]
Rodoni, B. C. [1 ]
机构
[1] Dept Primary Ind, Knoxfield, Vic 3156, Australia
[2] BSES Ltd, Burdekin Sugar Expt Stn, Ayr, Qld 4807, Australia
[3] S Australian Res & Dev Inst, Adelaide, SA 5001, Australia
关键词
nucleic acid extraction; sampling; viticulture; IMPROVED RNA EXTRACTION; VITIS-VINIFERA L; RT-PCR; SEROLOGICAL DETECTION; GRAPEVINE-LEAFROLL-ASSOCIATED-VIRUS-3; TRANSMISSION; VARIANTS; TISSUE; ELISA; CDNA;
D O I
10.1111/j.1755-0238.2012.00188.x
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Background and Aims: Australian certification programs that provide high-health planting material depend on accurate virus detection methods. The reliability of enzyme-linked immunosorbent assays (ELISAs) and reverse transcription-polymerase chain reaction (RT-PCR) tests for virus detection was compared in Australian conditions. Methods and Results: Replicate trials were established in a hot climate and a cool climate with grapevines that were uninoculated or inoculated with Grapevine virus A, Grapevine fleck virus, Grapevine leafroll-associated virus (GLRaV)-2 and GLRaV-3. Grapevines were tested monthly for virus during 3 years. RT-PCR detected viruses more frequently than ELISA, and the reliability of both tests increased after 12 months and up to 3 years post-inoculation in both climates. Conclusions: Viruses may not be consistently detected until 12 months after an infection event. RT-PCR is more reliable than ELISA for virus detection during spring and summer. However, detection of viruses was rarely 100% efficient, and retesting of grapevines is recommended to improve the rate of detection. Significance of the Study: Validated diagnostic procedures were developed to improve the reliability of grapevine virus detection in Australia.
引用
收藏
页码:239 / 244
页数:6
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