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| Authors: | T. Candresse, M. Lanneau, F. Revers, S. Kofalvi, G. Macquaire |
| Keywords: | detection, diagnostic, typing, sensitivity, specificity |
Abstract:
Ten years after the original reports demonstrating the feasibility of the detection of plant viruses and viroids by PCR-based techniques, a large body of literature describes the development of PCR primer pairs and of very sensitive assays for essentially all groups of viral pathogens.
The tests developed show, in general, a sensitivity in great excess (up to several thousand-fold) of that reported for serological assays.
Yet, the assays reported have so far and to a very large extent been confined to laboratory scale set-ups.
Transition from this situation to the real-life, large scale application of these techniques will require further validation as well as development of automated or semi-automated pre- and post-PCR steps.
Past and current achievements as well as future perspectives are discussed.
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