Polymerase chain reaction driven by sequence specific primers has become the most widely used diagnostic method to detect andidentify plant pathogens. The sensitive and cost-effective pathogen detection is exceptionally important in the production of propagatingmaterial. In this paper we have collected primer sequence data from the literature for the detection of the most important grapevine pathogensdisseminated by propagating stocks by conventional polymerase chain reaction. Basic protocols to obtain template nucleic acids have alsobeen briefly rewieved
