Detection and Quantification of in Seeds of Using Droplet Digital Polymerase Chain Reaction.

is an important seedborne pathogen of squash (). The aim of our work was to develop a rapid and sensitive diagnostic tool for detection and quantification of in squash seed samples, to be compared with blotter analysis, that is the current official seed test. In blotter analysis, 29 of 31 seed samples were identified as infected, with contamination from 1.5 to 65.4%. A new set of primers (DB1F/R) was validated and in conventional, quantitative real-time PCR (qPCR) and droplet digital (dd) PCR. The limit of detection of DNA for conventional PCR was ∼1.82 × 10 ng, with 17 of 19 seed samples positive. The limit of detection for ddPCR was 3.6 × 10 ng, which corresponded to 0.2 copies/μl. Detection carried out with artificial samples revealed no interference in the absolute quantification when the seed samples were diluted to 20 ng. All seed samples that showed contamination in the blotter analysis were highly correlated with the absolute quantification of DNA (copies/μl) in ddPCR ( = 0.986; ≤ 0.01). Our ddPCR protocol provided rapid detection and absolute quantification of , offering a useful support to the standard procedure.