This project demonstrates that the real-time assay had potential to enable the early prediction of skin spot levels during storage. The work presented in this report confirms that there was a good relationship between levels of P. pustulans DNA in peel at harvest and skin spot development in tubers following a 20-week storage duration
- Over two years of trials involving the testing of 106 sets of tuber samples, there wasa good relationship between P. pustulans DNA levels in tuber peel at harvest and skin spot incidence on tubers after storage. This relationship promises to enable skin spot risk assessment and management strategies to be made prior to storage.
- During the 2008-09 season, at the end of a 20-week storage period, 51% of 53 tuber samples developed visible symptoms resembling skin spot and 87% had detectable levels of P. pustulans DNA. During the 2009-10 season, 100% of a further 53 samples collected developed visible skin spot after storage and all samples had detectable levels of P. pustulans DNA.
- It is suggested that for samples tested at or around harvest, P. pustulans DNA levels of <103 pg DNA/g peel represents low skin spot risk; 103 to 104 pg DNA/g peel represents moderate skin spot risk; and > 104 pg DNA/g peel represents high skin spot risk.
- There was broad agreement between results presented in this report and those reported in a previous PCL-funded project (R294) for samples collected at or around harvest
- The discrimination between low and high risk samples, in terms of skin spot development, was good in progeny tubers collected at harvest. However, this disagrees with the findings of R294 where better discrimination was achieved when testing tubers at the end of a 20-week storage period. A likely reason for this is that tubers investigated in R294 developed higher skin spot severity than was found on tubers in this report.
- This work indicates that crop duration is a significant component of the disease epidemiology. This, as a factor, has been under-investigated.
- Future sampling should involve the removal and testing of peel from the entire surface of the tuber, or as a minimum include cores taken from around the stolon and eyes.
- It is recommended that further work is done to refine the relationship between pathogen DNA levels in peel and skin spot levels by considering factors such as cultivar, crop duration and geographical location of crop