Real-Time PCR Detection and QUantification of Soilborne Fungal Pathogens : the Case of Rosellinia necatrix, Phytophthora nicotianae, P. citrophthora and Verticillium dahliae

Abstract

Conventional and Scorpion primers were designed from the ITS regions to identify Rosellinia necatrix,
Phytophthora nicotianae, and P. citrophthora and from the IGS regions to identify Verticillium dahliae and V. alboatrum.
Specificity of primers and probes was assessed using genomic DNA from a large number of fungi from several
hosts and by means of BLAST analyses, to exclude the presence of similar sequences in other micro-organisms
among available DNA databases (GenBank). Simple and rapid procedures for DNA extraction from naturally infected
matrices (soils, roots, bark, and/or woody tissues) were utilised to yield DNA of a purity and quality suitable for
PCR assays. Combining these protocols with a double amplification (nested Scorpion-PCR), the real-time detection of
these pathogens was possible from naturally infested soils and from infected citrus roots (P. nicotianae and P.
citrophthora), from the roots and bark of stone fruits and olive (R. necatrix) and from olive branches (V. dahliae). For
target pathogens, the limit of detection was 1 pg µl-1 in Scorpion-PCR and 1 fg µl-1 in nested Scorpion-PCR. High and
significant correlations between pathogen propagule concentrations and real-time PCR cycle thresholds (Ct) were
obtained. Moreover, specific tests with R. necatrix seem to indicate that its DNA is quite rapidly degraded in the soil,
excluding the risk of false positives due to the presence of dead cells.