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Updated: May 13, 2025

Development of a Quantitative Recombinase Polymerase Amplification Assay with an Internal Positive Control
Published on: March 30, 2015
Development of a Quantitative SYBR Green Real-Time PCR for Trichoderma afroharzianum, Causal Agent of Ear Rot of
Martina Sanna1,2, Simone Bosco1, Monica Mezzalama1,2
1Department of Agricultural, Forestry and Food Sciences (DISAFA), University of Torino, Grugliasco 10095, Italy.
Abstract:
Trichoderma afroharzianum, the causal agent of Trichoderma ear rot, is an emerging pathogen of maize (Zea mays L.). It was recently reported as a maize pathogen in Germany, France, and in Italy. In 2023, nine seed lots from three farms in Northern Italy were tested for their phytosanitary conditions, revealing infection rates of up to 71% with Trichoderma spp. All seed lots showed symptoms of Trichoderma ear rot infection, and 26 out of 50 isolates were identified as T. afroharzianum. The study confirmed that T. afroharzianum infects maize seeds causing severe disease. Thirteen isolates from infected seeds were used to design species-specific primers on the translation elongation factor 1α gene and to develop a SYBR Green quantitative PCR to detect and quantify T. afroharzianum in maize seeds. The assay was validated following EPPO standard PM 7/98 guidelines, assessing analytical sensitivity, specificity, selectivity, repeatability, and reproducibility. The specificity of the method was validated using 19 T. afroharzianum strains and 16 nontarget species, including Trichoderma species belonging to the T. harzianum species complex. Only target DNA produced positive amplifications. Analytical sensitivity was tested using serial dilutions of T. afroharzianum DNA, revealing a detection limit of 50 fg, even in the presence of maize seed DNA. The assay enables specific and sensitive detection of target DNA in asymptomatic samples, providing a valuable tool for early target detection and quantification during seed certification.

