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Cerny"],"technology_type":["Mass Spectrometry","Bottom-up proteomics"],"software":[""],"submitter_keywords":["pedunculate oak","Quercus robur","forest nurseries","koch’s postulates","dual-culture","cadophora luteo-olivacea","trichoderma atroviride","contact-zone proteomics","Quercus robur; pedunculate oak; forest nurseries; trunk disease pathogens; cadophora luteo-olivacea; trichoderma atroviride; koch’s postulates; mycoparasitism; dual-culture; contact-zone proteomics; secretome; biocontrol","mycoparasitism","secretome","trunk disease pathogens","biocontrol"],"full_dataset_link":["https://www.ebi.ac.uk/pride/archive/projects/PXD073144"],"tissue":["Mycelium"],"sample_protocol":["Protein extraction from the protein-rich pellet followed (Berková et al., 2024). Briefly, pellets were resolubilized in 2% (w/v) SDS, 30% (w/v) sucrose, 5% (v/v) β-mercaptoethanol, 5 mM EDTA, and 100 mM Tris (pH 8.0), supplemented with 400 µL Tris-saturated phenol. Proteins were precipitated from the phenolic phase using 100 mM ammonium acetate in methanol, washed with 80% acetone, and solubilized in 8 M urea, 10 mM DTT, and 100 mM ammonium bicarbonate. Proteins were alkylated and digested with trypsin. Each sample (5 µg peptides) was analyzed by nanoflow reverse-phase LC–MS/MS using a 25 cm bioZen 2.6 µm Peptide XB-C18 (Phenomenex) column coupled to a Dionex Ultimate 3000 RSLC nano-UPLC and an Orbitrap Fusion Lumos Tribrid Mass Spectrometer equipped with a FAIMS Pro interface (Thermo Fisher Scientific) (Kopecká et al., 2025), using alternating FAIMS compensation voltages of −40, −50, and −75 V."],"repository":["Pride"],"quantification_method":[""],"modification":[""],"data_protocol":["MS/MS spectra were recalibrated and searched against the corresponding species-specific protein database using Proteome Discoverer 2.5 with Sequest HT, MS Amanda 2.0 (Dorfer et al., 2021), and MSFragger (Kong et al., 2017). Quantification was restricted to proteins identified by at least two unique peptides. In addition, de novo-assisted interpretation was performed using PEAKS 6.0 and Unipept for downstream interpretation (Chatterjee et al., 2019). Metabolomics (GC–MS)"],"omics_type":["Proteomics"],"labhead":["Martin Cerny"],"instrument_platform":[""],"submission_type":["PARTIAL"],"labhead_affiliation":["Mendel University in Brno"],"species":["Cadophora Luteo-olivacea","Trichoderma Atroviride"],"publication":["Not available"],"submitter_mail":["martincerny83@gmail.com"],"submitter_affiliation":["Mendel University in Brno"],"submitter_country":["Czech Republic"],"additional_accession":[]},"is_claimable":false,"name":"Unveiling Oak Endophyte Dynamics: Cadophora luteo-olivacea and Trichoderma atroviride from Pathogenicity Tests to Omics Insights","description":"Pedunculate oak (Quercus robur) is a foundation tree species in European forests and reforestation programs, and forest nurseries represent key phytosanitary bottlenecks where asymptomatic planting stock can disseminate cryptic pathogens. Cadophora luteo-olivacea is frequently associated with grapevine trunk diseases and has been recovered from diverse woody hosts, yet its pathogenic potential on oak and its interactions with antagonistic fungi remain unresolved.  Here, we combine pathogenicity testing, dual-culture confrontation assays and time-resolved, spatially resolved contact-zone proteomics and metabolomics to connect detection to causality and mechanism in an oak associated Cadophora–Trichoderma system. We fulfill Koch’s postulates for C. luteo-olivacea on Q. robur seedlings and quantify inhibition of Cadophora by a natural isolate of Trichoderma atroviride.  Contact-zone proteomics at 4 and 8 days post-contact reveals a staged, interface-localized antagonistic program dominated by fungal cell-wall targeting hydrolases (including chitinases and β-1,3-glucanases), secreted proteases, oxidoreductases, transporters and small secreted proteins, alongside factors consistent with adhesion and self-protection. Together, these complementary assays provide the first experimental evidence that C. luteo-olivacea is pathogenic on Q. robur and delineate mechanistic signatures of T. atroviride mycoparasitism at the interaction front. This framework links nursery-relevant pathogen screening to mechanistic readouts and informs evaluation of biocontrol potential in a foundation forest 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