Microbial communities play a critical role in determining both fruit health and fermentation outcomes along the grape-to-wine continuum, yet their diversity dynamics within holistic production systems remain poorly understood. In this study, we investigated the impact of pre-harvest interventions-specifically the application of Saccharomyces cerevisiae NX2320, Trichoderma harzianum, and fludioxonil-on microbial community trajectories and wine aroma profiles during spontaneous fermentation. We demonstrated that all treatments significantly suppressed grape pathogens compared to untreated controls, while simultaneously restructuring the microbial communities in grape juice. This restructuring influenced fermentation outcomes, leading to distinct volatile compound profiles in the final wines. Notably, the S. cerevisiae-treated group exhibited rapid dominance of Saccharomyces (initial abundance: 89.96 %), which accelerated ethanol production and elevated key esters such as isobutyl acetate and 1-butanol-3-methyl-acetate. These changes collectively enhanced fruity notes in the wines. Furthermore, fungal diversity inversely correlated with fermentation progression, reinforcing the role of Saccharomyces in simplifying the microbial ecosystem. Crucially, early microbial modulation (pre-fermentation) proved to be a pivotal factor in determining the sensory attributes of the final wines, with the timing and type of intervention significantly influencing the variability of volatile compounds. These findings establish a causal relationship between agricultural microbiome management and oenological quality, offering actionable strategies for optimizing wine microbiota engineering and achieving desired aromatic characteristics.
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Evidence ID | Analyze ID | Gene/Complex | Systematic Name/Complex Accession | Qualifier | Gene Ontology Term ID | Gene Ontology Term | Aspect | Annotation Extension | Evidence | Method | Source | Assigned On | Reference |
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Evidence ID | Analyze ID | Gene | Gene Systematic Name | Phenotype | Experiment Type | Experiment Type Category | Mutant Information | Strain Background | Chemical | Details | Reference |
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Evidence ID | Analyze ID | Gene | Gene Systematic Name | Disease Ontology Term | Disease Ontology Term ID | Qualifier | Evidence | Method | Source | Assigned On | Reference |
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Evidence ID | Analyze ID | Regulator | Regulator Systematic Name | Target | Target Systematic Name | Direction | Regulation of | Happens During | Regulator Type | Direction | Regulation Of | Happens During | Method | Evidence | Strain Background | Reference |
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Site | Modification | Modifier | Source | Reference |
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Evidence ID | Analyze ID | Interactor | Interactor Systematic Name | Interactor | Interactor Systematic Name | Allele | Assay | Annotation | Action | Phenotype | SGA score | P-value | Source | Reference | Note |
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Evidence ID | Analyze ID | Interactor | Interactor Systematic Name | Interactor | Interactor Systematic Name | Assay | Annotation | Action | Modification | Source | Reference | Note |
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Complement ID | Locus ID | Gene | Species | Gene ID | Strain background | Direction | Details | Source | Reference |
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Evidence ID | Analyze ID | Dataset | Description | Keywords | Number of Conditions | Reference |
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