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Biology subjects

Calcaterra, M.

Publications and source records attributed to Calcaterra, M..

2 recordsLinked to original sources

Comparative assessment of genomic, phenomic, and metabolomic prediction models in biparental grapevine breeding populations

Accelerating grapevine breeding for disease resistance and climate adaptation remains constrained by long generation cycles. We benchmarked genomic (SNP), phenomic (NIRS), and metabolomic (untargeted LC-MS) prediction for 24 agronomic traits in a biparental population phenotyped over three years. Seven statistical frameworks and four tissue x timepoint combinations (wood; vineyard leaves at budbreak and flowering; greenhouse leaves at flowering) were evaluated, together with feature-wise BLUPs across samples. Cross-year and cross-population analyses with two additional populations assessed temporal robustness and transferability. Genomic prediction was most accurate (up to r = 0.83), metabolomic prediction was intermediate (up to r = 0.59), and phenomic prediction was lowest (up to r = 0.39) despite its lower acquisition cost. Metabolite features were more heritable than NIR wavelengths, for which most unexplained variation remained residual under the fitted model. Multi-omics integration produced limited overall gains. These results support genomic selection as the primary approach, with metabolomic or phenomic screening considered only for traits and sampling designs that show reproducible predictive signal.

genomics↗

Immune-parenchymal multicellular niches are shared across distinct thyroid autoimmune diseases

Thyroid hormone, produced in the thyroid gland, regulates metabolism, development, and cardiac function. The thyroid is susceptible to autoimmune attack by both cellular and humoral immunity exemplified by Hashimotos thyroiditis (HT) and Graves Disease (GD), respectively. In HT, immune-mediated destruction impairs thyroid hormone production, while in GD, stimulating autoantibodies promote over-production. Here, we generated a multi-modal atlas of 604,076 human thyroid and blood cells from HT, GD, and control patients. We found that, despite markedly different clinical presentations and distinct antigenic triggers, HT and GD exhibit convergent cellular dynamics resulting in a shared continuum of immune infiltration. Along this continuum, a key feature is a thyrocyte niche containing CD8+ T cells that may segregate pathogenic T cells from regions with preserved thyroid hormone production. These findings of a shared disease continuum characterized by spatially defined immune niches provide a new framework for understanding tissue homeostasis in human autoimmune disease.

immunology↗