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Riera, C.

Publications and source records attributed to Riera, C..

3 recordsLinked to original sources

First outbreak of Lumpy Skin disease in Catalonia, Spain, 2025-2026

Lumpy skin disease (LSD) is an emerging cattle disease caused by lumpy skin disease virus (LSDV), with major impacts on the industry, being classified as a Category A disease. Although it was historically confined to Africa, LSD has expanded into the Middle East, Asia and Europe. Here, we report two LSDV genomes from the first outbreak detected in Catalonia, Spain, in October 2025. The genomes were assembled from high-throughput sequencing data generated from two homogenized skin nodules. Comparative phylogenetic analyses were performed using all available complete LSDV genomes and rpo30 gene sequences. These analyses placed the LSDV isolates detected in Catalonia within clade 1.2, closely related to the isolates recently reported in Sardinia, Italy. Our findings also support a connection between recent south-western Europe and central African strains, possibly through northern Africa, and highlight the need for more complete genomes to clarify the origin and connections among recent LSDV outbreaks.

genomics↗

The Role of Supraoptic Hypothalamic Arginine Vasopressin Neurons in Aging-Associated Water Balance and Thermoregulatory Deficits

Aging disrupts physiological homeostasis, impairing thermoregulation, metabolism, and water balance, but the underlying neural mechanisms remain unclear. Here, we identify arginine vasopressin (AVP) neurons in the supraoptic nucleus (SON) of the hypothalamus as a critical driver of these changes. Using single-nucleus RNA-sequencing of the anterior hypothalamus in young and aged mice, we found Avp to be one of the most upregulated neuronal transcripts with age. Aged SONAVP neurons displayed enlarged size and heightened excitability, features consistent with hyperactivity. Functionally, chemogenetic activation of SONAVP neurons in young mice reproduced aging-associated phenotypes including hypothermia, reduced energy expenditure, and suppressed water intake. Conversely, knockdown of Avp in the SON of aged mice restored water balance, partially improved thermoregulation and systemic metabolism. Pharmacological inhibition of AVP receptors revealed that neuroendocrine release of AVP drives homeostatic deficits, with distinct roles for V1A and V2 receptors. Senolytic drug treatment improved systemic metabolism and reduced inflammaging but does not rescue hypothalamic AVP dysfunction, underscoring a brain autonomous mechanism of age-related physiological failure. Together, our findings establish SONAVP neuronal hyperactivity as a driver of impaired homeostasis with age and suggest that targeted modulation of neuroendocrine AVP signaling may offer a therapeutic strategy to alleviate age-associated water balance defects.

physiology↗

Choosing variant interpretation tools for clinical applications: context matters

Our inability to solve the Variant Interpretation Problem (VIP) has become a bottleneck in the biomedical/clinical application of Next-Generation Sequencing. This situation has favored the development and use of bioinformatics tools for the VIP. However, choosing the optimal tool for our purposes is difficult because of the high variability of clinical contexts across and within countries. Here, we introduce the use of cost models as a new approach to compare pathogenicity predictors that considers clinical context. An interesting feature of this approach, absent in standard performance measures, is that it treats pathogenicity predictors as rejection classifiers. These classifiers, commonly found in machine learning applications to healthcare, reject low-confidence predictions. Finally, to explore whether context has any impact on predictor selection, we have developed a computational procedure that solves the problem of comparing an arbitrary number of tools across all possible clinical scenarios. We illustrate our approach using a set of seventeen pathogenicity predictors for missense variants. Our results show that there is no optimal predictor for all possible clinical scenarios. We also find that considering rejection gives a view of classifiers contrasting with that of standard performance measures. The Python code for comparing pathogenicity predictors across the clinical space using cost models is available to any interested user at: https://github.com/ClinicalTranslationalBioinformatics/clinical_space_partition SummariesJosu Aguirre earned his doctorate at the Clinical and Translational Bioinformatics group, at the Vall dHebron Institute of Research (VHIR). Natalia Padilla earned is a post-doctoral researcher at the Clinical and Translational Bioinformatics group, at the Vall dHebron Institute of Research (VHIR). Selen Ozkan is a Ph.D. student at the Clinical and Translational Bioinformatics group, at the Vall dHebron Institute of Research (VHIR). Casandra Riera earned her doctorate at the Clinical and Translational Bioinformatics group, at the Vall dHebron Institute of Research (VHIR). Lidia Feliubadalo earned her doctorate at the Universitat de Barcelona, presently she is a high-level technician working at the Catalan Institute of Oncology (ICO) in the diagnosis of hereditary cancers. Xavier de la Cruz is ICREA Research Professor at the Vall dHebron Institute of Research (VHIR). His research interests revolve around the application of machine learning methods to healthcare problems.

bioinformatics↗