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Biology subjects

Freitas, A.

Publications and source records attributed to Freitas, A..

5 recordsLinked to original sources

Predicting Lifespan-Extending Compounds Using Supervised Machine Learning

Identifying lifespan-extending compounds is an important objective in ageing research, but experimental screening remains costly and time consuming. This study evaluates supervised machine learning for predicting lifespan-extending compounds in Caenorhabditis elegans using compound-protein interaction features derived from the STITCH database. Three feature representations were compared: continuous interaction probabilities, binary features generated using a fixed threshold of 0.5, and binary features generated using an optimised threshold selected within cross-validation. Random Forest and XGBoost classifiers were evaluated using stratified 10-fold cross-validation, with performance assessed by accuracy, area under the receiver operating characteristic curve (AUROC), and area under the precision recall curve (AUPRC). Model interpretation was examined using Mean Decrease in Impurity (MDI), SHAP, TreeSHAP, and LIME, with Jaccard similarity used to compare the top-ranked protein features. Random Forest achieved its highest accuracy (78.84%), AUROC (0.7391), and AUPRC (0.5202) using the fixed threshold binary representation. XGBoost achieved its highest accuracy (80.36%) using the optimised threshold representation, whereas continuous features yielded its highest AUROC (0.7605) and AUPRC (0.5332). SHAP and TreeSHAP showed the strongest agreement in protein rankings, producing identical top-10 feature sets across all three XGBoost representations. These findings demonstrate that feature representation influences both predictive performance and model interpretation, highlighting the importance of evaluating classification metrics alongside explainability when prioritising candidate compounds for further ageing research.

bioinformatics↗

Short-Report: First whole-genome evidence of dengue virus in field-caught mosquitoes from southern Brazil

Dengue virus (DENV) is a major global health threat whose expansion into temperate regions has been facilitated by climate change and vector adaptation. Despite recurrent epidemics in Brazil, genomic surveillance in mosquitoes remains limited, particularly in the South. To address this gap, we implemented a novel urban mosquito-trapping strategy optimized for low-density and peri-domestic environments in Porto Alegre, Rio Grande do Sul. Between April and July 2023, were collected 4,768 Aedes aegypti samples across 16 neighborhoods, generating 2,022 pools. Among these, 41 pools tested positive for DENV, of which 33 pools exhibited RNA integrity suitable for sequencing. Whole-genome sequencing revealed 33 DENV-positive pools, including 29 DENV-1 (Genotype V) and 4 DENV-2 (Genotype II). Two pools contained both serotypes, highlighting the risk of sequential infections in humans. Phylogenetic analyses indicated sustained local transmission alongside multiple introductions, while recurrent mutations, particularly in NS1, NS2A, and NS5, suggested ongoing viral adaptation. These findings represent the first vector-based genomic data for dengue in southern Brazil and demonstrate the utility of mosquito genomics for early outbreak detection, serotype monitoring, and preparedness in emerging transmission zones. Author SummaryDengue virus (DENV) continues to expand into new regions, driven by climate change and mosquito adaptation. In Brazil, dengue epidemics are recurrent, but genomic surveillance of mosquitoes is still scarce, particularly in the southern states. To fill this gap, we implemented an urban mosquito-trapping strategy designed for low-density and peri-domestic environments in Porto Alegre, Rio Grande do Sul. From April to July 2023, we collected 4,768 Aedes aegypti samples across 16 neighborhoods, generating 2,022 pools. Among these, 41 pools were positive for DENV, of which 33 pools exhibited RNA integrity suitable for sequencing, mainly DENV-1 (Genotype V) and DENV-2 (Genotype II), with two pools showing co-circulation of both serotypes, raising concern for sequential infections in humans. Phylogenetic analysis revealed sustained local transmission combined with multiple virus introductions, and mutations in NS1, NS2A, and NS5 suggested ongoing viral adaptation. Our findings provide the first mosquito-based genomic data for dengue in southern Brazil and highlight how mosquito genomics can strengthen early outbreak detection, serotype monitoring, and epidemic preparedness.

molecular biology↗

High capacity of Brazilian Aedes aegypti populations to transmit a locally circulating lineage of Chikungunya virus

The global incidence of chikungunya has surged in recent decades, with South America, particularly Brazil, experiencing devastating outbreaks. The primary vector for transmitting CHIKV in urban areas is the mosquito species Aedes aegypti, which is very abundant in Brazil. However, little is known about the impact of locally circulating CHIKV genotypes and specific combinations of mosquito populations on vector competence. In this study, we analyzed and compared the infectivity and transmissibility of a recently isolated CHIKV-ECSA lineage from Brazil among four Ae. aegypti populations collected from different regions of the country. When exposed to CHIKV-infected mice for blood feeding, all mosquito populations showed high infection rates and dissemination efficiency. Moreover, using a mouse model to assess transmission rates in a manner that better mirrors natural cycles, we observed that these populations exhibit highly efficient transmission rates of CHIKV-ECSA. Our findings underscore the robust capability of Brazilian Ae. aegypti populations to transmit the locally circulating CHIKV-ECSA lineage, potentially explaining its higher prevalence compared to the Asian lineage also introduced in Brazil. Author SummaryChikungunya virus (CHIKV) is an alphavirus transmitted by mosquitoes, gaining attention due to its rapid global spread and public health impact. Initially isolated in Tanzania in 1952, it was confined to Africa, Asia, and the Indian subcontinent. Local transmission of CHIKV in the Americas began in December 2013, leading to a 2014 epidemic. The Aedes aegypti mosquito, prevalent in Brazil, is suspected as the primary vector. Yet, our understanding of how different mosquito populations and virus lineages impact spread is limited. In this Brazilian study, we collected mosquitoes from four regions, exposing them to the local African ECSA lineage of CHIKV. Remarkably, all mosquito populations exhibited high infection rates and efficient virus transmission to vertebrate hosts. This research sheds light on why the ECSA chikungunya lineage is spreading rapidly in Brazil. The Brazilian Ae. aegypti mosquitoes appear to possess exceptional capabilities in transmitting African ECSA lineage of CHIKV, potentially contributing to its rapid dissemination within the country and neighboring regions. Comprehending these dynamics is vital for developing strategies to control and mitigate the impact of chikungunya in affected areas.

immunology↗

Machine-learning-based predictions of caloricrestriction associations across ageing-related genes

Caloric restriction (CR) is the most studied pro-longevity intervention; however, a complete understanding of its underlying mechanisms remains elusive, and new research directions may emerge from the identification of novel CR-related genes and CR-related genetic features. This work used a Machine Learning (ML) approach to classify ageing-related genes as CR-related or NotCR-related using 9 different types of predictive features: PathDIP pathways, two types of features based on KEGG pathways, two types of Protein-Protein Interactions (PPI) features, Gene Ontology (GO) terms, Genotype-Tissue Expression (GTEx) expression features, Gene-Friends co-expression features and protein sequence descriptors. Our findings suggested that features biased towards curated knowledge (i.e. GO terms and biological pathways), had the greatest predictive power, while unbiased features (mainly gene expression and co-expression data) have the least predictive power. Moreover, a combination of all the feature types diminished the predictive power compared to predictions based on curated knowledge. Feature importance analysis on the two most predictive classifiers mostly corroborated existing knowledge and supported recent findings linking CR to the Nuclear Factor Erythroid 2-Related Factor 2 (NRF2) signalling pathway and G protein-coupled receptors (GPCR). We then used the two strongest combinations of feature type and ML algorithm to predict CR-relatedness among ageing-related genes currently lacking CR-related annotations in the data, resulting in a set of promising candidate CR-related genes (GOT2, GOT1, TSC1, CTH, GCLM, IRS2 and SESN2) whose predicted CR-relatedness remain to be validated in future wet-lab experiments.

bioinformatics↗

Protecting synapses from amyloid β-associated degeneration by manipulations of Wnt/planar cell polarity signaling

Synapse loss is an early event in Alzheimers disease and is thought to be associated with amyloid pathology and caused by Amyloid {beta} (A{beta}) oligomers. Whether and how A{beta} oligomers directly target signaling pathways for glutamatergic synapse maintenance is unknown. Glutamatergic synapse development is controlled by the opposing functions of Celsr3 and Vangl2, core components of the Wnt/planar cell polarity (PCP) signaling pathway, functioning directly in the synapses. Celsr3 promotes synapse formation, whereas Vangl2 inhibits synapse formation. Here we show that oligomeric A{beta} binds to Celsr3 and assists Vangl2 in disassembling synapses by disrupting the intercellular Celsr3/Frizzled3-Celsr3 complex, essential for PCP signaling. Together with Vangl2, a Wnt receptor, Ryk, is also required for A{beta} oligomer-induced synapse loss in a mouse model of Alzheimers disease, 5XFAD, where conditional Ryk knockout protected synapses and preserved cognitive function. Our study reveals a fine balance of Wnt/PCP signaling components in glutamatergic synapse maintenance and suggests that overproduced A{beta} oligomers may lead to excessive synapse loss by tipping this balance. Together with previous reports that an inhibitor of Wnt/Ryk signaling, WIF1, is found reduced in Alzheimers disease patients, our results suggest that the imbalance of PCP signaling in these patients may contribute to synapse loss in Alzheimers disease and manipulating Wnt/PCP signaling may preserve synapses and cognitive function.

neuroscience↗