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Biology subjects

Silva, B. M.

Publications and source records attributed to Silva, B. M..

6 recordsLinked to original sources

NoiTox: A Machine Learning Strategy for Peptide Toxicity Prediction Reveals Label Noise in Benchmark Datasets

Motivation: Peptide toxicity remains a major bottleneck in drug development, as small sequence variations can drastically alter cytotoxic profiles. Experimental assessment is costly and time-consuming, motivating computational predictors. Existing approaches often rely on single black-box architectures, limiting interpretability and obscuring the contribution of individual sequence features. Furthermore, benchmark datasets frequently define the negative class through annotation filters rather than direct experimental evidence, introducing structural label noise that can compromises training and evaluation. Results: We present NoiTox, a multi-model strategy for peptide toxicity prediction integrating three complementary architectures, evaluated as four model variants: NoiToxML (Bo/full), an Extremely Randomized Trees classifier with Boruta-selected or complete physicochemical, compositional, and atomic descriptors; NoiToxDP, a deep learning model leveraging ESM-2 protein language model embeddings; and NoiToxGP, a graph neural network that combines ESM-2 residue embeddings, a fully connected residue graph with attention, and the Boruta descriptors as global features. Averaged over five random seeds, the models approached the state-of-the-art predictor ToxiPep on CD-HIT-controlled test sets, and on an independent dataset the interpretable NoiToxML variants and a probability-averaging consensus of the four models exceeded it, showing that physicochemical descriptors are highly informative for toxicity prediction. Cross-referencing negative-labeled sequences against curated databases of hemolytic, cytotoxic, and neurotoxic peptides flagged a small set annotated as toxic elsewhere, consistent with label noise by omission. However, removing the sequences that all models contradicted did not improve, and for some models reduced, ranking performance, indicating that such sequences carry useful information and are better treated as candidates for curation than discarded automatically. Availability and implementation: https://github.com/goalmeida05/NoiTox.

bioinformatics↗

Pipeasm: a tool for automated large chromosome-scale genome assembly and evaluation

MotivationWith increasing initiatives to study biodiversity through high-quality reference genomes and the growing capacity of sequencing a wide range of organisms, there is a pressing need for an accessible, reproducible, and user-friendly tool that incorporates state-of-the-art methodologies for large genome assembly. ResultsWe introduce Pipeasm, a Snakemake pipeline designed for assembling vertebrate genomes using HiFi PacBio, ONT, and HiC data. By setting a configuration file with input information and suggested parameters, Pipeasm was able to assemble multiple-sized diploid genomes ready for manual curation. Availability and ImplementationPipeasm requires an environment with Snakemake and Singularity and is available at https://github.com/itvgenomics/pipeasm.

bioinformatics↗

The virome of the invasive Asian bush mosquito Aedes japonicus in Europe

BackgroundThe Asian bush mosquito Aedes japonicus is rapidly invading North America and Europe. Due to its potential to transmit multiple pathogenic arthropod-borne (arbo)viruses including Zika virus, West Nile virus and chikungunya virus, it is important to understand the biology of this vector mosquito in more detail. In addition to arboviruses, mosquitoes can also carry insect-specific viruses that receive increasing attention due to their potential effects on host physiology and arbovirus transmission. In this study, we characterized the collection of viruses, referred to as the virome, circulating in Ae. japonicus populations in the Netherlands and France. ResultsApplying a small RNA-based metagenomic approach to Ae. japonicus, we uncovered a distinct group of viruses present in samples from both the Netherlands and France. These included one known virus, Ae. japonicus narnavirus 1 (AejapNV1), and three new virus species that we named Ae. japonicus totivirus 1 (AejapTV1), Ae. japonicus anphevirus 1 (AejapAV1) and Ae. japonicus bunyavirus 1 (AejapBV1). We also discovered sequences that were presumably derived from two additional novel viruses: Ae. japonicus bunyavirus 2 (AejapBV2) and Ae. japonicus rhabdovirus 1 (AejapRV1). All six viruses induced strong RNA interference responses, including the production of 21 nucleotide sized small interfering RNAs, a signature of active replication in the host. Notably, AejapBV1 and AejapBV2 belong to different viral families, however, no RNA-dependent RNA polymerase sequence has been found for AejapBV2. Intriguingly, our small RNA-based approach identified a [~]1 kb long ambigrammatic RNA that is associated with AejapNV1 as a secondary segment but showed no similarity to any sequence in public databases. We confirmed the presence of AejapNV1 primary and secondary segments, AejapTV1, AejapAV1 and AejapBV1 by reverse-transcriptase PCR in wild-caught Ae. japonicus mosquitoes. AejapNV1 and AejapTV1 were found at high prevalence (87-100%) in adult females, adult males and larvae. ConclusionsUsing a small RNA-based, sequence-independent metagenomic strategy, we uncovered a conserved and prevalent virome among Ae. japonicus mosquito populations. The high prevalence of AejapNV1 and AejapTV1 across all tested mosquito life stages suggests that these viruses are intimately associated with Ae. japonicus and may affect different aspects of the physiology of this vector mosquito.

microbiology↗

Targeting C5aR1 signaling reduced neutrophil extracellular traps and ameliorates COVID-19 pathology

Patients with severe COVID-19 develop acute respiratory distress syndrome (ARDS) that may progress to cytokine storm syndrome, organ dysfunction, and death. Considering that complement component 5a (C5a), through its cellular receptor C5aR1, has potent proinflammatory actions, and plays immunopathological roles in inflammatory diseases, we investigated whether C5a/C5aR1 pathway could be involved in COVID-19 pathophysiology. C5a/C5aR1 signaling increased locally in the lung, especially in neutrophils of critically ill COVID-19 patients compared to patients with influenza infection, as well as in the lung tissue of K18-hACE2 Tg mice (Tg mice) infected with SARS-CoV-2. Genetic and pharmacological inhibition of C5aR1 signaling ameliorated lung immunopathology in Tg-infected mice. Mechanistically, we found that C5aR1 signaling drives neutrophil extracellular trap (NET)s-dependent immunopathology. These data confirm the immunopathological role of C5a/C5aR1 signaling in COVID-19 and indicate that antagonist of C5aR1 could be useful for COVID-19 treatment.

immunology↗

Targeting Neutrophils Extracellular Traps (NETs) reduces multiple organ injury in a COVID-19 mouse model

COVID-19 is characterized by severe acute lung injury, which is associated with neutrophils infiltration and release of neutrophil extracellular traps (NETs). COVID-19 treatment options are scarce. Previous work has shown an increase in NETs release in the lung and plasma of COVID-19 patients suggesting that drugs that prevent NETs formation or release could be potential therapeutic approaches for COVID-19 treatment. Here, we report the efficacy of NET-degrading DNase I treatment in a murine model of COVID-19. DNase I decreased detectable levels of NETs, improved clinical disease, and reduced lung, heart, and kidney injuries in SARS-CoV-2-infected K18-hACE2 mice. Furthermore, our findings indicate a potential deleterious role for NETs lung tissue in vivo and lung epithelial (A549) cells in vitro, which might explain part of the pathophysiology of severe COVID-19. This deleterious effect was diminished by the treatment with DNase I. Together, our results support the role of NETs in COVID-19 immunopathology and highlight NETs disruption pharmacological approaches as a potential strategy to ameliorate COVID-19 clinical outcomes.

pharmacology and toxicology↗

Workflow for Protein N-terminal Acetylation and C-terminal Amidation Application using CcpNmr Analysis v2.4 Platform and Aria2.3 Structure Calculation Software

Structural biology is a field that enables a better understanding of proteins from scratch. From the available techniques, solution NMR is one well established that provides structure, dynamics and protein-molecules interaction. In a NMR lab routine, from data acquisition until protein/mechanisms elucidation comes a process that can undergo months. During the past decades, different tools were developed for NMR data processing, peaks assignment, structure elucidation and data submission. Since many of these programs demand great computational skills, a few groups have tried to combine those programs and make them more friendly and useful, what can possibilite a faster process. Here we highlight CCPNMR2.4 analysis and ARIA2.3, responsible for peak assignment and structure calculation, respectively, and can work associated. Although being academic free and the possibility of working with a GUI interface, the common N-terminal acetylation and C-terminal amidation modifications are not implemented in a way that possibilities to work with them in combination, what results in a dilemma. This work brings visual data that evidences the low usability of CCPN and ARIA with N-terminal acetylated and C-terminal amidated proteins and propose a workflow to overcome this problem, which may improve the usage of both software in the mentioned versions and facilitate the lab users already used to these programs. As a proof of concept, we have chosen a N-terminal amidated peptide, L-Phenylseptin, whose structure has already been solved with other programs. Statistical data shows that no significant difference was found with the structure obtained with the new protocol. In conclusion, we exhibit a new protocol that can be used in combination with CCPNMR2.4 and ARIA2.3 for protein with the mentioned modifications and it successfully works and manipulates these molecules.

bioinformatics↗