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Nicolas, M. F.

Publications and source records attributed to Nicolas, M. F..

2 recordsLinked to original sources

Transcriptional Profiling and Co-expression Integration for the Filtering of Relevant Bacterial sRNA-mRNA Interactions: Application to Staphylococcus aureus Biofilm

Small regulatory RNAs (sRNAs) are fast-acting non-coding RNAs (ncRNAs), stress-responsive regulators that fine-tune bacterial gene expression, shaping virulence, antimicrobial resistance, metabolism, and biofilm development. At the post-transcriptional level, sRNAs pair with target mRNAs to block or enhance translation, remodel secondary structures, adjust transcript stability, and act as molecular sponges for other sRNAs. Staphylococcus aureus, a leading cause of hospital-acquired infections, relies on a multiple-layered regulatory network, including post-transcriptional mechanisms, to transition between planktonic and biofilm lifestyles. Here, we expand the cross-lineage sRNA repertoire of S. aureus by integrating newly generated RNA-seq data from the Brazilian ST239 strain Bmb9393 with public datasets from five USA-lineage strains previously uncharacterized for sRNAs. Using sequence homology and covariance models, we predicted and annotated candidate sRNA loci across all analyzed genomes, quantified their expression under planktonic and biofilm conditions, and assigned genomic context. Integration of differential-expression (DE) profiles with weighted gene co-expression network analysis (WGCNA) identified sRNAs associated with biofilm and virulence, in modules that include well-known regulators (sarA, mgrA, RNAIII) and the adhesin clfA. To prioritize functional target interactions, we combined DEG concordance, network features, and interaction-energy thresholds, depleting millions of initial predictions to thousands of high-confidence sRNA-mRNA pairs. Our integrative bioinformatics framework provides additional insights into sRNA-mediated regulation in S. aureus, highlighting biofilm- and resistance-linked candidates, and yields a ranked, reusable set of sRNA-mRNA interactions to guide hypothesis-driven experiments across diverse genetic backgrounds.

bioinformatics↗

CellHeap: A scRNA-seq workflow for large-scalebioinformatics data analysis

AbstractO_ST_ABSBackgroundC_ST_ABSSeveral hundred terabytes of single-cell RNA-seq (scRNA-seq) data are available in public repositories. These data refer to various research projects, from microbial population cells to multiple tissues, involving patients with a myriad of diseases and comorbidities. An increase to several Petabytes of scRNA-seq data available in public repositories is a realistic prediction for coming years. Therefore, thoughtful analysis of these data requires large-scale computing infrastructures and software systems optimized for such platforms to generate correct and reliable biological knowledge. ResultsThis paper presents CellHeap, a flexible, portable, and robust platform for analyzing large scRNA-seq datasets, with quality control throughout the execution steps, and deployable on platforms that support large-scale data, such as supercomputers or clouds. As a case study, we designed a workflow to study particular modulations of Fc receptors, considering mild and severe cases of COVID-19. This workflow, deployed in the Brazilian Santos Dumont supercomputer, processed dozens of Terabytes of COVID-19 scRNA-seq raw data. Our results show that most of the workflow total execution time is spent in its initial phases and that there is great potential for a parallel solution to speed up scRNA-seq data analysis significantly. Thus, this workflow includes an efficient solution to use parallel computational resources, improving total execution time. Our case study showed increased Fc receptors transcription in macrophages of patients with severe COVID-19 symptoms, especially FCGR1A, FCGR2A, and FCGR3A. Furthermore, diverse molecules associated with their signaling pathways were upregulated in severe cases, possibly associated with the prominent inflammatory response observed. ConclusionFrom the CellHeap platform, different workflows capable of analyzing large scRNA-seq datasets can be generated. Our case study, a workflow designed to study particular modulations of Fc receptors, considering mild and severe cases of COVID-19, deployed on the Brazilian supercomputer Santos Dumont, had a substantial reduction in total execution time when jobs are triggered simultaneously using the parallelization strategy described in this manuscript. Regarding biological results, our case study identified specific modulations comparing healthy individuals with COVID-19 patients with mild or severe symptoms, revealing an upregulation of several inflammatory pathways and an increase in the transcription of Fc receptors in severe cases.

bioinformatics↗