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Galan-Vasquez, E.

Publications and source records attributed to Galan-Vasquez, E..

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↗

RNA polymerases in strict endosymbiont bacteria with extreme genome reduction show distinct erosions that could result in limited and differential promoters recognition.

Strict endosymbiont bacteria with high degree of genome reduction retain smaller proteins and, in certain cases, lack complete functional domains compared to their free-living counterparts. Until now, the mechanisms underlying these genetic reductions are not well understood. However, it is thought that, in order to compensate for gene reduction, somehow hosts take over those vital functions that endosymbionts cannot perform. In the present study, the conservation of RNA polymerases, the essential machinery for gene expression, is analysed in bacteria with extreme genome reductions. For this purpose, comparative genomics, phylogenetic analysis and three-dimensional models of RNA polymerase subunits were done over four lineages of endosymbiotic proteobacteria with the smallest genomes known to date. Amino acids under positive selection in the subunit and loss of motifs in other subunits of RNA polymerase were observed. According to three-dimensional models, sites under positive selection might compensate the loss of motifs in subunit. In addition, variations in the {sigma} subunit were identified, some of them already studied in E. coli as a result of random mutagenesis. Amino acid changes in RNA polymerase suggest a possible modification in the binding specificity of the canonical -10 box (TATAAT) in some of these organisms. Furthermore, the {beta}-flap helix domain is absent in some Hodgkinia strains, as observed in RNA pol II of Archaea, thus lacking the capacity to bind to the -35 box. Here, we propose several RNA polymerases models for endosymbiont bacteria with extremely reduced genomes. Evidence suggests that RNA polymerases of each endosymbiont bacteria follow a unique evolutionary path, without necessarily following the same path as a lineage, this is probably influenced by the intimate interactions sustained with other endosymbionts and its hosts.

evolutionary biology↗