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Biology subjects

Marques, M. M.

Publications and source records attributed to Marques, M. M..

2 recordsLinked to original sources

Omics analysis of MRSA under antibiotic stress identifies conserved adaptive modules and candidate adjuvant targets

Methicillin-resistant Staphylococcus aureus (MRSA) survives antibiotic exposure through coordinated physiological adaptation that extends beyond canonical resistance determinants. Here, we used an untargeted multi-omics strategy integrating proteomics, post-translational modifications, and metabolomics to characterize MRSA ATCC 43300 responses to five mechanistically distinct antibiotics: ampicillin, methicillin, vancomycin, chloramphenicol, and ciprofloxacin. Cells were exposed to 0.5x, 1x, and 2x IC50, enabling comparison of graded stress responses across antibiotic classes. Across treatments, MRSA did not deploy fully distinct drug-specific programs. Instead, antibiotic exposure repeatedly converged on a limited set of conserved adaptive modules detectable across independent molecular layers. These included coupling of envelope stress with genome maintenance, recurrent remodeling of metal/cofactor and redox homeostasis, sustained pressure on nucleotide and folate metabolism, and reprogramming of transport and surface-associated functions. A particularly robust cross-antibiotic signature was the accumulation of MoO2-molybdopterin cofactor. Ciprofloxacin additionally induced compensatory envelope reinforcement, supporting tight coupling between DNA damage responses and cell-envelope maintenance. Overall, the data support a unified model in which MRSA buffers mechanistically distinct antibiotic stress through a compact set of conserved stress-response functions rather than through entirely separate adaptive programs. These recurrent modules highlight candidate adjuvant vulnerabilities, particularly in metal/cofactor handling, nucleotide supply and repair, and transport/envelope compensation pathways. As this was an exploratory design intended to identify candidate adaptive patterns, these vulnerabilities now require validation in biologically replicated cultures and targeted functional studies.

microbiology↗

p73 controls cell junction dynamics during sprouting angiogenesis and acts via Angiomotin

Preservation of blood vessels integrity, which is critical for normal physiology and organ function, is controlled at multiple levels, including endothelial junctions. However, the mechanism that controls the adequate assembly of endothelial cell junctions is not fully defined. Here we uncover TAp73 transcription factor as a vascular architect that orchestrates transcriptional programs involved in cell junction establishment and developmental blood vessel morphogenesis and identify Angiomotin (AMOT) as a TAp73 direct transcriptional target. Knockdown of p73 in endothelial cells not only results in decreased Angiomotin expression and localization at intercellular junctions, but also affects its downstream function regarding Yes-Associated Protein (YAP) cytoplasmic sequestration upon cell-cell contact. Analysis of adherens junctional morphology after p73-knockdown in human endothelial cells revealed striking alterations, particularly a sharp increase in serrated junctions and actin bundles appearing as stress fibers, both features associated with enhanced barrier permeability. In turn, stabilization of Angiomotin levels rescued those junctional defects, confirming that TAp73 controls endothelial junction dynamics, at least in part, through the regulation of Angiomotin. The observed defects in monolayer integrity were linked to hyperpermeability and reduced transendothelial electric resistance. Moreover, p73-knockout retinas showed a defective sprout morphology coupled to hemorrhages, highlighting the physiological relevance of p73 regulation in the maintenance of vessel integrity in vivo. We propose a new model in which TAp73 acts as a vascular architect integrating transcriptional programs that will impinge with Angiomotin/YAP signaling to maintain junctional dynamics and integrity, whilst balancing endothelial cell rearrangements in angiogenic vessels.

cell biology↗