RT Journal Article T1 Multiomics Assessment of Gene Expression in a Clinical Strain of CTX-M-15-Producing ST131 Escherichia coli A1 Pinto, Luís A1 Torres, Carmen A1 Gil, Concha A1 Nunes-Miranda, Júlio D A1 Santos, Hugo M A1 Borges, Vítor A1 Gomes, João P A1 Silva, Catarina A1 Vieira, Luís A1 Pereira, José E A1 Poeta, Patrícia A1 Igrejas, Gilberto AB Extended-spectrum beta-lactamase (ESBL)-producing strain C999 was isolated of a Spanish patient with urinary tract infection. Previous genotyping indicated that this strain presented a multidrug-resistance phenotype and carried beta-lactamase genes encoding CTX-M-15, TEM-1, and OXA-1 enzymes. The whole-cell proteome, and the membrane, cytoplasmic, periplasmic and extracellular sub-proteomes of C999 were obtained in this work by two-dimensional gel electrophoresis (2DE) followed by fingerprint sequencing through matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF/MS). A total of 602 proteins were identified in the different cell fractions, several of which are related to stress response systems, cellular responses, and antibiotic and drug responses, consistent with the multidrug-resistance phenotype. In parallel, whole genome sequencing (WGS) and RNA sequencing (RNA-Seq) was done to identify and quantify the genes present and expressing. The prediction following WGS confirmed our strain as being serotype O25:H4 and sequence type ST131. The presence of proteins related to antibiotic resistance and virulence in an O25:H4-ST131 clone are serious indicators of the continued threat of antibiotic resistance spread amongst healthcare institutions. On a positive note, a multiomics approach can facilitate surveillance and more detailed characterization of virulent bacterial clones from hospital environments. PB Frontiers Media SN 1664-302X YR 2019 FD 2019-05-03 LK https://hdl.handle.net/20.500.14352/13381 UL https://hdl.handle.net/20.500.14352/13381 LA eng NO Fundação para a Ciência e a Tecnologia and European Social Fund DS Docta Complutense RD 3 may 2024