Alejandro
Beceiro Casas
Hospital Universitario Son Espases
Palma, EspañaPublications in collaboration with researchers from Hospital Universitario Son Espases (22)
2024
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Impact of chromosomally encoded resistance mechanisms and transferable β-lactamases on the activity of cefiderocol and innovative β-lactam/β-lactamase inhibitor combinations against Pseudomonas aeruginosa
Journal of Antimicrobial Chemotherapy, Vol. 79, Núm. 10, pp. 2591-2597
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Impact of transferable β-lactamases and intrinsic AmpC amino acid substitutions on the activity of cefiderocol against wild-type and iron uptake-deficient mutants of Pseudomonas aeruginosa
The Journal of antimicrobial chemotherapy, Vol. 79, Núm. 11, pp. 3023-3028
2023
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Simultaneous and divergent evolution of resistance to cephalosporin/β-lactamase inhibitor combinations and imipenem/relebactam following ceftazidime/avibactam treatment of MDR Pseudomonas aeruginosa infections
The Journal of antimicrobial chemotherapy, Vol. 78, Núm. 5, pp. 1195-1200
2022
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Activity of cefiderocol, imipenem/relebactam, cefepime/taniborbactam and cefepime/zidebactam against ceftolozane/tazobactam- and ceftazidime/avibactam-resistant Pseudomonas aeruginosa
The Journal of antimicrobial chemotherapy, Vol. 77, Núm. 10, pp. 2809-2815
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Selection of AmpC β-Lactamase Variants and Metalloβ- Lactamases Leading to Ceftolozane/Tazobactam and Ceftazidime/Avibactam Resistance during Treatment of MDR/ XDR Pseudomonas aeruginosa Infections
Antimicrobial Agents and Chemotherapy, Vol. 66, Núm. 2
2021
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6-Halopyridylmethylidene Penicillin-Based Sulfones Efficiently Inactivate the Natural Resistance of Pseudomonas aeruginosa to β-Lactam Antibiotics
Journal of Medicinal Chemistry, Vol. 64, Núm. 9, pp. 6310-6328
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Molecular mechanisms driving the in vivo development of OXA-10-mediated resistance to ceftolozane/tazobactam and ceftazidime/avibactam during treatment of XDR Pseudomonas aeruginosa infections
The Journal of antimicrobial chemotherapy, Vol. 76, Núm. 1, pp. 91-100
2020
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Molecular and biochemical insights into the in vivo evolution of AmpC-mediated resistance to ceftolozane/tazobactam during treatment of an MDR Pseudomonas aeruginosa infection
The Journal of antimicrobial chemotherapy, Vol. 75, Núm. 11, pp. 3209-3217
2019
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Challenging antimicrobial susceptibility and evolution of resistance (oxa-681) during treatment of a long-term nosocomial infection caused by a pseudomonas aeruginosa ST175 Clone
Antimicrobial Agents and Chemotherapy, Vol. 63, Núm. 10
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Therapeutic Efficacy of LN-1-255 in Combination with Imipenem in Severe Infection Caused by Carbapenem-Resistant Acinetobacter baumannii
Antimicrobial Agents and Chemotherapy, Vol. 63, Núm. 10
2018
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Increased Antimicrobial Resistance in a Novel CMY-54 AmpC-Type Enzyme with a GluLeu217-218 Insertion in the Ω-Loop
Microbial Drug Resistance, Vol. 24, Núm. 5, pp. 527-533
2014
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Genetic and kinetic characterization of the novel AmpC β-lactamases DHA-6 and DHA-7
Antimicrobial Agents and Chemotherapy, Vol. 58, Núm. 11, pp. 6544-6549
2012
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Characterization of a novel IMP-28 metallo-β-lactamase from a Spanish Klebsiella oxytoca clinical isolate
Antimicrobial Agents and Chemotherapy, Vol. 56, Núm. 8, pp. 4540-4543
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Pan-β-lactam resistance development in Pseudomonas aeruginosa clinical strains: Molecular mechanisms, penicillin-binding protein profiles, and binding affinities
Antimicrobial Agents and Chemotherapy, Vol. 56, Núm. 9, pp. 4771-4778
2011
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False extended-spectrum β-lactamase phenotype in clinical isolates of escherichia coli associated with increased expression of OXA-1 or TEM-1 penicillinases and loss of porins
Journal of Antimicrobial Chemotherapy, Vol. 66, Núm. 9, pp. 2006-2010
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Phosphoethanolamine modification of lipid A in colistin-resistant variants of Acinetobacter baumannii mediated by the pmrAB two-component regulatory system
Antimicrobial Agents and Chemotherapy, Vol. 55, Núm. 7, pp. 3370-3379
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Role of changes in the L3 loop of the active site in the evolution of enzymatic activity of VIM-type metallo-β-lactamases-authors' response
Journal of Antimicrobial Chemotherapy
2010
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Clinical features of infections and colonization by Acinetobacter genospecies 3
Journal of Clinical Microbiology, Vol. 48, Núm. 12, pp. 4623-4626
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Role of changes in the L3 loop of the active site in the evolution of enzymatic activity of VIM-type metallo-β-lactamases
Journal of Antimicrobial Chemotherapy, Vol. 65, Núm. 9, pp. 1950-1954
2008
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Characterization of the new metallo-β-lactamase VIM-13 and its integron-borne gene from a Pseudomonas aeruginosa clinical isolate in Spain
Antimicrobial Agents and Chemotherapy, Vol. 52, Núm. 10, pp. 3589-3596