Rapid prediction of carbapenemases in Pseudomonas aeruginosa by imipenem/relebactam and MALDI-TOF MS

UDC.coleccionInvestigaciónes_ES
UDC.departamentoFisioterapia, Medicina e Ciencias Biomédicases_ES
UDC.grupoInvInvestigación en Microbiología (INIBIC)es_ES
UDC.institutoCentroINIBIC - Instituto de Investigacións Biomédicas de A Coruñaes_ES
UDC.issue5es_ES
UDC.journalTitleJournal of Clinical Microbiologyes_ES
UDC.startPagee0110524es_ES
UDC.volume63es_ES
dc.contributor.authorCandela, Ana
dc.contributor.authorFernández-Billón, María
dc.contributor.authorAja-Macaya, Pablo
dc.contributor.authorGonzález-Pinto, Lucía
dc.contributor.authorFraile-Ribot, Pablo Arturo
dc.contributor.authorViedma, Esther
dc.contributor.authorAlonso-García, Isaac
dc.contributor.authorBlanco Martín, Tania
dc.contributor.authorEstévez-Alfaya, Roberto
dc.contributor.authorFernández González, Ana
dc.contributor.authorBeceiro Casas, Alejandro
dc.contributor.authorLópez-Causapé, Carla
dc.contributor.authorOviaño, Marina
dc.contributor.authorBou, Germán
dc.contributor.authorOliver, Antonio
dc.contributor.authorArca-Suárez, Jorge
dc.date.accessioned2025-06-03T10:46:28Z
dc.date.available2025-06-03T10:46:28Z
dc.date.issued2025-03-25
dc.description.abstract[Abstract] Pseudomonas aeruginosa is a major nosocomial pathogen commonly involved in multidrug-resistant (MDR) infections that are very difficult to treat. Imipenem/relebactam is a new carbapenem/β-lactamase inhibitor combination with robust activity against P. aeruginosa. However, resistance is increasingly reported, and rapid detection is, therefore, crucial so that appropriate treatments can be prescribed. We have developed a rapid MALDI TOF-MS-based method that can accurately predict the presence of carbapenemases in P. aeruginosa using imipenem/relebactam. The method was developed using a retrospective and a prospective collection of 419 P. aeruginosa isolates (including recombinant isolates and WGS-characterized clinical strains) encompassing the most important β-lactam resistance mechanisms. The MALDI TOF-MS method is based on the detection of the hydrolysis of imipenem in the presence or absence of relebactam, measuring modifications in the mass spectra of imipenem after incubation with bacteria. The method was evaluated against a retrospective collection and then validated against 250 prospectively collected clinical isolates, showing a 98% (246/250) agreement between the phenotype and the MALDI-TOF MS hydrolysis result and a 100% accordance with the β-lactam resistance genotype. Some errors in detecting GES-producing isolates and in detecting different mutational resistance mechanisms associated with imipenem/relebactam resistance (MICs ranging from 4 to 8 mg/L) were observed. All results were obtained within 1 hour, positioning the MALDI-TOF-based test as a rapid and easy-to-perform method for detection of carbapenemases (except GES enzymes) in P. aeruginosa. Besides, implementation of the method in routine laboratory screening would facilitate the correct use of imipenem/relebactam to treat P. aeruginosa infections.IMPORTANCEWhile several rapid diagnostic methods have been developed for the detection of ESBLs and carbapenemases to improve treatment decision-making in Enterobacterales, there is a lack of approaches to rapidly identify resistance mechanisms and predict β-lactam susceptibility in Pseudomonas aeruginosa. Taking advantage of the mechanism of action and the high efficacy of the newly developed β-lactam/β-lactamase inhibitor combination imipenem/relebactam against P. aeruginosa, we developed a WGS-guided, MALDI-TOF-based algorithm that accurately predicts the presence of carbapenemase enzymes in this bacterium and aids in forecasting the imipenem/relebactam susceptibility profile. The implementation of this method in routine laboratory testing would provide significant support in the rapid decision-making for the use of imipenem/relebactam in severe P. aeruginosa infections.es_ES
dc.description.sponsorshipThis work was supported by the Instituto de Salud Carlos III through the projects: PI20/00686, PI23/00851, PI22/01212, PI20/01212, PI21/00017, and PI21/00704) and co-funded by the European Union. It was also supported by Merck Sharp & Dohme (MSD), through the Investigator Initiated Studies Program, and funded by the Centro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC: CB21/13/00055, and CB/13/00099). The study was also funded by the Axencia Galega de Innovación (GAIN), Consellería de Innovación, Consellería deEmprego de Emprego e Industria (IN607D2021/12 to A.B., IN607A 2016/22 to G.B. and IN607D2024/008 to J.A.-S.) and futherfurther supported by Personalized and precision medicine grant from the Instituto de Salud Carlos III (MePRAM Project, PMP22/00092), Instituto de Salud Carlos III, Ministerio de Ciencia e Innovación. A.C. was financially supported by the Río Hortega program (ISCIII-SERGAS, CM21/00165). M.F.-B. was financially supported by the Río Hortega program (CM23/00127). T.B.-M. was financially supported by the Río Hortega program (ISCIII, CM23/00095). L.G.-P. was financially supported by the PFIS program (ISCIII, FI23/00074). I.A.-G. was financially supported by the Juan Rodés program (ISCIII, JR23/00036). J.A.-S. was financially supported by the Juan Rodés program (ISCIII, JR21/00026). The Fundación Pública Galega de Investigación Biomédica INIBIC has paid the charges for the open access of the manuscript.es_ES
dc.description.sponsorshipinfo:eu-repo/grantAgreement/ISCIII/Programa Estatal de Generación de Conocimiento y Fortalecimiento del Sistema Español de I+D+I/PI20%2F00686/ES/DETECCION RAPIDA DE RESISTENCIAS ANTIBIOTICAS MEDIANTE ESPECTROMETRIA DE MASAS MALDI-TOFes_ES
dc.description.sponsorshipinfo:eu-repo/grantAgreement/ISCIII/Programa Estatal para impulsar la investigación científico-técnica y su transferencia/PI23%2F00851/ES/Actividad in vivo de nuevos inhibidores de carbapenemasas frente a patógenos críticos multirresistentes: K. pneumoniae productor de carbapenemasas y P. aeruginosa.es_ES
dc.description.sponsorshipinfo:eu-repo/grantAgreement/ISCIII/Programa Estatal para Impulsar la Investigación Científico-Técnica y su Transferencia/PI22%2F01212/ES/Inhibidores de carbapenemasas: actividad frente a Enterobacterales productores de carbapenemasas, mecanismos e impacto en la evolución de la resistencia antimicrobiana (PROTECT)es_ES
dc.description.sponsorshipinfo:eu-repo/grantAgreement/ISCIII/Programa Estatal de Generación de Conocimiento y Fortalecimiento del Sistema Español de I+D+I/PI20%2F01212/ES/DESARROLLO Y EVALUACION DE NUEVAS MOLECULAS ANTIMICROBIANAS DIRIGIDAS A PATOGENOS MULTIRRESISTENTES (INHIBIDORES DE ß-LACTAMASAS Y CONJUGADOS TETRACICLINAS-SIDEROFOROS). ESTUDIO NACIONAL ACINETOBACTER SPP.es_ES
dc.description.sponsorshipinfo:eu-repo/grantAgreement/ISCIII/Programa Estatal de Generación de Conocimiento y Fortalecimiento del Sistema Español de I+D+I/PI21%2F00017/ES/MONITORIZACION PERSONALIZADA DE LA RESISTENCIA A LOS ANTIBIOTICOS A TRAVES DE LA DETERMINACIÓN DE LA DINAMICA IN VIVO DEL RESISTOMA DE PSEUDOMONAS AERUGINOSAes_ES
dc.description.sponsorshipinfo:eu-repo/grantAgreement/ISCIII/Programa Estatal de Generación de Conocimiento y Fortalecimiento del Sistema Español de I+D+I/PI21%2F00704/ES/VACUNAS AUXOTROFAS ORALES PARA LA ERRADICACION DE BACTERIAS INTESTINALES: COLONIZACIÓN INTESTINAL POR KLEBSIELLA PNEUMONIAE MULTIRRESISTENTE COMO MODELOes_ES
dc.description.sponsorshipXunta de Galicia; IN607D2021/12es_ES
dc.description.sponsorshipXunta de Galicia; IN607A 2016/22es_ES
dc.description.sponsorshipXunta de Galicia; IN607D2024/008es_ES
dc.description.sponsorshipinfo:eu-repo/grantAgreement/ISCIII/Programa Estatal Para Afrontar las Prioridades de Nuestro Entorno/PMP22%2F00092/ES/La medicina de precisión contra la resistencia a antimicrobianos: Proyecto MePRAMes_ES
dc.identifier.citationCandela A, Fernández-Billón M, Aja-Macaya P, González-Pinto L, Fraile-Ribot PA, Viedma E, Alonso-García I, Blanco-Martín T, Estévez-Alfaya R, Fernández-González A, Beceiro A, López-Causapé C, Oviaño M, Bou G, Oliver A, Arca-Suárez J. Rapid prediction of carbapenemases in Pseudomonas aeruginosa by imipenem/relebactam and MALDI-TOF MS. J Clin Microbiol. 2025 May 14;63(5):e0110524es_ES
dc.identifier.doi10.1128/jcm.01105-24
dc.identifier.issn0095-1137
dc.identifier.urihttp://hdl.handle.net/2183/42144
dc.language.isoenges_ES
dc.publisherAmerican Society of Microbiologyes_ES
dc.relation.urihttps://doi.org/10.1128/jcm.01105-24es_ES
dc.rightsCreative Commons Attribution 4.0 International License (CC-BY 4.0)es_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectMALDI-TOFes_ES
dc.subjectPseudomonas aeruginosaes_ES
dc.subjectAntimicrobial resistancees_ES
dc.subjectClinical microbiologyes_ES
dc.subjectImipenem/relebactames_ES
dc.titleRapid prediction of carbapenemases in Pseudomonas aeruginosa by imipenem/relebactam and MALDI-TOF MSes_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublication909e08d1-6ed1-4b99-9e9e-c64eb72e7dea
relation.isAuthorOfPublication.latestForDiscovery909e08d1-6ed1-4b99-9e9e-c64eb72e7dea

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