Rapid prediction of carbapenemases in Pseudomonas aeruginosa by imipenem/relebactam and MALDI-TOF MS
| UDC.coleccion | Investigación | es_ES |
| UDC.departamento | Fisioterapia, Medicina e Ciencias Biomédicas | es_ES |
| UDC.grupoInv | Investigación en Microbiología (INIBIC) | es_ES |
| UDC.institutoCentro | INIBIC - Instituto de Investigacións Biomédicas de A Coruña | es_ES |
| UDC.issue | 5 | es_ES |
| UDC.journalTitle | Journal of Clinical Microbiology | es_ES |
| UDC.startPage | e0110524 | es_ES |
| UDC.volume | 63 | es_ES |
| dc.contributor.author | Candela, Ana | |
| dc.contributor.author | Fernández-Billón, María | |
| dc.contributor.author | Aja-Macaya, Pablo | |
| dc.contributor.author | González-Pinto, Lucía | |
| dc.contributor.author | Fraile-Ribot, Pablo Arturo | |
| dc.contributor.author | Viedma, Esther | |
| dc.contributor.author | Alonso-García, Isaac | |
| dc.contributor.author | Blanco Martín, Tania | |
| dc.contributor.author | Estévez-Alfaya, Roberto | |
| dc.contributor.author | Fernández González, Ana | |
| dc.contributor.author | Beceiro Casas, Alejandro | |
| dc.contributor.author | López-Causapé, Carla | |
| dc.contributor.author | Oviaño, Marina | |
| dc.contributor.author | Bou, Germán | |
| dc.contributor.author | Oliver, Antonio | |
| dc.contributor.author | Arca-Suárez, Jorge | |
| dc.date.accessioned | 2025-06-03T10:46:28Z | |
| dc.date.available | 2025-06-03T10:46:28Z | |
| dc.date.issued | 2025-03-25 | |
| 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.sponsorship | This 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.sponsorship | info: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-TOF | es_ES |
| dc.description.sponsorship | info: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.sponsorship | info: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.sponsorship | info: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.sponsorship | info: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 AERUGINOSA | es_ES |
| dc.description.sponsorship | info: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 MODELO | es_ES |
| dc.description.sponsorship | Xunta de Galicia; IN607D2021/12 | es_ES |
| dc.description.sponsorship | Xunta de Galicia; IN607A 2016/22 | es_ES |
| dc.description.sponsorship | Xunta de Galicia; IN607D2024/008 | es_ES |
| dc.description.sponsorship | info: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 MePRAM | es_ES |
| dc.identifier.citation | Candela 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):e0110524 | es_ES |
| dc.identifier.doi | 10.1128/jcm.01105-24 | |
| dc.identifier.issn | 0095-1137 | |
| dc.identifier.uri | http://hdl.handle.net/2183/42144 | |
| dc.language.iso | eng | es_ES |
| dc.publisher | American Society of Microbiology | es_ES |
| dc.relation.uri | https://doi.org/10.1128/jcm.01105-24 | es_ES |
| dc.rights | Creative Commons Attribution 4.0 International License (CC-BY 4.0) | es_ES |
| dc.rights.accessRights | open access | es_ES |
| dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
| dc.subject | MALDI-TOF | es_ES |
| dc.subject | Pseudomonas aeruginosa | es_ES |
| dc.subject | Antimicrobial resistance | es_ES |
| dc.subject | Clinical microbiology | es_ES |
| dc.subject | Imipenem/relebactam | es_ES |
| dc.title | Rapid prediction of carbapenemases in Pseudomonas aeruginosa by imipenem/relebactam and MALDI-TOF MS | es_ES |
| dc.type | journal article | es_ES |
| dc.type.hasVersion | VoR | es_ES |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | 909e08d1-6ed1-4b99-9e9e-c64eb72e7dea | |
| relation.isAuthorOfPublication.latestForDiscovery | 909e08d1-6ed1-4b99-9e9e-c64eb72e7dea |
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