New carbapenemase inhibitors: clearing the way for the β-lactams

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.issue23es_ES
UDC.journalTitleInternational Journal of Molecular Scienceses_ES
UDC.startPage9308es_ES
UDC.volume21es_ES
dc.contributor.authorVázquez-Ucha, Juan Carlos
dc.contributor.authorArca-Suárez, Jorge
dc.contributor.authorBou, Germán
dc.contributor.authorBeceiro Casas, Alejandro
dc.date.accessioned2025-02-20T10:29:23Z
dc.date.available2025-02-20T10:29:23Z
dc.date.issued2020-12-06
dc.descriptionReviewes_ES
dc.description.abstract[Abstract] Carbapenem resistance is a major global health problem that seriously compromises the treatment of infections caused by nosocomial pathogens. Resistance to carbapenems mainly occurs via the production of carbapenemases, such as VIM, IMP, NDM, KPC and OXA, among others. Preclinical and clinical trials are currently underway to test a new generation of promising inhibitors, together with the recently approved avibactam, relebactam and vaborbactam. This review summarizes the main, most promising carbapenemase inhibitors synthesized to date, as well as their spectrum of activity and current stage of development. We particularly focus on β-lactam/β-lactamase inhibitor combinations that could potentially be used to treat infections caused by carbapenemase-producer pathogens of critical priority. The emergence of these new combinations represents a step forward in the fight against antimicrobial resistance, especially in regard to metallo-β-lactamases and carbapenem-hydrolysing class D β-lactamases, not currently inhibited by any clinically approved inhibitor.es_ES
dc.description.sponsorshipThis work was supported by Projects PI15/00860 and PI18/00501 awarded to G.B. and PI17/01482 and PI20/1212 to A.B., all within in the National Plan for Scientific Research, Development and Technological Innovation 2013–2016 and funded by the ISCIII—General Subdirection of Assessment and Promotion of the Research—European Regional Development Fund (FEDER) “A way of making Europe”. The study was also funded by project IN607A 2016/22 (GAIN-Agencia Gallega de Innovación—Consellería de Economía, Emprego e Industria) awarded to G.B. This work was also supported by Planes Nacionales de I + D + i 2008–2011/2013–2016 and Instituto de Salud Carlos III, Subdirección General de Redes y Centros de Investigación Cooperativa, Ministerio de Economía y Competitividad, Spanish Network for Research in Infectious Diseases (REIPI RD16/0016/006) co-financed by European Development Regional Fund “A way to achieve Europe” and operative program Intelligent Growth 2014–2020. J.A.-S. was financially supported by the Rio Hortega program (ISCIII, CM19/00219) and J.C.V.-U was financially supported by the pFIS program (ISCIII, PI17/01482).es_ES
dc.description.sponsorshipinfo:eu-repo/grantAgreement/MINECO/Programa Estatal de I+D+I Orientada a los Retos de la Sociedad/PI15%2F00860/ES/Desarrollo de una plataforma universal de vacunas bacterianas vivas atenuadas auxótrofas para D-glutamato: prevención y erradicación de infecciones por bacterias multirresistenteses_ES
dc.description.sponsorshipinfo:eu-repo/grantAgreement/ISCIII/Programa Estatal de Fomento de la Investigación Científica y Técnica de Excelencia/PI18%2F00501/ES/DISEÑO Y DESARROLLO DE UNA VACUNA PARA LA PREVENCION Y ERRADICACION DE LAS INFECCIONES RESPIRATORIAS AGUDAS Y CRONICAS (FIBROSIS QUISTICA) CAUSADAS POR PSEUDOMONAS AERUGINOSAes_ES
dc.description.sponsorshipinfo:eu-repo/grantAgreement/ISCIII/Programa Estatal de Fomento de la Investigación Científica y Técnica de Excelencia/PI17%2F01482/ES/EVALUACION DE NUEVAS ESTRATEGIAS ANTIMICROBIANAS MEDIANTE SILENCIAMIENTO DE ARN VEHICULIZADO EN NANOCAPSULAS E INHIBIDORES ENZIMATICOSes_ES
dc.description.sponsorshipInstituto de Salud Carlos III; PI20/1212es_ES
dc.description.sponsorshipXunta de Galicia; IN607A 2016/22es_ES
dc.identifier.citationVázquez-Ucha JC, Arca-Suárez J, Bou G, Beceiro A. New carbapenemase inhibitors: clearing the way for the β-lactams. Int J Mol Sci. 2020 Dec 6;21(23):9308.es_ES
dc.identifier.doi10.3390/ijms21239308
dc.identifier.issn1422-0067
dc.identifier.urihttp://hdl.handle.net/2183/41223
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relation.urihttps://doi.org/10.3390/ijms21239308es_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.subjectAntibiotic resistancees_ES
dc.subjectCarbapenem resistancees_ES
dc.subjectCarbapenemasees_ES
dc.subjectInhibitores_ES
dc.subjectMetallo-β-lactamaseses_ES
dc.subjectSerine-β-lactamaseses_ES
dc.titleNew carbapenemase inhibitors: clearing the way for the β-lactamses_ES
dc.typejournal articlees_ES
dspace.entity.typePublication
relation.isAuthorOfPublication909e08d1-6ed1-4b99-9e9e-c64eb72e7dea
relation.isAuthorOfPublication.latestForDiscovery909e08d1-6ed1-4b99-9e9e-c64eb72e7dea

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