<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Blanco-Martin T</submitter><funding>Axencia Galega de Innovación (GAIN)</funding><funding>Centro de Investigación Biomédica en Red de Enfermedades Infecciosas</funding><funding>MEC | Instituto de Salud Carlos III</funding><funding>Axencia Galega de Innovación</funding><funding>MEC | Instituto de Salud Carlos III (ISCIII)</funding><funding>Centro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC)</funding><pagination>e0092424</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11539232</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>68(11)</volume><pubmed_abstract>We aimed to investigate the activity of and mechanisms of resistance to cefiderocol and innovative β-lactam/β-lactamase inhibitor combinations in a nationwide collection of double-carbapenemase-producing Enterobacterales. In all, 57 clinical isolates co-producing two carbapenemases collected from Spanish hospitals during the period 2017-2022 were analyzed. Minimum inhibitory concentration (MIC) values for ceftazidime, ceftazidime/avibactam, aztreonam, aztreonam/avibactam, aztreonam/nacubactam, cefiderocol, cefepime, cefepime/taniborbactam, cefepime/zidebactam, cefepime/nacubactam, imipenem, imipenem/relebactam, meropenem, meropenem/vaborbactam, meropenem/xeruborbactam, and meropenem/ANT3310 were determined by reference broth microdilution. Genetic drivers of resistance were analyzed by who</pubmed_abstract><journal>Antimicrobial agents and chemotherapy</journal><pubmed_title>Assessment of the activity and mechanisms of resistance to cefiderocol and combinations of β-lactams and the novel β-lactamase inhibitors avibactam, taniborbactam, zidebactam, nacubactam, xeruborbactam, and ANT3310 in emerging double-carbapenemase-producing Enterobacterales.</pubmed_title><pmcid>PMC11539232</pmcid><funding_grant_id>JR23/00036</funding_grant_id><funding_grant_id>CM21/00076</funding_grant_id><funding_grant_id>PI23/00851</funding_grant_id><funding_grant_id>PI22/01212</funding_grant_id><funding_grant_id>CM23/00104</funding_grant_id><funding_grant_id>IN607D 2021/12</funding_grant_id><funding_grant_id>IN607A 2016/22</funding_grant_id><funding_grant_id>JR21/00026</funding_grant_id><funding_grant_id>IN606A 2023/023</funding_grant_id><funding_grant_id>CB21/13/00012</funding_grant_id><funding_grant_id>CB21/13/00055</funding_grant_id><funding_grant_id>PI21/00704</funding_grant_id><funding_grant_id>PI20/01212</funding_grant_id><funding_grant_id>PI20/00686</funding_grant_id><funding_grant_id>CB21/13/00095</funding_grant_id><funding_grant_id>FI23/00074</funding_grant_id><funding_grant_id>IN606B 2022/009</funding_grant_id><funding_grant_id>CM23/00095</funding_grant_id><funding_grant_id>PMP22/00092</funding_grant_id><pubmed_authors>Aja-Macaya P</pubmed_authors><pubmed_authors>Aracil B</pubmed_authors><pubmed_authors>Oteo-Iglesias J</pubmed_authors><pubmed_authors>Gonzalez-Pinto L</pubmed_authors><pubmed_authors>Pascual A</pubmed_authors><pubmed_authors>Sanchez-Pena L</pubmed_authors><pubmed_authors>Lopez-Hernandez I</pubmed_authors><pubmed_authors>Rodriguez-Pallares S</pubmed_authors><pubmed_authors>Arca-Suarez J</pubmed_authors><pubmed_authors>Alonso-Garcia I</pubmed_authors><pubmed_authors>Blanco-Martin T</pubmed_authors><pubmed_authors>Perez-Vazquez M</pubmed_authors><pubmed_authors>Beceiro A</pubmed_authors><pubmed_authors>Bou G</pubmed_authors><pubmed_authors>Lopez-Cerero L</pubmed_authors><pubmed_authors>GEMARA-SEIMC/CIBERINFEC Study Group on the activity and resistance mechanisms to new β-lactams and β-lactamase inhibitors (PROTECT)</pubmed_authors><pubmed_authors>Outeda-Garcia M</pubmed_authors><pubmed_authors>Vazquez-Ucha JC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Assessment of the activity and mechanisms of resistance to cefiderocol and combinations of β-lactams and the novel β-lactamase inhibitors avibactam, taniborbactam, zidebactam, nacubactam, xeruborbactam, and ANT3310 in emerging double-carbapenemase-producing Enterobacterales.</name><description>We aimed to investigate the activity of and mechanisms of resistance to cefiderocol and innovative β-lactam/β-lactamase inhibitor combinations in a nationwide collection of double-carbapenemase-producing Enterobacterales. In all, 57 clinical isolates co-producing two carbapenemases collected from Spanish hospitals during the period 2017-2022 were analyzed. Minimum inhibitory concentration (MIC) values for ceftazidime, ceftazidime/avibactam, aztreonam, aztreonam/avibactam, aztreonam/nacubactam, cefiderocol, cefepime, cefepime/taniborbactam, cefepime/zidebactam, cefepime/nacubactam, imipenem, imipenem/relebactam, meropenem, meropenem/vaborbactam, meropenem/xeruborbactam, and meropenem/ANT3310 were determined by reference broth microdilution. Genetic drivers of resistance were analyzed by who</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2026-06-01T17:57:07.866Z</modification><creation>2025-07-14T03:02:42.221Z</creation></dates><accession>S-EPMC11539232</accession><cross_references><pubmed>39382274</pubmed><doi>10.1128/aac.00924-24</doi></cross_references></HashMap>