<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hobson CA</submitter><funding>ARC (association recherche contre le cancer) foundation</funding><funding>Fondation pour la Recherche Médicale</funding><pagination>e0044722</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9487638</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>66(9)</volume><pubmed_abstract>First variants of the Klebsiella pneumoniae carbapenemase (KPC), KPC-2 and KPC-3, have encountered a worldwide success, particularly in K. pneumoniae isolates. These beta-lactamases conferred resistance to most beta-lactams including carbapenems but remained susceptible to new beta-lactam/beta-lactamase inhibitors, such as ceftazidime-avibactam. After the marketing of ceftazidime-avibactam, numerous variants of KPC resistant to this association have been described among isolates recovered from clinical samples or derived from experimental studies. In KPC variants resistant to ceftazidime-avibactam, point mutations, insertions and/or deletions have been described in various hot spots. Deciphering the impact of these mutations is crucial, not only from a therapeutic point of view, but also t</pubmed_abstract><journal>Antimicrobial agents and chemotherapy</journal><pubmed_title>Klebsiella pneumoniae Carbapenemase Variants Resistant to Ceftazidime-Avibactam: an Evolutionary Overview.</pubmed_title><pmcid>PMC9487638</pmcid><funding_grant_id>EQU201903007848</funding_grant_id><funding_grant_id>DOC20190509066</funding_grant_id><pubmed_authors>Birgy A</pubmed_authors><pubmed_authors>Jacquier H</pubmed_authors><pubmed_authors>Pierrat G</pubmed_authors><pubmed_authors>Jaouen E</pubmed_authors><pubmed_authors>Hobson CA</pubmed_authors><pubmed_authors>Bonacorsi S</pubmed_authors><pubmed_authors>Bercot B</pubmed_authors><pubmed_authors>Tenaillon O</pubmed_authors></additional><is_claimable>false</is_claimable><name>Klebsiella pneumoniae Carbapenemase Variants Resistant to Ceftazidime-Avibactam: an Evolutionary Overview.</name><description>First variants of the Klebsiella pneumoniae carbapenemase (KPC), KPC-2 and KPC-3, have encountered a worldwide success, particularly in K. pneumoniae isolates. These beta-lactamases conferred resistance to most beta-lactams including carbapenems but remained susceptible to new beta-lactam/beta-lactamase inhibitors, such as ceftazidime-avibactam. After the marketing of ceftazidime-avibactam, numerous variants of KPC resistant to this association have been described among isolates recovered from clinical samples or derived from experimental studies. In KPC variants resistant to ceftazidime-avibactam, point mutations, insertions and/or deletions have been described in various hot spots. Deciphering the impact of these mutations is crucial, not only from a therapeutic point of view, but also t</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2026-06-13T06:11:35.789Z</modification><creation>2025-04-05T23:29:31.664Z</creation></dates><accession>S-EPMC9487638</accession><cross_references><pubmed>35980232</pubmed><doi>10.1128/aac.00447-22</doi></cross_references></HashMap>