<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ma W</submitter><funding>Natural Science Foundation of Shandong Province</funding><funding>Cultivate Fund from The First Affiliated Hospital of Shandong First Medical University &amp; Shandong Provincial Qianfoshan Hospital</funding><funding>Clinical &amp;amp; Medical Science and Technology Innovation Program of Jinan</funding><funding>Cultivate Fund from The First Affiliated Hospital of Shandong First Medical University &amp;amp; Shandong Provincial Qianfoshan Hospital</funding><funding>Clinical &amp; Medical Science and Technology Innovation Program of Jinan</funding><pagination>471-480</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9998317</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>42(4)</volume><pubmed_abstract>The widespread of different NDM variants in clinical Enterobacterales isolates poses a serious public health concern, which requires continuous monitoring. In this study, three E. coli strains carrying two novel bla&lt;sub>NDM&lt;/sub> variants of bla&lt;sub>NDM-36, -37&lt;/sub> were identified from a patient with refractory urinary tract infection (UTI) in China. We conducted antimicrobial susceptibility testing (AST), enzyme kinetics analysis, conjugation experiment, whole-genome sequencing (WGS), and bioinformatics analysis to characterize the bla&lt;sub>NDM-36, -37&lt;/sub> enzymes and their carrying strains. The bla&lt;sub>NDM-36, -37&lt;/sub> harboring E. coli isolates belonged to ST227, O9:H10 serotype and exhibited intermediate or resistance to all β-lactams tested except aztreonam and aztreonam/avibactam</pubmed_abstract><journal>European journal of clinical microbiology &amp; infectious diseases : official publication of the European Society of Clinical Microbiology</journal><pubmed_title>Genetic and enzymatic characterization of two novel bla&lt;sub>NDM-36, -37&lt;/sub> variants in Escherichia coli strains.</pubmed_title><pmcid>PMC9998317</pmcid><funding_grant_id>QYPY2022NSFC0802</funding_grant_id><funding_grant_id>ZR2021MH078</funding_grant_id><funding_grant_id>202134040</funding_grant_id><pubmed_authors>Cheng F</pubmed_authors><pubmed_authors>Dong X</pubmed_authors><pubmed_authors>Chen L</pubmed_authors><pubmed_authors>Hao M</pubmed_authors><pubmed_authors>Cui X</pubmed_authors><pubmed_authors>Zhu B</pubmed_authors><pubmed_authors>Shi X</pubmed_authors><pubmed_authors>Ma W</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Niu S</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Wang W</pubmed_authors><pubmed_authors>Ma J</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genetic and enzymatic characterization of two novel bla&lt;sub>NDM-36, -37&lt;/sub> variants in Escherichia coli strains.</name><description>The widespread of different NDM variants in clinical Enterobacterales isolates poses a serious public health concern, which requires continuous monitoring. In this study, three E. coli strains carrying two novel bla&lt;sub>NDM&lt;/sub> variants of bla&lt;sub>NDM-36, -37&lt;/sub> were identified from a patient with refractory urinary tract infection (UTI) in China. We conducted antimicrobial susceptibility testing (AST), enzyme kinetics analysis, conjugation experiment, whole-genome sequencing (WGS), and bioinformatics analysis to characterize the bla&lt;sub>NDM-36, -37&lt;/sub> enzymes and their carrying strains. The bla&lt;sub>NDM-36, -37&lt;/sub> harboring E. coli isolates belonged to ST227, O9:H10 serotype and exhibited intermediate or resistance to all β-lactams tested except aztreonam and aztreonam/avibactam</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Apr</publication><modification>2025-05-29T20:46:54.17Z</modification><creation>2024-11-07T08:46:02.831Z</creation></dates><accession>S-EPMC9998317</accession><cross_references><pubmed>36810726</pubmed><doi>10.1007/s10096-023-04576-y</doi></cross_references></HashMap>