{"title":"Genotypic Detection of New-Delhi Metallo-β-Lactamase Producing Carbapenem Resistant Escherichia coli in Holy Karbala Province-Iraq","authors":"Rasol Taqi, Oday Hadi","doi":"10.21608/eajbsc.2023.320708","DOIUrl":null,"url":null,"abstract":"Background: Carbapenem is a beta-lactam antibiotic that works similarly to Penicillins and Cephalosporins by binding to Penicillin-binding sites and subsequently inhibiting cell wall synthesis. Due to their high potency and extraordinarily broad antibacterial action, Carbapenem antibiotics, which belong to the most recent generation of β-lactam antibiotics, are frequently used in clinics to treat bacterial infections. The current study aimed to shed light on Escherichia coli 's resistance to β-lactam antibiotics, especially Carbapenem, and the potential link between Carbapenem resistance and the production of β-lactamase variants bla (NDM-1, NDM-2, NDM-3, NDM-4, NDM-5, GIM-1, VIM-1, SPM-1, and IMP-1) in Karbala province, Iraq. Materials and methods: Four hundred-eight isolates have been identified according to traditional methods (colonial morphology on MacConkey and Eosin methylene blue (EMB) agar, and biochemical reactions), and confirmed by the Vitek2® system. Carbapenem susceptibility was assayed by using the Vitek2® system. Isolates were subjected to multiplex PCR targeting β-lactamase variants genes. Results: Out of a total of 408 samples randomly collected from different clinical sources, 24 (19.51%) Escherichia coli isolates were diagnosed. Four (16.67%) of the Escherichia coli isolates tested positive for imipenem and meropenem resistance. PCR experiments indicated that only two (50%) isolates contained the blaNDM-1 gene and four (100%) carried the blaNDM-3 gene; no additional beta-lactamases were found.","PeriodicalId":52600,"journal":{"name":"Egyptian Academic Journal of Biological Sciences C Physiology and Molecular Biology","volume":"234 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Egyptian Academic Journal of Biological Sciences C Physiology and Molecular Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21608/eajbsc.2023.320708","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Carbapenem is a beta-lactam antibiotic that works similarly to Penicillins and Cephalosporins by binding to Penicillin-binding sites and subsequently inhibiting cell wall synthesis. Due to their high potency and extraordinarily broad antibacterial action, Carbapenem antibiotics, which belong to the most recent generation of β-lactam antibiotics, are frequently used in clinics to treat bacterial infections. The current study aimed to shed light on Escherichia coli 's resistance to β-lactam antibiotics, especially Carbapenem, and the potential link between Carbapenem resistance and the production of β-lactamase variants bla (NDM-1, NDM-2, NDM-3, NDM-4, NDM-5, GIM-1, VIM-1, SPM-1, and IMP-1) in Karbala province, Iraq. Materials and methods: Four hundred-eight isolates have been identified according to traditional methods (colonial morphology on MacConkey and Eosin methylene blue (EMB) agar, and biochemical reactions), and confirmed by the Vitek2® system. Carbapenem susceptibility was assayed by using the Vitek2® system. Isolates were subjected to multiplex PCR targeting β-lactamase variants genes. Results: Out of a total of 408 samples randomly collected from different clinical sources, 24 (19.51%) Escherichia coli isolates were diagnosed. Four (16.67%) of the Escherichia coli isolates tested positive for imipenem and meropenem resistance. PCR experiments indicated that only two (50%) isolates contained the blaNDM-1 gene and four (100%) carried the blaNDM-3 gene; no additional beta-lactamases were found.