Plasmid-mediated quinolone resistance in gram-negative pathogens isolated from cancer patients in Egypt
dc.Affiliation | October University for modern sciences and Arts (MSA) | |
dc.contributor.author | Hamed S.M. | |
dc.contributor.author | Aboshanab K.M.A. | |
dc.contributor.author | El-Mahallawy H.A. | |
dc.contributor.author | Helmy M.M. | |
dc.contributor.author | Ashour M.S. | |
dc.contributor.author | Elkhatib W.F. | |
dc.contributor.other | Department of Microbiology and Immunology | |
dc.contributor.other | Faculty of Pharmacy | |
dc.contributor.other | October University for Modern Sciences and Arts | |
dc.contributor.other | Egypt; Department of Microbiology and Immunology | |
dc.contributor.other | Faculty of Pharmacy | |
dc.contributor.other | Ain Shams University | |
dc.contributor.other | African Union Organization | |
dc.contributor.other | Abbassia | |
dc.contributor.other | Cairo | |
dc.contributor.other | 11566 | |
dc.contributor.other | Egypt; Department of Clinical Pathology | |
dc.contributor.other | National Cancer Institute | |
dc.contributor.other | Cairo University | |
dc.contributor.other | Cairo | |
dc.contributor.other | Egypt; Department of Microbiology and Immunology | |
dc.contributor.other | Faculty of Medicine | |
dc.contributor.other | Zagazig University | |
dc.contributor.other | Zagazig | |
dc.contributor.other | Egypt; Department of Microbiology and Immunology | |
dc.contributor.other | Faculty of Pharmacy | |
dc.contributor.other | Al-Azhar University | |
dc.contributor.other | Cairo | |
dc.contributor.other | Egypt | |
dc.date.accessioned | 2020-01-09T20:40:51Z | |
dc.date.available | 2020-01-09T20:40:51Z | |
dc.date.issued | 2018 | |
dc.description | Scopus | |
dc.description.abstract | Fluoroquinolones (FQs) are the drugs of choice for prophylaxis of bacterial infections in immunocompromised cancer patients. This study aimed to investigate FQ resistance and the prevalence of plasmid-mediated quinolone resistance (PMQR) determinants in 239 Gram-negative isolates collected at a tertiary care cancer hospital in Cairo, Egypt. Disc diffusion and broth microdilution tests showed that 70.7% of the isolates were nonsusceptible to ciprofloxacin (MIC50 = 64 ?g/ml). Polymerase chain reaction (PCR) revealed that 53.6% of the isolates carried at least one PMQR determinant, of which 23.4% were susceptible to ciprofloxacin. The most prevalent gene, aac(6?)-Ib-cr, was identified in 36.8% of the isolates, while qnr genes were harbored by 31.0% (qnrS, 24.3%; qnrB, 7.1%, and qnrA, 0.4%). The oqxAB genes were only detected in Klebsiella sp. isolates (92.5%). PMQR determinants were more likely detectable among isolates recovered from pediatric patients than adults (59.3% vs. 43.8%) and were significantly associated with ceftriaxone and gentamicin resistance. A combined genetic analysis using random amplified polymorphic DNA-PCR and enterobacterial repetitive intergenic consensus-PCR showed that most of the qnr-positive isolates were not clonal. Findings of the current study raised concerns about the efficacy of prophylactic use of FQs in cancer patients in our region. It also demonstrates the possible role of PMQR-positive ciprofloxacin-susceptible isolates in the dissemination of resistance to other antimicrobial agents and the urgent need to reconsider the existing FQ breakpoints defined by the Clinical and Laboratory Standards Institute. � Copyright 2018, Mary Ann Liebert, Inc., publishers 2018. | en_US |
dc.description.uri | https://www.scimagojr.com/journalsearch.php?q=19034&tip=sid&clean=0 | |
dc.identifier.doi | https://doi.org/10.1089/mdr.2017.0354 | |
dc.identifier.doi | PubMed ID 29653475 | |
dc.identifier.issn | 10766294 | |
dc.identifier.other | https://doi.org/10.1089/mdr.2017.0354 | |
dc.identifier.other | PubMed ID 29653475 | |
dc.identifier.uri | https://t.ly/mp3lr | |
dc.language.iso | English | en_US |
dc.publisher | Mary Ann Liebert Inc. | en_US |
dc.relation.ispartofseries | Microbial Drug Resistance | |
dc.relation.ispartofseries | 24 | |
dc.subject | جامعة أكتوبر للعلوم الحديثة والآداب | |
dc.subject | University of Modern Sciences and Arts | |
dc.subject | MSA University | |
dc.subject | cancer patients | en_US |
dc.subject | Egypt | en_US |
dc.subject | fluoroquinolones | en_US |
dc.subject | Gram negative | en_US |
dc.subject | PMQR | en_US |
dc.subject | amikacin | en_US |
dc.subject | aminoglycoside | en_US |
dc.subject | carbapenem derivative | en_US |
dc.subject | ceftriaxone | en_US |
dc.subject | cephalosporin derivative | en_US |
dc.subject | ciprofloxacin | en_US |
dc.subject | gentamicin | en_US |
dc.subject | imipenem | en_US |
dc.subject | levofloxacin | en_US |
dc.subject | nalidixic acid | en_US |
dc.subject | norfloxacin | en_US |
dc.subject | quinolone derivative | en_US |
dc.subject | antiinfective agent | en_US |
dc.subject | beta lactamase | en_US |
dc.subject | ciprofloxacin | en_US |
dc.subject | quinolone derivative | en_US |
dc.subject | aac(6') 1b gene | en_US |
dc.subject | adult | en_US |
dc.subject | antibiotic resistance | en_US |
dc.subject | antibiotic sensitivity | en_US |
dc.subject | Article | en_US |
dc.subject | bacterial gene | en_US |
dc.subject | bacterium isolation | en_US |
dc.subject | broth dilution | en_US |
dc.subject | cancer center | en_US |
dc.subject | cancer patient | en_US |
dc.subject | disk diffusion | en_US |
dc.subject | Egypt | en_US |
dc.subject | gene identification | en_US |
dc.subject | genetic analysis | en_US |
dc.subject | Gram negative bacterium | en_US |
dc.subject | human | en_US |
dc.subject | in vitro study | en_US |
dc.subject | Klebsiella | en_US |
dc.subject | MIC50 | en_US |
dc.subject | minimum inhibitory concentration | en_US |
dc.subject | nonhuman | en_US |
dc.subject | OqxA gene | en_US |
dc.subject | oqxAB gene | en_US |
dc.subject | OqxB gene | en_US |
dc.subject | pediatric patient | en_US |
dc.subject | plasmid | en_US |
dc.subject | prevalence | en_US |
dc.subject | priority journal | en_US |
dc.subject | QepA gene | en_US |
dc.subject | qnr gene | en_US |
dc.subject | qnrA gene | en_US |
dc.subject | qnrB gene | en_US |
dc.subject | QnrS gene | en_US |
dc.subject | random amplified polymorphic DNA | en_US |
dc.subject | tertiary health care | en_US |
dc.subject | drug effect | en_US |
dc.subject | genetics | en_US |
dc.subject | Gram negative bacterium | en_US |
dc.subject | Gram negative infection | en_US |
dc.subject | isolation and purification | en_US |
dc.subject | microbial sensitivity test | en_US |
dc.subject | microbiology | en_US |
dc.subject | multidrug resistance | en_US |
dc.subject | neoplasm | en_US |
dc.subject | plasmid | en_US |
dc.subject | Anti-Bacterial Agents | en_US |
dc.subject | beta-Lactamases | en_US |
dc.subject | Ciprofloxacin | en_US |
dc.subject | Drug Resistance, Multiple, Bacterial | en_US |
dc.subject | Egypt | en_US |
dc.subject | Fluoroquinolones | en_US |
dc.subject | Genes, Bacterial | en_US |
dc.subject | Gram-Negative Bacteria | en_US |
dc.subject | Gram-Negative Bacterial Infections | en_US |
dc.subject | Humans | en_US |
dc.subject | Microbial Sensitivity Tests | en_US |
dc.subject | Neoplasms | en_US |
dc.subject | Plasmids | en_US |
dc.subject | Quinolones | en_US |
dc.title | Plasmid-mediated quinolone resistance in gram-negative pathogens isolated from cancer patients in Egypt | en_US |
dc.type | Article | en_US |
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