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Effect of diclofenac sodium on the expression levels of adhesion-related genes (asa1 and efaA) and the EfrAB efflux pump genes in enterococcal clinical isolates / Abeer Khaled Mokhtar Abuelazayem ; Supervised Heba Hamed Arnaout , Marwa Salah Mostafa , Maha Mahmoud Kotb

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Abeer Khaled Mokhtar Abuelazayem , 2019Description: 117 P. : charts , facimiles ; 25cmOther title:
  • فى المكورات المعوية السريرية EfrAB وجينات مضخات efaA و asa1 تأثير ديكلوفيناك الصوديوم على مستويات التعبير عن الجينات المرتبطة بالالتصاق
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Dissertation note: Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Microbiology and Immunology Summary: Antimicrobial drug resistance has become an emerging threat and a matter of concern worldwide. Many steps are being taken to reduce this problem, like gradually limiting antibiotics administration against pathogenic bacteria and searching for non-antibiotic compounds that have antibacterial activity through different mechanisms. The aim of this work was to evaluate the antibacterial effect of diclofenac sodium on enterococcal growth, ciprofloxacin resistance and biofilm forming ability. The effect of exposure of enterococcal isolates to diclofenac sodium on their expression of efflux pump genes (efrA and efrB) and adherence-related genes (asa1 and efaA) was also investigated. Fifty Enterococcal isolates were retrieved from 36 urine and 14 pus specimens. Antimicrobial activity of diclofenac and ciprofloxacin was determined by agar dilution method.Their effect on biofilm formation was determined by tissue culture plate method. The expression of asa1, efaA, efrA and efrB genes was determined by RT-PCR before and after exposure to diclofenac. Ciprofloxacin resistance was reported in 54% of the enterococcal isolates. Diclofenac was found to have antibacterial activity, as it inhibited the growth of enterococcal isolates at MIC of 400-800æg/ml. Although diclofenac induced a statistically significant reduction in the expression of efflux pump genes (efrA and efrB) (P < 0.001), it failed to reduce either ciprofloxacin resistance rate or ciprofloxacin MICs. Biofilm formation was reported in 64% of the isolates
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Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.19.Ph.D.2019.Ab.E (Browse shelf(Opens below)) Not for loan 01010110080251000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.19.Ph.D.2019.Ab.E (Browse shelf(Opens below)) 80251.CD Not for loan 01020110080251000

Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Microbiology and Immunology

Antimicrobial drug resistance has become an emerging threat and a matter of concern worldwide. Many steps are being taken to reduce this problem, like gradually limiting antibiotics administration against pathogenic bacteria and searching for non-antibiotic compounds that have antibacterial activity through different mechanisms. The aim of this work was to evaluate the antibacterial effect of diclofenac sodium on enterococcal growth, ciprofloxacin resistance and biofilm forming ability. The effect of exposure of enterococcal isolates to diclofenac sodium on their expression of efflux pump genes (efrA and efrB) and adherence-related genes (asa1 and efaA) was also investigated. Fifty Enterococcal isolates were retrieved from 36 urine and 14 pus specimens. Antimicrobial activity of diclofenac and ciprofloxacin was determined by agar dilution method.Their effect on biofilm formation was determined by tissue culture plate method. The expression of asa1, efaA, efrA and efrB genes was determined by RT-PCR before and after exposure to diclofenac. Ciprofloxacin resistance was reported in 54% of the enterococcal isolates. Diclofenac was found to have antibacterial activity, as it inhibited the growth of enterococcal isolates at MIC of 400-800æg/ml. Although diclofenac induced a statistically significant reduction in the expression of efflux pump genes (efrA and efrB) (P < 0.001), it failed to reduce either ciprofloxacin resistance rate or ciprofloxacin MICs. Biofilm formation was reported in 64% of the isolates

Issued also as CD

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