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Prevalence of Extended-Spectrum B-Lactamase (ESBL) and Quinolone Resistance (qnr) Genes among Cytotoxic Necrotizing Factor-۱-Producing Uropathogenic Escherichia coli in Babylon, Iraq

عنوان مقاله: Prevalence of Extended-Spectrum B-Lactamase (ESBL) and Quinolone Resistance (qnr) Genes among Cytotoxic Necrotizing Factor-۱-Producing Uropathogenic Escherichia coli in Babylon, Iraq
شناسه ملی مقاله: JR_IEM-9-3_006
منتشر شده در در سال 1402
مشخصات نویسندگان مقاله:

Haidar Qasim Raheem - DNA Research center, University of Babylon, Al-Karameh Street-۵۱۰۰۱, Babylon state, Iraq
Lamiaa Al-Maliki - Department of Molecular and Medical biotechnology, college of Biotechnology Al-Nahrain University
Mohammed Alaa Abdolzahra - Department of Pharmacy, Al-Amal College For Medical Specialized Sciences, Karbala-۵۶۰۰۱, Iraq
Thaer Shafi Hussein - Department of Pharmacy, Al-Amal College For Medical Specialized Sciences, Karbala-۵۶۰۰۱, Iraq

خلاصه مقاله:
Background: Pathogenic Escherichia coli (E. coli) is usually known as the principal agent of hospital-acquired infections, particularly those related to urinary tract infections (UTIs). The purpose of tThis study aimedwas to determine ESBL (extended-spectrum B-lactamase) production and quinolone resistance (qnr) genes in cytotoxic necrotizing factor ۱ (CNF-۱)- producing E. coli isolatesd from UTIs in Iraq. Materials & Methods: A total of ۹۹۶ E. coli isolates were obtained from UTIs infections in two general hospitals in Hillah, Babylon, Iraq (during ۲۰۱۴-۲۰۲۲), and ۱۰۰ uropathogenic E. coli (UPEC) were cnf-۱ gene carriers. ESBL production was evaluated using the double-disk synergy -test. The qnr genes were detected using polymerase chain reaction (PCR). Findings: Nalidixic acid and chloramphenicol resistance wasincluded ۷۰% and ۳۰%, respectively. ESBL production was observed among ۴۶% of cnf-۱ -carriers isolates. The qnrA, qnrB, and qnrS genes were detected in ۱۸%, ۲۱%, and ۱۱% of the isolates, respectively. ESBL-producing isolates mainly carried the qnrB gene and showedhad the highest resistance levels to quinolones. Major risk factors of pathogenic E. coli isolation included older age (۶۸%, p= ۰.۰۳۱), previous hospitalization (۷۶%, p= ۰.۰۲۱), and urinary catheter (۸۳%, p= ۰.۰۱۸). Conclusion: Although the prevalenceexistence of the cnf-۱ gene was not high among UPEC isolates, its prevalencerate was high among quinolone-resistant and ESBL-producing isolates. The cContinuous investigation of virulence and resistance genes is essential tfor monitoring and controlling the infections and facilitate their control. ItMore investigation is necessary to determine the virulence  traits factors and resistance genes among UPEC in Iraq and to take in timely measures action to hinder the spread of resistance genes from spreading to other nosocomial isolates.

کلمات کلیدی:
UTIs, Virulence, Antibiotics, Quinolone resistance, Escherichia coli, ESBL

صفحه اختصاصی مقاله و دریافت فایل کامل: https://civilica.com/doc/1873314/