Assessment of Antibiotic Resistance Genes in Escherichia coli Isolates from Hospital Environments

Assessment of Antibiotic Resistance Genes in Escherichia coli Isolates from Hospital Environments


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نویسندگان: رضا قوطاسلو , سودا ذوقی , حامد ابراهیم زاده لیل آبادلو

عنوان کنگره / همایش: 24th Iran's International Congress of Microbiology , , تهران , 2023

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نویسنده ثبت کننده مقاله حامد ابراهیم زاده لیل آبادلو
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه بیماری های گوارش و کبد
کد مقاله 83113
عنوان فارسی مقاله Assessment of Antibiotic Resistance Genes in Escherichia coli Isolates from Hospital Environments
عنوان لاتین مقاله Assessment of Antibiotic Resistance Genes in Escherichia coli Isolates from Hospital Environments
نوع ارائه پوستر
عنوان کنگره / همایش 24th Iran's International Congress of Microbiology
نوع کنگره / همایش بین المللی
کشور محل برگزاری کنگره/ همایش
شهر محل برگزاری کنگره/ همایش تهران
سال انتشار/ ارائه شمسی 1402
سال انتشار/ارائه میلادی 2023
تاریخ شمسی شروع و خاتمه کنگره/همایش 1402/06/27 الی 1402/06/29
آدرس لینک مقاله/ همایش در شبکه اینترنت
آدرس علمی (Affiliation) نویسنده متقاضی Liver and Gastrointestinal Diseases Research Center, Tabriz University of Medical Sciences, Tabriz, Iran

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نویسنده نفر چندم مقاله
رضا قوطاسلواول
سودا ذوقیدوم
حامد ابراهیم زاده لیل آبادلوسوم

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عنوان متن
کلمات کلیدیE. coli, antibiotic resistant genes, PCR, Azerbaijan, Iran
خلاصه مقالهBACKGROUND AND OBJECTIVES Antibiotic resistance increases the prolonged consequences and mortality caused by E. coli infections. The emergence and expression of resistant genes is a potential factor for the stability of this pathogen against antibiotics. Hence, the present study was designed to investigate the prevalence of antibiotic resistance genes in E. coli isolates from Tabriz, Iran. MATERIALS AND METHODS In this study, 141 females and 78 males aged 1 to 89 from surgery, internal, intensive care unit, and pediatric wards of Tabriz hospitals were enrolled. E. coli was isolated from 219 biological samples (urine, blood, wounds, peritoneum, and respiratory tracts) by culture on sheep blood agar or MacConkey agar and microbial detection standards. The genomic DNA was extracted using cetyltrimethylammonium bromide and resistance genes were identified by polymerase chain reaction method. RESULTS AND DISCUSSION In the molecular investigation, at least 4 high risk genes inducing resistant for E. coli isolates were reported in each antibiotic group. The interpretation of data for each of the antibiotic groups indicates that blaCTXM-15 (70%) among positive beta-lactamases, tetB (31.6%) in tetracycline, fosC (40%) in fosfomycin, OqxB (34%) in fluoroquinolone, ArmA (12.96%) in aminoglycosides, and Sul1 (69.5%) in co-trimoxazole combination are genetic indexes of antibiotic resistance. CONCLUSION The genes encoding the destructive factors of antibiotics had a significant prevalence in E. coli isolates. The blaCTXM-15 inducing beta-lactam resistance was the most common gene among our clinical isolates. Due to the possibility of development of resistance genes with chromosomal or plasmid origin, the consumption of antibiotics based on approved global standards has a high priority.

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