Reza Ranjbar, Sajjad S Tolon, Mehrdad Sami, Reza Golmohammadi
{"title":"Detection of Plasmid-Mediated <i>qnr</i> Genes Among the Clinical Quinolone-Resistant <i>Escherichia coli</i> Strains Isolated in Tehran, Iran.","authors":"Reza Ranjbar, Sajjad S Tolon, Mehrdad Sami, Reza Golmohammadi","doi":"10.2174/1874285801812010248","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong><i>Escherichia coli</i> is one of the most important bacterial agents to cause urinary tract infections. Inappropriate and unnecessary administration of antibiotics has led to an increase in the appearance of multidrug-resistant <i>E. coli</i> isolates, limiting treatment options. The increase in a number of resistant strains of bacteria is a major concern of health authorities worldwide.</p><p><strong>Objective: </strong>The purpose of this study was to determine the presence of the <i>qnr</i> genes among <i>E. coli</i> isolated from UTIs of patients in Baqiyatallah hospital in Tehran province, Iran.</p><p><strong>Method: </strong>Clinical urine samples of patients with suspected urinary tract infection were collected by standard methods in sterile disposable containers. After analysis of urine, microscopic observations and culture analysis, the bacterial genome was extracted by boiling method. PCR for detection of <i>qnr</i> genes including <i>qnrA</i>, <i>qnrB</i> and <i>qnrS</i> was done by specific primers, then PCR products were run using gel electrophoresis and visualized by gel documentation system.</p><p><strong>Results: </strong>In the present study among the 95 isolates, 60 strains were resistant to nalidixic acid. PCR showed that 92 strains were positive for <i>qnrS</i>. The <i>qnrA</i> and <i>qnrB</i> genes were not found among the clinical isolates.</p><p><strong>Conclusion: </strong>Our finding indicates a high level of resistance against nalidixic acid among <i>E. coli</i> isolates recovered from the patients with UTI. Also, the high frequency of <i>qnrS</i> imposes the importance of survey of molecular and genetic analysis of mechanisms of quinolone resistance in <i>E. coli</i> strains.</p>","PeriodicalId":38953,"journal":{"name":"Open Microbiology Journal","volume":"12 ","pages":"248-253"},"PeriodicalIF":0.0000,"publicationDate":"2018-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6110078/pdf/","citationCount":"9","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Open Microbiology Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/1874285801812010248","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2018/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"Immunology and Microbiology","Score":null,"Total":0}
引用次数: 9
Abstract
Background: Escherichia coli is one of the most important bacterial agents to cause urinary tract infections. Inappropriate and unnecessary administration of antibiotics has led to an increase in the appearance of multidrug-resistant E. coli isolates, limiting treatment options. The increase in a number of resistant strains of bacteria is a major concern of health authorities worldwide.
Objective: The purpose of this study was to determine the presence of the qnr genes among E. coli isolated from UTIs of patients in Baqiyatallah hospital in Tehran province, Iran.
Method: Clinical urine samples of patients with suspected urinary tract infection were collected by standard methods in sterile disposable containers. After analysis of urine, microscopic observations and culture analysis, the bacterial genome was extracted by boiling method. PCR for detection of qnr genes including qnrA, qnrB and qnrS was done by specific primers, then PCR products were run using gel electrophoresis and visualized by gel documentation system.
Results: In the present study among the 95 isolates, 60 strains were resistant to nalidixic acid. PCR showed that 92 strains were positive for qnrS. The qnrA and qnrB genes were not found among the clinical isolates.
Conclusion: Our finding indicates a high level of resistance against nalidixic acid among E. coli isolates recovered from the patients with UTI. Also, the high frequency of qnrS imposes the importance of survey of molecular and genetic analysis of mechanisms of quinolone resistance in E. coli strains.
期刊介绍:
The Open Microbiology Journal is a peer-reviewed open access journal which publishes research articles, reviews/mini-reviews, case studies, guest edited thematic issues and short communications/letters covering theoretical and practical aspects of Microbial systematics, evolutionary microbiology, immunology, virology, parasitology , bacteriology, mycology, phycology, protozoology, microbial ecology, molecular biology, microbial physiology, biochemistry, microbial pathogenesis, host-microbe interaction, systems microbiology, synthetic microbiology, bioinformatics. The Open Microbiology Journal , a peer-reviewed journal, is an important and reliable source of current information on developments in the field. The emphasis will be on publishing quality papers rapidly and freely available to researchers worldwide.