[Home ] [Archive]   [ فارسی ]  
:: Main :: About :: Current Issue :: Archive :: Search :: Submit :: Contact ::
Main Menu
Home::
Journal Information::
Indexing Sources::
Guide for Authors::
Online Submission::
Ethics::
Articles archive::
For Reviewers::
Contact us::
AI::
::
Basic and Clinical Biochemistry and Nutrition
..
DOAJ
..
CINAHL
..
EBSCO
..
IMEMR
..
ISC
..
Search in website

Advanced Search
..
Receive site information
Enter your Email in the following box to receive the site news and information.
..
enamad
..
metrics
Journal volumes: 30
Journal issues: 154
Articles views: 20442922
Articles downloads: 7131482

Total authors: 7786
Unique authors: 5405
Repeated authors: 2381
Repeated authors percent: 31

Submitted articles: 5101
Accepted articles: 2180
Rejected articles: 2844
Published articles: 2071

Acceptance rate: 42.74
Rejection rate: 55.75

Average Time to Accept: 194 days
Average Time to First Review: 15.3 days
Average Time to Publish: 42.9 days

Last 3 years statistics:
Submitted articles: 615
Accepted articles: 203
Rejected articles: 339
Published articles: 203

Acceptance rate: 33.01
Rejection rate: 55.12

Average Time to Accept: 106 days
Average Time to First Review: 10.7 days
Average Time to Publish: 42.8 days
____
..
:: Volume 17, Issue 5 (Quarterly 2013) ::
Feyz Med Sci J 2013, 17(5): 488-494 Back to browse issues page
Detection of qnrA gene among quinolone-resistant Escherichia coli isolated from urinary tract infections in Khorram Abad during 2011-2012
Yuonos Soleimani-Asl , Mohammad Zibaei , Farzaneh Firoozeh *
Kashan University of Medical Sciences , ffiroozeh@ut.ac.ir
Abstract:   (9209 Views)

Background: Quinolone-resistance in Escherichia coli is ordinarily associated with mutations in the gyrA and parC genes. Plasmid-mediated quinolone resistance (PMQR) was increasingly identified in Enterobacteriaceae family worldwide. The aim of this study was to determine the prevalence of qnrA gene among quinolone-resistant E. coli isolates in Khorram Abad, Iran.

Materials and Methods: In this cross-sectional study, one-hundred forty E. coli isolates were collected from urine samples of the patients. Isolates were screened for ciprofloxacin and nalidixic acid resistance using disk diffusion method according to clinical and laboratory standards institute (CLSI) guidelines. Moreover, PCR was used to evaluate the presence of qnrA gene in quinolone-resistant isolates.

Results: One-hundred sixteen (82.8%) and 63 (43%) out of 140 E. coli isolates showed resistance to nalidixic acid and ciprofloxacin, respectively. The results showed that 14 (12.1%) nalidixic acid- resistant and 9 (14.3%) ciprofloxacin-resistant isolates were positive for qnrA gene.

Conclusion: The identification of qnrA gene among quinolone-resistant E. coli isolates shows that the emergence of PMQR in this region requires serious preventive measures.

Keywords: Escherichia coli, PMQR, qnrA, Ciprofloxacin, Urinary tract infection
Full-Text [PDF 276 kb]   (6973 Downloads)    
Type of Study: Research | Subject: medicine, paraclinic
Received: 2013/09/29 | Revised: 2017/06/28 | Accepted: 2013/10/19 | Published: 2013/10/19
Send email to the article author

Add your comments about this article
Your username or Email:

CAPTCHA


XML   Persian Abstract   Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Soleimani-Asl Y, Zibaei M, Firoozeh F. Detection of qnrA gene among quinolone-resistant Escherichia coli isolated from urinary tract infections in Khorram Abad during 2011-2012. Feyz Med Sci J 2013; 17 (5) :488-494
URL: http://feyz.kaums.ac.ir/article-1-2043-en.html


Creative Commons License
This open access journal is licensed under a Creative Commons Attribution-NonCommercial ۴.۰ International License. CC BY-NC ۴. Design and publishing by Kashan University of Medical Sciences.
Copyright ۲۰۲۳© Feyz Medical Sciences Journal. All rights reserved.
Volume 17, Issue 5 (Quarterly 2013) Back to browse issues page
مجله علوم پزشکی فیض Feyz Medical Sciences Journal
Persian site map - English site map - Created in 0.18 seconds with 48 queries by YEKTAWEB 4774