Molecular characterization of ESBL producing uropathogenic Escherichia coli. (Record no. 3084)

MARC details
000 -LEADER
fixed length control field 02666nam a22002297a 4500
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20230813141751.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 220621b ||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Description conventions NLM
060 ## - NATIONAL LIBRARY OF MEDICINE CALL NUMBER
Classification number THS-00614
100 ## - MAIN ENTRY--PERSONAL NAME
Personal name Thapa, Garima.
9 (RLIN) 4602
245 ## - TITLE STATEMENT
Title Molecular characterization of ESBL producing uropathogenic Escherichia coli.
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Date of publication, distribution, etc. c2021.
300 ## - PHYSICAL DESCRIPTION
Extent x,48p.
500 ## - GENERAL NOTE
General note Thesis Report.
520 ## - SUMMARY, ETC.
Summary, etc. ABSTRACT: <br/><br/>Background: Antibiotic resistance is a globally disappointing trend and challenging problem for researchers of all fields worldwide. Health and economic burdens are two factors provoked due to antibiotic resistance, and today's world is entering the same era. Both phenotypic and genotypic characterizations would be required to understand the molecular mechanisms generating resistance and their pathological consequences. The major goal of this study was to see how common the blaTEM and blacTX-M genes were in extended spectrum β=lactamase (ESBL) producing E. coli isolates. <br/><br/>Methodology: The E. coli isolated from urine samples of Urinary Tract Infection (UTI) diagnosed patients between October 2020 to August 2021 at Meridian Health Care Center and Abhiyan Pathology Lab were collected and included in this study. On the basis of colony appearance and biochemical characteristics, bacterial isolates were identified. The modified Kirby-Bauer disk diffusion method was used to screen clinical isolates for antimicrobial susceptibility testing (AST), while a combination disk diffusion method was used to identify ESBL producers. The ESBL genes blaTEM and blacts-M were detected using standard polymerase chain reaction (PCR) in ESBL positive isolates. <br/><br/>Results: After performing antibiotics susceptibility testing and phenotypic confirmatory tests of 54 isolates of E. Coli, we identifies a large frequency of multi-drug resistance and extended spectrum beta-lactamases producers, 57.4% and 46.3%, respectively. Similarly, the CTX-M gene was found to be more prevalent than the TEM gene following PCR amplification, with 72% and 56% occurrences, respectively. <br/><br/>Conclusion: Multi drug resistance (MDR) bacteria made up half of the isolates in our investigation. To maximize treatment and minimize antibiotic resistance, routine identification of and infecting pathogen followed by AST is crucial. <br/><br/>Key Words: Antibiotic resistance, Escherichia coli, Extended-spectrum β-lactamase.
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Antibiotic resistance.
9 (RLIN) 334
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Escherichia coli.
9 (RLIN) 4603
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Extended-spectrum β-lactamase.
9 (RLIN) 4604
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="http://nhrc.gov.np/contact/">http://nhrc.gov.np/contact/</a>
Link text Visit NHRC Library
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme National Library of Medicine
Koha item type Thesis Report
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Home library Current library Shelving location Date acquired Total Checkouts Full call number Barcode Date last seen Price effective from Koha item type
    National Library of Medicine     Nepal Health Research Council Nepal Health Research Council Reference 06/21/2022   THS00614/THA/2021 THS-00614 06/21/2022 06/21/2022 Thesis Report

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