<?xml version="1.0" encoding="utf-8"?>
<Journal>
<Journal-Info>
<name>International Journal of Pharma and Bio Sciences</name>
<website>ijpbs.net</website>
<email>editorijpbs@rediffmail.com (or) editorofijpbs@yahoo.com (or) prasmol@rediffmail.com</email>
</Journal-Info>
<article>
<article-id pub-id-type='other'>10.22376/ijpbs.2019.10.1.p1-12</article-id>
<issue_number>Volume 3 Issue 4</issue_number>
<issue_period>2012(October - December)</issue_period>
<title>OCCURRENCE OF CTX-M AND SHV GENES IN ESBL PRODUCING GRAM NEGATIVE ORGANISMS CAUSING PYOGENIC INFECTIONS IN A TERTIARY CARE HOSPITAL IN PUDUCHERRY. </title>
<abstract>An extended spectrum beta lactamase (ESBL) production among gram-negative bacilli has emerged as a significant mechanism of resistance to oxyimino-cephalosporin antibiotics during the last 3 decades. Detection of common ESBL genes such as CTX-M and SHV by molecular methods in ESBL-producing bacteria and their pattern of antimicrobial resistance can provide useful information about its epidemiology and aid in rational antimicrobial therapy. A total of 138 multi drug resistant clinical isolates of  lessThan i greaterThan Enterobacteriaceae lessThan /i greaterThan  family obtained from pyogenic lesions were included in the study. Antibiotic susceptibility test, Phenotypic confirmatory methods, Minimum inhibitory concentration and detection of CTX-M and SHV genes by Polymerase chain reaction were performed. Out of 138 samples, 84 were ESBL producers. Among the 84 isolates CTX-M gene was seen in 55 (65.5%) isolates, SHV was seen in 16 (19%) isolates and both CTX-M and SHV was seen in 14 (16.7%). A strict monitoring mechanism of antimicrobial resistance is necessary because of the high rate of prevalence of CTX-M and SHV genes among gram negative organisms causing clinically significant infections.</abstract>
<authors>DHANDAPANY SENTHIL PRAGASH, MANGAIYARKARASI, LATHA RAGUNATHAN, SAGEERA BANOO, VIJAYA RAYAPU   AND IVVALA ANAND SHAKER</authors>
<keywords>CTX-M, SHV, Extended spectrum beta lactamase, ESBL, Polymerase chain reaction.</keywords>
<pages>782-788</pages>
</article>
</Journal>
