ISSN: 0973-7510

E-ISSN: 2581-690X

A. Umasankar1 , T. Shobarani2 and D. Satyaranjan1
1Department of Microbiology, College of Science, GITAM Deemed University. Vishakapatnam – 530 045, India.
2Department of Microbiology, Rangaraya Medical College, Kakinada, India.
J Pure Appl Microbiol. 2008;2(2):427-430
© The Author(s). 2008
Received: 12/06/2008 | Accepted: 30/07/2008 | Published: 31/10/2008
Abstract

Extended spectrum beta lactometers are the enzymes, which were mainly occurred in hospital acquired infections (nosocomial infections) due to unhygienic conditions of the hospital environment. ESBL production is usually plasmid mediated, it is possible for one specimen to contain both ESBL producing and non ESBL producing cells of the same species. This suggests that for optimal detection, several colonies must be tested from a primary culture plate. In the process of detection of these enzymes, first we isolate the organism from wound based on the culture characters and biochemical characters and proceed for antibiotic sensitivity. If the organism shows resistant, then we have proceed for test for Beta lactamases, and confirmatory tests for ESBLs.The prevalence of ESBLs in government general hospitalk kakinada and surroundings places in kakinada district is 9.33%. It is much lower than other reports from India and abrod. In our study surprisingly out of 21% of esbl positive cases, 16% of the isolates were Proteus species. All the isolates were found sensitive to the  Carbapenem antibiotics.

Keywords

ESBLs – Extended Spectrum Beta-Lactamases, 3GC-third generation cephalosporins, TEM-Temonera (gene), SHV-sulphydril variable (gene) enzymes, CONS-Coagulase negative Staphylococci

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