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Ampc Beta Lactamases Among Gram Negative Clinical Isolates From A Tertiary Hospital, South India

AmpC β-lactamases are cephalosporinases that hydrolyze cephamycins as well as other extended-spectrum cephalosporins and are poorly inhibited by clavulanic acid. Although reported with increasing frequency, the true rate of occurrence of AmpC β-lactamases in different organisms, including members of...

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Autores principales: Mohamudha Parveen, R., Harish, B.N., Parija, S.C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Microbiologia 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3768642/
https://www.ncbi.nlm.nih.gov/pubmed/24031534
http://dx.doi.org/10.1590/S1517-83822010000300009
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author Mohamudha Parveen, R.,
Harish, B.N.
Parija, S.C.
author_facet Mohamudha Parveen, R.,
Harish, B.N.
Parija, S.C.
author_sort Mohamudha Parveen, R.,
collection PubMed
description AmpC β-lactamases are cephalosporinases that hydrolyze cephamycins as well as other extended-spectrum cephalosporins and are poorly inhibited by clavulanic acid. Although reported with increasing frequency, the true rate of occurrence of AmpC β-lactamases in different organisms, including members of Enterobacteriaceae, remains unknown. The present study was designed to determine the occurrence of AmpC enzyme-harbouring Gram-negative clinical isolates in a tertiary care hospital in Pondicherry state, South India. A total of 235 Gram negative clinical isolates were tested for resistance to cefoxitin, third generation cephalosporin (3GC) antibiotics, ampicillin, amikacin, co-trimoxazole, gentamicin, meropenem and tetracycline by disc diffusion method. Isolates found resistant to 3GC and cefoxitin were tested for the production of AmpC β -lactamases by three dimensional extraction method and AmpC disc method. Isolates found to sensitive to 3GC were subjected to disc antagonism test for inducible AmpC production. One hundred and thirty four (57%) strains were resistant to 3GC, among which 63(47%) were positive for plasmid-mediated AmpC beta lactamases production. Among the 101 strains sensitive to 3GC, 23 (22.7%) revealed the presence of inducible AmpC beta lactamases by disc approximation test. A total of 80.9% (51/63) of screen positive isolates were detected by Amp C disc test and 93.6% (59/63) by three dimensional extraction method. Out of the 86 AmpC producers, 67 (77.9%) were cefoxitin resistant .Inducible AmpC was not found in Esch.coli and Klebsiella spp. The AmpC producers also concurrently showed multidrug resistance pattern. AmpC producers were found to be prevalent in our hospital and though three dimensional extraction test detects AmpC better, the disk test is easier to perform routinely and is user- friendly.
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spelling pubmed-37686422013-09-12 Ampc Beta Lactamases Among Gram Negative Clinical Isolates From A Tertiary Hospital, South India Mohamudha Parveen, R., Harish, B.N. Parija, S.C. Braz J Microbiol Medical Microbiology AmpC β-lactamases are cephalosporinases that hydrolyze cephamycins as well as other extended-spectrum cephalosporins and are poorly inhibited by clavulanic acid. Although reported with increasing frequency, the true rate of occurrence of AmpC β-lactamases in different organisms, including members of Enterobacteriaceae, remains unknown. The present study was designed to determine the occurrence of AmpC enzyme-harbouring Gram-negative clinical isolates in a tertiary care hospital in Pondicherry state, South India. A total of 235 Gram negative clinical isolates were tested for resistance to cefoxitin, third generation cephalosporin (3GC) antibiotics, ampicillin, amikacin, co-trimoxazole, gentamicin, meropenem and tetracycline by disc diffusion method. Isolates found resistant to 3GC and cefoxitin were tested for the production of AmpC β -lactamases by three dimensional extraction method and AmpC disc method. Isolates found to sensitive to 3GC were subjected to disc antagonism test for inducible AmpC production. One hundred and thirty four (57%) strains were resistant to 3GC, among which 63(47%) were positive for plasmid-mediated AmpC beta lactamases production. Among the 101 strains sensitive to 3GC, 23 (22.7%) revealed the presence of inducible AmpC beta lactamases by disc approximation test. A total of 80.9% (51/63) of screen positive isolates were detected by Amp C disc test and 93.6% (59/63) by three dimensional extraction method. Out of the 86 AmpC producers, 67 (77.9%) were cefoxitin resistant .Inducible AmpC was not found in Esch.coli and Klebsiella spp. The AmpC producers also concurrently showed multidrug resistance pattern. AmpC producers were found to be prevalent in our hospital and though three dimensional extraction test detects AmpC better, the disk test is easier to perform routinely and is user- friendly. Sociedade Brasileira de Microbiologia 2010 2010-09-01 /pmc/articles/PMC3768642/ /pubmed/24031534 http://dx.doi.org/10.1590/S1517-83822010000300009 Text en © Sociedade Brasileira de Microbiologia http://creativecommons.org/licenses/by-nc/3.0/ All the content of the journal, except where otherwise noted, is licensed under a Creative Commons License
spellingShingle Medical Microbiology
Mohamudha Parveen, R.,
Harish, B.N.
Parija, S.C.
Ampc Beta Lactamases Among Gram Negative Clinical Isolates From A Tertiary Hospital, South India
title Ampc Beta Lactamases Among Gram Negative Clinical Isolates From A Tertiary Hospital, South India
title_full Ampc Beta Lactamases Among Gram Negative Clinical Isolates From A Tertiary Hospital, South India
title_fullStr Ampc Beta Lactamases Among Gram Negative Clinical Isolates From A Tertiary Hospital, South India
title_full_unstemmed Ampc Beta Lactamases Among Gram Negative Clinical Isolates From A Tertiary Hospital, South India
title_short Ampc Beta Lactamases Among Gram Negative Clinical Isolates From A Tertiary Hospital, South India
title_sort ampc beta lactamases among gram negative clinical isolates from a tertiary hospital, south india
topic Medical Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3768642/
https://www.ncbi.nlm.nih.gov/pubmed/24031534
http://dx.doi.org/10.1590/S1517-83822010000300009
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