Laboratory Identification of Metallo-beta-lactamase Producing Clinical Isolates of Pseudomonas aeruginosa: An Assessment of Different Phenotypic Methods
Background: Multidrug Resistant (MDR) Pseudomonas aeruginosa, an emerging superbug causing a wide spectrum of nosocomial infections. Carbapenem resistance among P. aeruginosa isolates is of grave concern and is mainly due to production of Metallobeta- lactamase (MBL) enzymes. Aim and Objectives...
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doaj-439eda2c2cb2412c89ebd470dbced4e02020-11-24T22:04:55ZengKrishna Institute of Medical Sciences UniversityJournal of Krishna Institute of Medical Sciences University2231-42612231-42612018-07-0107032734Laboratory Identification of Metallo-beta-lactamase Producing Clinical Isolates of Pseudomonas aeruginosa: An Assessment of Different Phenotypic MethodsAruna Siddabathuni0Department of Microbiology, GSL Medical College and General Hospital, Rajahmundry – 533296 (Andhra Pradesh) IndiaBackground: Multidrug Resistant (MDR) Pseudomonas aeruginosa, an emerging superbug causing a wide spectrum of nosocomial infections. Carbapenem resistance among P. aeruginosa isolates is of grave concern and is mainly due to production of Metallobeta- lactamase (MBL) enzymes. Aim and Objectives: To find out the prevalence of MBL producing P. aeruginosa isolates from various clinical samples and to evaluate the efficacy of different phenotypic tests employed in vitro for their detection. Material and Methods:Atotal of 358 P. aeruginosa strains obtained from different clinical samples were subjected to antimicrobial susceptibility testing by Kirby-Bauer's Disc Diffusion method. All the imipenem resistant isolates were further tested by Modified Hodge Test (MHT) to detect carbapenem resistance. MBL production was tested by screening with Combined Disc Test (CDT) and Double Disc Synergy Test (DDST). MBL production was confirmed by MBL Etest (Ab BioDisk). Results: Among 358 strains of P. aeruginosa recovered, 114 isolates showed resistance to imipenem. E test demonstrated 73 out of 114 isolates as MBL producers. Of MHT, CDT and DDST tests performed, DDST showed high sensitivity and specificity. Conclusion: DDST can be suggested as an economical option in place of expensive E test for routine screening of MDR P. aeruginosa isolates for MBL production in a clinical laboratory; which is crucial for planning better management protocols.http://www.jkimsu.com/jkimsu-vol7no3/JKIMSU,%20Vol.%207,%20No.%203,%20July-September%202018%20Page%2027-34.pdfModified Hodge TestCombined Disc TestDouble Disc Synergy TestMBLE-test |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Aruna Siddabathuni |
spellingShingle |
Aruna Siddabathuni Laboratory Identification of Metallo-beta-lactamase Producing Clinical Isolates of Pseudomonas aeruginosa: An Assessment of Different Phenotypic Methods Journal of Krishna Institute of Medical Sciences University Modified Hodge Test Combined Disc Test Double Disc Synergy Test MBLE-test |
author_facet |
Aruna Siddabathuni |
author_sort |
Aruna Siddabathuni |
title |
Laboratory Identification of Metallo-beta-lactamase Producing Clinical Isolates of Pseudomonas aeruginosa: An Assessment of Different Phenotypic Methods |
title_short |
Laboratory Identification of Metallo-beta-lactamase Producing Clinical Isolates of Pseudomonas aeruginosa: An Assessment of Different Phenotypic Methods |
title_full |
Laboratory Identification of Metallo-beta-lactamase Producing Clinical Isolates of Pseudomonas aeruginosa: An Assessment of Different Phenotypic Methods |
title_fullStr |
Laboratory Identification of Metallo-beta-lactamase Producing Clinical Isolates of Pseudomonas aeruginosa: An Assessment of Different Phenotypic Methods |
title_full_unstemmed |
Laboratory Identification of Metallo-beta-lactamase Producing Clinical Isolates of Pseudomonas aeruginosa: An Assessment of Different Phenotypic Methods |
title_sort |
laboratory identification of metallo-beta-lactamase producing clinical isolates of pseudomonas aeruginosa: an assessment of different phenotypic methods |
publisher |
Krishna Institute of Medical Sciences University |
series |
Journal of Krishna Institute of Medical Sciences University |
issn |
2231-4261 2231-4261 |
publishDate |
2018-07-01 |
description |
Background: Multidrug Resistant (MDR) Pseudomonas
aeruginosa, an emerging superbug causing a wide
spectrum of nosocomial infections. Carbapenem
resistance among P. aeruginosa isolates is of grave
concern and is mainly due to production of Metallobeta-
lactamase (MBL) enzymes. Aim and Objectives:
To find out the prevalence of MBL producing P.
aeruginosa isolates from various clinical samples and
to evaluate the efficacy of different phenotypic tests
employed in vitro for their detection. Material and
Methods:Atotal of 358 P. aeruginosa strains obtained
from different clinical samples were subjected to
antimicrobial susceptibility testing by Kirby-Bauer's
Disc Diffusion method. All the imipenem resistant
isolates were further tested by Modified Hodge Test
(MHT) to detect carbapenem resistance. MBL
production was tested by screening with Combined
Disc Test (CDT) and Double Disc Synergy Test
(DDST). MBL production was confirmed by MBL Etest
(Ab BioDisk). Results: Among 358 strains of P.
aeruginosa recovered, 114 isolates showed resistance
to imipenem. E test demonstrated 73 out of 114 isolates
as MBL producers. Of MHT, CDT and DDST tests
performed, DDST showed high sensitivity and
specificity. Conclusion: DDST can be suggested as an
economical option in place of expensive E test for
routine screening of MDR P. aeruginosa isolates for
MBL production in a clinical laboratory; which is
crucial for planning better management protocols. |
topic |
Modified Hodge Test Combined Disc Test Double Disc Synergy Test MBLE-test |
url |
http://www.jkimsu.com/jkimsu-vol7no3/JKIMSU,%20Vol.%207,%20No.%203,%20July-September%202018%20Page%2027-34.pdf |
work_keys_str_mv |
AT arunasiddabathuni laboratoryidentificationofmetallobetalactamaseproducingclinicalisolatesofpseudomonasaeruginosaanassessmentofdifferentphenotypicmethods |
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1725828168795815936 |