Combined Use of the Modified Hodge Test and Carbapenemase Inhibition Test for Detection of Carbapenemase-Producing Enterobacteriaceae and Metallo-beta-Lactamase-Producing Pseudomonas spp..
10.3343/alm.2015.35.2.212
- Author:
Wonkeun SONG
1
;
Seong Geun HONG
;
Dongeun YONG
;
Seok Hoon JEONG
;
Hyun Soo KIM
;
Han Sung KIM
;
Jae Seok KIM
;
Il Kwon BAE
Author Information
1. Department of Laboratory Medicine, Hallym University College of Medicine, Seoul, Korea. swonkeun@hallym.or.kr
- Publication Type:Evaluation Studies ; Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
Modified Hodge test;
Carbapenemase inhibition test;
Phenylboronic acid;
EDTA;
Enterobacteriaceae;
Pseudomonas spp.
- MeSH:
Bacterial Proteins/antagonists & inhibitors/*metabolism;
Boronic Acids/chemistry/pharmacology;
Disk Diffusion Antimicrobial Tests/*methods;
Edetic Acid/chemistry/pharmacology;
Enterobacteriaceae/drug effects/*enzymology;
Enterobacteriaceae Infections/diagnosis;
Humans;
Pseudomonas/drug effects/*enzymology;
Pseudomonas Infections/diagnosis;
Sensitivity and Specificity;
beta-Lactamases/chemistry/*metabolism
- From:Annals of Laboratory Medicine
2015;35(2):212-219
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND: We evaluated the combined use of the modified Hodge test (MHT) and carbapenemase inhibition test (CIT) using phenylboronic acid (PBA) and EDTA to detect carbapenemase-producing Enterobacteriaceae (CPE) and metallo-beta-lactamase (MBL)-producing Pseudomonas spp. METHODS: A total of 49 isolates of CPE (15 Klebsiella pneumoniae carbapenemase [KPC], 5 Guiana extended-spectrum beta-lactamase [GES]-5, 9 New Delhi metallo-beta-lactamase [NDM]-1, 5 Verona integron-encoded metallo-beta-lactamase [VIM]-2, 3 imipenem-hydrolyzing beta-lactamase [IMP], and 12 oxacillinase [OXA]-48-like), 25 isolates of MBL-producing Pseudomonas spp. (14 VIM-2 and 11 IMP), and 35 carbapenemase-negative controls were included. The MHT was performed for all isolates as recommended by the Clinical and Laboratory Standards Institute. Enhanced growth of the indicator strain was measured in mm with a ruler. The CIT was performed by directly dripping PBA and EDTA solutions onto carbapenem disks that were placed on Mueller-Hinton agar plates seeded with the test strain. RESULTS: Considering the results of the MHT with the ertapenem disk in Enterobacteriaceae and Pseudomonas spp., the CIT with the meropenem disk in Enterobacteriaceae, and the imipenem disk in Pseudomonas spp., three combined disk tests, namely MHT-positive plus PBA-positive, EDTA-positive, and MHT-positive plus PBA-negative plus EDTA-negative, had excellent sensitivity and specificity for the detection of KPC- (100% sensitivity and 100% specificity), MBL- (94% sensitivity and 100% specificity), and OXA-48-like-producing isolates (100% sensitivity and 100% specificity), respectively. CONCLUSIONS: Combined use of the MHT and CIT with PBA and EDTA, for the detection of CPE and MBL-producing Pseudomonas spp., is effective in detecting and characterizing carbapenemases in routine laboratories.
