Controlling False-Positive Results Obtained with the Hodge and Masuda Assays for Detection of Class A Carbapenemase in Species of Enterobacteriaceae by Incorporating Boronic Acid

被引:71
作者
Pasteran, Fernando [1 ]
Mendez, Tania [1 ]
Rapoport, Melina [1 ]
Guerriero, Leonor [1 ]
Corso, Alejandra [1 ]
机构
[1] INEI, ANLIS Dr Carlos G Malbran, Serv Antimicrobianos, Dept Bacteriol,Minist Salud & Ambiente, Buenos Aires, DF, Argentina
关键词
GRAM-NEGATIVE BACTERIA; KLEBSIELLA-PNEUMONIAE; BETA-LACTAMASES; ESCHERICHIA-COLI; RESISTANCE; IDENTIFICATION; MECHANISMS; ARGENTINA;
D O I
10.1128/JCM.01771-09
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The modified Hodge method (MHT) has been recommended by the CLSI for confirmation of suspected class A carbapenemase production in species of Enterobacteriaceae. This test and the Masuda method (MAS) have advantages over traditional phenotypic methods in that they directly analyze carbapenemase activity. In order to identify the potential interferences of these tests, we designed a panel composed of diverse bacterial genera with distinct carbapenem susceptibility patterns (42 carbapenemase producers and 48 nonproducers). About 25% of results among carbapenemase nonproducers, mainly strains harboring CTX-M and AmpC hyperproducers, were observed to be false positive. Subsequently, we developed an optimized approach for more-accurate detection of suspicious isolates of carbapenemase by addition of boronic acid (BA) derivatives (reversible inhibitor of class A carbapenemases and AmpC cephalosporinases) and oxacillin (inhibitor of AmpCs enzymes). The use of the modified BA-and oxacillin-based MHT and MAS resulted in high sensitivity (>90%) and specificity (100%) for class A carbapenemase detection. By use of these methodologies, isolates producing KPCs and GES, Sme, IMI, and NMC-A carbapenemases were successfully distinguished from those producing other classes of beta-lactamases (extended-spectrum beta-lactamases [ESBLs], AmpC beta-lactamases, metallo-beta-lactamases [MBLs], etc.). These methods will provide the fast and useful information needed for targeting of antimicrobial therapy and appropriate infection control.
引用
收藏
页码:1323 / 1332
页数:10
相关论文
共 26 条
  • [1] ANDERSON KF, 2009, 49 INT C ANT AG CHEM
  • [2] THE INHIBITION OF CLASS-C BETA-LACTAMASES BY BORONIC ACIDS
    BEESLEY, T
    GASCOYNE, N
    KNOTTHUNZIKER, V
    PETURSSON, S
    WALEY, SG
    JAURIN, B
    GRUNDSTROM, T
    [J]. BIOCHEMICAL JOURNAL, 1983, 209 (01) : 229 - 233
  • [3] A FUNCTIONAL CLASSIFICATION SCHEME FOR BETA-LACTAMASES AND ITS CORRELATION WITH MOLECULAR-STRUCTURE
    BUSH, K
    JACOBY, GA
    MEDEIROS, AA
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (06) : 1211 - 1233
  • [4] Cloverleaf test (modified Hodge test) for detecting carbapenemase production in Klebsiella pneumoniae: be aware of false positive results
    Carvalhaes, Cecilia G.
    Picao, Renata C.
    Nicoletti, Adriana G.
    Xavier, Danilo E.
    Gales, Ana C.
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2010, 65 (02) : 249 - 251
  • [5] Clinical and Laboratory Standards Institute, 2009, M100S20 CLSI
  • [6] Simple Disk-Based Method for Detection of Klebsiella pneumoniae Carbapenemase-Type β-Lactamase by Use of a Boronic Acid Compound
    Doi, Yohei
    Potoski, Brian A.
    Adams-Haduch, Jennifer M.
    Sidjabat, Hanna E.
    Pasculle, Anthony W.
    Paterson, David L.
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2008, 46 (12) : 4083 - 4086
  • [7] GOMEZ S, 2009, 49 INT C ANT AG CHEM
  • [8] Escherichia coli:: Development of carbapenem resistance during therapy
    Hong, T
    Moland, ES
    Abdalhamid, B
    Hanson, ND
    Wang, J
    Sloan, C
    Fabian, D
    Faraiallah, A
    Levine, J
    Thomson, KS
    [J]. CLINICAL INFECTIOUS DISEASES, 2005, 40 (10) : E84 - E86
  • [9] STATISTICAL-METHODS IN MICROBIOLOGY
    ILSTRUP, DM
    [J]. CLINICAL MICROBIOLOGY REVIEWS, 1990, 3 (03) : 219 - 226
  • [10] Molecular mechanisms of β-lactam resistance mediated by AmpC hyperproduction in Pseudomonas aeruginosa clinical strains
    Juan, C
    Maciá, MD
    Gutiérrez, O
    Vidal, C
    Pérez, JL
    Oliver, A
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (11) : 4733 - 4738