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. 2011 May 1;17(5):BR147–BR152. doi: 10.12659/MSM.881761

Table 1.

Criteria of positivity of the phenotypic tests used to detect ESBL and AmpC enzymes.

Test ESBL detection AmpC detection
mDDST* Extension of the inhibition zone towards the disk with the inhibitor and/or enlargement of the zone by more than 5 mm around the disk with the inhibitor (Figure 1)
mAmpC test** Enlargement of the inhibition zone by more than 5 mm as compared with the disk without 3-aminophenylboronic acid (Figure 2)
mMIC*** Cefoxitin MIC ≤16 mg/L and a ratio of MIC of cefoperazone and cefoperazone/sulbactam >2:1 Cefoxitin MIC ≥16 mg/L and a ratio of MIC of cefotaxime and cefotaxime/3-aminophenylboronic acid or MIC of ceftazidime and ceftazidime/3-aminophenylboronic acid >2:1
ESBL Etest At least 4-fold decrease of MIC of the particular third- or fourth-generation cephalosporin (cefotaxime and ceftazidime in case of E. coli and K. pneumoniae, and in addition cefepime in S. marcescens) in the presence of the inhibitor (cefotaxime/clavulanic acid and ceftazidime/clavulanic acid, and additionally cefepime/clavulanic acid in S. marcescens) (Figure 3)
*

Modified double-disk synergy test;

**

modified AmpC disk method;

***

modified microdilution method.