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. 2021 May 12;76(6):1487-1494.
doi: 10.1093/jac/dkab032.

Evaluation of methods for detection of β-lactamase production in MSSA

Robert Skov  1 , David R Lonsway  2 , Jesper Larsen  3 , Anders Rhod Larsen  3 , Jurgita Samulioniené  4 , Brandi M Limbago  2
Affiliations

Evaluation of methods for detection of β-lactamase production in MSSA

Robert Skov et al. J Antimicrob Chemother. .

Abstract

Objectives: Correct determination of penicillin susceptibility is pivotal for using penicillin in the treatment of Staphylococcus aureus infections. This study examines the performance of MIC determination, disc diffusion and a range of confirmatory tests for detection of penicillin susceptibility in S. aureus.

Methods: A total of 286 consecutive penicillin-susceptible S. aureus blood culture isolates as well as a challenge set of 62 MSSA isolates were investigated for the presence of the blaZ gene by PCR and subjected to penicillin-susceptibility testing using broth microdilution MIC determination, disc diffusion including reading of the zone edge, two nitrocefin tests and the cloverleaf test.

Results: Using PCR-based detection of blaZ as the gold standard, both broth microdilution MIC testing and disc diffusion testing resulted in a relatively low accuracy (82%-93%) with a sensitivity ranging from 49%-93%. Among the confirmatory tests, the cloverleaf test performed with 100% accuracy, while zone edge interpretation and nitrocefin-based tests increased the sensitivity of β-lactamase detection to 96%-98% and 82%-96% when using MIC determination or disc diffusion as primary test, respectively.

Conclusions: This investigation showed that reliable and accurate detection of β-lactamase production in S. aureus can be obtained by MIC determination or penicillin disc diffusion followed by interpretation of the zone edge as a confirmatory test for apparently penicillin-susceptible isolates. The more cumbersome cloverleaf test can also be used. Nitrocefin-based tests should not be used as the only test for confirmation of a presumptive β-lactamase-negative isolate.

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Figures

Figure 1.
Figure 1.
Cloverleaf patterns for a β-lactamase-negative isolate and a β-lactamase-positive isolate. (a) β-Lactamase-negative isolate. (b) β-Lactamase-positive isolate. This figure appears in colour in the online version of JAC and in black and white in the print version of JAC.
Figure 2.
Figure 2.
Zone edge patterns for a β-lactamase-negative isolate and a β-lactamase-positive isolate. (a) β-Lactamase-negative isolate. (b) β-Lactamase-positive isolate. This figure appears in colour in the online version of JAC and in black and white in the print version of JAC.
See this image and copyright information in PMC

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