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Updated: Jun 21, 2026

Direct Microbial Identification using An Automated Microbial Identification System to Facilitate the EUCAST RAST Method Without Mass Spectrometry
Published on: May 24, 2024
Erroneous reporting of vancomycin susceptibility for Staphylococcus spp. by Vitek software version 2.01.
Bijayini Behera1, Purva Mathur
1Microbiology Division, Department of Laboratory Medicine, Jai Prakash Narayan Apex Trauma Centre, All India Institute of Medical Sciences, New Delhi, India.
Automated vancomycin resistance testing in Staphylococcus species using Vitek 2.01 showed a 15% false resistance rate. Confirmatory testing with validated methods is crucial for accurate clinical decisions.
Area of Science:
- Clinical microbiology
- Antimicrobial resistance
- Medical diagnostics
Background:
- Vancomycin resistance in Staphylococcus species presents significant therapeutic and epidemiological challenges.
- Accurate susceptibility testing is vital for guiding patient treatment and monitoring resistance trends.
Purpose of the Study:
- To evaluate the performance of Vitek software version 2.01 for vancomycin susceptibility testing in Staphylococcus species.
- To compare Vitek 2.01 results against reference methods like broth dilution, vancomycin screen agar, and Etest.
Main Methods:
- Testing of 105 Staphylococcus isolates.
- Utilized CLSI-recommended broth dilution, CDC-recommended vancomycin screen agar, and Etest as reference methods.
- Compared results obtained from Vitek 2.01 automated system with reference methods.
Main Results:
- Vitek 2.01 incorrectly identified 16 out of 105 isolates (15%) as having intermediate or resistant vancomycin phenotypes.
- Discrepancies highlight potential inaccuracies in automated susceptibility testing for vancomycin resistance.
Conclusions:
- Automated systems like Vitek 2.01 may produce false vancomycin resistance reports in Staphylococcus species.
- Laboratories must implement validated confirmatory methods to verify vancomycin resistance detected by automated systems.
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