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Updated: Jan 29, 2026

Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus MRSA
Published on: February 9, 2011
Vancomycin MIC Distribution among Methicillin-Resistant Staphylococcus Aureus. Is Reduced Vancomycin Susceptibility
Hala B Othman1, Rania M Abdel Halim1, Fatma Alzahraa M Gomaa2
1Clinical Pathology Department, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Aim:
To determine the distribution of vancomycin MIC and the frequency of S. aureus strains with reduced vancomycin susceptibility among Methicillin-Resistant Staphylococcus aureus (MRSA) isolates.
Methods:
MRSA isolates (n = 100) were tested for reduced susceptibility to vancomycin using MIC broth microdilution method (BMD), vancomycin screening agar with different vancomycin concentrations with and without casein, and Vitek 2 system.
Results:
BMD detected (22%) vancomycin-intermediate S. aureus (VISA) and (78%) vancomycin-susceptible S. aureus (VSSA) but couldn't detect nine (Heterogeneous VISA) (hVISA) isolates (9%) with MIC ≤ 2 µg/ml that grew on screening agar 4 µg/ml or 6 µg/ml. Adding casein to vancomycin screening agar increased detection rate of VISA by 4.5%. Screening agar with 6 µg/ml vancomycin overall detection rate for VISA was 95.45%. Probable 'pre-hVISA'isolates (17%) showed growth on vancomycin screening agar 2 µg/ml with casein. Vitek 2 system failed to detect any VISA isolates.
Conclusion:
Vancomycin screening agar; 2 µg/ml and (4 and 6 µg/ml) were able to detect; probable "pre hVISA and (hVISA and VISA) isolates respectively based on their BMD MIC values. Decreased vancomycin susceptibility in MRSA isolates might be related to MIC creep. Analysis of vancomycin MIC values over longer periods is recommended to further study this phenomenon and its impact on vancomycin treatment failure.
Insights
Vancomycin screening agar effectively detects various levels of vancomycin resistance in Methicillin-Resistant Staphylococcus aureus (MRSA) isolates, including heterogeneous strains missed by other methods. This aids in understanding reduced vancomycin susceptibility in MRSA.
Area of Science:
- Clinical Microbiology
- Infectious Diseases
- Antimicrobial Resistance
Background:
- Methicillin-Resistant Staphylococcus aureus (MRSA) poses a significant treatment challenge, often requiring vancomycin as a last resort.
- Reduced vancomycin susceptibility in MRSA, including vancomycin-intermediate S. aureus (VISA) and heterogeneous VISA (hVISA), complicates treatment and necessitates accurate detection methods.
- Current methods for detecting vancomycin resistance in MRSA may not identify all resistant strains, potentially leading to treatment failures.
Purpose of the Study:
- To determine the distribution of vancomycin Minimum Inhibitory Concentration (MIC) values among MRSA isolates.
- To evaluate the frequency of MRSA strains exhibiting reduced vancomycin susceptibility.
- To assess the efficacy of different methods, including vancomycin screening agar, for detecting vancomycin resistance in MRSA.
Main Methods:
- One hundred MRSA isolates were tested using broth microdilution (BMD) for vancomycin MIC determination.
- Vancomycin screening agar with varying vancomycin concentrations, with and without casein, was employed to detect reduced susceptibility.
- The Vitek 2 system was also utilized for comparison in identifying vancomycin resistance.
Main Results:
- BMD identified 22% VISA and 78% VSSA, but failed to detect 9% hVISA isolates with MIC ≤ 2 µg/ml.
- Vancomycin screening agar detected hVISA (MIC ≤ 2 µg/ml) and VISA (MIC 4-6 µg/ml), with a 95.45% overall detection rate for VISA using 6 µg/ml concentration.
- Adding casein to screening agar improved VISA detection by 4.5%, and probable 'pre-hVISA' isolates (17%) were identified using 2 µg/ml with casein; Vitek 2 failed to detect any VISA.
Conclusions:
- Vancomycin screening agar, particularly with specific concentrations (2 µg/ml with casein for pre-hVISA, 4-6 µg/ml for hVISA/VISA), accurately detects reduced vancomycin susceptibility in MRSA.
- The Vitek 2 system demonstrated limitations in detecting VISA and hVISA isolates.
- Observed decreases in vancomycin susceptibility may be linked to 'MIC creep,' warranting long-term monitoring to understand its impact on treatment outcomes.
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