Reduced glycopeptide susceptibility in methicillin-resistant Staphylococcus aureus (MRSA)
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Updated: Jul 11, 2026

Biosensor for Detection of Antibiotic Resistant Staphylococcus Bacteria
Published on: May 8, 2013
1Hershey Medical Center, P.O. Box 850, Hershey, PA 17033, USA. pappelbaum@psu.edu
Abstract:
Vancomycin and other glycopeptide antibiotics are the current mainstay of therapy for infections caused by methicillin-resistant Staphylococcus aureus (MRSA). However, the high prevalence of MRSA has led to increased use of vancomycin in chronic and seriously ill patients and has resulted in the emergence of MRSA with reduced susceptibility to glycopeptides. Multiple MRSA phenotypes demonstrate reduced susceptibility to glycopeptides. According to the Clinical and Laboratory Standards Institute, vancomycin-intermediate S. aureus (VISA) are now those isolates with minimum inhibitory concentrations (MICs) between 4 microg/mL and 8 microg/mL, whilst heterogeneous VISA (hVISA) strains appear to be susceptible to vancomycin but contain a subpopulation of cells with reduced susceptibility to vancomycin (MICs > or = 4 microg/mL). At this time, MICs for these strains are reported to range between 1 microg/mL and 2 microg/mL. Vancomycin-resistant S. aureus (VRSA) are defined as those having MICs > or = 16 microg/mL. The detection of reduced susceptibility to vancomycin by routine susceptibility testing is unreliable and vancomycin non-susceptibility is most probably being underreported. Reports of reduced clinical efficacy associated with vancomycin MICs between 1 microg/mL and 2 microg/mL have been published. Patients most at risk of infection by hVISA, VISA and VRSA appear to be those with previous exposure to vancomycin. VRSA appears in the elderly and those with chronic leg or decubitus ulcers mainly containing vancomycin-resistant enterococci, which were probably the donor organism of the vanA gene to S. aureus. All MRSA strains recovered from patients whose infections do not respond to vancomycin treatment should be tested accurately for vancomycin susceptibility if these phenotypes are not to be missed. Treatment options for infections due to MRSA with reduced susceptibility to vancomycin are limited. Rapid identification of patients harbouring VRSA, VISA or hVISA as well as prompt isolation and adherence to infection control protocols are paramount in controlling the dissemination of these pathogens.
Insights
Methicillin-resistant Staphylococcus aureus (MRSA) is increasingly showing reduced susceptibility to vancomycin, a key antibiotic. Accurate detection and infection control are crucial for managing these challenging infections.
Area of Science:
- Infectious Diseases
- Microbiology
- Antimicrobial Resistance
Background:
- Vancomycin is the primary treatment for methicillin-resistant Staphylococcus aureus (MRSA) infections.
- Increased vancomycin use has led to the emergence of MRSA with reduced susceptibility.
- Vancomycin-intermediate S. aureus (VISA), heterogeneous VISA (hVISA), and vancomycin-resistant S. aureus (VRSA) are emerging phenotypes.
Purpose of the Study:
- To highlight the growing problem of vancomycin-non-susceptible MRSA.
- To discuss the challenges in detecting these resistant strains.
- To emphasize the need for improved management strategies.
Main Methods:
- Review of current definitions for VISA, hVISA, and VRSA.
- Discussion of the limitations of routine susceptibility testing.
- Analysis of patient risk factors and transmission pathways.
Main Results:
- Detection of vancomycin non-susceptibility in MRSA is often unreliable and underreported.
- Reduced vancomycin susceptibility is associated with clinical treatment failures.
- Patients with prior vancomycin exposure are at higher risk.
Conclusions:
- Accurate susceptibility testing for MRSA is essential, especially in treatment failures.
- Limited treatment options exist for infections caused by vancomycin-non-susceptible MRSA.
- Prompt identification, isolation, and infection control are critical to prevent spread.
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