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Updated: Jul 15, 2026

Biosensor for Detection of Antibiotic Resistant Staphylococcus Bacteria
Published on: May 8, 2013
Occurrence of vancomycin-intermediate-resistant Staphylococcus aureus in Japan
Hideaki Hanaki1, Yasuko Hososaka, Chie Yanagisawa
1Kitasato Research Center for Anti-infection Drugs, The Kitasato Institute, 5-9-1 Shirokane, Minato-ku, Tokyo, 108-0072, Japan. hanaki@lisci.kitasato-u.ac.jp
Abstract:
The Clinical and Laboratory Standards Institute (CLSI) amended the criteria for vancomycin susceptibility and resistance of Staphylococcus aureus in 2006. The earlier criteria had established that S. aureus with minimum inhibitory concentrations (MICs) of vancomycin of < or =4 microg/ml, 8 to 16 microg/ml, and > or =32 microg/ml were vancomycin-susceptible, -intermediate-resistant and -resistant, respectively. The revised recommendation states that bacteria showing vancomycin MICs of < or =2 microg/ml, 4 to 8 microg/ml, and > or =16 microg/ml are -susceptible, -intermediate-resistant, and -resistant, respectively. We examined, based on these new criteria, the vancomycin susceptibility of methicillin-resistant S. aureus (MRSA) strains isolated in Japan from 1978 through 2005 at 17 general hospitals. The results showed that, among 2446 MRSA isolates tested, 8 were classified as intermediate-vancomycin-resistant (VISA). Re-examination of vancomycin susceptibility in these 8 strains in 2006 revealed that 6 strains showed a vancomycin MIC of 4 microg/ml, as tested by the agar dilution method, broth dilution methods, and E-test; the 2 other strains had lost the vancomycin resistance. Pulsed-field gel electrophoresis (PFGE) of the chromosomal DNA of these strains exhibited five unique profiles; 2 strains isolated from the same hospital were identical. These results revealed that at least five different types of VISA strains could be identified in Japan so far according to the new CLSI criteria. All these VISA strains had type II staphylococcal cassette chromosome, mec. This study revealed, for the first time in Japan, the presence of intermediate vancomycin-resistant MRSA in this country.
Insights
The Clinical and Laboratory Standards Institute revised vancomycin resistance criteria in 2006. This study identified intermediate vancomycin-resistant methicillin-resistant Staphylococcus aureus (MRSA) in Japan, revealing at least five distinct VISA strains.
Area of Science:
- Microbiology
- Infectious Diseases
- Clinical Laboratory Science
Background:
- The Clinical and Laboratory Standards Institute (CLSI) updated vancomycin susceptibility criteria for Staphylococcus aureus in 2006.
- Previous criteria classified vancomycin MICs differently than the revised recommendations.
- Methicillin-resistant Staphylococcus aureus (MRSA) poses a significant public health threat.
Purpose of the Study:
- To evaluate vancomycin susceptibility of MRSA strains in Japan using the new CLSI criteria.
- To identify and characterize intermediate vancomycin-resistant MRSA (VISA) strains.
- To determine the genetic diversity of identified VISA strains.
Main Methods:
- Analysis of 2446 MRSA isolates collected in Japan between 1978 and 2005.
- Application of the revised 2006 CLSI vancomycin susceptibility criteria.
- Determination of vancomycin MICs using agar dilution, broth dilution, and E-test methods.
- Pulsed-field gel electrophoresis (PFGE) for chromosomal DNA analysis.
Main Results:
- Eight MRSA isolates were classified as intermediate vancomycin-resistant (VISA) based on the new criteria.
- Re-testing confirmed vancomycin MICs of 4 microg/ml for six strains; two strains lost resistance.
- PFGE identified five distinct VISA strain profiles, with two isolates from the same hospital being identical.
- All identified VISA strains possessed the type II staphylococcal cassette chromosome mec.
Conclusions:
- This study reports the first identification of intermediate vancomycin-resistant MRSA in Japan.
- At least five different VISA strain types were identified according to the updated CLSI guidelines.
- The findings highlight the evolving landscape of antibiotic resistance in MRSA.
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