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Antimicrobial Agents and Chemotherapy, July 2001, p. 1955-1963, Vol. 45, No. 7
Department of Bacteriology, Faculty of
Medicine, Juntendo University, Tokyo, Japan
Received 5 September 2000/Returned for modification 26 December
2000/Accepted 6 April 2001
We report on the structural diversity of mecA gene
complexes carried by 38 methicillin-resistant Staphylococcus
aureus and 91 methicillin-resistant coagulase-negative
Staphylococcus strains of seven different species with a
special reference to its correlation with phenotypic expression of
methicillin resistance. The most prevalent and widely disseminated
mec complex had the structure mecI-mecR1-mecA-IS431R (or
IS431mec), designated the class A mecA gene
complex. In contrast, in S. haemolyticus, mecA was
bracketed by two copies of IS431, forming the structure
IS431L-mecA-IS431R. Of the 38 S. haemolyticus strains, 5 had low-level methicillin resistance
(MIC, 1 to 4 mg/liter) and characteristic heterogeneous methicillin
resistance as judged by population analysis. In these five strains,
IS431L was located to the left of an intact
mecI gene, forming the structure IS431L-class A
mecA-gene complex. In other S. haemolyticus
strains, IS431L was associated with the deletion of
mecI and mecR1, forming the structure
IS431L-
0066-4804/01/$04.00+0 DOI: 10.1128/AAC.45.7.1955-1963.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Genetic Organization of the Chromosome Region
Surrounding mecA in Clinical Staphylococcal Strains: Role of
IS431-Mediated mecI Deletion in Expression of
Resistance in mecA-Carrying, Low-Level
Methicillin- Resistant Staphylococcus
haemolyticus
mecR1-mecA-IS431mec, designated the class C mecA gene complex. Mutants with the
class C mecA gene complex were obtained in vitro by
selecting strain SH621, containing the IS431L-class A
mecA gene complex with low concentrations of methicillin (1 and 3 mg/liter). The mutants had intermediate level of methicillin
resistance (MIC, 16 to 64 mg/liter). The mecA gene
transcription was shown to be derepressed in a representative mutant
strain, SH621-37. Our study indicated that the mecI-encoded
repressor function is responsible for the low-level methicillin
resistance of some S. haemolyticus clinical strains and
that the IS431-mediated mecI gene deletion
causes the expression of methicillin resistance through the
derepression of mecA gene transcription.
*
Corresponding author. Mailing address: Department of
Bacteriology, Faculty of Medicine, Juntendo University, 2-1-1 Hongo, Bunkyo-ku, Tokyo, Japan 113-8421. Phone: 81-3-5802-1040. Fax: 81-3-5684-7830. E-mail: hiram{at}med.juntendo.ac.jp.
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