Journal
INTERNATIONAL JOURNAL OF MEDICAL MICROBIOLOGY
Volume 298, Issue 7-8, Pages 607-617Publisher
ELSEVIER GMBH, URBAN & FISCHER VERLAG
DOI: 10.1016/j.ijmm.2008.01.015
Keywords
Methicillin-resistant Staphylococcus aureus (MRSA); mecA; Promoter mutation; beta-Lactam resistance levels
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Funding
- Swiss National Science Foundation [NF31-105390/1]
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The reason for the extremely low-level oxacillin resistance in a so-called 'drug clone', a methicillin-resistant Staphylococcus aureus circulating among injection drug users in Zurich, Switzerland, could be traced back to the mecA Promoter sequence and particularly to the strain's genetic background. Sequencing of its nice complex identified a point Mutation (TATACT to TATATT), creating a perfect palindrome in the -10 region of the mecA promoter/operator region containing the binding sites For the mecA repressors MecI and BlaI. Two strains with vastly different beta-lactam resistance phenotypes, the low-level resistant drug Clone type strain CHE482 and the highly homogeneously resistant strain COLn, were cured of their SCCmec elements and subsequently transformed with plasmids containing mecA under the control of either the wild-type or mutant promoter. Expression Studies showed that this mutation had significant effects on both mecA transcription and corresponding PBP2a production, but only small effects on beta-lactam resistance levels within a given genetic background. A Further mutation in the mecA ribosomal binding site (GGAGG to GGAGT). common to SCCmec type IV strains, was found to have no discernable effect oil me(A transcription and PBP2a content, and only minimal effects on beta-lactam resistance. Factors associated with the genetic backgrounds into which these differently controlled mecA genes were introduced had a Much higher impact on P-lactam resistance levels than the rates of mecA transcription. The tight repression of mecA expression this drug clone the absence of beta-lactams Could contribute to the apparent fitness of this Fast growing strain. (C) 2008 Elsevier GmbH. All rights reserved.
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