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Antimicrobial Agents and Chemotherapy, July 2001, p. 1982-1989, Vol. 45, No. 7
0066-4804/01/$04.00+0   DOI: 10.1128/AAC.45.7.1982-1989.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Inducible Macrolide Resistance in Corynebacterium jeikeium

Adriana E. Rosato,dagger Bonnie S. Lee, and Kevin A. Nash*

Childrens Hospital Los Angeles and University of Southern California, Los Angeles, California

Received 3 August 2000/Returned for modification 10 November 2000/Accepted 6 April 2001

Corynebacterium jeikeium is an opportunistic pathogen primarily of immunocompromised (neutropenic) patients. Broad-spectrum resistance to antimicrobial agents is a common feature of C. jeikeium clinical isolates. We studied the profiles of susceptibility of 20 clinical strains of C. jeikeium to a range of antimicrobial agents. The strains were separated into two groups depending on the susceptibility to erythromycin (ERY), with one group (17 strains) representing resistant organisms (MIC > 128 µg/ml) and the second group (3 strains) representing susceptible organisms (MIC <=  0.25 µg/ml). The ERY resistance crossed to other members of the macrolide-lincosamide-streptogramin B (MLSb) group. Furthermore, this resistance was inducible with MLSb agents but not non-MLSb agents. Expression of ERY resistance was linked to the presence of an allele of the class X erm genes, erm(X)cj, with >93% identity to other erm genes of this class. Our evidence indicates that erm(X)cj is integrated within the chromosome, which contrasts with previous reports for the plasmid-associated erm(X) genes found in C. diphtheriae and C. xerosis. In 40% of C. jeikeium strains, erm(X)cj is present within the transposon, Tn5432. However, in the remaining strains, the components of Tn5432 (i.e., the erm and transposase genes) have separated within the chromosome. The rearrangement of Tn5432 leads to the possibility that the other drug resistance genes have become included in a new composite transposon bound by the IS1249 elements.


* Corresponding author. Mailing address: Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, 4650 Sunset Blvd., Mailstop 103, Los Angeles, CA 90027. Phone: (323) 669-5670. Fax: (323) 671-3871. E-mail: kanash{at}hsc.usc.edu.

dagger Present address: Department of Internal Medicine, Division of Infectious Diseases, Virginia Commonwealth University, Richmond, VA 23298.


Antimicrobial Agents and Chemotherapy, July 2001, p. 1982-1989, Vol. 45, No. 7
0066-4804/01/$04.00+0   DOI: 10.1128/AAC.45.7.1982-1989.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



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