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Antimicrobial Agents and Chemotherapy, January 2007, p. 231-238, Vol. 51, No. 1
0066-4804/07/$08.00+0     doi:10.1128/AAC.00576-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

High-Level Vancomycin-Resistant Staphylococcus aureus Isolates Associated with a Polymicrobial Biofilm{triangledown}

Linda M. Weigel,1* Rodney M. Donlan,1 Dong Hyeon Shin,1,{dagger} Bette Jensen,1 Nancye C. Clark,1 Linda K. McDougal,1 Wenming Zhu,1 Kimberlee A. Musser,2 Jill Thompson,2 Donna Kohlerschmidt,2 Nellie Dumas,2 Ronald J. Limberger,2 and Jean B. Patel1

Division of Healthcare Quality Promotion, Centers for Disease Control and Prevention, Atlanta, Georgia,1 Wadsworth Center, New York State Department of Health, Albany, New York2

Received 10 May 2006/ Returned for modification 21 July 2006/ Accepted 18 October 2006

Glycopeptides such as vancomycin are the treatment of choice for infections due to methicillin-resistant Staphylococcus aureus. This study describes the identification of high-level vancomycin-resistant S. aureus (VRSA) isolates in a polymicrobial biofilm within an indwelling nephrostomy tube in a patient in New York. S. aureus, Enterococcus faecalis, Enterococcus faecium, Micrococcus species, Morganella morganii, and Pseudomonas aeruginosa were isolated from the biofilm. For VRSA isolates, vancomycin MICs ranged from 32 to >128 µg/ml. VRSA isolates were also resistant to aminoglycosides, fluoroquinolones, macrolides, penicillin, and tetracycline but remained susceptible to chloramphenicol, linezolid, rifampin, and trimethoprim-sulfamethoxazole. The vanA gene was localized to a plasmid of ~100 kb in VRSA and E. faecium isolates from the biofilm. Plasmid analysis revealed that the VRSA isolate acquired the 100-kb E. faecium plasmid, which was then maintained without integration into the MRSA plasmid. The tetracycline resistance genes tet(U) and tet(S), not previously detected in S. aureus isolates, were identified in the VRSA isolates. Additional resistance elements in the VRSA isolate included a multiresistance gene cluster, ermB-aadE-sat4-aphA-3, msrA (macrolide efflux), and the bifunctional aminoglycoside resistance gene aac(6')-aph(2")-Ia. Multiple combinations of resistance genes among the various isolates of staphylococci and enterococci, including vanA, tet(S), and tet(U), illustrate the dynamic nature of gene acquisition and loss within and between bacterial species throughout the course of infection. The potential for interspecies transfer of antimicrobial resistance genes, including resistance to vancomycin, may be enhanced by the microenvironment of a biofilm.

* Corresponding author. Mailing address: NCID/DHQP/ELB MS:G-08, Centers for Disease Control and Prevention, 1600 Clifton Road, N.E., Atlanta, GA 30333. Phone: (404) 639-1497. Fax: (404) 639-1381. E-mail: lweigel{at}cdc.gov.

{triangledown} Published ahead of print on 30 October 2006.

{dagger} Present address: Department of Infectious Diseases, Chonnam National University Medical School, Gwangju, Korea.

Antimicrobial Agents and Chemotherapy, January 2007, p. 231-238, Vol. 51, No. 1
0066-4804/07/$08.00+0     doi:10.1128/AAC.00576-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.



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