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Molecular Typing and Antimicrobial Susceptibility of Vancomycin-Resistant Enterococcus faecium in Brazil

Published online by Cambridge University Press:  02 January 2015

Rosangela F. Cereda
Affiliation:
Division of Infectious Diseases, Universidade Federal Sao Paulo, Brazil
Ana C. Gales
Affiliation:
Division of Infectious Diseases, Universidade Federal Sao Paulo, Brazil
Suzane Silbert
Affiliation:
Division of Infectious Diseases, Universidade Federal Sao Paulo, Brazil
Ronald N. Jones
Affiliation:
Department of Pathology, University of Iowa College of Medicine, Iowa City, Iowa
Helio S. Sader*
Affiliation:
Division of Infectious Diseases, Universidade Federal Sao Paulo, Brazil
*
Laboratório Especial de Microbiologia Clínica, Infectious Disease Division, Federal University of Sao Paulo, Rua Botucatu, 740. Sao Paulo, SP- CEP 04023-063 – Brazil

Abstract

Objectives:

To characterize vancomycin-resistant enterococci (VRE) isolates and to evaluate the mode of dissemination of this pathogen in Brazil.

Design:

We collected 22 vancomycin-resistant Enterococcus faecium isolates from 6 medical centers in Sao Paulo, Brazil, and 1 isolate from a medical center in Curitiba, Brazil.

Participants:

All Brazilian hospitals that had identified vancomycin-resistant E. faecium up to the beginning of this study (late 1999) contributed isolates to the study.

Methods:

The isolates were susceptibility tested using the broth microdilution method and the E-test. The presence of vancomycin resistance genes (vanA, vanB, vanC1, vanC2-3, and vanD) was evaluated by polymerase chain reaction; molecular typing was performed by pulsed-field gel electrophoresis (PFGE).

Results:

The vanA gene was demonstrated in all vancomycin-resistant E. faecium, except for 1 isolate. None of the vancomycin resistance genes cited above was detected in the isolate from Curitiba, which was the first vancomycin-resistant E. faecium described in Brazil. All isolates were resistant to ampicillin and teicoplanin. The main clone remains susceptible to doxycycline and chloramphenicol, but intermediate to quinupristin-dalfopristin. PFGE analysis demonstrated 7 major PFGE patterns. A unique PFGE pattern with 4 subtypes was detected in 17 isolates from 4 different hospitals.

Conclusion:

The results of our study indicate the occurrence of intra- and interhospital dissemination of VRE in Sao Paulo, Brazil.

Type
Original Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 2002

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References

1.Sastry, V, Brennan, PJ, Levy, MM, et al. Vancomycin-resistant enterococci: an emerging pathogen in immunosuppressed transplant recipients. Transplant Proc 1995;27:954955.Google ScholarPubMed
2.Leclerq, R, Courvalin, P. Resistance to glycopeptides in enterococci. Clin Infect Dis 1997;24:545546.CrossRefGoogle Scholar
3.Cereda, RF, Pignatari, AC, Hashimoto, A, Sader, HS. In vitro antimicrobial activity against enterococci isolated in a university hospital in São Paulo, Brazil. Brazilian Journal of Infectious Diseases 1997;1:8390.Google Scholar
4.Pfaller, MA, Jones, RN, Doern, GV, Kugler, K, SENTRY Participants Group. Bacterial pathogens isolated from patients with bloodstream infection: frequencies of occurrence and antimicrobial susceptibility patterns from the SENTRY Antimicrobial Surveillance Program (United States and Canada, 1997). Antimicrob Agents Chemother 1998;42:17621770.CrossRefGoogle Scholar
5.Pfaller, MA, Jones, RN, Doern, GV, et al. Survey of blood stream infections attributable to gram-positive cocci: frequency of occurrence and antimicrobial susceptibility of isolates collected in 1997 in the United States, Canada, and Latin America from the SENTRY Antimicrobial Surveillance Program. Diagn Microbiol Infect Dis 1999;33:283297.CrossRefGoogle ScholarPubMed
6.Sader, HS, Sampaio, JLM, Zoccoli, C, Jones, RN. Results of the SENTRY Antimicrobial Surveillance Program in three Brazilian medical centers for 1997. Brazilian Journal of Infectious Diseases 1999;3:6379.Google ScholarPubMed
7.Dalla-Costa, LM, Souza, DC, Martins, LTF, et al. Vancomycin-resistant Enterococcus faecium: first case in Brazil. Brazilian Journal of Infectious Diseases 1998;2:160163.Google Scholar
8.Sader, HS, Jones, RN, Ballow, CH, Biedenbach, DJ, Cereda, RF. Antimicrobial susceptibility of quinupristin-dalfopristin tested against gram positive cocci from Latin America: results from the Global SMART (GSMART) Surveillance Study. Brazilian Journal of Infectious Diseases 2001;5:2130.CrossRefGoogle ScholarPubMed
9.Facklam, R, Sahm, DA, Teixeira, LM. Enterococcus. In: Murray, PR, Baron, EJ, Pfaller, MA, Tenover, FC, Yolken, RH, eds. Manual of Clinical Microbiology, 7th ed. Washington, DC: American Society for Microbiology; 1999:297305.Google Scholar
10.National Committee for Clinical Laboratory Standards (NCCLS). Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria That Grow Aerobically, 5th ed. Approved Standard, M7-A5. Wayne, PA: National Committee for Clinical Laboratory Standards; 2000.Google Scholar
11.National Committee for Clinical Laboratory Standards (NCCLS). Performance Standards for Antimicrobial Susceptibility Testing: Tenth Informational Supplement M100-S10. Wayne, PA: National Committee for Clinical Laboratory Standards; 2000.Google Scholar
12.National Committee for Clinical Laboratory Standards (NCCLS). Performance Standards for Antimicrobial Susceptibility Testing: Eighth Informational Supplement M100-S8. Wayne, PA: National Committee for Clinical Laboratory Standards; 1998.Google Scholar
13.Dutka-Malen, S, Evers, S, Courvalin, P. Detection of glycopeptide resistance genotypes and identification to the species level of clinically relevant enterococci by PCR. J Clin Microbiol 1995;30:16211624.Google Scholar
14.Soltani, M, Beighton, D, Philpott-Howard, J, Woodford, N. Mechanisms of resistance to quinupristin-dalfopristin among isolates of Enterococcus faecium from animals, raw meat, and hospital patients in Western Europe. Antimicrob Agents Chemother 2000;44:433436.CrossRefGoogle ScholarPubMed
15.Werner, G, Witte, W. Characterization of a new enterococcal gene, satG, encoding a putative acetyltransferase conferring resistance to streptogramin A compounds. Antimicrob Agents Chemother 1999;43:18131814.CrossRefGoogle ScholarPubMed
16.Pfaller, MA, Sader, HS, Hollis, RJ. Chromosomal restriction fragment analysis by pulsed-field gel electrophoresis. In: Isenberg, HD, ed. Clinical Microbiology Procedures Handbook. Washington, DC: American Society for Microbiology; 1992:112.Google Scholar
17.Jones, RN, Ballow, CH, Biedenbach, DJ, Deinhart, JA, Schentag, JJ. Antimicrobial activity of quinupristin-dalfopristin (RP 59500, Synercid) tested against over 28,000 recent clinical isolates from 200 medical centers in the United States and Canada. Diagn Microbiol Infect Dis 1998;31:437451.CrossRefGoogle Scholar
18.Dalla-Costa, LM, Reynolds, PE, Souza, AHM, Souza, DC, Palepou, MPI, Woodford, N. Characterization of a divergent vanD-type resistance element from the first glycopeptide-resistant strain of Enterococcus faecium in Brazil. Antimicrob Agents Chemother 2000;44:34443446.CrossRefGoogle ScholarPubMed
19.Vannuffel, P, Cocito, C. Mechanism of action of streptogramins and macrolides. Drugs 1996;51(suppl 1):2030.CrossRefGoogle ScholarPubMed
20.Sader, HS, Pignatari, AC, Hollis, RJ, Jones, RN. Evaluation of interhospital spread of methicillin-resistant Staphylococcus aureus in São Paulo, Brazil, using pulsed-field gel electrophoresis of chromosomal DNA. Infect Control Hosp Epidemiol 1994;15:320323.CrossRefGoogle Scholar
21.Cereda, RF, Vinagre, A, Hashimoto, A, et al. Low prevalence of patients colonized with vancomycin-resistant enterococci in spite of high use of vancomycin. Presented at the 98th General Meeting of the American Society for Microbiology; May 17-21, 1998; Atlanta, GA, Abstract C-356.Google Scholar
22.Centers for Disease Control and Prevention (CDC). Recommendations for preventing the spread of vancomycin resistance: recommendations of the Hospital Infection Clinical Practices Advisory Committee (HICPAC), United States, 1995. MMWR 1995;44(RR-12):113.Google Scholar
23.Sader, HS, Pfaller, MA, Tenover, FC, Hollis, RJ, Jones, RN. Evaluation and characterization of multiresistant Enterococcus faecium from twelve U.S. medical centers. J Clin Microbiol 1994;32:28402842.CrossRefGoogle Scholar