This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Oh, W. S.
Right arrow Articles by Woo, G.-J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Oh, W. S.
Right arrow Articles by Woo, G.-J.

 Previous Article  |  Next Article 

Antimicrobial Agents and Chemotherapy, December 2005, p. 5176-5178, Vol. 49, No. 12
0066-4804/05/$08.00+0     doi:10.1128/AAC.49.12.5176-5178.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

High Rate of Resistance to Quinupristin-Dalfopristin in Enterococcus faecium Clinical Isolates from Korea

Won Sup Oh,1,{dagger} Kwan Soo Ko,1,2,{dagger} Jae-Hoon Song,1,2* Mi Young Lee,2 Sulhee Park,2 Kyong Ran Peck,1 Nam Yong Lee,3 Choon-Kwan Kim,4 Hyuck Lee,5 Shin-Woo Kim,6 Hyun-Ha Chang,6 Yeon-Sook Kim,7 Sook-In Jung,8 Jun Seong Son,9 Joon-Sup Yeom,10 Hyun Kyun Ki,11 and Gun-Jo Woo12

Division of Infectious Diseases,1 Department of Laboratory Medicine, Samsung Medical Center, Seoul,3 Kangbuk Samsung Hospital, Seoul,10 Sungkyunkwan University School of Medicine, Asian-Pacific Research Foundation for Infectious Diseases (ARFID), Seoul,2 Seoul Veterans Hospital, Seoul,4 Dong-A University Hospital, Busan,5 Kyungpook National University Hospital, Daegu,6 Chungnam National University Hospital, Daejeon,7 Chonnam National University Medical School, Gwangju,8 Chungbuk National University Hospital, Chungju,9 Konkuk University Hospital, Seoul,11 Division of Food Microbiology, Korean Food & Drug Administration, Seoul, Korea,12

Received 14 July 2005/ Returned for modification 19 August 2005/ Accepted 20 September 2005


arrow
ABSTRACT
 
We tested the in vitro susceptibilities of 603 enterococcal isolates from eight tertiary-care hospitals in Korea. The quinupristin-dalfopristin resistance rate in Enterococcus faecium was very high (25 isolates, 10.0%). It was suggested that both clonal spread and the sporadic emergence of quinupristin-dalfopristin-resistant isolates may explain the high prevalence of quinupristin-dalfopristin resistance in Korea.


arrow
TEXT
 
Enterococci have become a more important cause of nosocomial infections with the emergence of multidrug-resistant strains in recent years (17). For instance, infections caused by vancomycin-resistant enterococci have resulted in increased morbidity and mortality due to limited treatment options (15). According to recent nationwide surveillance studies in Korea, the rate of vancomycin-resistant Enterococcus faecium (VREF) isolates has increased from 4% in 1997 to 16% in 2002 (11, 12). Quinupristin-dalfopristin (QD) could be useful in clinical practice as one of a few therapeutic options. Although several surveillance studies have reported increases in resistance to QD, the resistance rate still remains low in most parts (8, 13, 18). This recent multicenter surveillance study reports a high prevalence of QD resistance among E. faecium isolates from Korea.

Enterococcal isolates. As part of a multicenter surveillance study during 2 months (August and September) in 2004, a total of 603 nonduplicate enterococcal isolates (330 Enterococcus faecalis isolates, 249 E. faecium isolates, and 24 other isolates) were collected from eight tertiary-care hospitals in various regions of Korea. In vitro susceptibility testing was performed by a broth microdilution test according to CLSI guidelines (2). Eleven antimicrobial agents were tested: vancomycin, teicoplanin, ampicillin, tetracycline, erythromycin, ciprofloxacin, chloramphenicol, rifampin, QD, streptomycin, and gentamicin. For streptomycin (1,000 mg/liter) and gentamicin (500 mg/liter), high-level resistance was tested. Susceptibility interpretive criteria used were those established in CLSI standard M100-S15 (2). E. faecalis strain ATCC 29212 and Staphylococcus aureus strain ATCC 29213 were used as control strains. The chi-square test and Fisher's exact test were used to determine the significance of resistance differences where appropriate.

Molecular characterization. Multilocus sequence typing was performed as described previously (4, 9). To determine the number of variations in the esp A and C repeats, two different primer combinations were used, espfs7F-espfm5R and espfm5F-espfs3R, respectively (10). A genotypic clone was defined by coupling sequence type in multilocus sequence typing and the number of esp A and C repeats (9). Two virulence genes of E. faecium, enterococcal surface protein (esp) and hyaluronidase (hyl) genes, were detected by the duplex PCR method as described previously (23).

The results of the antimicrobial susceptibility test are summarized in Table 1. Sixty-three (25.3%) of 249 E. faecium isolates were resistant to vancomycin, while only 6 (1.8%) of 330 E. faecalis isolates were resistant to vancomycin. Resistance rates to vancomycin in E. faecium markedly varied by hospital, ranging from 0% to 54.7%. Isolates of VREF showed significantly higher resistance rates than vancomycin-susceptible E. faecium strains (VSEF) to teicoplanin, ampicillin, tetracycline, ciprofloxacin, and chloramphenicol (Table 2).


View this table:
[in this window]
[in a new window]
 
TABLE 1. Antibiotic resistance of E. faecium and E. faecalis isolates


View this table:
[in this window]
[in a new window]
 
TABLE 2. Comparison of antimicrobial resistance between VREF and VSEF isolates

In this study, the most prominent piece of data was a high rate of resistance to QD in E. faecium isolates in Korea (10.0%). This rate was significantly higher than those in North America, South America, and Europe, which ranged from 0% to 3.8% (7, 13, 19, 20, 22). Previous data from Korea with 56 E. faecium isolates also showed that only one isolate was resistant to QD (6). Based on previous reports, Taiwan showed very high rates of resistance to QD in E. faecium isolates, ranging from 9% to 51% (5, 14). Recent data from the SENTRY project in the Asian-Pacific region confirmed the high QD resistance rate in E. faecium from Taiwan (19.0%) and also showed increasing resistance to QD (29.4%) in Korea, with 17 isolates of E. faecium (J. M. Bell and J. D. Turnidge, Abstr. 44th Intersci. Conf. Antimicrob. Agents Chemother., abstr. C2-1361, 2004). Our study confirmed the increasing tendency of QD resistance in E. faecium isolates in Korea. Such high QD resistance rates in E. faecium in Taiwan and Korea were not observed in other Asian-Pacific countries (Bell and Turnidge, 44th ICAAC, abstr. C2-1361).

Our data showed a much higher QD resistance rate (12.9%) in VSEF than in VREF (3.2%), which was consistent with previous data (1). This implies that the QD resistance in E. faecium is not associated with the recent use of QD in the hospital for the treatment of vancomycin-resistant enterococci. Actually, the emergence of QD resistance even before its commercial use in the United States suggests that QD resistance might be linked with other reasons. Luh et al. (14) inferred that the high QD resistance rate in E. faecium in Taiwan was due to the use of virginiamycin in animal husbandry for many years. In Korea, virginiamycin has also been frequently used as a growth promoter in food animals, which could partly explain the high prevalence of QD resistance in E. faecium. However, the use of virginiamycin may not be the sole reason for the high rate of resistance to QD in Korea and Taiwan because Europe and the United States, where virginiamycin has also been used in animal husbandry, showed a low rate of QD resistance (16, 21). In addition, transmission of antibiotic-resistant E. faecium isolates from animals to humans is not common (3).

The QD resistance rate in E. faecium isolates was the highest at the Samsung Medical Center (16 of 64 isolates). In this hospital, two clones, ST192-A5-C6 in seven isolates and STnew-A0-C0 in two isolates, were identified (Table 3). This may suggest the clonal spread of the resistant strain within that hospital. In addition, two isolates in the Seoul Veterans Hospital also belonged to the same clone. However, there was no evidence that QD-resistant E. faecium isolates from other Korean hospitals have been clonally disseminated.


View this table:
[in this window]
[in a new window]
 
TABLE 3. Genotypic characteristics and antimicrobial resistance in 25 QD-resistant E. faecium isolates from Korea

Of 249 E. faecium isolates, esp and hyl genes were detected in 184 (73.9%) and 169 (67.9%) isolates, respectively. The esp gene was more frequently found in VREF (58/63 isolates, 92.1%) than in VSEF (67.7%) isolates. The hyl gene was present in 37 (58.7%) and 232 (71.0%) VREF and VSEF isolates, respectively. A dual presence of esp and hyl genes was observed among 31 VREF (49.2%) and 108 VSEF (58.1%) isolates.

In summary, the present study documented a high rate of QD resistance in E. faecium from Korea due to both clonal spread and sporadic emergence. Given the clinical importance of multidrug-resistant enterococci, continuous surveillance of QD resistance in E. faecium is strongly warranted if QD is to be used to treat E. faecium.


arrow
ACKNOWLEDGMENTS
 
This study was partly supported by the Korean Food & Drug Administration (KFDA) and the Asian-Pacific Research Foundation for Infectious Diseases (ARFID).

The eight tertiary-care hospitals participating in this study were the Samsung Medical Center (SMC, Seoul), Seoul Veterans Hospital (Seoul), Kangbuk Samsung Hospital (Seoul), Dong-A University Hospital (Busan), Kyungpook National University Hospital (Daegu), Chungnam National University Hospital (Daejeon), Chonnam National University Hospital (Gwangju), and Chungbuk National University Hospital (Chungju).


arrow
FOOTNOTES
 
* Corresponding author. Mailing address: Division of Infectious Diseases, Samsung Medical Center, Sungkyunkwan University School of Medicine, Asian-Pacific Research Foundation for Infectious Diseases (ARFID), 50 Ilwon-dong, Kangnam-ku, Seoul 135-710, Korea. Phone: 82-2-3410-0320. Fax: 82-2-3410-0328. E-mail: jhsong{at}smc.samsung.co.kr. Back

{dagger} W.S.O and K.S.K. contributed equally as joint first authors. Back


arrow
REFERENCES
 
    1
  1. Ballow, C. H., R. N. Jones, and D. J. Biedenbach. 2002. A multicenter evaluation of linezolid antimicrobial activity in North America. Diagn. Microbiol. Infect. Dis. 43:75-83.[CrossRef][Medline]
  2. 2
  3. Clinical and Laboratory Standards Institute. 2005. Performance standards for antimicrobial susceptibility testing, 15th informational supplement. Document M100-S15. CLSI, Wayne, Pa.
  4. 3
  5. Coque, T. M., R. J. L. Willems, J. Fortún, J. Top, S. Diz, E. Loza, R. Cantón, and F. Baquero. 2005. Population structure of Enterococcus faecium causing bacteremia in a Spanish university hospital: setting the scene for a future increase in vancomycin resistance? Antimicrob. Agents Chemother. 49:2693-2700.[Abstract/Free Full Text]
  6. 4
  7. Homan, W. L., D. Tribe, S. Poznanski, M. Li, G. Hogg, E. Spalburg, J. D. A. van Embden, and R. J. L. Willems. 2002. Multilocus sequence typing scheme for Enterococcus faecium. J. Clin. Microbiol. 40:1963-1971.[Abstract/Free Full Text]
  8. 5
  9. Hsueh, P. R., W. H. Chen, L. J. Teng, and K. T. Luh. 2005. Nosocomial infections due to methicillin-resistant Staphylococcus aureus and vancomycin-resistant enterococci at a university hospital in Taiwan from 1991 to 2003: resistance trends, antibiotic usage and in vitro activities of newer antimicrobial agents. Int. J. Antimicrob. Agents 26:43-49.[CrossRef][Medline]
  10. 6
  11. Hwang, S. H., M. N. Kim, C. H. Pai, D. H. Huh, and W. S. Shin. 2000. In vitro activities of quinupristin/dalfopristin and eight other antimicrobial agents against 360 clinical isolates from Korea. Yensei Med. J. 41:563-569.
  12. 7
  13. Jevitt, L. A., A. J. Smith, P. P. Williams, P. M. Raney, J. E. McGowan, Jr., and F. C. Tenover. 2003. In vitro activities of daptomycin, linezolid, and quinupristin-dalfopristin against a challenge panel of staphylococci and enterococci, including vancomycin-intermediate Staphylococcus aureus and vancomycin-resistant Enterococcus faecium. Microb. Drug Resist. 9:389-393.[CrossRef][Medline]
  14. 8
  15. Jones, R. N., C. H. Ballow, D. J. Biedenbach, J. A. Deinhart, and J. J. Schentag. 1998. 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. 31:437-451.[CrossRef][Medline]
  16. 9
  17. Ko, K. S., J. Y. Baek, J.-Y. Lee, W. S. Oh, K. R. Peck, N. Y. Lee, W. G. Lee, K. Lee, and J.-H. Song. 2005. Molecular characterization of vancomycin-resistant Enterococcus faecium isolates from Korea. J. Clin. Microbiol. 43:2303-2306.[Abstract/Free Full Text]
  18. 10
  19. Leavis, H., J. Top, N. Shankar, K. Borgen, M. Bonten, J. van Embden, and R. J. L. Willems. 2004. A novel putative enterococcal pathogenicity island linked to the esp virulence gene of Enterococcus faecium and associated with epidemicity. J. Bacteriol. 186:672-682.[Abstract/Free Full Text]
  20. 11
  21. Lee, K., S. J. Jang, H. J. Lee, N. Ryoo, M. Kim, S. G. Hong, and Y. Chong. 2004. Increasing prevalence of vancomycin-resistant Enterococcus faecium, expanded-spectrum cephalosporin-resistant Klebsiella pneumoniae, and imipenem-resistant Pseudomonas aeruginosa in Korea: KONSAR study in 2001. J. Kor. Med. Sci. 19:8-14.
  22. 12
  23. Lee, K., Y. A. Kim, Y. J. Park, H. S. Lee, M. Y. Kim, E. C. Kim, D. Yong, and Y. Chong. 2004. Increasing prevalence of vancomycin-resistant enterococci and cefoxitin-, imipenem- and fluoroquinolone-resistant gram-negative bacilli: a KONSAR study in 2002. Yensei Med. J. 45:598-608.
  24. 13
  25. Low, D. E., N. Keller, A. Barth, and R. N. Jones. 2001. Clinical prevalence, antimicrobial susceptibility, and geographic resistance patterns of enterococci: results from the SENTRY antimicrobial surveillance program, 1997-1999. 32(Suppl. 2):S133-S145.
  26. 14
  27. Luh, K. T., P. R. H. Hsueh, L. J. Teng, H. J. Pan, Y. C. Chen, J. J. Lu, J. J. Wu, and S. W. Ho. 2000. Quinupristin-dalfopristin resistance among gram-postive bacteria in Taiwan. Antimicrob. Agents Chemother. 44:3374-3380.[Abstract/Free Full Text]
  28. 15
  29. Malathum, K., and B. E. Murray. 1999. Vancomycin-resistant enterococci: recent advances in genetics, epidemiology and therapeutic options. Drug Resist. Updates 2:224-243.[CrossRef][Medline]
  30. 16
  31. McDonald, L. C., S. Rossiter, C. Mackinson, Y. Y. Wang, S. Johnson, M. Sullivan, R. Sokolow, E. Debess, L. Gilbert, J. A. Benson, B. Hill, and F. J. Angulo. 2001. Quinupristin-dalfopristin-resistant Enterococcus faecium on chicken and in human stool specimens. N. Engl. J. Med. 345:1155-1160.[Abstract/Free Full Text]
  32. 17
  33. Murray, B. E. 1990. The life and times of the Enterococcus. Clin. Microbiol. Rev. 3:46-65.[Abstract/Free Full Text]
  34. 18
  35. Mutnick, A. H., D. J. Biedenbach, and R. N. Jones. 2003. Geographic variations and trends in antimicrobial resistance among Enterococcus faecalis and Enterococcus faecium in the SENTRY Antimicrobial Surveillance Program (1997-2000). Diagn. Microbiol. Infect. Dis. 46:63-68.[CrossRef][Medline]
  36. 19
  37. Sader, H. S., R. N. Jones, C. H. Ballow, D. J. Biedenbach, R. F. Cered, and the GSMART Latin America Study Group. 2001. Antimicrobial susceptibility of quinupristin/dalfopristin tested against gram-positive cocci from Latin America: results from the global SMART (GSMART) surveillance study. Braz. J. Infect. Dis. 5:21-31.[Medline]
  38. 20
  39. Simonsen, G. S., K. Bergh, L. Bevanger, A. Digranes, P. Gaustad, K. K. Melby, and E. A. Hoiby. 2004. Susceptibility to quinupristin-dalfopristin and linezolid in 839 clinical isolates of Gram-positive cocci from Norway. Scand. J. Infect. Dis. 36:254-258.[CrossRef][Medline]
  40. 21
  41. Soltani, M., D. Beighton, J. Philpott-Howard, and N. Woodford. 2000. Mechanisms of resistance to quinupristin-dalfopristin among isolates of Enterococcus faecium from animals, raw meat, and hospital patients in Western Europe. Antimicrob. Agents Chemother. 44:433-436.[Abstract/Free Full Text]
  42. 22
  43. Torres-Vierak, C., and L.-M. Dembry. 2004. Approaches to vancomycin-resistant enterococci. Curr. Opin. Infect. Dis. 17:541-547.[CrossRef][Medline]
  44. 23
  45. Vankerchhoven, V., T. V. Autgaerden, C. Vael, C. Lammens, S. Chapelle, R. Rossi, D. Jabes, and H. Goossens. 2004. Development of a multiplex PCR for the detection of asa1, gelE, cylA, esp, and hyl genes in enterococci and survey for virulence determinants among European hospital isolates of Enterococcus faecium. J. Clin. Microbiol. 42:4473-4479.[Abstract/Free Full Text]


Antimicrobial Agents and Chemotherapy, December 2005, p. 5176-5178, Vol. 49, No. 12
0066-4804/05/$08.00+0     doi:10.1128/AAC.49.12.5176-5178.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Hwang, I. Y., Ku, H. O., Lim, S. K., Park, C. K., Jung, G. S., Jung, S. C., Nam, H. M. (2009). Species distribution and resistance patterns to growth-promoting antimicrobials of enterococci isolated from pigs and chickens in Korea. jvdi 21: 858-862 [Abstract] [Full Text]  
  • Song, J.-H., Ko, K. S., Suh, J. Y., Oh, W. S., Kang, C.-I., Chung, D. R., Peck, K. R., Lee, N. Y., Lee, W. G. (2008). Clinical implications of vancomycin-resistant Enterococcus faecium (VRE) with VanD phenotype and vanA genotype. J Antimicrob Chemother 61: 838-844 [Abstract] [Full Text]  
  • Korczynska, M., Mukhtar, T. A., Wright, G. D., Berghuis, A. M. (2007). Structural basis for streptogramin B resistance in Staphylococcus aureus by virginiamycin B lyase. Proc. Natl. Acad. Sci. USA 104: 10388-10393 [Abstract] [Full Text]  
  • Van Wamel, W. J. B., Hendrickx, A. P. A., Bonten, M. J. M., Top, J., Posthuma, G., Willems, R. J. L. (2007). Growth Condition-Dependent Esp Expression by Enterococcus faecium Affects Initial Adherence and Biofilm Formation. Infect. Immun. 75: 924-931 [Abstract] [Full Text]  
  • Kim, Y.-R., Kim, S.-I., Hur, J.-A., Kim, Y.-J., Wie, S.-H., Park, Y.-J., Kang, M.-W. (2007). Comparison of the MicroScan System and the Agar Dilution Assay for Quinupristin/Dalfopristin Susceptibility of Enterococcus faecium. Annals of Clinical & Laboratory Science 37: 260-262 [Abstract] [Full Text]  
  • French, G. L. (2006). Bactericidal agents in the treatment of MRSA infections--the potential role of daptomycin. J Antimicrob Chemother 58: 1107-1117 [Abstract] [Full Text]  

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Oh, W. S.
Right arrow Articles by Woo, G.-J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Oh, W. S.
Right arrow Articles by Woo, G.-J.