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Monitoring Persistence of Coagulase-Negative Staphylococci in a Hematology Department Using Phenotypic and Genotypic Strategies

Published online by Cambridge University Press:  02 January 2015

Alex van Belkum*
Affiliation:
Department of Bacteriology, University Hospital Dijkzigt, Rotterdam, The Netherlands
Jan Kluijtmans
Affiliation:
Department of Bacteriology, University Hospital Dijkzigt, Rotterdam, The Netherlands
Willem van Leeuwen
Affiliation:
Department of Bacteriology, University Hospital Dijkzigt, Rotterdam, The Netherlands
Wil Goessens
Affiliation:
Department of Bacteriology, University Hospital Dijkzigt, Rotterdam, The Netherlands
Ellen ter Averst
Affiliation:
Department of Bacteriology, University Hospital Dijkzigt, Rotterdam, The Netherlands
Jenne Wielenga
Affiliation:
Department of Hematology, University Hospital Dijkzigt, Rotterdam, The Netherlands
Henri Verbrugh
Affiliation:
Department of Bacteriology, University Hospital Dijkzigt, Rotterdam, The Netherlands
*
University Hospital Dijkzigt, Department of Bacteriology, Dr Molewaterplein 40, 3015 GD Rotterdam, The Netherlands

Abstract

Objective:

To determine persistence of coagulase-negative staphylococci (CNS) on a hematology-oncology ward and to determine the value of phenotypic and genotypic procedures for establishing clonality among CNS isolates.

Design:

Strains of CNS isolated from bacteremic patients (n=139) were typed by biochemical reactivity, antibiotic susceptibility, DNA macrorestriction analysis by pulsed-field gel electrophoresis (PFGE), and arbitrary primed polymerase chain reaction (AP PCR). Coagulase-negative staphylococci were subgrouped in a random collection (n=20) used for the evaluation of the typing procedures and a collection of 119 CNS isolates from hematologic patients displaying multiple bacteremic episodes.

Results:

Analysis of the reference collection demonstrated the usefulness of the DNA typing procedures, indicating that AP PCR and PFGE can be used for epidemiologic typing of CNS in a concordant fashion. Certain strains appeared to be permanent colonizers of the hematology ward or ward-related personnel. In individual patients, persistent colonization by a single type was demonstrated. However, a number of patients also experienced bacteremic episodes caused by CNS belonging to different types.

Conclusion:

We conclude that monitoring of CNS infections on a hematology ward by various genotypic techniques provides insight into nosocomial epidemiology and elucidates the complexity of the infections taking place. DNA typing is preferred over phenotypic procedures and can identify persistent CNS strains in a given location.

Type
Original Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 1996 

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References

1. Kloos, WE, Bannerman, TL. Update on clinical significance of coagulase negative staphylococci. Clin Microbiol Rev 1994;7:117140.10.1128/CMR.7.1.117CrossRefGoogle ScholarPubMed
2. Kloos, WE, Musselwhite, MS. Distribution and persistence of Staphylococcus and Micrococcus species and other aerobic bacteria on human skin. Appl Microbiol 1975;30:381395.10.1128/am.30.3.381-395.1975CrossRefGoogle ScholarPubMed
3. Jarvis, WR, Martone, WJ. Predominant pathogens in hospital infections. J Antimicrob Chemother 1992;29(suppl A):1924.10.1093/jac/29.suppl_A.19CrossRefGoogle ScholarPubMed
4. Schaberg, DR, Culver, DH, Gaynes, RP. Major trends in the microbial etiology of nosocomial infection. Am J Med 1991;91(suppl 3B):7275.10.1016/0002-9343(91)90346-YCrossRefGoogle ScholarPubMed
5. Van de Leur, JJJPM, Dofferhoff, ASM, Van Turnhout, JM, Vollaard, EJ, Clasener, HA. Colonization of oropharynx with staphylococci after penicillin in neutropenic patients. Lancet 1992;340:861862.10.1016/0140-6736(92)92747-4CrossRefGoogle ScholarPubMed
6. Vandenesch, F, Lina, B, Lebeau, C, Greenland, TB, Etienne, J. Epidemiological markers of coagulase-negative staphylococci. Intensive Care Med 1993;19:311315.10.1007/BF01694703CrossRefGoogle ScholarPubMed
7. Izard, NC, Hachler, H, Grehn, M, Kayser, FH. Ribotyping of coag-ulase-negative staphylococci with special emphasis on intraspecific typing of Staphylococcus epidermidis . J Clin Microbiol 1992;30:817823.10.1128/jcm.30.4.817-823.1992CrossRefGoogle Scholar
8. Wilton, J, Jung, K, Vedin, I, Aronsson, B, Flock, JI. Comparative evaluation of a new molecular method for typing Staphylococcus epidermidis . Eur J Clin Microbiol Infect Dis 1992;11:515521.10.1007/BF01960806CrossRefGoogle ScholarPubMed
9. Nesin, M, Projan, SJ, Kreiswirth, B, Bolt, Y, Novick, RP. Molecular epidemiology of Staphylococcus epidermidis blood isolates from neonatal intensive care unit patients. J Hosp Infect 1995;31:111121.10.1016/0195-6701(95)90166-3CrossRefGoogle ScholarPubMed
10. Boom, R, Sol, CJA, Salimans, MMM, Jansen, CL, Wertheim-van Dillen, PME, Van der Noorda, J. Rapid and simple method for purification of nucleic acids. J Clin Microbiol 1990;28:495503.10.1128/jcm.28.3.495-503.1990CrossRefGoogle ScholarPubMed
11. Struelens, MJ, Bax, R, Deplano, A, Quint, WGV, van Belkum, A. Concordant clonal delineation of methicillin resistant Staphylococcus aureus by macrorestriction analysis and polymerase chain reaction genome fingerprinting. J Clin Microbiol 1993;31:19641970.10.1128/jcm.31.8.1964-1970.1993CrossRefGoogle ScholarPubMed
12. van Belkum, A, Bax, R, Peerbooms, P, Goessens, WHF, van Leeuwen, N, Quint, WGV. Comparison of phage typing and DNA fingerprinting by PCR for discrimination of methicillin resistant Staphylococcus aureus isolates. J Clin Microbiol 1993;31:798803.10.1128/jcm.31.4.798-803.1993CrossRefGoogle Scholar
13. van Belkum, A, Bax, R, Prevost, G. Comparison of four genotyping assays for epidemiological study of methicillin resistant Staphylococcus aureus . Eur J Clin Microbiol Infect Dis 1994;13:420424.10.1007/BF01972002CrossRefGoogle ScholarPubMed
14. Versalovic, J, Koeuth, T, Lupski, JR. Distribution of repetitive DNA sequences in eubacteria and application to fingerprinting of bacterial genomes. Nucleic Acids Res 1991;19:68236831.10.1093/nar/19.24.6823CrossRefGoogle ScholarPubMed
15. Sambrook, J, Fritsch, EF, Maniatis, T. Molecular Cloning: A Laboratory Manual. 2nd ed. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory; 1989.Google Scholar
16. Goering, RV, Winters, A. Rapid method for epidemiological evaluation of gram-positive cocci by field inversion gel electrophoresis. J Clin Microbiol 1992;77:2735.Google Scholar
17. Prevost, G, Jaulhac, B, Piemont, Y. DNA fingerprinting by pulsed field gel electrophoresis is more effective than ribotyping for distinguishing among methicillin resistant Staphylococcus aureus isolates. J Clin Microbiol 1992;30:967973.10.1128/jcm.30.4.967-973.1992CrossRefGoogle ScholarPubMed
18. Ludlam, HA, Noble, WC, Marples, RR, Bayston, R, Phillips, I. The epidemiology of peritonitis caused by coagulase negative staphylococci in continuous ambulatory peritoneal dialysis. J Med Microbiol 1991;30:167174.10.1099/00222615-30-3-167CrossRefGoogle Scholar
19. Beard-Pegles, MA, Gabelish, CL, Stubbs, E, Harbour, C. Prevalence of peritonitis associated coagulase negative staphylococci on the skin of continuous ambulatory peritoneal dialysis patients. Epidemiol Infect 1989;102:365378.10.1017/S0950268800030089CrossRefGoogle Scholar
20. Moller, JK. Observations on multiple drug resistance in coagulase negative staphylococci isolated from hospitals from 1975 to 1985. J Hosp Infect 1988;11:2635.10.1016/0195-6701(88)90036-9CrossRefGoogle ScholarPubMed
21. Moller, JK. Epidemiology of coagulase negative staphylococci in the hospital. In: Espersen, F, Thamdrup-Rosdahl, V, Moller, N, eds. Coagulase Negative Staphylococci, An Increasing Problem in Hospital-Acquired Infection. Bogtrykkergaarden, Denmark: Slagslunde; 1993.Google Scholar
22. Boyce, JM, Potter-Bynoe, G, Opal, SM, Dziobek, R, Medeiros, AA. Common source outbreak of Staphylococcus epidermidis infections among patients undergoing cardiac surgery. J Infect Dis 1990;161:493499.10.1093/infdis/161.3.493CrossRefGoogle ScholarPubMed
23. Huebner, J, Pier, GB, Maslow, JN, et al. Endemic nosocomial transmission of Staphylococcus epidermidis bacteremia isolates in a neonatal intensive care unit over 10 years. J Infect Dis 1994;169:526531.10.1093/infdis/169.3.526CrossRefGoogle Scholar
24. Lyytikainen, O, Saxen, H, Ryhanen, R, Vaara, M, Vuopio-Varkila, J. Persistence of a multi-resistant Staphylococcus epidermidis clone in a neonatal intensive care unit for a 4-year period. In: Abstract from the third international meeting on Bacterial Epidemiological Markers; April 6-9, 1994; Cambridge, UK. Abstract PA 13.Google Scholar
25. Tan, TQ, Musser, JM, Shulman, RJ, Mason, EO, Mahoney, DH, Kaplan, SL. Molecular epidemiology of coagulase negative Staphylococcus blood isolates from neonates with persistent bacteremia and children with central venous catheter infections. J Infect Dis 1994;169:13931397.10.1093/infdis/169.6.1393CrossRefGoogle ScholarPubMed
26. Chetchotisakd, P, Phelps, CL, Hartstein, AI. Assessment of bacterial cross-transmission as a cause of infections in patients in intensive care units. J Infect Dis 1994;18:929937.Google ScholarPubMed
27. Archer, GL. Molecular epidemiology of multiresistant Staphylococcus epidermidis . J Antimicrob Chemother 1988;21:133138.10.1093/jac/21.suppl_C.133CrossRefGoogle ScholarPubMed