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Characterization of Nosocomial Strains of Enterobacter aerogenes by Arbitrarily Primed-PCR Analysis and Ribotyping

Published online by Cambridge University Press:  02 January 2015

Florence Grattard*
Affiliation:
Laboratory of Bacteriology-Virology, University of Medicine, Saint-Etienne, France
Bruno Pozzetto
Affiliation:
Laboratory of Bacteriology-Virology, University of Medicine, Saint-Etienne, France
Lionel Tabard
Affiliation:
Laboratory of Bacteriology-Virology, University of Medicine, Saint-Etienne, France
Marianne Petit
Affiliation:
Laboratory of Bacteriology-Virology, University of Medicine, Saint-Etienne, France
Alain Ros
Affiliation:
Laboratory of Bacteriology-Virology, University of Medicine, Saint-Etienne, France
Odette G. Gaudin
Affiliation:
Laboratory of Bacteriology-Virology, University of Medicine, Saint-Etienne, France
*
Laboratoire de Bactéiologie-Vologie, Faclté de Médecine J. Lisfranc, rue A. Paré, 42023 Saint-Etienne Cedex 2, France

Abstract

Objective:

To study the spread of strains of Enterobacter aerogenes in our hospital in 1992 and 1993 by using two genotypic markers, and to evaluate these methods for the epidemiological investigation of this species.

Design:

Ribotyping (using two endonucleases) and arbitrarily primed (AP)-PCR (using two different 10-mer primers) were applied to the epidemiological typing of clinical strains of E aerogenes isolated from hospitalized patients.

Setting and Patients:

The intensive care unit (ICU; 5 patients, 13 isolates), nephrology units (3 patients, 5 isolates), and surgery units (2 patients, 2 isolates) of the university hospital of Saint-Etienne (France).

Results:

Eight epidemiologically unrelated isolates, chosen as controls, exhibited distinct profiles, both by AP-PCR and ribotyping. Two clones of E aerogenes circulated in the ICU; both were isolated successively from samples of a single patient who stayed in the unit for almost 1 year. A third clone was recovered from patients of surgery units. A fourth clone was shown to have infected patients of nephrology units.

Conclusions:

Ribotyping and AP-PCR appear to be reliable methods for typing E aerogenes strains implicated in nosocomial infection. The spread of independent clones of E aerogenes in different units of our hospital in 1992 and 1993 was demonstrated by both methods. This study emphasizes the need to choose the endonucleases or primers with care to obtain high discriminatory results in genotypic investigations.

Type
Original Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 1995

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References

1. Gaston, MA. Enterobacter: an emerging nosocomial pathogen. J Hosp Infect 1988;11:197208.10.1016/0195-6701(88)90098-9CrossRefGoogle ScholarPubMed
2. Flynn, DM, Weinstein, RA, Nathan, C, Gaston, MA, Kabins, SA. Patients' endogenous flora as the source of ‘nosocomial’ Enterobacter in cardiac surgery. J Infect Dis 1987;156:363368.Google Scholar
3. Griffith, BP, Kormos, RL, Hardesty, RL, Armitage, JM, Dummer, JS. The artificial heart: infection-related morbidity and its effect on transplantation. Ann Thorac Surg 1988;45:409414.Google Scholar
4. de Champs, C, Guelon, D, Joyon, D, Sirot, D, Chanal, M, Sirot, J. Treatment of a meningitis due to Enterobacter aerogenes producing a derepressed cephalosporinase and a Klebsiella pneumoniae producing an extended-spectrum beta-lactamase. Infection 1991;19:181183.Google Scholar
5. Mellencamp, MA, Roccaforte, JS, Preheim, LC, Sanders, CC, Anene, CA, Bittner, MJ. Isolation of Enterobacter aerogenes susceptible to beta-lactam antibiotics despite high level beta-lactamase production. Eur J Clin Microbial Infect Dis 1990;9:827830.Google Scholar
6. de Champs, C, Henquell, C, Guelon, D, Sirot, D, Gazuy, N, Sirot, J. Clinical and bacteriological study of nosocomial infections due to Enterobacter aerogenes resistant to imipenem. J Clin Microbiol 1993;31:123127.Google Scholar
7. Jaroux, E, Collet, L, Bellon, O, et al. Emergence of Enterobacter aerogenes strains with an extended-spectrum betalactamase in Provence. 3rd International Conference on the Prevention of Infection, Nice, April 4-5, 1994, abstract MCBG.Google Scholar
8. Markowitz, SM, Smith, SM, Williams, DS. Retrospective analysis of plasmid patterns in a study of bum unit outbreaks of infection due to Enterobucter cloacae . J Infect Dis 1983;148:1823.10.1093/infdis/148.1.18Google Scholar
9. Haertl, R, Bandlow, G. Epidemiological fingerprinting of Enterobacter cloacae by small-fragment restriction endonuclease analysis and pulsed-field gel electrophoresis of genomic restriction fragments. J Clin Microbial 1993;31:128133.Google Scholar
10. Grattard, F, Pozzetto, B, Berthelot, PH, et al. Arbitrarily primed PCR, ribotyping, and plasmid pattern analysis applied to investigation of a nosocomial outbreak due to Enterobacter cloacae in a neonatal intensive care unit. J Clin Microbiol 1994;32:596602.10.1128/jcm.32.3.596-602.1994Google Scholar
11. Garaizar, J, Kaufmann, ME, Pitt, TL. Comparison of ribotyping with conventional methods for the type identification of Enterobucter cloacae . J Clin Microbiol 1991;29:13031307.CrossRefGoogle ScholarPubMed
12. Poilane, I, Cruaud, P, Lachassinne, E, et al. Enterobacter cloacae cross-colonization in neonates demonstrated by ribotyping. Eur J Clin Microbiol Infect Dis 1993;12:820826.CrossRefGoogle ScholarPubMed
13. Gaston, MA, Strickland, MA, Ayling-Smith, BA, Pitt, TL. Epidemiological typing of Enterobucter aerogenes . J Clin Microbiol 1989;27:564565.Google Scholar
14. Grattard, F, Pozzetto, B, Ros, A, Gaudin, OG. Differentiation of Pseudomonas aeruginosa strains by ribotyping: high discriminatory power by using a single restriction endonuclease. J Med Microbiol 1994;40:275282.10.1099/00222615-40-4-275Google Scholar
15. Williams, JGK, Kubelick, AR, Livak, KJ, Rafalski, JA, Tingey, SV. DNA polymorphisms amplified by arbitrary primers are useful genetic markers. Nucleic Acids Res 1990;18:65316535.CrossRefGoogle Scholar
16. Van Belkum, A, Bax, R, Peerbooms, P, Goessens, WHF, Van Leeuwen, N, Quint, WGV. Comparison of phage typing and DNA fingerprinting by polymerase chain reaction for discrimination of methicillin-resistant Staphylococcus aureus strains. J Clin Microbiol 1993;31:798803.Google Scholar
17. MacPherson, JM, Eckstein, PE, Scoles, GJ, Gajadhar, AA. Variability of random amplified polymorphic DNA assay among thermal cyclers, and effects of primer and DNA concentration. Mol Cell Probes 1993;7:293299.10.1006/mcpr.1993.1043Google Scholar
18. Meunier, JR, Grimont, PAD. Factors affecting reproducibility of random amplified polymorphic DNA fingerprinting. Res Microbiol 1993;144:373379.Google Scholar