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Plasmid DNA Profiles of Acinetobacter Baumannii: Clinical Application in a Complex Endemic Setting

Published online by Cambridge University Press:  02 January 2015

Harald Seifert*
Affiliation:
Institute of Medical Microbiology and Hygiene, Klinikum Merheim, Cologne, Germany
Bertil Boullon
Affiliation:
University of Cologne, and the Department of Surgery, Klinikum Merheim, Cologne, Germany
Andrea Schulze
Affiliation:
Institute of Medical Microbiology and Hygiene, Klinikum Merheim, Cologne, Germany
Gerhard Pulverer
Affiliation:
Institute of Medical Microbiology and Hygiene, Klinikum Merheim, Cologne, Germany
*
Institut fur Medizinische Mikrobiologie und Hygiene, Goldenfelsstr. 19-21, 50935 Koln, Germany

Abstract

Objective:

To study the epidemiological, microbiological, and clinical features of infections due to Acinetobacter baumannii in a complex endemic situation over an 18-month period and to determine the clinical usefulness of plasmid DNA analysis of A baumannii in epidemiological investigations.

Design:

Review of medical and laboratory records. Antibiotic resistance patterns, biotyping, and plasmid profile analysis were used to characterize clinical and environmental isolates. Pulsed-field gel electrophoresis (PFGE) of chromosomal DNA was performed to verify results obtained with the other typing methods.

Setting:

Four different intensive care units of an 800-bed tertiary care center in Cologne, Germany.

Results:

240 patients were colonized or infected with A baumannii during the study period. No seasonal variations were observed. The majority of isolates (53%) were recovered from the respiratory tract. Major infections occurred in 61 patients; these included 48 bacteremias and eight pulmonary infections. Five different epidemic strains were identified: one each was A baumannii biotype 2 and 6, and three were biotype 9. A baumannii biotype 9 accounted for the vast majority of isolates (88%), which were clustered into three epidemic strains demonstrating distinct plasmid profiles. Two of these were considered genetically related as shown by PFGE. Epidemic strains were multidrug resistant, being uniformly susceptible to imipenem only. An epidemiological investigation failed to identify any point source of infection. Barrier precautions and improved handwashing were instituted in three of the four units and significantly reduced the incidence of colonization and infection in these units. Attack rates remained unchanged, however, in the burn unit where control measures were not implemented.

Conclusion:

Acinetobacter strains representing multiple biotypes and plasmid types were present in this endemic setting. Multidrug resistance in A baumannii is an important concern. Plasmid DNA analysis proved to be useful in epidemiological typing of A baumannii strains and may serve as a complementary typing system to traditional epidemiological methods.

Type
Original Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 1994

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References

1. Hartstein, AI, Rashad, AL, Liebler, JM, et al. Multiple intensive care unit outbreak of Acinetobacter calcoaceticus subspecies anitrutus respiratory infection and colonization associated with contaminated, reusable ventilator circuits and resuscitation bags. Am J Med 1988;85:624631.CrossRefGoogle ScholarPubMed
2. Beck-Sague, CM, Jarvis, WR, Brook, JH, et al. Epidemic bacteremia due to Acinetobacter baumannii in five intensive care units. Am J Epidemiol 1990;132:723733.CrossRefGoogle ScholarPubMed
3. Sakata, H, Fujita, K, Maruyama, S, Kakehashi, H, Mori, Y Yoshioka, H. Acinetobacter calcoaceticus biovar anitrutus septicaemia in a neonatal intensive care unit: epidemiology and control. J Hosp Infect 1989;14:1522.CrossRefGoogle Scholar
4. Jarvis, WR, Mattone, WJ. Predominant pathogens in hospital infection. J Anti microb Chemother 1992;29(suppl A):1924.CrossRefGoogle Scholar
5. Patterson, JE, Vecchio, J, Pantelick, EL, et al. Association of contaminated gloves with transmission of Acinetobacter cal-coaceticus var. anitrutus in an intensive care unit. Am J Med 1991;91:479483.CrossRefGoogle Scholar
6. Sherertz, RJ, Sullivan, ML. An outbreak of infections with Acinetobacter culcoaceticus in bum patients: contamination of patients' mattresses. J Infect Dis 1985; 151:252258.CrossRefGoogle Scholar
7. Vandenbroucke-Grauls, CM, Kerver, AJ, Rommes, JH, Jansen, R, den-Dekker, C. Verhoef, J. Endemie Acinetobucter anitratus in a surgical intensive care unit: mechanical ventilators as reservoir. Eur J Clin Microbiol Infect Dis 1988;7:485489.CrossRefGoogle Scholar
8. Cefai, C. Richards, J, Gould, FK. McPeake, I? An outbreak of Acinetoducter respiratory tract infection resulting from incomplete disinfection of ventilatory equipment. J Hosp Infect 1990;15:177182.Google Scholar
9. Contant, J, Kemeny, E, Oxley, C, Perry, E, Garber, G. Investigation of an outbreak of Acinetobactev calcoaceticus var. anitratus infections in an adult intensive care unit. Am J Infect Control 1990;18:288291.Google Scholar
10. Peacock, JE, Sorrell, L, Sortile, FD, Price, LC, Rutala, WA Nosocomial respiratory tract colonization and infection with aminogly-coside-resistant Acinetobacter calcouceticus var. anitratus: epidemiologic characteristics and clinical significance. Infect Control Hosp Epidemiol 1988;9:302308.CrossRefGoogle ScholarPubMed
11. Buxton, AE, Anderson, RL, Werdegar, D, Atlas, E. Nosocomial respiratory tract infection and colonization with Acinetobacter calcoaceticus. Epidemiologic characteristics. Am J Med 1978;65:507513.CrossRefGoogle ScholarPubMed
12. French, GL, Casewell, MW Roncoroni, AJ, Knight, S, Phillips, I. A hospital outbreak of antibiotic-resistant Acinetobactev anitratus: epidemiology and control. J Hosp Infect 1980;1:125131.CrossRefGoogle Scholar
13. Seifert, H. Baginski, R, Schulze, A. Pulverer, G. Antimicrobial susceptibility of Acinetobacter species. Antimicrob Agents Chemother 1993;37:750753.CrossRefGoogle ScholarPubMed
14. Joly-Guillou, ML, Bergogne-Berezin, E, Vieu, JE Epidemiologie et resistance aux antibiotiques des Acinetobacter en milieu hospitalier. Presse Médicale 1990;19:357–61.Google Scholar
15. Baumann, I? Isolation of Acinetobucter from soil and water. J Bacteriol 1968;96:3942.Google Scholar
16. Taplin, D, Rebell, G, Zaiab, N. The human skin as a source of Mima-Herella infections. JAMA 1963;186:166168.CrossRefGoogle ScholarPubMed
17. Alexander, M, Rahman, M, Taylor, M, Noble, WC. A study of the value of electrophoretic and other techniques for typing Acinetobacter culcouceticus. J Hosp Infect 1988;12:273287.CrossRefGoogle Scholar
18. Joly-Guillou, ML, Bergogne-Berezin, E, Vieu, JE A study of the relationships between antibiotic resistance phenotypes, phage-typing and biotyping of 117 clinical isolates of Acinetobacter spp. J Hosp Infect 1990;16:4958.CrossRefGoogle ScholarPubMed
19. Bouvet, PJ, Grimont, PA Identification and biotyping of clinical isolates of Acinetobuctes Ann Znst Risteur Microbiol 1987;138:569578.Google Scholar
20. Bouvet, PJ, Jeanjean, S, Vieu, JF, Dijkshoom, L. Species, biotype, and bacteriophage type determinations compared with cell envelope protein profiles for typing Acinetobucter strains. J Clin Microbiol 1990;28:170176.CrossRefGoogle ScholarPubMed
21. Dijkshoorn, L, Aucken, HM, Gemer-Smidt, P, Kaufmann, ME, Ursing, J, Pitt, TL. Correlation of typing methods for Acinetobacter isolates from hospital outbreaks. J Clin Microbiol 1993;31:702705.CrossRefGoogle ScholarPubMed
22. Traub, WH. Acinetobacter baumunnii serotyping for delineation of outbreaks of nosocomial cross-infection. J Clin Microbiol 1989;27:27132716.CrossRefGoogle ScholarPubMed
23. Hartstein, AI, Morthland, VH, Rourke, JW, et al. Plasmid DNA fingerprinting of Acinetobacter calcoaceticus subspecies anitratus from intubated and mechanically ventilated patients. Infect Control Hosp Epidemiol 1990;11:531538.CrossRefGoogle ScholarPubMed
24. Picard, B, Goullet, P. Epidemiological typing of Acinetobacter strains by esterase electrophoresis. FEMS Microbiol Lett 1990;72:229234.Google Scholar
25. Gouby, A, Carles-Nurit, MJ, Bouziges, N, Bourg, G, Mesnard, R, Bouvet, PJ. Use of pulsed-field gel electrophoresis for investigation of hospital outbreaks of Acinetobacter baumannii . J Clin Microbiol 1992;30:15881591.CrossRefGoogle ScholarPubMed
26. Gerner-Smidt, I? Ribotyping of the Acinetobacter calcoaceticus-Acinetobacter baumannii complex. J Clin Microbiol 1992;30:26802685.CrossRefGoogle ScholarPubMed
27. Gräser, Y, Klare, I, Halle, E, et al. Epidemiological study of an Acinetobacter baumannii outbreak by using polymerase chain reaction fingerprinting. J Clin Microbiol 1993;31:24172420.CrossRefGoogle ScholarPubMed
28. Johnson, DR, Love-Dixon, MA, Brown, WJ, Levine, DR Downes, FR Hall, WN. Delayed detection of an increase in resistant Acinetobacter at a Detroit hospital. Infect Control Hosp Epidemiol 1992;13:394398.Google Scholar
29. Garner, JS, Jarvis, WR, Emori, TG, Horan, TC, Hughes, JM. CDC definitions for nosocomial infections. Am J Infect Control 1988;16:128140.Google Scholar
30. Juni, E. Interspecies transformation of Acinetobacter: genetic evidence for a ubiquitous genus. J Bacteriol 1972;112:917931.CrossRefGoogle ScholarPubMed
31. Seifert, H, Schulze, A, Baginski, R, Pulverer, G. Plasmid DNA fingerprinting of Acinetobacter species other than Acinetobacter baumannii . J Clin Microbiol 1994;32:8286.CrossRefGoogle ScholarPubMed
32. Tjemberg, I, Ursing, J. Clinical strains of Acinetobacter classified by DNA-DNA hybridization. APMIS 1989;97:595605.CrossRefGoogle Scholar
33. Schumacher-Perdreau, F, Jansen, B, Seifert, H, Peters, G, Pulverer, G. Outbreak of methicillin-resistant Staphylococcus aureus in a teaching hospital-epidemiological and microbiological surveillance. Zentralblatt für Bakteriologie 1994;280:550559.CrossRefGoogle Scholar
34. Bouvet, PJ. Grimont, PA. Taxonomy of the genus Acinetobacter with the recognition of Acinetobacter baumannii sp.nov., Acinetobacter haemolyticus sp.nov., Acinetobacter johnsonii sp.nov., and Acinetobacter junii sp.nov., and emended description of Acinetobacter calcoaceticus and Acinetobacter Iwoffii . Int J Syst Bacteriol 1986;36:228240.Google Scholar
35. Mayer, LW. Use of plasmid profiles in epidemiologic surveillance of disease outbreaks and in tracing the transmission of antibiotic resistance. Clin Microbiol Rev 1988;1:228243.Google Scholar
36. Vila, J, Almela, M, Jimenez-de-Anta, MT Laboratory investigation of hospital outbreak caused by two different multiresistant Acinetobacter calcoaceticus subsp. anitratus strains. J Clin Microbiol 1989;27:10861089.Google Scholar
37. Noel, GJ, Kreiswirth, BN, Edelson, PJ, et al. Multiple methicillin-resistant Staphylococcus aureus strains as a cause for a single outbreak of severe disease in hospitalized neonates. Bediatr Infect Dis 1992;11:184188.Google Scholar
38. Getchell-White, SI, Donowitz, LG, Groschel, DH. The inanimate environment of an intensive care unit as a potential source of nosocomial bacteria: evidence for long survival of Acinetobacter calcoaceticus . Infect Control Hosp Epidemiol 1989;10:402407.Google ScholarPubMed