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. 1981 Dec;42(6):1093–1102. doi: 10.1128/aem.42.6.1093-1102.1981

Prolonged survival of Serratia marcescens in chlorhexidine.

T J Marrie, J W Costerton
PMCID: PMC244159  PMID: 7032422

Abstract

During an outbreak of Serratia marcescens infections at our hospital, we discovered widespread contamination of the 2% chlorhexidine hand-washing solution by S. marcescens. Examination by electron microscopy of the sides of bottles in which this solution was stored revealed that microorganisms were embedded in a fibrous matrix. Bacteria, free in the liquid, were morphologically abnormal, showing cell wall disruption or cytoplasmic changes. Furthermore, bacteria adherent to the walls of the storage jugs and embedded in this fibrous matrix also had morphologically abnormal cytoplasm. Despite these changes, viable S. marcescens organisms were recovered from the fluid during a storage period of 27 months. The concentration of chlorhexidine required to inhibit these strains of Serratia was 1,024 microgram/ml; however, the organism could survive in concentrations of up to 20,000 micrograms/ml. Additional studies are needed to define the mechanism(s) that allows such bacteria to contaminate and survive in disinfectants.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bassett D. C. The effect of pH on the multiplication of a pseudomonad in chlorhexidine and cetrimide. J Clin Pathol. 1971 Nov;24(8):708–711. doi: 10.1136/jcp.24.8.708. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Burdon D. W., Whitby J. L. Contamination of hospital disinfectants with Pseudomonas species. Br Med J. 1967 Apr 15;2(5545):153–155. doi: 10.1136/bmj.2.5545.153. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Burdon K. L. Fatty Material in Bacteria and Fungi Revealed by Staining Dried, Fixed Slide Preparations. J Bacteriol. 1946 Dec;52(6):665–678. doi: 10.1128/jb.52.6.665-678.1946. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Hennessey T. D. Antibacterial properties of Hibitane. J Clin Periodontol. 1977 Dec;4(5):36–48. doi: 10.1111/j.1600-051x.1977.tb00050.x. [DOI] [PubMed] [Google Scholar]
  5. Lovell D. J., Bibel D. J. Tween 80 medium for differentiating nonpigmented Serratia from other Enterobacteriaceae. J Clin Microbiol. 1977 Feb;5(2):245–247. doi: 10.1128/jcm.5.2.245-247.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Luft J. H. Ruthenium red and violet. II. Fine structural localization in animal tissues. Anat Rec. 1971 Nov;171(3):369–415. doi: 10.1002/ar.1091710303. [DOI] [PubMed] [Google Scholar]
  7. Malick L. E., Wilson R. B. Modified thiocarbohydrazide procedure for scanning electron microscopy: routine use for normal, pathological, or experimental tissues. Stain Technol. 1975 Jul;50(4):265–269. doi: 10.3109/10520297509117069. [DOI] [PubMed] [Google Scholar]
  8. Richards R. M., Cavill R. H. Electron-microscope study of the effect of chlorhexidine on Pseudomonas aeruginosa. Microbios. 1979;26(104):85–93. [PubMed] [Google Scholar]
  9. Stickler D. J., Thomas B. Antiseptic and antibiotic resistance in Gram-negative bacteria causing urinary tract infection. J Clin Pathol. 1980 Mar;33(3):288–296. doi: 10.1136/jcp.33.3.288. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Thomas B., Stickler D. J. Chlorhexidine resistance and the lipids of Providencia stuartii. Microbios. 1979;24(97-98):141–150. [PubMed] [Google Scholar]
  11. Wishart M. M., Riley T. V. Infection with Pseudomonas maltophilia hospital outbreak due to contaminated disinfectant. Med J Aust. 1976 Nov 6;2(19):710–712. doi: 10.5694/j.1326-5377.1976.tb128238.x. [DOI] [PubMed] [Google Scholar]

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