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Use of colistin and sorbitol for better isolation of Serratia marcescens in clinical samples

Published online by Cambridge University Press:  15 May 2009

G. M Grasso
Affiliation:
Institute of Hygiene and Preventive Medicine, 2nd Medical School, University of Naples, via S. Pansini 5, 80131 Naples, Italy
M. M D'errico
Affiliation:
Institute of Hygiene and Preventive Medicine, 2nd Medical School, University of Naples, via S. Pansini 5, 80131 Naples, Italy
F Schioppa
Affiliation:
Institute of Hygiene and Preventive Medicine, 2nd Medical School, University of Naples, via S. Pansini 5, 80131 Naples, Italy
F Romano
Affiliation:
Institute of Hygiene, Medical School, University of Reggio Calabria, via T. Campanella, 88100 Catanzaro, Italy
D Montanaro
Affiliation:
Institute of Hygiene and Preventive Medicine, 2nd Medical School, University of Naples, via S. Pansini 5, 80131 Naples, Italy
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A comparison was made of different culture media and procedures for detection of Serratia marcescens from faecal, pharyngeal and ocular swabs collected from 213 neonates. MacConkey agar and MacConkey agar with sorbitol (1%) and/or colistin (200 i.u./ml) were used both for primary isolation and after enrichment using Mossel Enterobacteriaceae broth with colistin (200 i.u./ml). The use of MacConkey agar supplemented with colistin for primary isolation improved considerably the isolation rate of S. marcescens from faecal swabs but not from pharyngeal swabs; the number of ocular isolations were insufficient to demonstrate differences between procedures. Moreover the enrichment procedures consistently increased the number of S. marcescens isolates especially from pharyngeal and ocular swabs. Use of sorbitol made detection of S'. marcescens from clinical specimens easier and time– and cost–efficient.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1988

References

Burger, S. C. & Bennett, J. W. (1985). Droplet enrichment factors of pigmented and nonpigmented Serratia marcescens: possible selective function for prodigiosin. Applied and Environmental Microbiology 50, 487490.CrossRefGoogle ScholarPubMed
Cochran, W. G. (1950). The comparison of percentages in matched samples. Biometrika 37, 256266.CrossRefGoogle ScholarPubMed
Dalbke, G. R. & Lynch, D. L. (1984). A procedure for isolation and speciation of Serratia from water samples. Microbios Letters 25, 105112.Google Scholar
Farmer, J. J. III, Silva, F. & Williams, D. R. (1973). Isolation of Serratia marcescens on deoxyribonuclease-toluidine blue cephalothin agar. Applied Microbiology 25, 151152.CrossRefGoogle ScholarPubMed
Fleiss, J. L. (1965). A note on Cochran's Q test. Biometrics 21, 10081010.CrossRefGoogle Scholar
Grimont, P. A. D. & Grimont, F. (1984). Genus VIII. Serratia. In Bergey's Manual of Systematic Bacteriology, vol. i (ed. Krieg, N. R.Holt, J. G.), pp. 477484. Baltimore: Williams & Wilkins.Google Scholar
Kelly, M. T., Brenner, D. J. & Farmer, J. J. III (1985). Enterobacteriaceae. In Manual of Clinical Microbiology, 4th ed. (ed. Lennette, E. H.Balows, A.Hausler, W. J. Jr. Shadomy, H. J.), pp. 263277. Washington, D. C.: American Society for Microbiology.Google Scholar
Lovell, D. J. & Bibel, D. J. (1977). Tween 80 medium for differentiating nonpigmented Serratia from other Enterobacteriaceae. Journal of Clinical Microbiology 5, 245247.CrossRefGoogle ScholarPubMed
Lynch, D. L. & Kenealy, W. R. (1976). A selective medium for the isolation of Serratia sp. from raw sewage. Microbios Letters 1, 3537.Google Scholar
Montanaro, D., Grasso, G. M., AnninoI., De I., DeRuggiero, N., Scarcella, A. & Schioppa, F. (1984). Epidemiological and bacteriological investigation of Serratia marcescens epidemic in a nursery and in a neonatal intensive care unit. Journal of Hygiene 93, 6778.CrossRefGoogle Scholar
Neuman, M. (1979). Vade-mecum des antibiotiques et agents chimiothérapiques anti-infectieux, 4th ed.Paris, France. Libraire Maloine.Google Scholar
Schreier, J. B. (1969). Modification of deoxyribonuclease test medium for rapid identification of Serratia marcescens. American Journal of Clinical Pathology 51, 711716.CrossRefGoogle ScholarPubMed
Slotnick, I. J. & Dougherty, M. (1972). Erythritol as a selective substrate for the growth of Serratia marcescens. Applied Microbiology 24. 292293.CrossRefGoogle ScholarPubMed
Starr, M. P., Grimont, P. A. D., Grimont, F. & Starr, P. B. (1976). Caprylate-thallous agar medium for selectively isolation Serratia and its utility in the clinical laboratory. Journal of Clinical Microbiology 4, 270276.CrossRefGoogle ScholarPubMed
Traub, W. H. & Kleber, I. (1975). In vitro additive effect of polymyxin B and rifampin against Serratia marcescens. Antimicrobial Agents Chemotherapy 7, 874876.CrossRefGoogle Scholar