Warianty tytułu
Języki publikacji
Abstrakty
The development of rapid and simple typing methods is required in order to identify possible sources of human exposure to opportunistic pathogens. Klebsiella spp. belongs to a group of bacteria that are opportunistic pathogens responsible for an increasing number of multi-resistant infections in hospitals. Recently, we showed the high genetic diversity of K. oxytoca using a large collection of strains isolated from the patients of several hospitals in Poland over a 50-year period. Our results showed that the internal transcribed spacer polymerase chain reaction method (ITS-PCR) is useful for the phylogenetic delineation of genetic groups in K. oxytoca and the high discriminatory power of the PCR melting profiles (PCR MP) method can be useful for epidemiological studies of K. oxytoca. In the present study the usefulness of PCR MP was tested on two sets of strains isolated from a single unit over a short period of time. The results revealed that PCR MP has a high discriminatory power and can be useful for epidemiological studies of closely related strains of K. oxytoca isolated from a single unit over a short period of time to identify the source, reservoirs and the tract of infection spread. The advantage of PCR MP for the above application was shown by using the procedure at increasing denaturation temperature during PCR to confirm genotyping results. Considering this feature and the high discriminatory power of PCR MP, as shown in this report for determination of the genetic similarities of consecutive K. oxytoca strains, we propose that PCR MP is one of the best techniques for short-term epidemiology analysis.
Wydawca
Czasopismo
Rocznik
Tom
Numer
Strony
247-253
Opis fizyczny
p.247-253,fig.,ref.
Twórcy
autor
- Gdansk University of Technology, Narutowicza 11/12, 80-952 Gdansk, Poland
autor
autor
Bibliografia
- Bingen E.H., P. Desjardins, G. Arlet, F. Bourgeois, P. Mariani Kurkdjian, N.Y. Lambert-Zechovsky, E. Denamur, A. Philippon and J. Elion. 1993. Molecular epidemiology of plasmid spread among extended broad-spectrum beta-lactamase-producing Klebsiella pneumoniae isolates in a pediatric hospital. J. Clin. Microbiol. 31: 179-184.
- Brisse S. and J. Verhoef. 2001. Phylogenetic diversity of Klebsiella pneumoniae and Klebsiella oxytoca clinical isolates revealed by randomly amplified polymorphic DNA, gyrA and parC genes sequencing and automated ribotyping. Int. J. Syst. Evol. Microbiol. 51: 915-924.
- Carrico, J. A., F.R. Pinto, C. Simas, S. Nunes, N.G. Sousa, N. Frazao, H. de Lencastre and J.S. Almeida. 2005. Assessment of bandbased similarity coefficients for automatic type and subtype classification of microbial isolates analyzed by pulsed-field gel electrophoresis. J. Clin. Microbiol. 43: 5483-5490.
- Combe M.L., J.L. Pons, R. Sesboue and J.P. Martin. 1994. Electrophoretic transfer from polyacrylamide gel to nitrocellulose sheets, a new method to characterize multi locus enzyme genotypes of Klebsiella strains. Appl. Environ. Microbiol. 60: 26-30.
- Ferragut C, K. Kersters and J. De Ley. 1989. Protein electrophoretic and DNA homology analysis of Klebsiella strains. Syst. Appl. Microbiol. 11: 121-127.
- Fevre C, M. Jbel, V. Passet, F.X. Weill, P.A.D. Grimont and S. Brisse. 2005. Six groups of the OXY beta-lactamase evolved over millions of years in Klebsiella oxytoca. Antimicrob. Agents. Chemother. 49: 3453-3462.
- Fournier B., P.H. Roy, P.H. Lagrange and A. Philippon. 1996. Chromosomal beta-lactamase genes of Klebsiella oxytoca are divided into two main groups, blaOXY-1 and blaOXY-2. Antimicrob. Agents. Chemother. 40: 454-459.
- Garcia de la Torre M., J. Romero-Vivas, J. Martinez-Beltran, A .Guerrero, M. Meseguer and E. Bouza. 1985. Klebsiella bacteremia: an analysis of 100 episodes. Rev. Infect. Dis. 7: 143-150.
- Hansen D.S., A. Gottschau and H.J. Kolmos. 1998. Epidemiology of Klebsiella bacteraemia: a case control study using Escherichia coli bacteraemia as control. J. Hosp. Infect. 38: 119-132.
- Holt J.G., N.R. Krieg, P.H.A. Sneath, J.T. Staley and S.T. Williams. 1994. Bergey's Manual of Determinative Bacteriology. The Williams & Wilkins Co., Baltimore, Md.
- Jensen M.A., J.A. Webster and N. Straus. 1993. Rapid identification of bacteria on the basis of polymerase chain reaction-amplified ribosomal DNA spacer polymorphisms. Appl. Environ. Microbiol. 59: 945- 952.
- Kałużewski S. 1967. Taxonomic position of indole-positive strains of Klebsiella. Exper. Med. Microbiol. 19: 327-35.
- Korvick JA, C.S. Bryan, B. Farber, T.R. Beam Jr, L. Schenfeld, R.R. Muder, D. Weinbaum, R. Lumish, D.N. Gerding, M.M. Wagener, et al. 1992. Prospective observational study of Klebsiella bacteremia in 230 patients: outcome for antibiotic combinations versus monotherapy. Antimicrob. Agents. Chemother. 36: 2639-2644.
- Krawczyk B, A. Samet, J. Leibner, A. Sledzinska and J. Kur. 2006. Evaluation of a PCR Melting Profile Technique for Bacterial Strain Differentiation. J. Clin. Microbiol. 44: 2327-32.
- Livermore D.M. 1995. b-Lactamases in laboratory and clinical resistance. Clin. Microbiol. Rev 8: 557-584.
- Mizuta K, M. Ohta, M. Mori, T. Hasegawa, I. Nakashima and N. Kato. 1983. Virulence for mice of Klebsiella strains belonging to the O1 group: relationship to their capsular (K) types. Infect. Immun. 40: 56-61.
- Morgan M.E., CA. Hart and R.W. Cooke. 1984. Klebsiella infection in a neonatal intensive care unit: role of bacteriological surveillance. J. Hosp. Infect. 5: 377-385.
- Ørskov I. and F. Ørskov. 1984. Serotyping of Klebsiella. In: T. Bergan (ed.) Methods in Microbiology, Vol. 14, Academic Press Inc. New York, NY, pp. 143-164.
- Ransjo U., Z. Good, K. Jalakas, I. Kuhn, I. Siggelkow, B. Aberg and E. Anjou. 1992. An outbreak of Klebsiella oxytoca septicemia associated with the use of invasive blood pressure monitoring equipment. Acta. Anaesthesiol. Scand. 36: 289-291.
- Rennie R.P. and I.B.R. Duncan. 1974. Combined biochemical and serological typing of clinical isolates of Klebsiella. Appl. Microbiol. 28: 534-539.
- Stojowska K., B. Krawczyk, S. Kałużewski and J. Kur. 2009. Retrospective analysis of the genetic diversity of Klebsiella oxytoca isolated in Poland over a 50-year period. Eur. J. Clin. Microbiol. Infect. Dis. (in press)
- Toldos C.M., G. Ortiz, M. Camara and M Segovia. 1997. Application of pulsed-field gel electrophoresis in an outbreak of infection due to Klebsiella oxytoca. J. Med. Microbiol. 46: 889-890.
- Van Belkum A., W. van Leeuwen, M.E. Kaufmann, B. Cookson, F. Forey, J. Etienne, R. Goering, F. Tenover, C. Steward, F. O'Brein, et al. 1998. Assessment of resolution and intercenter reproducibility of results of genotyping Staphylococcus aureus by pulsed-field gel electrophoresis of Smal macrorestriction fragments: a multicenter multicenter study. J. Clin. Microbiol. 36: 1653-1659.
- Watanakunakorn C. and J. Jura. 1991. Klebsiella bacteremia: a review of 196 episodes during a decade (1980-1989). Scand. J. Infect. Dis. 23: 399-405.
- Yinnon A.M., A. Butnaru, D. Ravch, Z. Jerassy and B. Rudensky. 1996. Klebsiella bacteraemia: community versus nosocomial infection. QJM. 89: 933-941.
Typ dokumentu
Bibliografia
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Identyfikator YADDA
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