Intercenter reproducibility of binary typing for Staphylococcus aureus
The reproducibility of the binary typing (BT) protocol developed for epidemiological typing of Staphylococcus aureus was analyzed in a biphasic multicenter study. In a Dutch multicenter pilot study, 10 genetically unique isolates of methicillin-resistant S. aureus (MRSA) were characterized by the BT...
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Published in: | Journal of microbiological methods Vol. 51; no. 1; pp. 19 - 28 |
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01-09-2002
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Abstract | The reproducibility of the binary typing (BT) protocol developed for epidemiological typing of
Staphylococcus aureus was analyzed in a biphasic multicenter study. In a Dutch multicenter pilot study, 10 genetically unique isolates of methicillin-resistant
S. aureus (MRSA) were characterized by the BT assay as presented by van Leeuwen et al. [J. Clin. Microbiol. 2001 39 (1) 328]. The BT assay, including a standardized DNA extraction protocol was performed in duplicate in eleven medical microbiology laboratories. Two different hybridization detection procedures were applied and a prelabeled DNA sample as process control was included. Only three laboratories accurately identified all strains. Divergence in technical procedures resulted in misinterpretation due to an increasing number of faint or absent hybridization signals in combination with high background staining. The binary type of the process control was determined correctly by all participating laboratories. The feasibility of the BT protocol was related directly to the skill of the laboratory personnel. On the basis of the national study, we concluded that the DNA extraction protocol needed modification to improve DNA yield and purity.
Subsequently, seven European laboratories participated in an international study to determine the reproducibility of the modified BT protocol. Each center was asked to analyze 10 DNA samples previously extracted from 10 MRSA strains (phase 1) and, additionally, to analyze 10 MRSA strains, using the standardized or their in-house DNA isolation protocol (phase 2). A prelabeled DNA process control sample was included again. The binary types of all DNA samples were identified correctly by all but one laboratories. This latter laboratory diverged from the protocol by adding an excess of labeled DNA to the hybridization mixture, resulting in a high background and, therefore, noninterpretable BT results. All centers produced identical BT results for the process control. Five of the seven centers correctly identified the binary types of all 10 MRSA strains in phase 2 of the international study. Three of these centers used their in-house DNA extraction protocol. Divergence from the standard BT protocol in the remaining two centers resulted in no interpretable BT data for the 10 MRSA strains. The study demonstrated that each center that followed the BT protocol to the letter could generate reproducible results, irrespective whether or not an in-house DNA isolation protocol was used. The current BT protocol thus represents a simple method generating robust, reproducible genotype data for
S. aureus strains. |
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AbstractList | The reproducibility of the binary typing (BT) protocol developed for epidemiological typing of Staphylococcus aureus was analyzed in a biphasic multicenter study. In a Dutch multicenter pilot study, 10 genetically unique isolates of methicillin-resistant S. aureus (MRSA) were characterized by the BT assay as presented by van Leeuwen et al. [J. Clin. Microbiol. 2001 39 (1) 328]. The BT assay, including a standardized DNA extraction protocol was performed in duplicate in eleven medical microbiology laboratories. Two different hybridization detection procedures were applied and a prelabeled DNA sample as process control was included. Only three laboratories accurately identified all strains. Divergence in technical procedures resulted in misinterpretation due to an increasing number of faint or absent hybridization signals in combination with high background staining. The binary type of the process control was determined correctly by all participating laboratories. The feasibility of the BT protocol was related directly to the skill of the laboratory personnel. On the basis of the national study, we concluded that the DNA extraction protocol needed modification to improve DNA yield and purity. Subsequently, seven European laboratories participated in an international study to determine the reproducibility of the modified BT protocol. Each center was asked to analyze 10 DNA samples previously extracted from 10 MRSA strains (phase 1) and, additionally, to analyze 10 MRSA strains, using the standardized or their in-house DNA isolation protocol (phase 2). A prelabeled DNA process control sample was included again. The binary types of all DNA samples were identified correctly by all but one laboratories. This latter laboratory diverged from the protocol by adding an excess of labeled DNA to the hybridization mixture, resulting in a high background and, therefore, noninterpretable BT results. All centers produced identical BT results for the process control. Five of the seven centers correctly identified the binary types of all 10 MRSA strains in phase 2 of the international study. Three of these centers used their in-house DNA extraction protocol. Divergence from the standard BT protocol in the remaining two centers resulted in no interpretable BT data for the 10 MRSA strains. The study demonstrated that each center that followed the BT protocol to the letter could generate reproducible results, irrespective whether or not an in-house DNA isolation protocol was used. The current BT protocol thus represents a simple method generating robust, reproducible genotype data for S. aureus strains. The reproducibility of the binary typing (BT) protocol developed for epidemiological typing of Staphylococcus aureus was analyzed in a biphasic multicenter study. In a Dutch multicenter pilot study, 10 genetically unique isolates of methicillin-resistant S. aureus (MRSA) were characterized by the BT assay as presented by van Leeuwen et al. [J. Clin. Microbiol. 2001 39 (1) 328]. The BT assay, including a standardized DNA extraction protocol was performed in duplicate in eleven medical microbiology laboratories. Two different hybridization detection procedures were applied and a prelabeled DNA sample as process control was included. Only three laboratories accurately identified all strains. Divergence in technical procedures resulted in misinterpretation due to an increasing number of faint or absent hybridization signals in combination with high background staining. The binary type of the process control was determined correctly by all participating laboratories. The feasibility of the BT protocol was related directly to the skill of the laboratory personnel. On the basis of the national study, we concluded that the DNA extraction protocol needed modification to improve DNA yield and purity. Subsequently, seven European laboratories participated in an international study to determine the reproducibility of the modified BT protocol. Each center was asked to analyze 10 DNA samples previously extracted from 10 MRSA strains (phase 1) and, additionally, to analyze 10 MRSA strains, using the standardized or their in-house DNA isolation protocol (phase 2). A prelabeled DNA process control sample was included again. The binary types of all DNA samples were identified correctly by all but one laboratories. This latter laboratory diverged from the protocol by adding an excess of labeled DNA to the hybridization mixture, resulting in a high background and, therefore, noninterpretable BT results. All centers produced identical BT results for the process control. Five of the seven centers correctly identified the binary types of all 10 MRSA strains in phase 2 of the international study. Three of these centers used their in-house DNA extraction protocol. Divergence from the standard BT protocol in the remaining two centers resulted in no interpretable BT data for the 10 MRSA strains. The study demonstrated that each center that followed the BT protocol to the letter could generate reproducible results, irrespective whether or not an in-house DNA isolation protocol was used. The current BT protocol thus represents a simple method generating robust, reproducible genotype data for S. aureus strains. |
Author | Boers, Miranda Landegent, Jim Renders, Nicole Zaat, Sebastiaan Tuip, Anita Veenendaal, Dick van der Reyden, Tanny Lynch, Alisson van der Zwaluw, Kim van der Riet, Daniëlle van Duyn, Inge van der Werken-Libregts, Christel van der Zee, Anneke Talens, Adriaan Noordhoek, Gerda T. Kluytmans, Jan Gits, Etty Verbrugh, Henri A. Lunter, Bjorn Heck, Max Mulder, Sije Fiett, Janusz van Belkum, Alex Bakker, Nancy Vernez, Isabelle Cuny, Christa Bik, Elisabeth Dijkshoorn, Lenie Blanc, Dominique Snoeijers, Sandor Witte, Wolfgang Egberink, Diane de Proost, Monique Hryniewicz, Waleria Struelens, Marc Deplano, Ariane Wannet, Wim Kooistra, Mirjam van Leeuwen, Willem B. Cookson, Barry |
Author_xml | – sequence: 1 givenname: Willem B. surname: van Leeuwen fullname: van Leeuwen, Willem B. email: vanleeuwen@bacl.azr.nl organization: Erasmus MC, Department of Medical Microbiology and Infectious Diseases, Dr. Molewaterplein 40, 3015 GD Rotterdam, The Netherlands – sequence: 2 givenname: Sandor surname: Snoeijers fullname: Snoeijers, Sandor organization: KREATECH Diagnostics, Amsterdam, The Netherlands – sequence: 3 givenname: Christel surname: van der Werken-Libregts fullname: van der Werken-Libregts, Christel organization: KREATECH Diagnostics, Amsterdam, The Netherlands – sequence: 4 givenname: Anita surname: Tuip fullname: Tuip, Anita organization: KREATECH Diagnostics, Amsterdam, The Netherlands – sequence: 5 givenname: Anneke surname: van der Zee fullname: van der Zee, Anneke organization: Department of Molecular Microbiology, St. Elisabeth Hospital Tilburg, Tilburg, The Netherlands – sequence: 6 givenname: Diane surname: Egberink fullname: Egberink, Diane organization: Department of Molecular Microbiology, St. Elisabeth Hospital Tilburg, Tilburg, The Netherlands – sequence: 7 givenname: Monique surname: de Proost fullname: de Proost, Monique organization: Department of Molecular Microbiology, St. Elisabeth Hospital Tilburg, Tilburg, The Netherlands – sequence: 8 givenname: Elisabeth surname: Bik fullname: Bik, Elisabeth organization: Department of Medical Microbiology and Immunology, St. Antonius Hospital Nieuwegein, Nieuwegein, The Netherlands – sequence: 9 givenname: Bjorn surname: Lunter fullname: Lunter, Bjorn organization: Department of Medical Microbiology and Immunology, St. Antonius Hospital Nieuwegein, Nieuwegein, The Netherlands – sequence: 10 givenname: Jan surname: Kluytmans fullname: Kluytmans, Jan organization: Laboratory of Medical Microbiology, Ignatius Hospital Breda, Breda, The Netherlands – sequence: 11 givenname: Etty surname: Gits fullname: Gits, Etty organization: Laboratory of Medical Microbiology, Ignatius 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Noordhoek fullname: Noordhoek, Gerda T. organization: Public Health Laboratory Friesland, Leeuwarden, The Netherlands – sequence: 17 givenname: Sije surname: Mulder fullname: Mulder, Sije organization: Public Health Laboratory Friesland, Leeuwarden, The Netherlands – sequence: 18 givenname: Nicole surname: Renders fullname: Renders, Nicole organization: Department of Medical Microbiology, Bosch Medical Center, 's-Hertogenbosch, The Netherlands – sequence: 19 givenname: Miranda surname: Boers fullname: Boers, Miranda organization: Department of Medical Microbiology, Bosch Medical Center, 's-Hertogenbosch, The Netherlands – sequence: 20 givenname: Sebastiaan surname: Zaat fullname: Zaat, Sebastiaan organization: Department of Medical Microbiology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands – sequence: 21 givenname: Daniëlle surname: van der Riet fullname: van der Riet, Daniëlle organization: Department of Medical Microbiology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands – sequence: 22 givenname: Mirjam surname: Kooistra fullname: Kooistra, Mirjam organization: Regional Laboratory for Public Health Groningen, Groningen, The Netherlands – sequence: 23 givenname: Adriaan surname: Talens fullname: Talens, Adriaan organization: Regional Laboratory for Public Health Groningen, Groningen, The Netherlands – sequence: 24 givenname: Lenie surname: Dijkshoorn fullname: Dijkshoorn, Lenie organization: Department of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands – sequence: 25 givenname: Tanny surname: van der Reyden fullname: van der Reyden, Tanny organization: Department of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands – sequence: 26 givenname: Dick surname: Veenendaal fullname: Veenendaal, Dick organization: Laboratory for Medical Microbiology, Regional Laboratory for Public Health Haarlem, Haarlem, The Netherlands – sequence: 27 givenname: Nancy 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Verbrugh, Henri A. organization: Erasmus MC, Department of Medical Microbiology and Infectious Diseases, Dr. Molewaterplein 40, 3015 GD Rotterdam, The Netherlands – sequence: 40 givenname: Alex surname: van Belkum fullname: van Belkum, Alex organization: Erasmus MC, Department of Medical Microbiology and Infectious Diseases, Dr. Molewaterplein 40, 3015 GD Rotterdam, The Netherlands |
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Keywords | Binary typing Library typing Multicenter study MRSA Nervous system diseases Typing Consciousness impairment β-Lactams Method Experimental protocol Meticillin Infection Penicillin derivatives Reproducibility Bacteriosis Bacteria Micrococcales Micrococcaceae Neurological disorder Staphylococcal infection Staphylococcus aureus |
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Staphylococcus aureus was analyzed in a biphasic multicenter... The reproducibility of the binary typing (BT) protocol developed for epidemiological typing of Staphylococcus aureus was analyzed in a biphasic multicenter... |
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SubjectTerms | Bacterial diseases Bacterial Typing Techniques - methods Bacterial Typing Techniques - standards Bacteriology Binary typing Biological and medical sciences DNA, Bacterial - chemistry DNA, Bacterial - genetics Europe Experimental bacterial diseases and models Fundamental and applied biological sciences. Psychology Infectious diseases Library typing Medical sciences Methicillin Resistance Microbiology MRSA Multicenter study Nucleic Acid Hybridization - methods Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains Pilot Projects Reproducibility of Results Staphylococcus aureus - classification Staphylococcus aureus - genetics |
Title | Intercenter reproducibility of binary typing for Staphylococcus aureus |
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