Literature DB >> 9399496

Multicenter study using standardized protocols and reagents for evaluation of reproducibility of PCR-based fingerprinting of Acinetobacter spp.

H J Grundmann1, K J Towner, L Dijkshoorn, P Gerner-Smidt, M Maher, H Seifert, M Vaneechoutte.   

Abstract

Seven laboratories in six European countries examined 40 isolates belonging to the Acinetobacter calcoaceticus-Acinetobacter baumannii complex to investigate whether standardized protocols and quality-controlled reagents could produce reliable, discriminatory, and reproducible PCR-based fingerprinting results. Four PCR protocols with different primers (primers DAF4, ERIC-2, M13, and REP1 + REP2) were used. The epidemiological conclusions reached by the participating laboratories were substantially correct, with 96.4% of the total isolate grouping allocations agreeing with the consensus view. All laboratories identified the main epidemiological clusters, and each laboratory also identified two non-outbreak-related isolates. There were no significant differences between the isolate grouping results obtained by the different protocols and with the different primers. Visual comparison indicated that the standardized protocols and reagents yielded reproducible fingerprint patterns, but with some variations in particular band intensities. Minor variations in fingerprint profiles were detected, but computer-assisted analysis of PCR fingerprints obtained on agarose gels demonstrated that 88.3 to 91.6% (depending on the source of DNA) of the patterns clustered correctly, while 96.4 to 98.9% of the patterns clustered correctly following automated high-resolution laser fluorescence analysis. Correlation of the patterns for isogenic isolates ranged from 83.3 to 86.6% but was slightly better (mean correlation, 87.1%) for centrally prepared DNA extracts than for DNA extracts prepared by individual laboratories (mean correlation, 84.7%). It was concluded that independently produced PCR fingerprint patterns can be obtained reproducibly for Acinetobacter spp. at the practical level if (i) quality-controlled reagents, (ii) standardized extraction of DNA, and (iii) standardized amplification conditions are used.

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Year:  1997        PMID: 9399496      PMCID: PMC230124          DOI: 10.1128/jcm.35.12.3071-3077.1997

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  20 in total

1.  Comparison of rapid automated laser fluorescence analysis of DNA fingerprints with four other computer-assisted approaches for studying relationships between Acinetobacter baumannii isolates.

Authors:  C A Webster; K J Towner; H Humphreys; B Ehrenstein; D Hartung; H Grundmann
Journal:  J Med Microbiol       Date:  1996-03       Impact factor: 2.472

2.  Automated laser fluorescence analysis of randomly amplified polymorphic DNA: a rapid method for investigating nosocomial transmission of Acinetobacter baumannii.

Authors:  H Grundmann; C Schneider; H V Tichy; R Simon; I Klare; D Hartung; F D Daschner
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3.  Multiple mismatch annealing: basis for random amplified polymorphic DNA fingerprinting.

Authors:  G Venugopal; S Mohapatra; D Salo; S Mohapatra
Journal:  Biochem Biophys Res Commun       Date:  1993-12-30       Impact factor: 3.575

Review 4.  Molecular epidemiology: application of contemporary techniques to the typing of microorganisms.

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5.  Multicenter evaluation of arbitrarily primed PCR for typing of Staphylococcus aureus strains.

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6.  Characterization of Acinetobacter type strains and isolates obtained from wastewater treatment plants by PCR fingerprinting.

Authors:  M Wiedmann-al-Ahmad; H V Tichy; G Schön
Journal:  Appl Environ Microbiol       Date:  1994-11       Impact factor: 4.792

7.  Analysis of relationships among isolates of Citrobacter diversus by using DNA fingerprints generated by repetitive sequence-based primers in the polymerase chain reaction.

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8.  A comparative study of different PCR-based DNA fingerprinting techniques for typing of the Acinetobacter calcoaceticus-A. baumannii complex.

Authors:  J Vila; M A Marcos; M T Jimenez de Anta
Journal:  J Med Microbiol       Date:  1996-06       Impact factor: 2.472

9.  Factors affecting reproducibility of random amplified polymorphic DNA fingerprinting.

Authors:  J R Meunier; P A Grimont
Journal:  Res Microbiol       Date:  1993-06       Impact factor: 3.992

10.  Nosocomial colonization and infection with multiresistant Acinetobacter baumannii: outbreak delineation using DNA macrorestriction analysis and PCR-fingerprinting.

Authors:  M J Struelens; E Carlier; N Maes; E Serruys; W G Quint; A van Belkum
Journal:  J Hosp Infect       Date:  1993-09       Impact factor: 3.926

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  49 in total

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5.  Endemic carbapenem resistance associated with OXA-40 carbapenemase among Acinetobacter baumannii isolates from a hospital in northern Spain.

Authors:  F Lopez-Otsoa; L Gallego; K J Towner; L Tysall; N Woodford; D M Livermore
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6.  Comparative evaluation of three different genotyping methods for investigation of nosocomial outbreaks of Legionnaires' disease in hospitals.

Authors:  D Jonas; H G Meyer; P Matthes; D Hartung; B Jahn; F D Daschner; B Jansen
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7.  Prevalence of group A streptococcal carriers in asymptomatic children and clonal relatedness among isolates in Malatya, Turkey.

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8.  Extended-spectrum beta-lactamases in Ireland, including a novel enzyme, TEM-102.

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9.  First isolation of bla(VIM-2) in Klebsiella oxytoca clinical isolates from Portugal.

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10.  Activity of meropenem with and without ciprofloxacin and colistin against Pseudomonas aeruginosa and Acinetobacter baumannii.

Authors:  Glenn A Pankuch; Gengrong Lin; Harald Seifert; Peter C Appelbaum
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