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

被引:160
作者
Grundmann, HJ
Towner, KJ
Dijkshoorn, L
GernerSmidt, P
Maher, M
Seifert, H
Vaneechoutte, M
机构
[1] UNIV NOTTINGHAM HOSP,DEPT MICROBIOL,NOTTINGHAM NG7 2UH,ENGLAND
[2] UNIV NOTTINGHAM HOSP,PHLS LAB,NOTTINGHAM NG7 2UH,ENGLAND
[3] UNIV FREIBURG,INST ENVIRONM MED & HOSP HYG,D-79106 FREIBURG,GERMANY
[4] UNIV LEIDEN HOSP,DEPT MED MICROBIOL,NL-2300 RC LEIDEN,NETHERLANDS
[5] STATENS SERUM INST,DIV MICROBIOL,DK-2300 COPENHAGEN S,DENMARK
[6] UNIV COLL,NATL DIAGNOST CTR,GALWAY,IRELAND
[7] UNIV COLOGNE,NATL DIAGNOST CTR,D-50935 COLOGNE,GERMANY
[8] UNIV HOSP,DEPT CLIN CHEM MICROBIOL & IMMUNOL,B-9000 GHENT,BELGIUM
关键词
D O I
10.1128/JCM.35.12.3071-3077.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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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页码:3071 / 3077
页数:7
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