TY - JOUR
T1 - Oligonucleotide microarray for identification of Enterococcus species
AU - Lehner, Angelika
AU - Loy, Alexander
AU - Behr, Thomas
AU - Gaenge, Helga
AU - Ludwig, Wolfgang
AU - Wagner, Michael
AU - Schleifer, Karl-Heinz
N1 - Zeitschrift: FEMS Microbiology Letters
DOI: 10.1016/j.femsle.2005.04.002
Coden: FMLED
Affiliations: Department of Microbiology, Technical University of Munich, D-85350 Freising, Germany; Department of Microbial Ecology, University of Vienna, Althanstr. 14, A-1090 Wien, Austria; Inst. for Food Safety and Hygiene, Vetsuisse Faculty, University of Zurich, CH-8057 Zurich, Switzerland
Adressen: Loy, A.; Department of Microbial Ecology; University of Vienna; Althanstr. 14 A-1090 Wien, Austria; email: [email protected]
Import aus Scopus: 2-s2.0-18144376284
24.08.2007: Datenanforderung 1832 (Import Sachbearbeiter)
PY - 2005
Y1 - 2005
N2 - For detection of most members of the Enterococcaceae, the specificity of a novel oligonucleotide microarray (ECC-PhyloChip) consisting of 41 hierarchically nested 16S or 23S rRNA gene-targeted probes was evaluated with 23 pure cultures (including 19 Enterococcus species). Target nucleic acids were prepared by PCR amplification of a 4.5-kb DNA fragment containing large parts of the 16S and 23S rRNA genes and were subsequently labeled fluorescently by random priming. Each tested member of the Enterococcaceae was correctly identified on the basis of its unique microarray hybridization pattern. The evaluated ECC-PhyloChip was successfully applied for identification of Enterococcus faecium and Enterococcus faecalis in artificially contaminated milk samples demonstrating the utility of the ECC-PhyloChip for parallel identification and differentiation of Enterococcus species in food samples. Œ 2005 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
AB - For detection of most members of the Enterococcaceae, the specificity of a novel oligonucleotide microarray (ECC-PhyloChip) consisting of 41 hierarchically nested 16S or 23S rRNA gene-targeted probes was evaluated with 23 pure cultures (including 19 Enterococcus species). Target nucleic acids were prepared by PCR amplification of a 4.5-kb DNA fragment containing large parts of the 16S and 23S rRNA genes and were subsequently labeled fluorescently by random priming. Each tested member of the Enterococcaceae was correctly identified on the basis of its unique microarray hybridization pattern. The evaluated ECC-PhyloChip was successfully applied for identification of Enterococcus faecium and Enterococcus faecalis in artificially contaminated milk samples demonstrating the utility of the ECC-PhyloChip for parallel identification and differentiation of Enterococcus species in food samples. Œ 2005 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
M3 - Article
SN - 0378-1097
VL - 246
SP - 133
EP - 142
JO - FEMS Microbiology Letters
JF - FEMS Microbiology Letters
IS - 1
ER -