Rapid quantification and taxonomic classification of environmental DNA from both prokaryotic and eukaryotic origins using a microarray

被引:74
作者
DeSantis, TZ
Stone, CE
Murray, SR
Moberg, JP
Andersen, GL
机构
[1] Lawrence Berkeley Natl Lab, Ctr Environm Biotechnol, Berkeley, CA 94720 USA
[2] Def Sci & Technol Lab, Salisbury SP4 0JQ, Wilts, England
关键词
rRNA; microarray; oligonucleotide; aerosol; probe; extraction;
D O I
10.1016/j.femsle.2005.03.016
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A microarray has been designed using 62,358 probes matched to both prokaryotic and eukaryotic small-subunit ribosomal RNA genes. The array categorized environmental DNA to specific phylogenetic clusters in under 9 h. To a background of DNA generated from natural outdoor aerosols, known quantities of rRNA gene copies from distinct organisms were added producing corresponding hybridization intensity scores that correlated well with their concentrations (r = 0.917). Reproducible differences in microbial community composition were observed by altering the genomic DNA extraction method. Notably, gentle extractions produced peak intensities for Mycoplasmatales and Burkholderiales, whereas a vigorous disruption produced peak intensities for Vibrionales, Clostridiales, and Bacillales. (c) 2005 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:271 / 278
页数:8
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