High-Density Microarray of Small-Subunit Ribosomal DNA Probes

ABSTRACT Ribosomal DNA sequence analysis, originally conceived as a way to provide a universal phylogeny for life forms, has proven useful in many areas of biological research. Some of the most promising applications of this approach are presently limited by the rate at which sequences can be analyzed. As a step toward overcoming this limitation, we have investigated the use of photolithography chip technology to perform sequence analyses on amplified small-subunit rRNA genes. The GeneChip (Affymetrix Corporation) contained 31,179 20-mer oligonucleotides that were complementary to a subalignment of sequences in the Ribosomal Database Project (RDP) (B. L. Maidak et al., Nucleic Acids Res. 29:173-174, 2001). The chip and standard Affymetrix software were able to correctly match small-subunit ribosomal DNA amplicons with the corresponding sequences in the RDP database for 15 of 17 bacterial species grown in pure culture. When bacteria collected from an air sample were tested, the method compared favorably with cloning and sequencing amplicons in determining the presence of phylogenetic groups. However, the method could not resolve the individual sequences comprising a complex mixed sample. Given these results and the potential for future enhancement of this technology, it may become widely useful.

[1]  George E. Fox,et al.  Comparative Cataloging of 16S Ribosomal Ribonucleic Acid: Molecular Approach to Procaryotic Systematics , 1977 .

[2]  N. Pace,et al.  Rapid determination of 16S ribosomal RNA sequences for phylogenetic analyses. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[3]  U. Göbel,et al.  Synthetic oligonucleotide probes complementary to rRNA for group- and species-specific detection of mycoplasmas. , 1987, Israel journal of medical sciences.

[4]  C. Woese,et al.  Bacterial evolution , 1987, Microbiological reviews.

[5]  E. Delong,et al.  Phylogenetic stains: ribosomal RNA-based probes for the identification of single cells. , 1989, Science.

[6]  H. Neimark,et al.  Broad range DNA probes for detecting and amplifying eubacterial nucleic acids. , 1989, FEMS microbiology letters.

[7]  H. Weetall,et al.  Antibodies immobilized on inorganic supports , 1989, Applied biochemistry and biotechnology.

[8]  K. Wilson,et al.  Amplification of bacterial 16S ribosomal DNA with polymerase chain reaction , 1990, Journal of clinical microbiology.

[9]  S Falkow,et al.  The agent of bacillary angiomatosis. An approach to the identification of uncultured pathogens. , 1990, The New England journal of medicine.

[10]  S. P. Fodor,et al.  Light-directed, spatially addressable parallel chemical synthesis. , 1991, Science.

[11]  C. Woese,et al.  Phylogenetic analysis of the spirochetes , 1991, Journal of bacteriology.

[12]  E. Delong,et al.  Analysis of a marine picoplankton community by 16S rRNA gene cloning and sequencing , 1991, Journal of bacteriology.

[13]  K. Wilson,et al.  Phylogeny of the Whipple's-disease-associated bacterium , 1991, The Lancet.

[14]  G. Fox,et al.  Comparative sequence analyses on the 16S rRNA (rDNA) of Bacillus acidocaldarius, Bacillus acidoterrestris, and Bacillus cycloheptanicus and proposal for creation of a new genus, Alicyclobacillus gen. nov. , 1992, International journal of systematic bacteriology.

[15]  N. Pace,et al.  Remarkable archaeal diversity detected in a Yellowstone National Park hot spring environment. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[16]  K. Wilson,et al.  Human colonic biota studied by ribosomal DNA sequence analysis , 1996, Applied and environmental microbiology.

[17]  D. Lockhart,et al.  Expression monitoring by hybridization to high-density oligonucleotide arrays , 1996, Nature Biotechnology.

[18]  Ross A. Overbeek,et al.  The Ribosomal Database Project (RDP) , 1996, Nucleic Acids Res..

[19]  N. Pace A molecular view of microbial diversity and the biosphere. , 1997, Science.

[20]  P Green,et al.  Base-calling of automated sequencer traces using phred. II. Error probabilities. , 1998, Genome research.

[21]  P. Green,et al.  Base-calling of automated sequencer traces using phred. I. Accuracy assessment. , 1998, Genome research.

[22]  A. Berno,et al.  Simultaneous genotyping and species identification using hybridization pattern recognition analysis of generic Mycobacterium DNA arrays. , 1998, Genome research.

[23]  D. E. Schultz,et al.  Performance of the Gen-Probe AMPLIFIED Chlamydia Trachomatis Assay in Detecting Chlamydia trachomatis in Endocervical and Urine Specimens from Women and Urethral and Urine Specimens from Men Attending Sexually Transmitted Disease and Family Planning Clinics , 1998, Journal of Clinical Microbiology.

[24]  John Dunbar,et al.  Levels of Bacterial Community Diversity in Four Arid Soils Compared by Cultivation and 16S rRNA Gene Cloning , 1999, Applied and Environmental Microbiology.

[25]  N. Yamamoto,et al.  Microarray fabrication with covalent attachment of DNA using Bubble Jet technology , 2000, Nature Biotechnology.

[26]  T. McMeekin,et al.  Diversity and community structure within anoxic sediment from marine salinity meromictic lakes and a coastal meromictic marine basin, Vestfold Hilds, Eastern Antarctica. , 2000, Environmental microbiology.

[27]  B L Maidak,et al.  The RDP-II (Ribosomal Database Project) , 2001, Nucleic Acids Res..

[28]  U. Alon,et al.  Transcriptional gene expression profiles of colorectal adenoma, adenocarcinoma, and normal tissue examined by oligonucleotide arrays. , 2001, Cancer research.