16S rRNA Gene-Based Oligonucleotide Microarray for Environmental Monitoring of the Betaproteobacterial Order “Rhodocyclales”

ABSTRACT For simultaneous identification of members of the betaproteobacterial order “Rhodocyclales” in environmental samples, a 16S rRNA gene-targeted oligonucleotide microarray (RHC-PhyloChip) consisting of 79 probes was developed. Probe design was based on phylogenetic analysis of available 16S rRNA sequences from all cultured and as yet uncultured members of the “Rhodocyclales.” The multiple nested probe set was evaluated for microarray hybridization with 16S rRNA gene PCR amplicons from 29 reference organisms. Subsequently, the RHC-PhyloChip was successfully used for cultivation-independent “Rhodocyclales” diversity analysis in activated sludge from an industrial wastewater treatment plant. The implementation of a newly designed “Rhodocyclales”-selective PCR amplification system prior to microarray hybridization greatly enhanced the sensitivity of the RHC-PhyloChip and thus enabled the detection of “Rhodocyclales” populations with relative abundances of less than 1% of all bacteria (as determined by fluorescence in situ hybridization) in the activated sludge. The presence of as yet uncultured Zoogloea-, Ferribacterium/Dechloromonas-, and Sterolibacterium-related bacteria in the industrial activated sludge, as indicated by the RHC-PhyloChip analysis, was confirmed by retrieval of their 16S rRNA gene sequences and subsequent phylogenetic analysis, demonstrating the suitability of the RHC-PhyloChip as a novel monitoring tool for environmental microbiology.

[1]  N. Stralis-Pavese,et al.  Optimization of diagnostic microarray for application in analysing landfill methanotroph communities under different plant covers. , 2004, Environmental microbiology.

[2]  Daniel B. Oerther,et al.  The oligonucleotide probe database , 1996, Applied and environmental microbiology.

[3]  J. Coates,et al.  Ubiquity and Diversity of Dissimilatory (Per)chlorate-Reducing Bacteria , 1999, Applied and Environmental Microbiology.

[4]  F. Sanger,et al.  DNA sequencing with chain-terminating inhibitors. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[5]  E. Stackebrandt,et al.  Nucleic acid techniques in bacterial systematics , 1991 .

[6]  N. Stralis-Pavese,et al.  Development and validation of a diagnostic microbial microarray for methanotrophs. , 2003, Environmental microbiology.

[7]  John J. Kelly,et al.  Optimization of Single-Base-Pair Mismatch Discrimination in Oligonucleotide Microarrays , 2003, Applied and Environmental Microbiology.

[8]  David A. Stahl,et al.  Development and application of nucleic acid probes , 1991 .

[9]  R. Amann,et al.  Combination of 16S rRNA-targeted oligonucleotide probes with flow cytometry for analyzing mixed microbial populations , 1990, Applied and environmental microbiology.

[10]  Michael Wagner,et al.  probeBase: an online resource for rRNA-targeted oligonucleotide probes , 2003, Nucleic Acids Res..

[11]  G. Grinstein,et al.  Modeling of DNA microarray data by using physical properties of hybridization , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[12]  E. Southern,et al.  Parallel analysis of oligodeoxyribonucleotide (oligonucleotide) interactions. I. Analysis of factors influencing oligonucleotide duplex formation. , 1992, Nucleic acids research.

[13]  M. Wagner,et al.  Fluorescence in situ hybridization for the detection of prokaryotes , 2004 .

[14]  P. Hugenholtz,et al.  Identification of Polyphosphate-Accumulating Organisms and Design of 16S rRNA-Directed Probes for Their Detection and Quantitation , 2000, Applied and Environmental Microbiology.

[15]  Michael Wagner,et al.  Bacterial community composition and function in sewage treatment systems. , 2002, Current opinion in biotechnology.

[16]  K. Schleifer,et al.  Combined Molecular and Conventional Analyses of Nitrifying Bacterium Diversity in Activated Sludge: Nitrosococcus mobilis and Nitrospira-Like Bacteria as Dominant Populations , 1998, Applied and Environmental Microbiology.

[17]  K. Schleifer,et al.  In situ visualization of high genetic diversity in a natural microbial community , 1996, Journal of bacteriology.

[18]  M. Wagner,et al.  The microbial community composition of a nitrifying-denitrifying activated sludge from an industrial sewage treatment plant analyzed by the full-cycle rRNA approach. , 2002, Systematic and applied microbiology.

[19]  H. Yukawa,et al.  Aerobic and Anaerobic Toluene Degradation by a Newly Isolated Denitrifying Bacterium, Thauera sp. Strain DNT-1 , 2004, Applied and Environmental Microbiology.

[20]  Rudolf Amann,et al.  Optimization Strategies for DNA Microarray-Based Detection of Bacteria with 16S rRNA-Targeting Oligonucleotide Probes , 2003, Applied and Environmental Microbiology.

[21]  F. Brockman,et al.  Direct Detection of 16S rRNA in Soil Extracts by Using Oligonucleotide Microarrays , 2001, Applied and Environmental Microbiology.

[22]  E. Stackebrandt,et al.  Phylogenetic and metabolic diversity of bacteria degrading aromatic compounds under denitrifying conditions, and description of Thauera phenylacetica sp. nov., Thauera aminoaromatica sp. nov., and Azoarcus buckelii sp. nov. , 2002, Archives of Microbiology.

[23]  D. Stahl,et al.  Monitoring the enrichment and isolation of sulfate-reducing bacteria by using oligonucleotide hybridization probes designed from environmentally derived 16S rRNA sequences , 1993, Applied and environmental microbiology.

[24]  U. Göbel,et al.  Phylogenetic Analysis of an Anaerobic, Trichlorobenzene-Transforming Microbial Consortium , 1999, Applied and Environmental Microbiology.

[25]  R. Amann,et al.  Anaerobic utilization of alkylbenzenes and n-alkanes from crude oil in an enrichment culture of denitrifying bacteria affiliating with the beta-subclass of Proteobacteria. , 1999, Environmental microbiology.

[26]  James R. Cole,et al.  The Ribosomal Database Project (RDP-II): previewing a new autoaligner that allows regular updates and the new prokaryotic taxonomy , 2003, Nucleic Acids Res..

[27]  J. Coates,et al.  Dechloromonas agitata gen. nov., sp. nov. and Dechlorosoma suillum gen. nov., sp. nov., two novel environmentally dominant (per)chlorate-reducing bacteria and their phylogenetic position. , 2001, International journal of systematic and evolutionary microbiology.

[28]  Dorothea K. Thompson,et al.  Development and Evaluation of Functional Gene Arrays for Detection of Selected Genes in the Environment , 2001, Applied and Environmental Microbiology.

[29]  K. Schleifer,et al.  The domain-specific probe EUB338 is insufficient for the detection of all Bacteria: development and evaluation of a more comprehensive probe set. , 1999, Systematic and applied microbiology.

[30]  T. Hurek,et al.  Preferential occurrence of diazotrophic endophytes, Azoarcus spp., in wild rice species and land races of Oryza sativa in comparison with modern races. , 2000, Environmental microbiology.

[31]  A. Mirzabekov,et al.  Parallel multiplex thermodynamic analysis of coaxial base stacking in DNA duplexes by oligodeoxyribonucleotide microchips. , 2001, Nucleic acids research.

[32]  K. Schleifer,et al.  The abundance of Zoogloea ramigera in sewage treatment plants , 1995, Applied and environmental microbiology.

[33]  T. Hurek,et al.  Identification of grass-associated and toluene-degrading diazotrophs, Azoarcus spp., by analyses of partial 16S ribosomal DNA sequences , 1995, Applied and environmental microbiology.

[34]  A. Mirzabekov,et al.  Parallel thermodynamic analysis of duplexes on oligodeoxyribonucleotide microchips. , 1998, Nucleic acids research.

[35]  B. Hoste,et al.  Azoarcus gen. nov., Nitrogen-Fixing Proteobacteria Associated with Roots of Kallar Grass (Leptochloa fusca (L.) Kunth), and Description of Two Species, Azoarcus indigens sp. nov. and Azoarcus communis sp. nov. , 1993 .

[36]  B. Ward,et al.  Oligonucleotide Microarray for the Study of Functional Gene Diversity in the Nitrogen Cycle in the Environment , 2003, Applied and Environmental Microbiology.

[37]  K. Schleifer,et al.  Phylogenetic Oligodeoxynucleotide Probes for the Major Subclasses of Proteobacteria: Problems and Solutions , 1992 .

[38]  Gary L. Andersen,et al.  High-Density Microarray of Small-Subunit Ribosomal DNA Probes , 2002, Applied and Environmental Microbiology.

[39]  Petr Dráber,et al.  New specificity and yield enhancer of polymerase chain reactions , 2000, Nucleic Acids Res..

[40]  D A Stahl,et al.  Oligonucleotide microchips as genosensors for determinative and environmental studies in microbiology , 1997, Applied and environmental microbiology.

[41]  K. Schleifer,et al.  ARB: a software environment for sequence data. , 2004, Nucleic acids research.

[42]  D A Stahl,et al.  Fluorescent-oligonucleotide probing of whole cells for determinative, phylogenetic, and environmental studies in microbiology , 1990, Journal of bacteriology.

[43]  K. Schleifer,et al.  Oligonucleotide Microarray for 16S rRNA Gene-Based Detection of All Recognized Lineages of Sulfate-Reducing Prokaryotes in the Environment , 2002, Applied and Environmental Microbiology.

[44]  K. Schleifer,et al.  Molecular evidence for genus level diversity of bacteria capable of catalyzing anaerobic ammonium oxidation. , 2000, Systematic and applied microbiology.

[45]  D. Stahl,et al.  Direct Profiling of Environmental Microbial Populations by Thermal Dissociation Analysis of Native rRNAs Hybridized to Oligonucleotide Microarrays , 2003, Applied and Environmental Microbiology.

[46]  R. Griffiths,et al.  Rapid Method for Coextraction of DNA and RNA from Natural Environments for Analysis of Ribosomal DNA- and rRNA-Based Microbial Community Composition , 2000, Applied and Environmental Microbiology.

[47]  Michael Zuker,et al.  Mfold web server for nucleic acid folding and hybridization prediction , 2003, Nucleic Acids Res..

[48]  K. Strimmer,et al.  Quartet Puzzling: A Quartet Maximum-Likelihood Method for Reconstructing Tree Topologies , 1996 .

[49]  L. Kerkhof,et al.  Characterization of halobenzoate-degrading, denitrifying Azoarcus and Thauera isolates and description of Thauera chlorobenzoica sp. nov. , 2001, International journal of systematic and evolutionary microbiology.

[50]  J. R. van der Meer,et al.  Enrichment, phylogenetic analysis and detection of a bacterium that performs enhanced biological phosphate removal in activated sludge. , 1999, Systematic and applied microbiology.

[51]  Alexander Loy,et al.  DNA Microarray Technology for Biodiversity Inventories of Sulfate-Reducing Prokaryotes , 2003 .

[52]  L. Bodrossy,et al.  Oligonucleotide microarrays in microbial diagnostics. , 2004, Current opinion in microbiology.

[53]  D A Stahl,et al.  Optimization of an oligonucleotide microchip for microbial identification studies: a non-equilibrium dissociation approach. , 2001, Environmental microbiology.

[54]  Thomas Ludwig,et al.  AxML: a fast program for sequential and parallel phylogenetic tree calculations based on the maximum likelihood method , 2002, Proceedings. IEEE Computer Society Bioinformatics Conference.

[55]  Jizhong Zhou Microarrays for bacterial detection and microbial community analysis. , 2003, Current opinion in microbiology.

[56]  J. Zeyer,et al.  In situ analysis of denitrifying toluene- and m-xylene-degrading bacteria in a diesel fuel-contaminated laboratory aquifer column , 1997, Applied and environmental microbiology.

[57]  D. Kelly,et al.  The prokaryotes: an evolving electronic resource for the microbiological community - , 2002 .

[58]  H Meier,et al.  A nested array of rRNA targeted probes for the detection and identification of enterococci by reverse hybridization. , 2000, Systematic and applied microbiology.

[59]  G. Garrity,et al.  The Road Map to the Manual , 2022 .

[60]  M. Wagner,et al.  Phylogeny of All Recognized Species of Ammonia Oxidizers Based on Comparative 16S rRNA and amoA Sequence Analysis: Implications for Molecular Diversity Surveys , 2000, Applied and Environmental Microbiology.

[61]  M Weizenegger,et al.  Bacterial phylogeny based on comparative sequence analysis (review) , 1998, Electrophoresis.