Identification of novel Archaea in bacterioplankton of a boreal forest lake by phylogenetic analysis and fluorescent in situ hybridization(1).

We report here on novel groups of Archaea in the bacterioplankton of a small boreal forest lake studied by the culture-independent analysis of the 16S rRNA genes amplified directly from lake water in combination with fluorescent in situ hybridization (FISH). Polymerase chain reaction products were cloned and 28 of the 160 Archaea clones with around 900-bp-long 16S rRNA gene inserts, were sequenced. Phylogenetic analysis, including 642 Archaea sequences, confirmed that none of the freshwater clones were closely affiliated with known cultured Archaea. Twelve Archaea sequences from lake Valkea Kotinen (VAL) belonged to Group I of uncultivated Crenarchaeota and affiliated with environmental sequences from freshwater sediments, rice roots and soil as well as with sequences from an anaerobic digestor. Eight of the Crenarchaeota VAL clones formed a tight cluster. Sixteen sequences belonged to Euryarchaeota. Four of these formed a cluster together with environmental sequences from freshwater sediments and peat bogs within the order Methanomicrobiales. Five were affiliated with sequences from marine sediments situated close to marine Group II and three formed a novel cluster VAL III distantly related to the order Thermoplasmales. The remaining four clones formed a distinct clade within a phylogenetic radiation characterized by members of the orders Methanosarcinales and Methanomicrobiales on the same branch as rice cluster I, detected recently on rice roots and in anoxic bulk soil of flooded rice microcosms. FISH with specifically designed rRNA-targeted oligonucleotide probes revealed the presence of Methanomicrobiales in the studied lake. These observations indicate a new ecological niche for many novel 'non-extreme' environmental Archaea in the pelagic water of a boreal forest lake.

[1]  P. Martikainen,et al.  CH4, CO2 and N2O supersaturation in 12 Finnish lakes before and after ice-melt , 2000 .

[2]  James R. Cole,et al.  The RDP (Ribosomal Database Project) continues , 2000, Nucleic Acids Res..

[3]  R. Amann,et al.  Bacterioplankton Compositions of Lakes and Oceans: a First Comparison Based on Fluorescence In Situ Hybridization , 1999, Applied and Environmental Microbiology.

[4]  L. Arvola,et al.  Stable isotope analysis of zooplankton carbon nutrition in humic lakes , 1999 .

[5]  G. Jurgens,et al.  Diversity of soil Archaea in boreal forest before, and after clear-cutting and prescribed burning , 1999 .

[6]  W. Liesack,et al.  Vertical Distribution of Methanogens in the Anoxic Sediment of Rotsee (Switzerland) , 1999, Applied and Environmental Microbiology.

[7]  Peter G. Brewer,et al.  Methane-consuming archaebacteria in marine sediments , 1999, Nature.

[8]  E. Delong,et al.  Everything in moderation: archaea as 'non-extremophiles'. , 1998, Current opinion in genetics & development.

[9]  W. Liesack,et al.  Novel Euryarchaeotal Lineages Detected on Rice Roots and in the Anoxic Bulk Soil of Flooded Rice Microcosms , 1998, Applied and Environmental Microbiology.

[10]  R. Amann,et al.  Seasonal Community and Population Dynamics of Pelagic Bacteria and Archaea in a High Mountain Lake , 1998, Applied and Environmental Microbiology.

[11]  T. Schmidt,et al.  Phylogenetic Analysis of Nonthermophilic Members of the Kingdom Crenarchaeota and Their Diversity and Abundance in Soils , 1998, Applied and Environmental Microbiology.

[12]  J. Saunders,et al.  Bacteria in post-glacial freshwater sediments. , 1998, Microbiology.

[13]  R. Amann,et al.  Microbial Community Composition of Wadden Sea Sediments as Revealed by Fluorescence In Situ Hybridization , 1998, Applied and Environmental Microbiology.

[14]  J. Doré,et al.  Recovery and phylogenetic analysis of archaeal rRNA sequences from continental shelf sediments. , 1998, FEMS microbiology letters.

[15]  L. Tranvik,et al.  Aquatic humic substances : ecology and biogeochemistry , 1998 .

[16]  I. Bergström The integrated monitoring programme in Finland , 1998 .

[17]  K. Salonen,et al.  Long-term fluctuations in environmental conditions, plankton and macrophytes in a humic lake, Valkea-Kotinen , 1998 .

[18]  D. B. Nedwell,et al.  Phylogenetic diversity of Archaea in sediment samples from a coastal salt marsh , 1997, Applied and environmental microbiology.

[19]  R. Moss,et al.  The regional impacts of climate change : an assessment of vulnerability , 1997 .

[20]  L. Forney,et al.  Distribution of bacterioplankton in meromictic Lake Saelenvannet, as determined by denaturing gradient gel electrophoresis of PCR-amplified gene fragments coding for 16S rRNA , 1997, Applied and environmental microbiology.

[21]  R. Moletta,et al.  Molecular microbial diversity of an anaerobic digestor as determined by small-subunit rDNA sequence analysis , 1997, Applied and environmental microbiology.

[22]  J. Fuhrman,et al.  Widespread Archaea and novel Bacteria from the deep sea as shown by 16S rRNA gene sequences , 1997 .

[23]  D. Stahl,et al.  Copyright � 1997, American Society for Microbiology Crenarchaeota in Lake Michigan Sediment† , 1996 .

[24]  K. Lindström,et al.  Novel group within the kingdom Crenarchaeota from boreal forest soil , 1997, Applied and environmental microbiology.

[25]  E. Delong,et al.  Vertical distribution and phylogenetic characterization of marine planktonic Archaea in the Santa Barbara Channel , 1997, Applied and environmental microbiology.

[26]  C. Schleper,et al.  Recovery of crenarchaeotal ribosomal DNA sequences from freshwater-lake sediments , 1997, Applied and environmental microbiology.

[27]  N. Pace,et al.  Wide diversity of Crenarchaeota , 1996, Nature.

[28]  R. Conrad,et al.  Soil microorganisms as controllers of atmospheric trace gases (H2, CO, CH4, OCS, N2O, and NO). , 1996, Microbiological reviews.

[29]  Frank Oliver Glöckner,et al.  An in situ hybridization protocol for detection and identification of planktonic bacteria , 1996 .

[30]  J. Saunders,et al.  Isolation and identification of methanogen-specific DNA from blanket bog peat by PCR amplification and sequence analysis , 1996, Applied and environmental microbiology.

[31]  J. D. Elsas,et al.  Extraction and analysis of microbial DNA from soil , 1995 .

[32]  R. Amann In situ identification of micro-organisms by whole cell hybridization with rRNA-targeted nucleic acid probes , 1995 .

[33]  R. Amann,et al.  Identifying members of the domain Archaea with rRNA-targeted oligonucleotide probes , 1994, Applied and environmental microbiology.

[34]  Hideo Matsuda,et al.  fastDNAmL: a tool for construction of phylogenetic trees of DNA sequences using maximum likelihood , 1994, Comput. Appl. Biosci..

[35]  Robert C. Harriss,et al.  Review and assessment of methane emissions from wetlands , 1993 .

[36]  R. Kolter,et al.  The stationary phase of the bacterial life cycle. , 1993, Annual review of microbiology.

[37]  R. Amann,et al.  Optimizing fluorescent in situ hybridization with rRNA-targeted oligonucleotide probes for flow cytometric identification of microorganisms. , 1993, Cytometry.

[38]  M. Khalil,et al.  Atmospheric Methane: Sources, Sinks, and Role in Global Change , 1993, NATO ASI Series.

[39]  E. Delong Archaea in coastal marine environments. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[40]  C R Woese,et al.  A definition of the domains Archaea, Bacteria and Eucarya in terms of small subunit ribosomal RNA characteristics. , 1991, Systematic and applied microbiology.

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

[42]  K. Salonen,et al.  Heat uptake and resistance to mixing in small humic forest lakes in Southern Finland , 1990 .

[43]  R. Colwell,et al.  Survival strategies of bacteria in the natural environment. , 1987, Microbiological reviews.

[44]  T. Jukes CHAPTER 24 – Evolution of Protein Molecules , 1969 .