Literature DB >> 8787398

Identification in situ and dynamics of bacteria on limnetic organic aggregates (lake snow).

P Weiss1, B Schweitzer, R Amann, M Simon.   

Abstract

Microbial assemblages on large organic aggregates (lake snow) of Lake Constance, Germany, were analyzed with rRNA-directed fluorescent oligonucleotide probes specific for the domain Bacteria and the alpha-, beta-, and gamma-subclasses of the class Proteobacteria. Lake snow aggregates were either collected in situ by SCUBA diving or in a sediment trap at 50 m or formed of natural lake water incubated in rolling cylinders under simulated in situ conditions. For the latter aggregates, the time course of the microbial colonization was also examined. The natural aggregates and those made in rolling cylinders were composed of the particulate organic material present in the lake and thus reflected the composition of the ambient plankton community. All types of lake snow aggregates examined were heavily colonized by microbial cells and harbored between 0.5 x 10(6) and > 2 x 10(6) cells aggregate -1. Between 55 and 100% of the microbial cells stained with 4', 6-diamidino-2-phenylindole (DAPI) could be visualized with the domain Bacteria-specific probe. In most samples, beta-subclass proteobacteria dominated the microbial community, constituting 27 to 42% of total cells as counted by DAPI staining, irrespective of the composition of the aggregates. During the time course experiments with the laboratory-made aggregates, the fraction of beta-subclass proteobacteria usually increased over time. Except for a few samples, alpha- and gamma-subclass proteobacteria were far less abundant than beta-subclass proteobacteria, constituting 11 to 25 and 9 to 33% of total cells, respectively. Therefore, we assume that a specific aggregate-adapted microbial community was established on the aggregates. Because the compositions of the microbial assemblages on natural and laboratory-made aggregates were similar, we conclude that aggregates made in rolling cylinders are good model system with which to examine the formation and microbial colonization of macroscopic organic aggregates.

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Year:  1996        PMID: 8787398      PMCID: PMC167978          DOI: 10.1128/aem.62.6.1998-2005.1996

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  13 in total

1.  Molecular and microscopic identification of sulfate-reducing bacteria in multispecies biofilms.

Authors:  R I Amann; J Stromley; R Devereux; R Key; D A Stahl
Journal:  Appl Environ Microbiol       Date:  1992-02       Impact factor: 4.792

2.  Heterotrophic bacteria and bacterivorous protozoa in oceanic macroaggregates.

Authors:  D A Caron; P G Davis; L P Madin; J M Sieburth
Journal:  Science       Date:  1982-11-19       Impact factor: 47.728

Review 3.  Phylogenetic identification and in situ detection of individual microbial cells without cultivation.

Authors:  R I Amann; W Ludwig; K H Schleifer
Journal:  Microbiol Rev       Date:  1995-03

4.  Use of rRNA fluorescence in situ hybridization for measuring the activity of single cells in young and established biofilms.

Authors:  L K Poulsen; G Ballard; D A Stahl
Journal:  Appl Environ Microbiol       Date:  1993-05       Impact factor: 4.792

5.  Phylogenetic diversity of subsurface marine microbial communities from the Atlantic and Pacific Oceans.

Authors:  J A Fuhrman; K McCallum; A A Davis
Journal:  Appl Environ Microbiol       Date:  1993-05       Impact factor: 4.792

6.  Phylogenetic stains: ribosomal RNA-based probes for the identification of single cells.

Authors:  E F DeLong; G S Wickham; N R Pace
Journal:  Science       Date:  1989-03-10       Impact factor: 47.728

7.  Fluorescent-oligonucleotide probing of whole cells for determinative, phylogenetic, and environmental studies in microbiology.

Authors:  R I Amann; L Krumholz; D A Stahl
Journal:  J Bacteriol       Date:  1990-02       Impact factor: 3.490

8.  In situ identification of bacteria in drinking water and adjoining biofilms by hybridization with 16S and 23S rRNA-directed fluorescent oligonucleotide probes.

Authors:  W Manz; U Szewzyk; P Ericsson; R Amann; K H Schleifer; T A Stenström
Journal:  Appl Environ Microbiol       Date:  1993-07       Impact factor: 4.792

9.  Genetic diversity in Sargasso Sea bacterioplankton.

Authors:  S J Giovannoni; T B Britschgi; C L Moyer; K G Field
Journal:  Nature       Date:  1990-05-03       Impact factor: 49.962

10.  Probing activated sludge with oligonucleotides specific for proteobacteria: inadequacy of culture-dependent methods for describing microbial community structure.

Authors:  M Wagner; R Amann; H Lemmer; K H Schleifer
Journal:  Appl Environ Microbiol       Date:  1993-05       Impact factor: 4.792

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  34 in total

1.  Diversity and distribution of DNA sequences with affinity to ammonia-oxidizing bacteria of the beta subdivision of the class Proteobacteria in the Arctic Ocean.

Authors:  N Bano; J T Hollibaugh
Journal:  Appl Environ Microbiol       Date:  2000-05       Impact factor: 4.792

2.  Bacterioplankton compositions of lakes and oceans: a first comparison based on fluorescence in situ hybridization.

Authors:  F O Glöckner; B M Fuchs; R Amann
Journal:  Appl Environ Microbiol       Date:  1999-08       Impact factor: 4.792

3.  Community composition of marine bacterioplankton determined by 16S rRNA gene clone libraries and fluorescence in situ hybridization.

Authors:  M T Cottrell; D L Kirchman
Journal:  Appl Environ Microbiol       Date:  2000-12       Impact factor: 4.792

4.  Biofilm community structure in polluted rivers: abundance of dominant phylogenetic groups over a complete annual cycle.

Authors:  I H Brümmer; W Fehr; I Wagner-Döbler
Journal:  Appl Environ Microbiol       Date:  2000-07       Impact factor: 4.792

5.  Changes in bacterial community composition and dynamics and viral mortality rates associated with enhanced flagellate grazing in a mesoeutrophic reservoir.

Authors:  K Simek; J Pernthaler; M G Weinbauer; K Hornák; J R Dolan; J Nedoma; M Masín; R Amann
Journal:  Appl Environ Microbiol       Date:  2001-06       Impact factor: 4.792

6.  Processing deep-sea particle-rich water samples for fluorescence in situ hybridization: consideration of storage effects, preservation, and sonication.

Authors:  Phyllis Lam; James P Cowen
Journal:  Appl Environ Microbiol       Date:  2004-01       Impact factor: 4.792

7.  Dynamics of microcystin-degrading bacteria in mucilage of Microcystis.

Authors:  T Maruyama; K Kato; A Yokoyama; T Tanaka; A Hiraishi; H D Park
Journal:  Microb Ecol       Date:  2003-08       Impact factor: 4.552

8.  Temporal patterns in bacterial communities in three temperate lakes of different trophic status.

Authors:  A C Yannarell; A D Kent; G H Lauster; T K Kratz; E W Triplett
Journal:  Microb Ecol       Date:  2003-08-14       Impact factor: 4.552

9.  Characterization of the Cricket Hindgut Microbiota with Fluorescently Labeled rRNA-Targeted Oligonucleotide Probes.

Authors:  J W Santo Domingo; M G Kaufman; M J Klug; J M Tiedje
Journal:  Appl Environ Microbiol       Date:  1998-02       Impact factor: 4.792

10.  Bacterioplankton community structure in a maritime antarctic oligotrophic lake during a period of holomixis, as determined by denaturing gradient gel electrophoresis (DGGE) and fluorescence in situ hybridization (FISH).

Authors:  D A Pearce
Journal:  Microb Ecol       Date:  2003-05-13       Impact factor: 4.552

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