Literature DB >> 11823205

Comparison of fluorescently labeled oligonucleotide and polynucleotide probes for the detection of pelagic marine bacteria and archaea.

Annelie Pernthaler1, Christina M Preston, Jakob Pernthaler, Edward F DeLong, Rudolf Amann.   

Abstract

We compared the detection of bacteria and archaea in the coastal North Sea and at Monterey Bay, Calif., after fluorescence in situ hybridization (FISH) either with rRNA-targeted oligonucleotide probes monolabeled with the cyanin dye Cy3 (oligoFISH) or with fluorescein-labeled polyribonucleotide probes (polyFISH). During an annual cycle in German Bight surface waters, the percentages of bacteria visualized by polyFISH (annual mean, 77% of total counts) were significantly higher than those detected by oligoFISH (53%). The fraction of total bacteria visualized by oligoFISH declined during winter, whereas cell numbers determined by polyFISH remained constant throughout the year. Depth profiles from Monterey Bay showed large differences in the fraction of bacterial cells visualized by polyFISH and oligoFISH in the deeper water layers irrespective of the season. Image-analyzed microscopy indicated that the superior detection of cells by polyFISH with fluorescein-labeled probes in bacterioplankton samples was less a consequence of higher absolute fluorescence intensities but was rather related to quasi-linear bleaching dynamics and to a higher signal-to-background ratio. The relative abundances of archaea in North Sea and Monterey Bay spring samples as determined by oligoFISH were on average higher than those determined by polyFISH. However, simultaneous hybridizations with oligonucleotide probes for bacteria and archaea suggested that the oligoFISH probe ARCH915 unspecifically stained a population of bacteria. Using either FISH technique, blooms of archaea were observed in North Sea surface waters during the spring and summer months. Marine group II archaea (Euryarchaeota) reached >30% of total picoplankton abundances, as determined by polyFISH. We suggest that studies of pelagic microbial community structure using oligoFISH with monolabeled probes should focus on environments that yield detections > or =70% of total cell counts, e.g., coastal surface waters during spring and summer.

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Year:  2002        PMID: 11823205      PMCID: PMC126737          DOI: 10.1128/AEM.68.2.661-667.2002

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


  34 in total

1.  Natural assemblages of marine proteobacteria and members of the Cytophaga-Flavobacter cluster consuming low- and high-molecular-weight dissolved organic matter.

Authors:  M T Cottrell; D L Kirchman
Journal:  Appl Environ Microbiol       Date:  2000-04       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.  Succession of pelagic marine bacteria during enrichment: a close look at cultivation-induced shifts.

Authors:  H Eilers; J Pernthaler; R Amann
Journal:  Appl Environ Microbiol       Date:  2000-11       Impact factor: 4.792

5.  Growth patterns of two marine isolates: adaptations to substrate patchiness?

Authors:  A Pernthaler; J Pernthaler; H Eilers; R Amann
Journal:  Appl Environ Microbiol       Date:  2001-09       Impact factor: 4.792

6.  Identification of Whole Fixed Bacterial Cells with Nonradioactive 23S rRNA-Targeted Polynucleotide Probes.

Authors:  K Trebesius; R Amann; W Ludwig; K Mühlegger; K H Schleifer
Journal:  Appl Environ Microbiol       Date:  1994-09       Impact factor: 4.792

7.  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

8.  Culturability and In situ abundance of pelagic bacteria from the North Sea.

Authors:  H Eilers; J Pernthaler; F O Glöckner; R Amann
Journal:  Appl Environ Microbiol       Date:  2000-07       Impact factor: 4.792

9.  Influence of growth rate and starvation on fluorescent in situ hybridization of Rhodopseudomonas palustris.

Authors: 
Journal:  FEMS Microbiol Ecol       Date:  2000-06-01       Impact factor: 4.194

10.  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

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  57 in total

1.  Phylogenetic composition of Arctic Ocean archaeal assemblages and comparison with Antarctic assemblages.

Authors:  Nasreen Bano; Shomari Ruffin; Briana Ransom; James T Hollibaugh
Journal:  Appl Environ Microbiol       Date:  2004-02       Impact factor: 4.792

2.  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

3.  Combining catalyzed reporter deposition-fluorescence in situ hybridization and microautoradiography to detect substrate utilization by bacteria and Archaea in the deep ocean.

Authors:  Eva Teira; Thomas Reinthaler; Annelie Pernthaler; Jakob Pernthaler; Gerhard J Herndl
Journal:  Appl Environ Microbiol       Date:  2004-07       Impact factor: 4.792

4.  Reliability of CARD-FISH procedure for enumeration of Archaea in deep-sea surficial sediments.

Authors:  Massimiliano Molari; Elena Manini
Journal:  Curr Microbiol       Date:  2011-12-11       Impact factor: 2.188

5.  The metatranscriptome of a deep-sea hydrothermal plume is dominated by water column methanotrophs and lithotrophs.

Authors:  Ryan A Lesniewski; Sunit Jain; Karthik Anantharaman; Patrick D Schloss; Gregory J Dick
Journal:  ISME J       Date:  2012-06-14       Impact factor: 10.302

6.  Bacterial abundance, activity, and viability in the eutrophic River Warnow, northeast Germany.

Authors:  H M Freese; U Karsten; R Schumann
Journal:  Microb Ecol       Date:  2006-01-11       Impact factor: 4.552

7.  Anaerobic microbial communities in Lake Pavin, a unique meromictic lake in France.

Authors:  Anne-C Lehours; Corinne Bardot; Aurelie Thenot; Didier Debroas; Gerard Fonty
Journal:  Appl Environ Microbiol       Date:  2005-11       Impact factor: 4.792

8.  Contribution of Archaea to total prokaryotic production in the deep Atlantic Ocean.

Authors:  Gerhard J Herndl; Thomas Reinthaler; Eva Teira; Hendrik van Aken; Cornelius Veth; Annelie Pernthaler; Jakob Pernthaler
Journal:  Appl Environ Microbiol       Date:  2005-05       Impact factor: 4.792

9.  rRNA sequence-based scanning electron microscopic detection of bacteria.

Authors:  Takehiko Kenzaka; Ai Ishidoshiro; Nobuyasu Yamaguchi; Katsuji Tani; Masao Nasu
Journal:  Appl Environ Microbiol       Date:  2005-09       Impact factor: 4.792

Review 10.  Fate of heterotrophic microbes in pelagic habitats: focus on populations.

Authors:  Jakob Pernthaler; Rudolf Amann
Journal:  Microbiol Mol Biol Rev       Date:  2005-09       Impact factor: 11.056

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