Literature DB >> 8919803

Development and field application of a quantitative method for examining natural assemblages of protists with oligonucleotide probes.

E L Lim1, D A Caron, E F Delong.   

Abstract

A fluorescent in situ hybridization method that uses rRNA-targeted oligonucleotide probes for counting protists in cultures and environmental water samples is described. Filtration, hybridization, and enumeration of fixed cells with biotinylated eukaryote-specific probes and fluorescein isothiocyanate-conjugated avidin were performed directly on 0.4-microns-pore-size polycarbonate filters of Transwell cell culture inserts (Costar Corp., Cambridge, Mass.). Counts of various species of cultured protists by this probe hybridization method were not significantly different from counts obtained by the 4',6-diamidino-2-phenylindole (DAPI) and acridine orange (AO) staining methods. However, counts of total nanoplankton (TNAN) based on probe hybridizations in several field samples and in samples collected from a mesocosm experiment were frequently higher than TNAN counts obtained by staining with DAPI or AO. On the basis of these results, 25 to 70% of the TNAN determined with probes were not detectable by DAPI or AO staining. The underestimation of TNAN abundances in samples stained with DAPI or AO was attributed to the existence of small nanoplanktonic cells which could be detected with probes but not DAPI or AO and the difficulty associated with distinguishing DAPI- or AO-stained protists attached to or embedded in aggregates. We conclude from samples examined in this study that enumeration of TNAN with oligonucleotide probes provides estimates of natural TNAN abundances that are at least as high as (and in some cases higher than) counts obtained with commonly employed fluorochrome stains. The quantitative in situ hybridization method we have described here enables the direct enumeration of free-living protists in water samples with oligonucleotide probes. When combined with species-specific probes, this method will enable quantitative studies of the abundance and distribution of specific protistan taxa.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8919803      PMCID: PMC167908          DOI: 10.1128/aem.62.4.1416-1423.1996

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


  14 in total

1.  Use of monodispersed, fluorescently labeled bacteria to estimate in situ protozoan bacterivory.

Authors:  B F Sherr; E B Sherr; R D Fallon
Journal:  Appl Environ Microbiol       Date:  1987-05       Impact factor: 4.792

Review 2.  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

3.  Quantification of methanogenic groups in anaerobic biological reactors by oligonucleotide probe hybridization.

Authors:  L Raskin; L K Poulsen; D R Noguera; B E Rittmann; D A Stahl
Journal:  Appl Environ Microbiol       Date:  1994-04       Impact factor: 4.792

4.  Phylogenetic group-specific oligodeoxynucleotide probes for identification of single microbial cells.

Authors:  S J Giovannoni; E F DeLong; G J Olsen; N R Pace
Journal:  J Bacteriol       Date:  1988-02       Impact factor: 3.490

5.  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

6.  Use of nuclepore filters for counting bacteria by fluorescence microscopy.

Authors:  J E Hobbie; R J Daley; S Jasper
Journal:  Appl Environ Microbiol       Date:  1977-05       Impact factor: 4.792

Review 7.  Structural diversity of eukaryotic small subunit ribosomal RNAs. Evolutionary implications.

Authors:  M L Sogin; J H Gunderson
Journal:  Ann N Y Acad Sci       Date:  1987       Impact factor: 5.691

8.  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

9.  Design and application of rRNA-targeted oligonucleotide probes for the dissimilatory iron- and manganese-reducing bacterium Shewanella putrefaciens.

Authors:  T J DiChristina; E F DeLong
Journal:  Appl Environ Microbiol       Date:  1993-12       Impact factor: 4.792

10.  In situ identification of Legionellaceae using 16S rRNA-targeted oligonucleotide probes and confocal laser scanning microscopy.

Authors:  W Manz; R Amann; R Szewzyk; U Szewzyk; T A Stenström; P Hutzler; K H Schleifer
Journal:  Microbiology       Date:  1995-01       Impact factor: 2.777

View more
  11 in total

1.  Quantitative assessment of picoeukaryotes in the natural environment by using taxon-specific oligonucleotide probes in association with tyramide signal amplification-fluorescence in situ hybridization and flow cytometry.

Authors:  Isabelle C Biegala; Fabrice Not; Daniel Vaulot; Nathalie Simon
Journal:  Appl Environ Microbiol       Date:  2003-09       Impact factor: 4.792

2.  Quantitative fluorescence in situ hybridization of Aureobasidium pullulans on microscope slides and leaf surfaces.

Authors:  S Li; R N Spear; J H Andrews
Journal:  Appl Environ Microbiol       Date:  1997-08       Impact factor: 4.792

3.  Visualization and enumeration of marine planktonic archaea and bacteria by using polyribonucleotide probes and fluorescent in situ hybridization.

Authors:  E F DeLong; L T Taylor; T L Marsh; C M Preston
Journal:  Appl Environ Microbiol       Date:  1999-12       Impact factor: 4.792

4.  Development of molecular identification method for genus Alexandrium (Dinophyceae) using whole-cell FISH.

Authors:  Choong-Jae Kim; Chang-Hoon Kim; Yoshihiko Sako
Journal:  Mar Biotechnol (NY)       Date:  2005-05-17       Impact factor: 3.619

5.  Combination of competitive quantitative PCR and constant-denaturant capillary electrophoresis for high-resolution detection and enumeration of microbial cells.

Authors:  E L Lim; A V Tomita; W G Thilly; M F Polz
Journal:  Appl Environ Microbiol       Date:  2001-09       Impact factor: 4.792

6.  Molecular detection of harmful algal blooms (HABs) using locked nucleic acids and bead array technology.

Authors:  Mara R Diaz; James W Jacobson; Kelly D Goodwin; Sherry A Dunbar; Jack W Fell
Journal:  Limnol Oceanogr Methods       Date:  2010-06-01       Impact factor: 2.634

7.  Importance of passive diffusion in the uptake of polychlorinated biphenyls by phagotrophic protozoa.

Authors:  E B Kujawinski; J W Farrington; J W Moffett
Journal:  Appl Environ Microbiol       Date:  2000-05       Impact factor: 4.792

8.  Grazing of Tetrahymena sp. on adhered bacteria in percolated columns monitored by in situ hybridization with fluorescent oligonucleotide probes.

Authors:  H Eisenmann; H Harms; R Meckenstock; E I Meyer; A J Zehnder
Journal:  Appl Environ Microbiol       Date:  1998-04       Impact factor: 4.792

9.  An investigation of the fine structure, cell surface carbohydrates, and appeal of the diatom Extubocellulus sp. as prey for small flagellates.

Authors:  M Martin-Cereceda; R Williams; A Guinea; G Novarino
Journal:  Protoplasma       Date:  2007-12-24       Impact factor: 3.356

10.  Flow Cytometric Analysis of Characteristics of Hybridization of Species-Specific Fluorescent Oligonucleotide Probes to rRNA of Marine Nanoflagellates.

Authors:  J Rice; M A Sleigh; P H Burkill; G A Tarran; C D O'connor; M V Zubkov
Journal:  Appl Environ Microbiol       Date:  1997-03       Impact factor: 4.792

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.