Literature DB >> 9435059

Detection of toxin-producing cyanobacteria by use of paramagnetic beads for cell concentration and DNA purification.

K Rudi1, F Larsen, K S Jakobsen.   

Abstract

Early detection of water blooms caused by potential toxin-producing cyanobacteria is important in environmental monitoring. We present a new nucleic acid-based method for detection of cyanobacteria in water that utilizes the same paramagnetic solid phase (beads) for both bacterial cell concentration and subsequent DNA purification. In the cell concentration step, the beads were attracted to a magnet after cell adsorption (in an alcohol- and salt-containing solution), and the supernatant was removed. For DNA purification, a buffer containing guanidine thiocyanate and Sarkosyl lysed the concentrated cells. The addition of alcohol precipitated the released DNA onto the same solid phase as was used for the cell concentration. Finally, to remove PCR inhibitors, the DNA was washed twice in alcohol while bound to the beads. All of the bead-DNA complex was used in the subsequent PCR amplification. The detection limit, as measured by 16S rDNA PCR amplification, was 50 cells in a 0.5-ml water sample, which is considerably lower than the limit (500 cells/ml) of toxic cyanobacteria tolerated in drinking water (New South Wales Blue-Green Algae Task Force, 1992). Testing of water from natural habitats showed a detection limit in the same range as that for the defined samples. The detection limits and the simplicity of the method (paramagnetic beads can be handled in automated systems) suggest that our method is suitable for routine environmental monitoring.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9435059      PMCID: PMC124668     

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


  13 in total

Review 1.  Polymerase chain reaction: applications in environmental microbiology.

Authors:  R J Steffan; R M Atlas
Journal:  Annu Rev Microbiol       Date:  1991       Impact factor: 15.500

2.  Tangential flow filtration and preliminary phylogenetic analysis of marine picoplankton.

Authors:  S J Giovannoni; E F DeLong; T M Schmidt; N R Pace
Journal:  Appl Environ Microbiol       Date:  1990-08       Impact factor: 4.792

3.  Amplification of DNA from whole cells of cyanobacteria using PCR.

Authors:  C A Howitt
Journal:  Biotechniques       Date:  1996-07       Impact factor: 1.993

4.  Strain characterization and classification of oxyphotobacteria in clone cultures on the basis of 16S rRNA sequences from the variable regions V6, V7, and V8.

Authors:  K Rudi; O M Skulberg; F Larsen; K S Jakobsen
Journal:  Appl Environ Microbiol       Date:  1997-07       Impact factor: 4.792

5.  Detection of Legionella species in reclaimed water and air with the EnviroAmp Legionella PCR kit and direct fluorescent antibody staining.

Authors:  C J Palmer; G F Bonilla; B Roll; C Paszko-Kolva; L R Sangermano; R S Fujioka
Journal:  Appl Environ Microbiol       Date:  1995-02       Impact factor: 4.792

6.  Evaluation of commercial amplification kit for detection of Legionella pneumophila in clinical specimens.

Authors:  P Matsiota-Bernard; E Pitsouni; N Legakis; C Nauciel
Journal:  J Clin Microbiol       Date:  1994-06       Impact factor: 5.948

7.  Rapid, universal method to isolate PCR-ready DNA using magnetic beads.

Authors:  K Rudi; M Kroken; O J Dahlberg; A Deggerdal; K S Jakobsen; F Larsen
Journal:  Biotechniques       Date:  1997-03       Impact factor: 1.993

8.  Use of degenerate oligonucleotides for amplification of the nifH gene from the marine cyanobacterium Trichodesmium thiebautii.

Authors:  J P Zehr; L A McReynolds
Journal:  Appl Environ Microbiol       Date:  1989-10       Impact factor: 4.792

9.  Evaluation of a PCR based assay for specific detection of Campylobacter jejuni in chicken washes.

Authors:  D K Winters; M F Slavik
Journal:  Mol Cell Probes       Date:  1995-10       Impact factor: 2.365

10.  Specific detection of Salmonella spp. by multiplex polymerase chain reaction.

Authors:  J S Way; K L Josephson; S D Pillai; M Abbaszadegan; C P Gerba; I L Pepper
Journal:  Appl Environ Microbiol       Date:  1993-05       Impact factor: 4.792

View more
  6 in total

1.  Application of sequence-specific labeled 16S rRNA gene oligonucleotide probes for genetic profiling of cyanobacterial abundance and diversity by array hybridization.

Authors:  K Rudi; O M Skulberg; R Skulberg; K S Jakobsen
Journal:  Appl Environ Microbiol       Date:  2000-09       Impact factor: 4.792

2.  Molecular characterization of potential microcystin-producing cyanobacteria in Lake Ontario embayments and nearshore waters.

Authors:  A M Hotto; M F Satchwell; G L Boyer
Journal:  Appl Environ Microbiol       Date:  2007-05-25       Impact factor: 4.792

3.  Molecular phylogeny of Anabaena circinalis and its identification in environmental samples by PCR.

Authors:  K M Fergusson; C P Saint
Journal:  Appl Environ Microbiol       Date:  2000-09       Impact factor: 4.792

4.  Application of 5'-nuclease PCR for quantitative detection of Listeria monocytogenes in pure cultures, water, skim milk, and unpasteurized whole milk.

Authors:  H K Nogva; K Rudi; K Naterstad; A Holck; D Lillehaug
Journal:  Appl Environ Microbiol       Date:  2000-10       Impact factor: 4.792

5.  Direct real-time PCR quantification of Campylobacter jejuni in chicken fecal and cecal samples by integrated cell concentration and DNA purification.

Authors:  Knut Rudi; Hilde Kristin Høidal; Tone Katla; Birgit Klungseth Johansen; John Nordal; Kjetill S Jakobsen
Journal:  Appl Environ Microbiol       Date:  2004-02       Impact factor: 4.792

6.  Quantification of toxic cyanobacteria in water by use of competitive PCR followed by sequence-specific labeling of oligonucleotide probes.

Authors:  K Rudi; O M Skulberg; F Larsen; K S Jakobsen
Journal:  Appl Environ Microbiol       Date:  1998-07       Impact factor: 4.792

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.