Literature DB >> 8031237

Chemiluminescent detection of Fiji disease virus with biotinylated DNA probes.

G R Smith1, M L Clarke, R Van de Velde, J L Dale.   

Abstract

Biotinylated Fiji disease fijivirus specific cDNA probes detected the presence of the virus in total nucleic acid extracts from infected sugarcane plants. Hybridised biotinylated probes were detected with streptavidin-alkaline phosphatase conjugate and the light generating substrate AMPPD. Samples were either blotted manually, or by alkaline capillary transfer using 100 mM NaOH. Transfer of nucleic acids to charge modified nylon with sodium hydroxide was superior to denaturation with glyoxal or formamide and salt-citrate buffer transfer as the bands were clearly resolved and no degradation of the FDV dsRNA was observed. Transfer of either total nucleic acid extracts or purified dsRNA in manifold blots generated false positive signals with the non-radio-active chemiluminescent detection systems tested. Manual or northern blots had a limit of detection for purified target double-stranded RNA of approximately 10 pg and 0.5 pg respectively. Manual blots were tested for practical application to screen germplasma for FDV infection. The virus was detected in leaf samples from FDV-infected plants, in some instances prior to development of the characteristic gall symptom.

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Year:  1994        PMID: 8031237     DOI: 10.1007/bf01321061

Source DB:  PubMed          Journal:  Arch Virol        ISSN: 0304-8608            Impact factor:   2.574


  9 in total

1.  Adapting the polymerase chain reaction to a double-stranded RNA genome.

Authors:  V S Davis; J A Boyle
Journal:  Anal Biochem       Date:  1990-08-15       Impact factor: 3.365

2.  A method to produce six alkaline northern blots of viral dsRNA within one hour.

Authors:  B Parker; J K Li
Journal:  Biotechniques       Date:  1988-01       Impact factor: 1.993

3.  Detection of Fiji disease virus in infected sugarcane by nucleic acid hybridization.

Authors:  A H Skotnicki; J L Dale; M L Skotnicki
Journal:  J Virol Methods       Date:  1986-04       Impact factor: 2.014

4.  Molecular cloning and characterization of the genome of wound tumor virus: a tumor-inducing plant reovirus.

Authors:  T Asamizu; D Summers; M B Motika; J V Anzola; D L Nuss
Journal:  Virology       Date:  1985-07-30       Impact factor: 3.616

5.  Rapid and efficient method for cloning of blunt-ended DNA fragments.

Authors:  P Upcroft; A Healey
Journal:  Gene       Date:  1987       Impact factor: 3.688

6.  A simple and very efficient method for generating cDNA libraries.

Authors:  U Gubler; B J Hoffman
Journal:  Gene       Date:  1983-11       Impact factor: 3.688

7.  Molecular cloning and comparative sequence analyses of bluetongue virus S1 segments by selective synthesis of specific full-length DNA copies of dsRNA genes.

Authors:  T F Kowalik; Y Y Yang; J K Li
Journal:  Virology       Date:  1990-08       Impact factor: 3.616

8.  PCR amplification of a specific double-stranded RNA region of Fiji disease virus from diseased sugarcane.

Authors:  G R Smith; R Van de Velde; J L Dale
Journal:  J Virol Methods       Date:  1992-09       Impact factor: 2.014

9.  Electrophoretic separation of dsRNA genome segments from Fiji disease and maize rough dwarf viruses.

Authors:  D V Reddy; G Boccardo; R Outridge; D S Teakle; L M Black
Journal:  Virology       Date:  1975-01       Impact factor: 3.616

  9 in total

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