Literature DB >> 16348420

Use of Polymerase Chain Reaction To Detect the Take-All Fungus, Gaeumannomyces graminis, in Infected Wheat Plants.

K Schesser1, A Luder, J M Henson.   

Abstract

Gaeumannomyces graminis, the causative agent of take-all disease of wheat, barley, and oats, was detected in infected wheat seedlings by using the polymerase chain reaction to amplify Gaeumannomyces-specific DNA fragments. Nested primers and two rounds of amplification were used to amplify two fragments, approximately 287 and 188 bp in size, from G. graminis-infected wheat seedlings. The use of nested primers greatly decreased the number of nonspecific amplification products. Polymerase chain reaction products were not obtained with DNA from seedlings infected with several other phytopathogenic fungi or with DNA from uninfected seedlings. Amplified products were visualized on agarose gels, and their identities were confirmed by DNA hybridization. This method did not require culturing the fungus and has potential for detecting G. graminis in infested wheat, barley, or oat fields.

Entities:  

Year:  1991        PMID: 16348420      PMCID: PMC182747          DOI: 10.1128/aem.57.2.553-556.1991

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


  11 in total

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Authors:  F Rollo; R Salvi; P Torchia
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2.  Colorimetric detection of specific DNA segments amplified by polymerase chain reactions.

Authors:  D J Kemp; D B Smith; S J Foote; N Samaras; M G Peterson
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3.  Detection of specific sequences among DNA fragments separated by gel electrophoresis.

Authors:  E M Southern
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4.  DNA Probe for Identification of the Take-All Fungus, Gaeumannomyces graminis.

Authors:  J M Henson
Journal:  Appl Environ Microbiol       Date:  1989-02       Impact factor: 4.792

5.  Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia.

Authors:  R K Saiki; S Scharf; F Faloona; K B Mullis; G T Horn; H A Erlich; N Arnheim
Journal:  Science       Date:  1985-12-20       Impact factor: 47.728

6.  Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase.

Authors:  R K Saiki; D H Gelfand; S Stoffel; S J Scharf; R Higuchi; G T Horn; K B Mullis; H A Erlich
Journal:  Science       Date:  1988-01-29       Impact factor: 47.728

7.  A rapid alkaline extraction procedure for screening recombinant plasmid DNA.

Authors:  H C Birnboim; J Doly
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8.  DNA amplification to enhance detection of genetically engineered bacteria in environmental samples.

Authors:  R J Steffan; R M Atlas
Journal:  Appl Environ Microbiol       Date:  1988-09       Impact factor: 4.792

9.  Rapid transfer of DNA from agarose gels to nylon membranes.

Authors:  K C Reed; D A Mann
Journal:  Nucleic Acids Res       Date:  1985-10-25       Impact factor: 16.971

10.  One-step preparation of competent Escherichia coli: transformation and storage of bacterial cells in the same solution.

Authors:  C T Chung; S L Niemela; R H Miller
Journal:  Proc Natl Acad Sci U S A       Date:  1989-04       Impact factor: 11.205

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  8 in total

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2.  A simple, sensitive, and rapid method for detecting seed contaminated with highly virulent Leptosphaeria maculans.

Authors:  J L Taylor
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Authors:  K Groppe; T Boller
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4.  Comparison of fungi within the Gaeumannomyces-Phialophora complex by analysis of ribosomal DNA sequences.

Authors:  G T Bryan; M J Daniels; A E Osbourn
Journal:  Appl Environ Microbiol       Date:  1995-02       Impact factor: 4.792

5.  Isolation of a species-specific mitochondrial DNA sequence for identification of Tilletia indica, the Karnal bunt of wheat fungus.

Authors:  M A Ferreira; P W Tooley; E Hatziloukas; C Castro; N W Schaad
Journal:  Appl Environ Microbiol       Date:  1996-01       Impact factor: 4.792

6.  PCR amplification of species-specific DNA sequences can distinguish among Phytophthora species.

Authors:  T Ersek; J E Schoelz; J T English
Journal:  Appl Environ Microbiol       Date:  1994-07       Impact factor: 4.792

7.  Optimization of Production Conditions for Protoplasts and Polyethylene Glycol-Mediated Transformation of Gaeumannomyces tritici.

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8.  Species-specific fungal DNA in airborne dust as surrogate for occupational mycotoxin exposure?

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  8 in total

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