Literature DB >> 7509585

Identification of Erwinia stewartii by a ligase chain reaction assay.

W J Wilson1, M Wiedmann, H R Dillard, C A Batt.   

Abstract

A PCR-coupled ligase chain reaction (LCR) assay was developed to distinguish the plant pathogenic bacterium Erwinia stewartii from other erwiniae. This new technique allows discrimination to the species level on the basis of a single-base-pair difference in the 16S rRNA gene which is unique to E. stewartii. Portions of the 16S rRNA genes of E. stewartii and the closely related Erwinia herbicola were sequenced. From comparison of the two 16S rRNA gene regions, two primer pairs were constructed such that only E. stewartii DNA gave a product in the LCR assay. The ligated product was separated from the radioactively labelled primers by denaturing polyacrylamide gel electrophoresis and visualized by autoradiography. Twenty-four different Erwinia species and strains were tested by PCR-coupled LCR to verify the specificity of the assay, and only E. stewartii strains gave a positive reaction. In addition, infected and healthy plant material was also assayed. E. stewartii was detected in infected plant material, even when large populations of epiphytic bacteria were present. No enrichment was necessary for detection of the pathogen in corn leaves. This assay has potential as a diagnostic technique for the detection of E. stewartii in infected plant and vector material.

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Year:  1994        PMID: 7509585      PMCID: PMC201300          DOI: 10.1128/aem.60.1.278-284.1994

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


  13 in total

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Authors:  F Barany
Journal:  PCR Methods Appl       Date:  1991-08

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Journal:  Proc Natl Acad Sci U S A       Date:  1978-10       Impact factor: 11.205

4.  The pUC plasmids, an M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primers.

Authors:  J Vieira; J Messing
Journal:  Gene       Date:  1982-10       Impact factor: 3.688

5.  On the evolutionary descent of organisms and organelles: a global phylogeny based on a highly conserved structural core in small subunit ribosomal RNA.

Authors:  M W Gray; D Sankoff; R J Cedergren
Journal:  Nucleic Acids Res       Date:  1984-07-25       Impact factor: 16.971

6.  Detection of Listeria monocytogenes with a nonisotopic polymerase chain reaction-coupled ligase chain reaction assay.

Authors:  M Wiedmann; F Barany; C A Batt
Journal:  Appl Environ Microbiol       Date:  1993-08       Impact factor: 4.792

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Authors:  L Birkenmeyer; A S Armstrong
Journal:  J Clin Microbiol       Date:  1992-12       Impact factor: 5.948

8.  Genetic disease detection and DNA amplification using cloned thermostable ligase.

Authors:  F Barany
Journal:  Proc Natl Acad Sci U S A       Date:  1991-01-01       Impact factor: 11.205

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Authors:  F Sanger; S Nicklen; A R Coulson
Journal:  Proc Natl Acad Sci U S A       Date:  1977-12       Impact factor: 11.205

10.  Discrimination of Listeria monocytogenes from other Listeria species by ligase chain reaction.

Authors:  M Wiedmann; J Czajka; F Barany; C A Batt
Journal:  Appl Environ Microbiol       Date:  1992-11       Impact factor: 4.792

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  1 in total

1.  Identification of the corn pathogen Pantoea stewartii by mass spectrometry of whole-cell extracts and its detection with novel PCR primers.

Authors:  Annette Wensing; Stefan Zimmermann; Klaus Geider
Journal:  Appl Environ Microbiol       Date:  2010-07-23       Impact factor: 4.792

  1 in total

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