Literature DB >> 24788585

Rapid and sensitive detection of Sclerotium rolfsii associated with collar rot disease of Amorphophallus paeoniifolius by species-specific polymerase chain reaction assay.

V Pravi1, M L Jeeva, P V Archana.   

Abstract

Collar rot disease caused by Sclerotium rolfsii is an economically important disease prevailing in all Amorphophallus growing areas. The pathogen propagules surviving in soil and planting material are the major sources of inoculum. A nested PCR assay has been developed for specific detection of S. rolfsii in soil and planting material. The PCR detection limit was 10 pg in conventional assay whereas 0.1 pg in nested assay. The primers designed were found to be highly specific and could be used for accurate identification of pathogen up to species level. The protocol was standardized for detection of the pathogen in artificially and naturally infected field samples.

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Year:  2014        PMID: 24788585     DOI: 10.1007/s12033-014-9757-x

Source DB:  PubMed          Journal:  Mol Biotechnol        ISSN: 1073-6085            Impact factor:   2.695


  9 in total

1.  A greedy algorithm for aligning DNA sequences.

Authors:  Z Zhang; S Schwartz; L Wagner; W Miller
Journal:  J Comput Biol       Date:  2000 Feb-Apr       Impact factor: 1.479

Review 2.  Molecular diagnostics for fungal plant pathogens.

Authors:  H Alastair McCartney; Simon J Foster; Bart A Fraaije; Elaine Ward
Journal:  Pest Manag Sci       Date:  2003-02       Impact factor: 4.845

3.  Advances in molecular-based diagnostics in meeting crop biosecurity and phytosanitary issues.

Authors:  Norman W Schaad; Reid D Frederick; Joe Shaw; William L Schneider; Robert Hickson; Michael D Petrillo; Douglas G Luster
Journal:  Annu Rev Phytopathol       Date:  2003       Impact factor: 13.078

4.  Length heterogeneity in ITS 2 and the methylation status of CCGG and GCGC sites in the rRNA genes of the genus Peronosclerospora.

Authors:  C Yao; R A Frederiksen; C W Magill
Journal:  Curr Genet       Date:  1992-11       Impact factor: 3.886

5.  The polymerase chain reaction and plant disease diagnosis.

Authors:  J M Henson; R French
Journal:  Annu Rev Phytopathol       Date:  1993       Impact factor: 13.078

6.  Detection of Ralstonia solanacearum strains with a quantitative, multiplex, real-time, fluorogenic PCR (TaqMan) assay.

Authors:  S A Weller; J G Elphinstone; N C Smith; N Boonham; D E Stead
Journal:  Appl Environ Microbiol       Date:  2000-07       Impact factor: 4.792

7.  A simple method of preparing plant samples for PCR.

Authors:  H Wang; M Qi; A J Cutler
Journal:  Nucleic Acids Res       Date:  1993-08-25       Impact factor: 16.971

8.  PCR amplification of ribosomal DNA for species identification in the plant pathogen genus Phytophthora.

Authors:  J B Ristaino; M Madritch; C L Trout; G Parra
Journal:  Appl Environ Microbiol       Date:  1998-03       Impact factor: 4.792

9.  Polymerase Chain Reaction Detection of Ustilago hordei in Leaves of Susceptible and Resistant Barley Varieties.

Authors:  D A Willits; J E Sherwood
Journal:  Phytopathology       Date:  1999-03       Impact factor: 4.025

  9 in total

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