15 research outputs found

    Development of a recombinant antibody ELISA test for the detection of Polymyxa betae and its use in resistance screening

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    An ELISA test was developed for the quantitative detection of the obligate parasite Polymyxa betae, the vector of Beet necrotic yellow vein virus (BNYVV), in infected sugarbeet roots. The test used monoclonal and polyclonal antibodies raised to a recombinantly expressed glutathione-S-transferase (GST) from P. betae. A close correlation was found between the number of P. betae zoospores in serially diluted suspensions and absorbance values in the ELISA test. Time-course studies of plants grown in naturally infested soils in controlled environment tests demonstrated the value of the ELISA test in screening for P. betae resistance. In preliminary tests, P. betae-resistant accessions of the wild sea beet (Beta vulgaris ssp. maritima), which might be used to restrict the transmission of BNYVV, were identifiedPeer reviewe

    Screening for genetic elements involved in the non-host response of sugar beet to the plasmodiophorid cereal root parasite Polymyxa graminis by representational difference analysis

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    Representational difference analysis (RDA) was used to select and clone cDNA fragments of genes whose steady state transcription was upregulated in sugar beet challenged with the nonhost parasite Polymyxa graminis. In silico analysis revealed that sequences with similarities to plant defence genes as well as genes of unknown function were represented amongst the cloned cDNAs. The utility of RDA was verified when, in material from the nonhost interaction, semiquantitative RT-PCR confirmed transcriptional upregulation of at least 10 of 17 genes randomly selected from the RDA library. Time-course transcriptional analysis of two plant defence gene-like sequences demonstrated that, in sugar beet, both were upregulated within 1 h in response to P. graminis but not to P. betae. This work comprises the first report of an active response by sugar beet to P. graminisPeer reviewe
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