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dc.contributor.authorPoudel, B.
dc.contributor.authorEllwood, Simon
dc.contributor.authorTesta, A.
dc.contributor.authorMcLean, M.
dc.contributor.authorSutherland, M.
dc.contributor.authorMartin, A.
dc.date.accessioned2017-07-27T05:21:57Z
dc.date.available2017-07-27T05:21:57Z
dc.date.created2017-07-26T11:11:19Z
dc.date.issued2017
dc.identifier.citationPoudel, B. and Ellwood, S. and Testa, A. and McLean, M. and Sutherland, M. and Martin, A. 2017. Rare pyrenophora teres hybridization events revealed by development of sequence-specific PCR markers. Phytopathology. 107 (7): pp. 878-884.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/54684
dc.identifier.doi10.1094/PHYTO-11-16-0396-R
dc.description.abstract

Pyrenophora teres f. teres and P. teres f. Maculata cause net form and spot form, respectively, of net blotch on barley (Hordeum vulgare). The two forms reproduce sexually, producing hybrids with genetic and pathogenic variability. Phenotypic identification of hybrids is challenging because lesions induced by hybrids on host plants resemble lesions induced by either P. teres f. teres or P. teres f. Maculata. In this study, 12 sequence-specific polymerase chain reaction markers were developed based on expressed regions spread across the genome. The primers were validated using 210 P. teres isolates, 2 putative field hybrids (WAC10721 and SNB172), 50 laboratory-produced hybrids, and 7 isolates collected from barley grass (H. leporinum). The sequence-specific markers confirmed isolate WAC10721 as a hybrid. Only four P. teres f. teres markers amplified on DNA of barley grass isolates. Amplified fragment length polymorphism markers suggested that P. teres barley grass isolates are genetically different from P. teres barley isolates and that the second putative hybrid (SNB172) is a barley grass isolate. We developed a suite of markers which clearly distinguish the two forms of P. teres and enable unambiguous identification of hybrids.

dc.publisherAmerican Phytopathological Society
dc.titleRare pyrenophora teres hybridization events revealed by development of sequence-specific PCR markers
dc.typeJournal Article
dcterms.source.volume107
dcterms.source.number7
dcterms.source.startPage878
dcterms.source.endPage884
dcterms.source.issn0031-949X
dcterms.source.titlePhytopathology
curtin.departmentCentre for Crop Disease Management
curtin.accessStatusFulltext not available


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