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    Quantitative variation in effector activity of ToxA isoforms from Stagonospora nodorum and Pyrenophora tritici-repentis

    Access Status
    Fulltext not available
    Authors
    Tan, Kar-Chun
    Ferguson-Hunt, M.
    Rybak, K.
    Waters, O.
    Stanley, W.
    Bond, C.
    Stukenbrock, E.
    Friesen, T.
    Faris, J.
    McDonald, B.
    Oliver, Richard
    Date
    2012
    Type
    Journal Article
    
    Metadata
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    Citation
    Tan, K. and Ferguson-Hunt, M. and Rybak, K. and Waters, O. and Stanley, W. and Bond, C. and Stukenbrock, E. et al. 2012. Quantitative variation in effector activity of ToxA isoforms from Stagonospora nodorum and Pyrenophora tritici-repentis. Molecular Plant - Microbe Interactions. 25 (4): pp. 515-522.
    Source Title
    Molecular Plant - Microbe Interactions
    DOI
    10.1094/MPMI-10-11-0273
    ISSN
    08940282
    School
    Department of Environment and Agriculture
    URI
    http://hdl.handle.net/20.500.11937/10700
    Collection
    • Curtin Research Publications
    Abstract

    ToxA is a proteinaceous necrotrophic effector produced by Stagonospora nodorum and Pyrenophora tritici-repentis. In this study, all eight mature isoforms of the ToxA protein were purified and compared. Circular dichroism spectra indicated that all isoforms were structurally intact and had indistinguishable secondary structural features. ToxA isoforms were infiltrated into wheat lines that carry the sensitivity gene Tsn1. It was observed that different wheat lines carrying identical Tsn1 alleles varied in sensitivity to ToxA. All ToxA isoforms induced necrosis when introduced into any Tsn1 wheat line but we observed quantitative variation in effector activity, with the least-active version found in isolates of P. tritici-repentis. Pathogen sporulation increased with higher doses of ToxA. The isoforms that induced the most rapid necrosis also induced the most sporulation, indicating that pathogen fitness is affected by differences in ToxA activity. We show that differences in toxin activity encoded by a single gene can contribute to the quantitative inheritance of necrotrophic virulence. Our findings support the hypothesis that the variation at ToxA results from selection that favors increased toxin activity.

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