PR-1 protein inhibits the differentiation of rust infection hyphae in leaves of acquired resistant broad bean

dc.contributor.authorRauscher, Martinadeu
dc.contributor.authorAdam, Attiladeu
dc.contributor.authorWirtz, Sabinedeu
dc.contributor.authorGuggenheim, Richarddeu
dc.contributor.authorMendgen, Kurt
dc.contributor.authorDeising, Holgerdeu
dc.date.accessioned2011-03-24T17:28:14Zdeu
dc.date.available2011-03-24T17:28:14Zdeu
dc.date.issued1999deu
dc.description.abstractTreatment of broad bean leaves with salicylic acid (SA) or 2,6-dichloro-isonicotinic acid (DCINA) induces resistance against the rust fungus Uromyces fabae resulting in reduced rust pustule density. Lightmicroscopy studies showed that in induced resistant plants the rust fungus is inhibited immediately after penetration through the stomatal pore. The differentiation of infection structures growing within the intercellular space of the leaf, i.e. infection hyphae and haustorial mother cells, is inhibited. Furthermore, low-temperature scanning electron microscopy studies of freeze fractures revealed protrusions at the tips of infection hyphae growing in induced resistant broad bean leaves. Treatment of in vitro-differentiating rust infection structures with intercellular fluids (IFs) from induced resistant plants confirmed that the fungus is sensitive towards an apoplastic anti-fungal activity only after having formed appressoria. Other legume rusts such as U. vignae and U. appendiculatus were likewise inhibited in the presence of IF from SA-treated broad bean leaves. Heterologous antibodies were used to study changes in the extracellular pathogenesis-related (PR) protein pattern after resistance induction. Western blots indicated that chitinases and ß-1,3-glucanases were present in both induced and control plants. In contrast, PR-1 proteins were newly synthesized in response to SA or DCINA application. The major induced PR-1 protein was purified and exhibited strong differentiation inhibiting activity towards U. fabae infection structures.We conclude that the inhibition of rust infection hyphae in acquired resistant broad bean plants is mainly due to the anti-fungal activity of this induced basic PR-1 protein.eng
dc.description.versionpublished
dc.format.mimetypeapplication/pdfdeu
dc.identifier.citationFirst publ. in: The Plant Journal 19 (1999), 6, pp. 625-633deu
dc.identifier.doi10.1046/j.1365-313x.1999.00545.x
dc.identifier.ppn273205587deu
dc.identifier.urihttp://kops.uni-konstanz.de/handle/123456789/6672
dc.language.isodeudeu
dc.legacy.dateIssued2007deu
dc.rightsAttribution-NonCommercial-NoDerivs 2.0 Generic
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/
dc.subjectPR-1 proteindeu
dc.subjectrust infectiondeu
dc.subject.ddc570deu
dc.titlePR-1 protein inhibits the differentiation of rust infection hyphae in leaves of acquired resistant broad beandeu
dc.typeJOURNAL_ARTICLEdeu
dspace.entity.typePublication
kops.citation.bibtex
@article{Rauscher1999prote-6672,
  year={1999},
  doi={10.1046/j.1365-313x.1999.00545.x},
  title={PR-1 protein inhibits the differentiation of rust infection hyphae in leaves of acquired resistant broad bean},
  number={6},
  volume={19},
  issn={0960-7412},
  journal={The Plant Journal},
  pages={625--633},
  author={Rauscher, Martina and Adam, Attila and Wirtz, Sabine and Guggenheim, Richard and Mendgen, Kurt and Deising, Holger}
}
kops.citation.iso690RAUSCHER, Martina, Attila ADAM, Sabine WIRTZ, Richard GUGGENHEIM, Kurt MENDGEN, Holger DEISING, 1999. PR-1 protein inhibits the differentiation of rust infection hyphae in leaves of acquired resistant broad bean. In: The Plant Journal. 1999, 19(6), pp. 625-633. ISSN 0960-7412. eISSN 1365-313X. Available under: doi: 10.1046/j.1365-313x.1999.00545.xdeu
kops.citation.iso690RAUSCHER, Martina, Attila ADAM, Sabine WIRTZ, Richard GUGGENHEIM, Kurt MENDGEN, Holger DEISING, 1999. PR-1 protein inhibits the differentiation of rust infection hyphae in leaves of acquired resistant broad bean. In: The Plant Journal. 1999, 19(6), pp. 625-633. ISSN 0960-7412. eISSN 1365-313X. Available under: doi: 10.1046/j.1365-313x.1999.00545.xeng
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    <dcterms:abstract xml:lang="eng">Treatment of broad bean leaves with salicylic acid (SA) or 2,6-dichloro-isonicotinic acid (DCINA) induces resistance against the rust fungus Uromyces fabae resulting in reduced rust pustule density. Lightmicroscopy studies showed that in induced resistant plants the rust fungus is inhibited immediately after penetration through the stomatal pore. The differentiation of infection structures growing within the intercellular space of the leaf, i.e. infection hyphae and haustorial mother cells, is inhibited. Furthermore, low-temperature scanning electron microscopy studies of freeze fractures revealed protrusions at the tips of infection hyphae growing in induced resistant broad bean leaves. Treatment of in vitro-differentiating rust infection structures with intercellular fluids (IFs) from induced resistant plants confirmed that the fungus is sensitive towards an apoplastic anti-fungal activity only after having formed appressoria. Other legume rusts such as U. vignae and U. appendiculatus were likewise inhibited in the presence of IF from SA-treated broad bean leaves. Heterologous antibodies were used to study changes in the extracellular pathogenesis-related (PR) protein pattern after resistance induction. Western blots indicated that chitinases and ß-1,3-glucanases were present in both induced and control plants. In contrast, PR-1 proteins were newly synthesized in response to SA or DCINA application. The major induced PR-1 protein was purified and exhibited strong differentiation inhibiting activity towards U. fabae infection structures.We conclude that the inhibition of rust infection hyphae in acquired resistant broad bean plants is mainly due to the anti-fungal activity of this induced basic PR-1 protein.</dcterms:abstract>
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kops.sourcefieldThe Plant Journal. 1999, <b>19</b>(6), pp. 625-633. ISSN 0960-7412. eISSN 1365-313X. Available under: doi: 10.1046/j.1365-313x.1999.00545.xdeu
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kops.sourcefield.plainThe Plant Journal. 1999, 19(6), pp. 625-633. ISSN 0960-7412. eISSN 1365-313X. Available under: doi: 10.1046/j.1365-313x.1999.00545.xeng
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