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Journal of Experimental Botany 2009 60(15):4287-4300; doi:10.1093/jxb/erp269
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© 2009 The Author(s).
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. This paper is available online free of all access charges (see
http://jxb.oxfordjournals.org/open_access.html for further details)


RESEARCH PAPER

Effects of β-1,3-glucan from Septoria tritici on structural defence responses in wheat

Nandini P. Shetty1, Jens D. Jensen1, Anne Knudsen2, Christine Finnie3, Naomi Geshi2, Andreas Blennow2, David B. Collinge1 and Hans J. Lyngs Jørgensen1,*

1Department of Plant Biology and Biotechnology, Faculty of Life Sciences, University of Copenhagen, Thorvaldsensvej 40, DK-1871 Frederiksberg C, Denmark
2Villum Kann Rasmussen Research Centre Pro-Active Plants, Molecular Plant Biology, Department of Plant Biology and Biotechnology, Faculty of Life Sciences, University of Copenhagen, Thorvaldsensvej 40, DK-1871 Frederiksberg C, Denmark
3Enzyme and Protein Chemistry, Department of Systems Biology, Building 224, Technical University of Denmark, DK-2800 Kgs. Lyngby, Denmark

* To whom correspondence should be addressed: E-mail: hjo{at}life.ku.dk

The accumulation of the pathogenesis-related (PR) proteins β-1,3-glucanase and chitinase and structural defence responses were studied in leaves of wheat either resistant or susceptible to the hemibiotrophic pathogen Septoria tritici. Resistance was associated with an early accumulation of β-1,3-glucanase and chitinase transcripts followed by a subsequent reduction in level. Resistance was also associated with high activity of β-1,3-glucanase, especially in the apoplastic fluid, in accordance with the biotrophic/endophytic lifestyle of the pathogen in the apoplastic spaces, thus showing the highly localized accumulation of defence proteins in the vicinity of the pathogen. Isoform analysis of β-1,3-glucanase from the apoplastic fluid revealed that resistance was associated with the accumulation of an endo-β-1,3-glucanase, previously implicated in defence against pathogens, and a protein with identity to ADPG pyrophosphatase (92%) and germin-like proteins (93%), which may be involved in cell wall reinforcement. In accordance with this, glycoproteins like extensin were released into the apoplast and callose accumulated to a greater extent in cell walls, whereas lignin and polyphenolics were not found to correlate with defence. Treatment of a susceptible wheat cultivar with purified β-1,3-glucan fragments from cell walls of S. tritici gave complete protection against disease and this was accompanied by increased gene expression of β-1,3-glucanase and the deposition of callose. Collectively, these data indicate that resistance is dependent on a fast, initial recognition of the pathogen, probably due to β-1,3-glucan in the fungal cell walls, and this results in the accumulation of β-1,3-glucanase and structural defence responses, which may directly inhibit the pathogen and protect the host against fungal enzymes and toxins.

Key words: ADPG pyrophosphatase, callose, chitinase, extensin, β-1,3-glucanase, Mycosphaerella graminicola, PAMPs/MAMPs, Septoria tritici, wheat

Received 25 May 2009; Revised 8 August 2009 Accepted 11 August 2009


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