期刊论文详细信息
BMC Genomics
Secretome analysis reveals effector candidates associated with broad host range necrotrophy in the fungal plant pathogen Sclerotinia sclerotiorum
Sylvain Raffaele1  Dominique Roby1  Claudine Balagué1  Koanna Guyon1 
[1] CNRS, Laboratoire des Interactions Plantes-Microorganismes (LIPM), UMR2594, F-31326, Castanet-Tolosan, France
关键词: Arabidopsis thaliana;    Pathogen;    Necrotrophic fungal;    Secretome;    Gene expression;    Sclerotinia sclerotiorum. Effectors;   
Others  :  1217295
DOI  :  10.1186/1471-2164-15-336
 received in 2014-02-03, accepted in 2014-04-27,  发布年份 2014
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【 摘 要 】

Background

The white mold fungus Sclerotinia sclerotiorum is a devastating necrotrophic plant pathogen with a remarkably broad host range. The interaction of necrotrophs with their hosts is more complex than initially thought, and still poorly understood.

Results

We combined bioinformatics approaches to determine the repertoire of S. sclerotiorum effector candidates and conducted detailed sequence and expression analyses on selected candidates. We identified 486 S. sclerotiorum secreted protein genes expressed in planta, many of which have no predicted enzymatic activity and may be involved in the interaction between the fungus and its hosts. We focused on those showing (i) protein domains and motifs found in known fungal effectors, (ii) signatures of positive selection, (iii) recent gene duplication, or (iv) being S. sclerotiorum-specific. We identified 78 effector candidates based on these properties. We analyzed the expression pattern of 16 representative effector candidate genes on four host plants and revealed diverse expression patterns.

Conclusions

These results reveal diverse predicted functions and expression patterns in the repertoire of S. sclerotiorum effector candidates. They will facilitate the functional analysis of fungal pathogenicity determinants and should prove useful in the search for plant quantitative disease resistance components active against the white mold.

【 授权许可】

   
2014 Guyon et al.; licensee BioMed Central Ltd.

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