Genome analysis of the sugar beet pathogen Rhizoctonia solani AG2-2IIIB revealed high numbers in secreted proteins and cell wall degrading enzymes

被引:65
|
作者
Wibberg, Daniel [1 ]
Andersson, Louise [2 ,3 ]
Tzelepis, Georgios [3 ]
Rupp, Oliver [4 ]
Blom, Jochen [4 ]
Jelonek, Lukas [4 ]
Puehler, Alfred [1 ]
Fogelqvist, Johan [3 ]
Varrelmann, Mark [5 ]
Schlueter, Andreas [1 ]
Dixelius, Christina [3 ]
机构
[1] Univ Bielefeld, Inst Genome Res & Syst Biol, CeBiTec, D-33501 Bielefeld, Germany
[2] Syngenta Seeds AB, Sabyholmsvagen 24, S-26191 Landskrona, Sweden
[3] Swedish Univ Agr Sci, Dept Plant Biol, Uppsala BioCtr, Linnean Ctr Plant Biol, POB 7080S-75007, Uppsala, Sweden
[4] Univ Giessen, Bioinformat & Syst Biol, D-35392 Giessen, Germany
[5] IfZ, Inst Sugar Beet Res, Gottingen, Germany
来源
BMC GENOMICS | 2016年 / 17卷
基金
瑞典研究理事会;
关键词
Beta vulgaris; Carbohydrate active enzymes; Carbohydrate esterases; Sugar beet pathogens; Glycoside hydrolases; Polysaccharide lyases; Rhizoctonia solani; RICH PECTIC POLYSACCHARIDES; FERULIC ACID; AG1-IB; 7/3/14; SEQUENCE; EVOLUTION; FUNGUS; GENES; DATABASE; TRANSCRIPTOME; ANASTOMOSIS;
D O I
10.1186/s12864-016-2561-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Sugar beet (Beta vulgaris) is a crop cultivated for its high content in sugar, but it is vulnerable to many soil-borne pathogens. One of them is the basidiomycete Rhizoctonia solani. This fungal species has a compatibility system regulating hyphal fusions (anastomosis). Consequently, R. solani species are categorized in anastomosis groups (AGs). AG2-2IIIB isolates are most aggressive on sugar beet. In the present study, we report on the draft genome of R. solani AG2-2IIIB using the Illumina technology. Genome analysis, interpretation and comparative genomics of five sequenced R. solani isolates were carried out. Results: The draft genome of R. solani AG2-2IIIB has an estimated size of 56.02 Mb. In addition, two normalized EST libraries were sequenced. In total 20,790 of 21,980 AG2-2IIIB isotigs (transcript isoforms) were mapped on the genome with more than 95 % sequence identity. The genome of R. solani AG2-2IIIB was predicted to harbor 11,897 genes and 4908 were found to be isolate-specific. R. solani AG2-2IIIB was predicted to contain 1142 putatively secreted proteins and 473 of them were found to be unique for this isolate. The R. solani AG2-2IIIB genome encodes a high number of carbohydrate active enzymes. The highest numbers were observed for the polysaccharide lyases family 1 (PL-1), glycoside hydrolase family 43 (GH-43) and carbohydrate estarase family 12 (CE-12). Transcription analysis of selected genes representing different enzyme clades revealed a mixed pattern of up-and down-regulation six days after infection on sugar beets featuring variable levels of resistance compared to mycelia of the fungus grown in vitro. Conclusions: The established R. solani AG2-2IIIB genome and EST sequences provide important information on the gene content, gene structure and transcriptional activity for this sugar beet pathogen. The enriched genomic platform provides an important platform to enhance our understanding of R. solani biology.
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页数:12
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