期刊论文详细信息
PLoS Pathogens
Genomic and Proteomic Analyses of the Fungus Arthrobotrys oligospora Provide Insights into Nematode-Trap Formation
Jianping Xu1  Yanlu Luo2  Jinkui Yang2  Lianming Liang2  Yajun Liu2  Guohong Li2  Yu Liu2  Lu Feng2  Wei Zhou2  Haiyan Wang2  Min Qiao2  Juan Li2  Qili Mi2  Chenggang Zou2  Lei Li2  Xinglai Ji2  Kaifang Ji2  Zefen Yu2  Yan Ren3  Ke-Qin Zhang3  Lei Wang3  Xuemei Niu3  Xiaomin Li3  Yun Feng3  Shuqun Liu3  Xiaowei Huang3  Junli Wu4 
[1] Department of Biology, McMaster University, Hamilton, Ontario, Canada;Laboratory for Conservation and Utilization of Bio-Resources, and Key Laboratory of Microbial Diversity in Southwest China, Ministry of Education, Yunnan University, Kunming, P. R. China;TEDA School of Biological Sciences and Biotechnology, Nankai University, Tianjin, P. R. China;Yunnan Academy of Tobacco Science, Kunming, P. R. China
关键词: Fungal genomics;    Fungi;    Fungal genetics;    Fungal pathogens;    Phylogenetic analysis;    Comparative genomics;    Rice blast fungus;    Pathogenesis;   
DOI  :  10.1371/journal.ppat.1002179
学科分类:生物科学(综合)
来源: Public Library of Science
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【 摘 要 】

Nematode-trapping fungi are “carnivorous” and attack their hosts using specialized trapping devices. The morphological development of these traps is the key indicator of their switch from saprophytic to predacious lifestyles. Here, the genome of the nematode-trapping fungus Arthrobotrys oligospora Fres. (ATCC24927) was reported. The genome contains 40.07 Mb assembled sequence with 11,479 predicted genes. Comparative analysis showed that A. oligospora shared many more genes with pathogenic fungi than with non-pathogenic fungi. Specifically, compared to several sequenced ascomycete fungi, the A. oligospora genome has a larger number of pathogenicity-related genes in the subtilisin, cellulase, cellobiohydrolase, and pectinesterase gene families. Searching against the pathogen-host interaction gene database identified 398 homologous genes involved in pathogenicity in other fungi. The analysis of repetitive sequences provided evidence for repeat-induced point mutations in A. oligospora. Proteomic and quantitative PCR (qPCR) analyses revealed that 90 genes were significantly up-regulated at the early stage of trap-formation by nematode extracts and most of these genes were involved in translation, amino acid metabolism, carbohydrate metabolism, cell wall and membrane biogenesis. Based on the combined genomic, proteomic and qPCR data, a model for the formation of nematode trapping device in this fungus was proposed. In this model, multiple fungal signal transduction pathways are activated by its nematode prey to further regulate downstream genes associated with diverse cellular processes such as energy metabolism, biosynthesis of the cell wall and adhesive proteins, cell division, glycerol accumulation and peroxisome biogenesis. This study will facilitate the identification of pathogenicity-related genes and provide a broad foundation for understanding the molecular and evolutionary mechanisms underlying fungi-nematodes interactions.

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