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感染过程与基因组组装为了解具有宿主特异性的破坏性真菌寄生菌的致病机制提供了见解。

Infection Process and Genome Assembly Provide Insights into the Pathogenic Mechanism of Destructive Mycoparasite with Host Specificity.

作者信息

Liu Qing, Xu Yanyan, Zhang Xiaoling, Li Kuan, Li Xiao, Wang Fen, Xu Fangxu, Dong Caihong

机构信息

State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.

University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

J Fungi (Basel). 2021 Oct 28;7(11):918. doi: 10.3390/jof7110918.

Abstract

is the pathogen in the white mildew disease of , one of the popular mushrooms. This disease frequently occurs and there is no effective method for disease prevention and control. In the present study, is found to be the only host of , indicating strict host specificity. The infection process was monitored by fluorescent labeling and scanning and transmission electron microscopes. can invade into the gaps among hyphae of the fruiting bodies of the host and fill them gradually. It can degrade the hyphae of the host by both direct contact and noncontact. The parasitism is initially biotrophic, and then necrotrophic as mycoparasitic interaction progresses. The approximate chromosome-level genome assembly of yielded an N50 length of 5.45 Mbp and a total size of 34.51 Mbp, encoding 10,443 proteins. Phylogenomic analysis revealed that is phylogenetically close to its specific host, A comparative genomic analysis showed that the number of CAZymes of was much less than in other mycoparasites, which might be attributed to its host specificity. Secondary metabolite cluster analysis disclosed the great biosynthetic capabilities and potential mycotoxin production capability. This study provides insights into the potential pathogenesis and interaction between mycoparasite and its host.

摘要

是流行蘑菇之一的白霉病中的病原体。这种疾病经常发生,并且没有有效的疾病预防和控制方法。在本研究中,发现是唯一的宿主,表明严格的宿主特异性。通过荧光标记以及扫描和透射电子显微镜监测感染过程。可以侵入宿主子实体菌丝之间的间隙并逐渐填充它们。它可以通过直接接触和非接触两种方式降解宿主的菌丝。寄生作用最初是活体营养型的,然后随着真菌寄生相互作用的进展变为死体营养型。的近似染色体水平基因组组装产生了5.45 Mbp的N50长度和34.51 Mbp的总大小,编码10,443种蛋白质。系统基因组分析表明,在系统发育上与其特定宿主接近。比较基因组分析表明,的碳水化合物活性酶数量比其他真菌寄生物少得多,这可能归因于其宿主特异性。次生代谢物簇分析揭示了其巨大的生物合成能力和潜在的霉菌毒素产生能力。本研究为真菌寄生物与其宿主之间的潜在发病机制和相互作用提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c89e/8620734/d9fe1a3cedb5/jof-07-00918-g001.jpg

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