昆虫病原真菌Conidiobolus coronatus (Entomophthoromycotina)广泛宿主适应性分子基础的基因组学见解。

IF 4.2 2区 生物学 Q2 MICROBIOLOGY
Fan Bai, Tian Yang, Lvhao Zhang, Jiaqi Yang, Xinyu Chen, Xiang Zhou
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引用次数: 0

摘要

冠状孢子虫(Conidiobolus coronatus)是一种具有广泛寄主范围的真菌病原体,在生物防治方面具有广阔的应用前景。利用PacBio长读测序技术对一株冠状冠状螺旋体(C. coronatus)进行测序,以阐明其广泛宿主适应性的分子基础。新组装的44.21 Mb基因组具有较高的完整性(BUSCO评分:93.45%),编码11,128个蛋白质编码基因,其中23.1%预测介导病原体-宿主相互作用。与蚜虫专性病原体C. obscurus的比较基因组学发现,与宿主适应机制相关的基因家族显著扩增,包括宿主识别、转录调节、宿主成分降解、解毒和免疫逃避。功能注释强调了细胞成分组织和能量代谢的富集。Pfam注释鉴定了125个7跨膜受体(假定的gpcr), 67个真菌特异性转录因子,361个肽酶(198个丝氨酸蛋白酶和103个金属蛋白酶),127个细胞色素P450单加氧酶(P450), 35个富含半胱氨酸的分泌蛋白和55个酪氨酸酶。此外,还鉴定了6个主要模块中的430种碳水化合物活性酶(CAZymes)。非靶向代谢组学检测到22种高表达的萜类化合物,与基因组中的萜类生物合成基因簇一致。总的来说,这些扩展通过实现跨宿主信号解码和基因表达重编程,打破多种宿主物理化学屏障,扩大其化学生态位,巩固了冠状冠冠状冠的广泛宿主范围。这项研究为昆虫病原真菌广泛的宿主适应性提供了基因组学的见解,有助于进一步了解病原体与宿主的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genomic Insights into the Molecular Basis of Broad Host Adaptability of the Entomopathogenic Fungus Conidiobolus coronatus (Entomophthoromycotina).

Conidiobolus coronatus (Entomophthorales), a fungal pathogen with a broad insect host range, is a promising candidate for biocontrol applications. We sequenced a C. coronatus strain isolated from a Rhopalomyia sp. cadaver using PacBio long-read sequencing to elucidate the molecular basis of its wide host adaptability. The newly assembled 44.21 Mb genome exhibits high completeness (BUSCO score: 93.45%) and encodes 11,128 protein-coding genes, with 23.1% predicted to mediate pathogen-host interactions. Comparative genomics with the aphid-obligate pathogen C. obscurus revealed significant expansions in gene families associated with host adaptation mechanisms, including host recognition, transcriptional regulation, degradation of host components, detoxification, and immune evasion. Functional annotation highlighted enrichment in cellular component organization and energy metabolism. Pfam annotation identified one hundred twenty-five seven-transmembrane receptors (putative GPCRs), sixty-seven fungus-specific transcription factors, three hundred sixty-one peptidases (one hundred ninety-eight serine proteases and one hundred three metalloproteases), one hundred twenty-seven cytochrome P450 monooxygenases (P450s), thirty-five cysteine-rich secretory proteins, and fifty-five tyrosinases. Additionally, four hundred thirty carbohydrate-active enzymes (CAZymes) across six major modules were characterized. Untargeted metabolomics detected 22 highly expressed terpenoids, consistent with terpenoid biosynthesis gene clusters in the genome. Collectively, these expansions underpin the broad host range of C. coronatus by enabling cross-host signal decoding and gene expression reprogramming, breaching diverse host physicochemical barriers, and expanding its chemical ecological niche. This study provides genomic insights into broad host adaptability in entomopathogenic fungi, facilitating further understanding of pathogen-host interactions.

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来源期刊
Journal of Fungi
Journal of Fungi Medicine-Microbiology (medical)
CiteScore
6.70
自引率
14.90%
发文量
1151
审稿时长
11 weeks
期刊介绍: Journal of Fungi (ISSN 2309-608X) is an international, peer-reviewed scientific open access journal that provides an advanced forum for studies related to pathogenic fungi, fungal biology, and all other aspects of fungal research. The journal publishes reviews, regular research papers, and communications in quarterly issues. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on paper length. Full experimental details must be provided so that the results can be reproduced.
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