Temporal dynamics, microdiversity, and ecological functions of viral communities during cyanobacterial blooms in Lake Taihu.

IF 9.2 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Tianyi Chen, Yanxuan Xiong, Jinhong Zhang, Qiue Zhang, Jiang Wu, Nan Xu, Tang Liu
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Abstract

Harmful cyanobacterial blooms pose severe threats to aquatic ecosystems. Bloom-forming cyanobacteria form cyanobacterial aggregates (CAs) that create a phycosphere supporting diverse microbial interactions. Here, longitudinal metagenomics and metatranscriptomics were employed to explore the temporal variation of CA-attached viral communities throughout cyanobacterial blooms in Lake Taihu. Viral communities, represented by 5613 viral operational taxonomic units, showed increased relative abundance (RPKM) with the expansion of bloom areas. Among 1791 virus‒host linkages, host shifts followed the succession of two dominant cyanobacterial genera, Microcystis and Dolichospermum. Viruses demonstrated high virus‒host abundance ratios within all host genera and showed elevated transcriptional activities infecting Dolichospermum during the late bloom stage. Viruses featured high microdiversity and positively selected replication-associated genes in response to abundant host genera and variable trophic status. This study uncovered diverse active viral auxiliary metabolism associated with photosynthesis, biochemical cycling, and DNA biosynthesis, and highlighted the significant role of phycosphere-associated viruses during cyanobacterial blooms.

太湖蓝藻水华期间病毒群落的时间动态、微多样性和生态功能。
有害的蓝藻繁殖对水生生态系统构成严重威胁。形成开花的蓝藻形成蓝藻聚集体(CAs),创造一个支持多种微生物相互作用的藻球。本文采用纵向宏基因组学和亚转录组学研究了太湖蓝藻华中ca附着病毒群落的时间变化。病毒群落的相对丰度(RPKM)随着开花面积的扩大而增加,以5613个病毒操作分类单位为代表。在1791个病毒-宿主联系点中,宿主的转移伴随着两个优势蓝藻属的演替,微囊藻属和Dolichospermum。病毒在所有寄主属中均表现出较高的病毒-寄主丰度比,并且在开花后期表现出较高的转录活性。病毒具有高度的微多样性和正向选择复制相关基因,以响应丰富的宿主属和可变的营养状态。本研究揭示了与光合作用、生化循环和DNA生物合成相关的多种活性病毒辅助代谢,并强调了藻球相关病毒在蓝藻华中的重要作用。
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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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