Tracking putative Microcystis viruses and virus-host associations across distinct phases of a Microcystis-dominated bloom.

IF 4.6 2区 生物学 Q1 MICROBIOLOGY
mSystems Pub Date : 2025-09-22 DOI:10.1128/msystems.00575-25
A J Wing, Bridget Hegarty, G Eric Bastien, Vincent J Denef, Jacob Evans, Gregory J Dick, Melissa B Duhaime
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引用次数: 0

Abstract

Viruses significantly impact microbial community composition and function. Yet their role in the fate of freshwater cyanobacterial harmful algal blooms (cHABs), an increasing threat to freshwater systems, remains poorly understood. Here, we address this with a metagenomic analysis of viruses of bloom-forming Microcystis aeruginosa through a seasonal cHAB in the western basin of Lake Erie. We identified globally distributed Microcystis viruses in Lake Erie based on sequence homology to well-studied isolates. A machine-learning model was then used to predict associations between uncharacterized viral populations and the Microcystis and non-Microcystis hosts of the cHAB. Size fractionation of water samples allowed us to identify significant fraction-specific trends in Microcystis viral diversity that corresponded with Microcystis genetic diversity. Viral diversity was highest in the non-colony-associated fraction and lowest in the colony-associated fraction, suggesting that colony formation may lead to bottlenecks in viral diversity in cHABs. Significant turnover of predicted Microcystis virus populations was observed through time, but not between stations miles apart. The virus-host networks revealed extensive interconnectivity and the potential for virus-mediated cross-species genetic exchange. The networks predicted that Lake Erie Microcystis viruses infect hosts spanning phyla, in agreement with lab studies in other systems but challenging previous notions of "narrow" host-virus associations in this genus. Abundant Microcystis virus genes revealed a potential role in key metabolic pathways and host adaptation. These findings advance our understanding of Microcystis viruses and their potential influence on host metabolism, species interactions, and coevolution in Microcystis-dominated cHABs.IMPORTANCEUnderstanding associations between viruses, their hosts, and environmental factors is key for identifying the mechanisms behind the rise and fall of cyanobacterial harmful algal blooms. This study explores the diversity and host ranges of viruses predicted to infect Microcystis, reporting how these properties vary over time, across sample stations in western Lake Erie, and among different filter size fractions. We found that Microcystis virus diversity is highest in non-colony-associated fractions and the lowest in colony-associated fractions, suggesting a link between Microcystis colony formation and reduced viral diversity. We identify abundant genes belonging to predicted Microcystis viruses and their potential roles in key metabolic pathways and adaptation to environmental changes. These findings enhance our understanding of the interplay among viruses, Microcystis, and co-occurring bacteria in cHABs, offering insights into the mechanisms driving bloom dynamics, species interactions, and coevolutionary processes.

在微囊藻为主的华花的不同阶段追踪假定的微囊藻病毒和病毒与宿主的关联。
病毒显著影响微生物群落组成和功能。然而,它们在淡水蓝藻有害藻华(cHABs)的命运中所起的作用,对淡水系统的威胁越来越大,仍然知之甚少。在这里,我们通过伊利湖西部盆地的季节性cHAB对形成华花的铜绿微囊藻病毒进行了宏基因组分析。我们根据序列同源性确定了伊利湖全球分布的微囊虫病毒。然后使用机器学习模型来预测非特征病毒种群与cHAB的微囊藻和非微囊藻宿主之间的关联。水样的大小分级使我们能够确定微囊藻病毒多样性的显著部分特异性趋势,这与微囊藻的遗传多样性相对应。病毒多样性在非集落相关部分中最高,在集落相关部分中最低,这表明集落形成可能导致chab病毒多样性的瓶颈。随着时间的推移,观察到预测的微囊藻病毒种群的显著更替,但在相隔数英里的站点之间却没有。病毒-宿主网络揭示了广泛的互联性和病毒介导的跨物种遗传交换的潜力。该网络预测伊利湖微囊虫病毒感染跨门的宿主,这与其他系统的实验室研究一致,但挑战了以前在该属中“狭隘”宿主-病毒关联的概念。丰富的微囊藻病毒基因揭示了其在关键代谢途径和宿主适应中的潜在作用。这些发现促进了我们对微囊藻病毒及其对宿主代谢、物种相互作用和微囊藻主导的cHABs共同进化的潜在影响的理解。了解病毒、宿主和环境因素之间的联系是确定蓝藻有害藻华兴衰背后机制的关键。本研究探讨了预计感染微囊藻的病毒的多样性和宿主范围,报告了这些特性如何随着时间的推移而变化,在伊利湖西部的样本站中,以及在不同的过滤器大小分数中。我们发现微囊藻病毒多样性在非菌落相关部分中最高,而在菌落相关部分中最低,这表明微囊藻菌落形成与病毒多样性降低之间存在联系。我们发现了大量属于预测微囊虫病毒的基因,以及它们在关键代谢途径和适应环境变化中的潜在作用。这些发现增强了我们对cHABs中病毒、微囊藻和共生细菌之间相互作用的理解,为驱动水华动力学、物种相互作用和共同进化过程的机制提供了见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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