蓝藻有害藻华的微生物多样性、基因组学和噬菌体-宿主相互作用。

IF 5 2区 生物学 Q1 MICROBIOLOGY mSystems Pub Date : 2024-07-23 Epub Date: 2024-06-10 DOI:10.1128/msystems.00709-23
Lauren E Krausfeldt, Elizaveta Shmakova, Hyo Won Lee, Viviana Mazzei, Keith A Loftin, Robert P Smith, Emily Karwacki, P Eric Fortman, Barry H Rosen, Hidetoshi Urakawa, Manoj Dadlani, Rita R Colwell, Jose V Lopez
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引用次数: 0

摘要

蓝藻有害藻华(cyanoHABs)的发生与其物理和化学环境有关。然而,人们对其相关的微生物相互作用和过程却知之甚少。本研究将蓝藻有害藻华作为一个微生物生态系统进行分析,使用了一年的 16S rRNA 测序和在藻华季节从奥基乔比湖(美国佛罗里达州)收集的 70 个元基因组。在微生物群落组成和功能方面观察到的生物地理模式反映了物理和化学参数不同的生态区,这些生态区在主要入湖口附近形成了水华 "热点"。随着水华严重程度的增加,多个门类中类群的相对丰度也发生了变化。与水华严重程度增加相关的功能途径包括有机氮和磷的利用、营养物质的储存、遗传物质的交换、噬菌体的防御以及对氧化应激的保护,这表明微生物的相互作用可能会促进蓝藻水华的恢复能力。蓝藻群落具有高度的多样性,其中微囊藻无处不在,有时数量最多,尤其是在没有藻华的情况下。新型水华形成蓝藻的鉴定和基因组比较表明,蓝藻群落的功能多种多样,它们利用蓝藻素储存氮的能力以及利用 CRISPR 和限制性修饰系统抵御噬菌体的能力也各不相同。从微生物生态系统及其在自然界中的相互作用的角度来考虑蓝藻水华,提出了支持蓝藻水华增殖和稳定的生理机制和相互作用,包括噬菌体感染皮蓝藻的作用。这项研究展示了 "组学 "在揭示重要生物过程方面的威力,可为有效管理和预测蓝藻有害藻华提供支持:蓝藻有害藻华对水生生态系统和人类健康构成重大威胁。尽管人们对水生系统中促进藻华发展的物理和化学条件进行了深入研究,但对蓝藻藻华产生的微生物生态系统的生物学认识还存在根本性的差距。高通量测序被用来确定自然界中蓝藻藻华的驱动因素。研究发现了蓝藻水华生态学中需要考虑的多种功能和相互作用。藻华的微生物生物多样性揭示了蓝藻种群之间的微生物功能、基因组特征和相互作用,这些可能参与藻华的稳定性,并能更一致地定义蓝藻藻华。我们的研究结果强调了将蓝藻水华视为一个微生物生态系统来预测、预防和缓解蓝藻水华的重要性。
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Microbial diversity, genomics, and phage-host interactions of cyanobacterial harmful algal blooms.

The occurrence of cyanobacterial harmful algal blooms (cyanoHABs) is related to their physical and chemical environment. However, less is known about their associated microbial interactions and processes. In this study, cyanoHABs were analyzed as a microbial ecosystem, using 1 year of 16S rRNA sequencing and 70 metagenomes collected during the bloom season from Lake Okeechobee (Florida, USA). Biogeographical patterns observed in microbial community composition and function reflected ecological zones distinct in their physical and chemical parameters that resulted in bloom "hotspots" near major lake inflows. Changes in relative abundances of taxa within multiple phyla followed increasing bloom severity. Functional pathways that correlated with increasing bloom severity encoded organic nitrogen and phosphorus utilization, storage of nutrients, exchange of genetic material, phage defense, and protection against oxidative stress, suggesting that microbial interactions may promote cyanoHAB resilience. Cyanobacterial communities were highly diverse, with picocyanobacteria ubiquitous and oftentimes most abundant, especially in the absence of blooms. The identification of novel bloom-forming cyanobacteria and genomic comparisons indicated a functionally diverse cyanobacterial community with differences in its capability to store nitrogen using cyanophycin and to defend against phage using CRISPR and restriction-modification systems. Considering blooms in the context of a microbial ecosystem and their interactions in nature, physiologies and interactions supporting the proliferation and stability of cyanoHABs are proposed, including a role for phage infection of picocyanobacteria. This study displayed the power of "-omics" to reveal important biological processes that could support the effective management and prediction of cyanoHABs.

Importance: Cyanobacterial harmful algal blooms pose a significant threat to aquatic ecosystems and human health. Although physical and chemical conditions in aquatic systems that facilitate bloom development are well studied, there are fundamental gaps in the biological understanding of the microbial ecosystem that makes a cyanobacterial bloom. High-throughput sequencing was used to determine the drivers of cyanobacteria blooms in nature. Multiple functions and interactions important to consider in cyanobacterial bloom ecology were identified. The microbial biodiversity of blooms revealed microbial functions, genomic characteristics, and interactions between cyanobacterial populations that could be involved in bloom stability and more coherently define cyanobacteria blooms. Our results highlight the importance of considering cyanobacterial blooms as a microbial ecosystem to predict, prevent, and mitigate them.

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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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