病毒对刺藻赤石异星藻的感染影响了海岸原核生物群落的胞内有机物组成和动态。

IF 4.6 2区 生物学 Q1 MICROBIOLOGY
mSystems Pub Date : 2025-09-22 DOI:10.1128/msystems.00816-25
Hiroaki Takebe, Haruna Hiromoto, Tetsuhiro Watanabe, Keigo Yamamoto, Keizo Nagasaki, Ryoma Kamikawa, Takashi Yoshida
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引用次数: 0

摘要

微藻在海洋生态系统中发挥着至关重要的作用,为异养原核生物提供溶解的有机物,介导微生物循环。微藻经常被病毒感染,在被感染的细胞(病毒细胞)中,病毒调节并经常改变宿主的代谢以进行繁殖和内代谢物。然而,藻类病毒细胞对原核生物群落的影响尚不完全清楚。在这项研究中,我们研究了一种全球普遍存在的形成水华的raphiophycean藻类——赤石异源藻(Heterosigma akashiwo)的病毒细胞裂解物是否会引起原核生物群落结构的变化,以及病毒裂解物中的哪些代谢化合物可能会影响周围的原核生物种群。通过微观实验,我们培养了含有赤窝H.病毒溶解部分(VDF)的原核生物群落。结果表明,某些原核生物种群被指定为鱼类和甲壳类致病性弧菌,对VDF有特异性的反应。这些弧菌具有支链氨基酸转运蛋白基因模块,通过气相色谱-质谱分析发现该基因模块富含VDF。总之,我们的研究结果表明,病毒感染引起的赤石芽孢杆菌细胞生化特性的变化可以促进分类和代谢不同的原核生物群体的生长,潜在地影响海洋生态系统中更高营养水平的消费者。海洋微藻的初级生产和原核生物对其产生的有机物的消耗对生物地球化学循环起着重要作用。微藻经常被病毒感染,在被感染的细胞(病毒细胞)中,病毒调节宿主的代谢以进行繁殖和内代谢物。然而,微藻病毒细胞对原核生物群落的影响尚不完全清楚。本研究研究了一种分布于全球的有害水华形成型刺藻——赤石异sigma akashhiwo病毒细胞裂解物对原核生物群落的影响。我们的数据表明,H. akashhiwo病毒细胞生化特性的变化促进了特定细菌群的生长,这些细菌群似乎具有代谢能力,可以利用裂解物中富含的某些有机化合物。此外,由于这些种群中含有鱼类致病菌,我们认为病毒感染赤石黑藻会间接影响海洋生态系统中更高营养水平的消费者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Viral infection to the raphidophycean alga Heterosigma akashiwo affects both intracellular organic matter composition and dynamics of a coastal prokaryotic community.

Marine microalgae play a crucial role in the marine ecosystem by supplying dissolved organic matter to heterotrophic prokaryotes, which mediate the microbial loop. Microalgae are often infected by viruses, and in infected cells (virocells), the viruses modulate and often change the host metabolism for propagation and endo-metabolites. However, the impact of algal virocells on prokaryotic communities is not fully understood. In this study, we investigated whether lysates from virocells of Heterosigma akashiwo, a globally prevalent bloom-forming raphidophycean alga, cause shifts in prokaryotic community structure, and which metabolic compounds in the viral lysate might affect the surrounding prokaryotic populations. Using microcosm experiments, we cultured prokaryotic communities with a viral dissolved fraction (VDF) of H. akashiwo. Results revealed that certain prokaryotic populations assigned as Vibrio spp. pathogenic to fish and crustaceans grew specifically in response to the VDF. These Vibrio species possessed a gene module for branched-chain amino acids transporters, which were revealed to be enriched in VDF by gas chromatography-mass spectrometry analysis. Altogether, our findings suggest that viral infection-induced changes in biochemical properties of H. akashiwo cells can promote the growth of taxonomically and metabolically different prokaryotic populations, potentially impacting higher trophic-level consumers in marine ecosystems.IMPORTANCEThe primary production by marine microalgae and the consumption of the produced organic matter by prokaryotes significantly contribute to biogeochemical cycling. Microalgae are often infected by viruses, and in infected cells (virocells), the viruses modulate host metabolism for propagation and endo-metabolites. However, the impact of microalgal virocells on prokaryotic communities is not fully understood. This study investigates effects of lysates from virocells of Heterosigma akashiwo, a globally distributed harmful bloom-forming raphidophycean alga, on the prokaryotic community. Our data suggest that changes in biochemical properties in H. akashiwo virocells promoted the growth of specific bacterial populations that appeared to have metabolic capacity to utilize certain organic compounds enriched in the lysate. Additionally, as those populations included fish-pathogenic bacteria, we propose that viral infection to H. akashiwo can indirectly affect higher trophic-level consumers in marine ecosystems.

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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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