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可视化活跃的病毒感染揭示了藻类水华同步衰亡过程中不同的细胞命运。

Visualizing active viral infection reveals diverse cell fates in synchronized algal bloom demise.

机构信息

Department of Plant and Environmental Sciences, Weizmann Institute of Science, 7610001 Rehovot, Israel.

Flow Cytometry Unit, Life Sciences Core Facilities, Weizmann Institute of Science, 7610001 Rehovot, Israel.

出版信息

Proc Natl Acad Sci U S A. 2021 Mar 16;118(11). doi: 10.1073/pnas.2021586118.

Abstract

Marine viruses are the most abundant biological entity in the ocean and are considered as major evolutionary drivers of microbial life [C. A. Suttle, 5, 801-812 (2007)]. Yet, we lack quantitative approaches to assess their impact on the marine ecosystem. Here, we provide quantification of active viral infection in the bloom forming single-celled phytoplankton infected by the large virus EhV, using high-throughput single-molecule messenger RNA in situ hybridization (smFISH) of both virus and host transcripts. In natural samples, viral infection reached only 25% of the population despite synchronized bloom demise exposing the coexistence of infected and noninfected subpopulations. We prove that photosynthetically active cells chronically release viral particles through nonlytic infection and that viral-induced cell lysis can occur without viral release, thus challenging major assumptions regarding the life cycle of giant viruses. We could also assess active infection in cell aggregates linking viral infection and carbon export to the deep ocean [C. P. Laber , 3, 537-547 (2018)] and suggest a potential host defense strategy by enrichment of infected cells in sinking aggregates. Our approach can be applied to diverse marine microbial systems, opening a mechanistic dimension to the study of biotic interactions in the ocean.

摘要

海洋病毒是海洋中最丰富的生物实体,被认为是微生物生命的主要进化驱动因素[C. A. Suttle,5,801-812(2007)]。然而,我们缺乏定量方法来评估它们对海洋生态系统的影响。在这里,我们使用高通量单分子信使 RNA 原位杂交(smFISH)技术对受大型病毒 EhV 感染的形成浮游植物的单细胞进行了活跃病毒感染的定量,该技术同时检测了病毒和宿主转录本。在自然样本中,尽管同步爆发导致大量种群死亡,暴露出感染和未感染的亚种群共存,但病毒感染仅达到了种群的 25%。我们证明了光合作用活跃的细胞通过非溶细胞感染持续释放病毒颗粒,并且病毒诱导的细胞裂解可以在没有病毒释放的情况下发生,从而挑战了关于巨型病毒生命周期的主要假设。我们还可以评估通过病毒感染将碳输出与深海联系起来的细胞聚集体中的活跃感染[C. P. Laber,3,537-547(2018)],并通过富含感染细胞的下沉聚集体提出一种潜在的宿主防御策略。我们的方法可应用于多种海洋微生物系统,为海洋生物相互作用的研究开辟了一个新的机制维度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ec/7980383/d5d5dce99e57/pnas.2021586118fig02.jpg

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