波罗的海夏季浮游植物群落中游动孢子寄生虫的动态。

IF 3.2 3区 生物学 Q2 MICROBIOLOGY
Silke Van den Wyngaert, Ali Nawaz, Elisabet Alacid, Steffaney M Wood-Rocca, Albert Reñé, Esther Garcés, Anke Kremp, Christian Wurzbacher
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引用次数: 0

摘要

游动孢子寄生虫通过感染各种浮游植物类群对水生生态系统产生重大影响,但它们在微咸生态系统中的相互作用在很大程度上尚未被探索。本研究探讨了波罗的海北部六个半咸淡水海岸地点的微生物群落和寄生与夏季浮游植物群落的相互作用。我们假设环境条件下的小尺度空间异质性会导致微生物群落和浮游植物-寄生虫相互作用的不同组合。通过结合DNA元条形码、单细胞测序和显微镜技术,首次对波罗的海夏季浮游植物的虫孢寄生虫进行了群落水平的定性和定量评估。不同地点的微生物群落差异显著,盐度是真核生物多样性的主要驱动因素。以壶菌为主,主要侵染绿藻、硅藻和丝状蓝藻,侵染率高达浮游植物生物量的5.8%。来自半咸淡壶菌的序列与来自淡水环境的序列聚集在一起,反映了与宿主分类群相关的多系模式。浮游植物-寄生虫相互作用受寄主丰度和特定地点条件的影响,相关分析表明某些壶菌种类的寄主范围更广,可能具有通才性。此外,一种未识别的卵菌感染了高达85%的有毒结核蓝藻。该研究强调了波罗的海游动孢子寄生虫的生态相关性,并强调了进一步研究它们在浮游植物华流动力学中的作用的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dynamics of zoosporic parasites in summer phytoplankton communities of the Baltic Sea.

Zoosporic parasites significantly influence aquatic ecosystems by infecting various phytoplankton taxa, but their interactions in brackish ecosystems remain largely unexplored. This study explores microbial communities and parasitic interactions with summer phytoplankton communities at six brackish coastal sites in the northern Baltic Sea. We hypothesized that small-scale spatial heterogeneity in environmental conditions would lead to distinct assemblages of microbial communities and phytoplankton-parasite interactions. By combining DNA metabarcoding, single-cell sequencing, and microscopy, we provide the first community-level qualitative and quantitative assessment of zoosporic parasites infecting summer phytoplankton in the Baltic Sea. Microbial communities varied significantly across sites, with salinity as primary driver of eukaryotic diversity. Chytrid fungi were the dominant parasites, infecting green algae, diatoms, and filamentous cyanobacteria, with infection rates up to 5.8% of phytoplankton biomass. Sequences from brackish chytrids clustered with those from freshwater environments, reflecting polyphyletic patterns linked to host taxa. Phytoplankton-parasite interactions were influenced by host abundance and site-specific conditions with correlation analysis suggesting broader host ranges and potential generalist behavior in some chytrid species. Additionally, an unidentified oomycete infected up to 85% of the toxic bloom-forming cyanobacterium Nodularia spp. This study highlights the ecological relevance of zoosporic parasites in the Baltic Sea and emphasizes the need for further research into their role in phytoplankton bloom dynamics.

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来源期刊
FEMS microbiology ecology
FEMS microbiology ecology 生物-微生物学
CiteScore
7.50
自引率
2.40%
发文量
132
审稿时长
3 months
期刊介绍: FEMS Microbiology Ecology aims to ensure efficient publication of high-quality papers that are original and provide a significant contribution to the understanding of microbial ecology. The journal contains Research Articles and MiniReviews on fundamental aspects of the ecology of microorganisms in natural soil, aquatic and atmospheric habitats, including extreme environments, and in artificial or managed environments. Research papers on pure cultures and in the areas of plant pathology and medical, food or veterinary microbiology will be published where they provide valuable generic information on microbial ecology. Papers can deal with culturable and non-culturable forms of any type of microorganism: bacteria, archaea, filamentous fungi, yeasts, protozoa, cyanobacteria, algae or viruses. In addition, the journal will publish Perspectives, Current Opinion and Controversy Articles, Commentaries and Letters to the Editor on topical issues in microbial ecology. - Application of ecological theory to microbial ecology - Interactions and signalling between microorganisms and with plants and animals - Interactions between microorganisms and their physicochemical enviornment - Microbial aspects of biogeochemical cycles and processes - Microbial community ecology - Phylogenetic and functional diversity of microbial communities - Evolutionary biology of microorganisms
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