Phagotrophy in the nitrogen-fixing haptophyte Braarudosphaera bigelowii

IF 3.6 4区 生物学 Q2 ENVIRONMENTAL SCIENCES
Esther Wing Kwan Mak, Kendra A. Turk-Kubo, David A. Caron, Rachel C. Harbeitner, Jonathan D. Magasin, Tyler H. Coale, Kyoko Hagino, Yoshihito Takano, Tomohiro Nishimura, Masao Adachi, Jonathan P. Zehr
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Abstract

Biological nitrogen fixation provides fixed nitrogen for microbes living in the oligotrophic open ocean. UCYN-A2, the previously known symbiont of Braarudosphaera bigelowii, now believed to be an early-stage B. bigelowii organelle that exchanges fixed nitrogen for fixed carbon, is globally distributed. Indirect evidence suggested that B. bigelowii might be a mixotrophic (phagotrophic) phototrophic flagellate. The goal of this study was to determine if B. bigelowii can graze on bacteria using several independent approaches. The results showed that B. bigelowii grazed on co-occurring bacteria at a rate of 5–7 cells/h/B. bigelowii and that the overall grazing rate was significantly higher at nighttime than at daytime. Bacterial abundance changes, assessed with 16S rRNA gene amplicon sequencing analysis, may have indicated preferential grazing by B. bigelowii on specific bacterial genotypes. In addition, Lysotracker™ staining of B. bigelowii suggested digestive activity inside B. bigelowii. Carbon and nitrogen fixation measurements revealed that the carbon demand of B. bigelowii could not be fulfilled by photosynthesis alone, implying supplementation by heterotrophy. These independent lines of evidence together revealed that B. bigelowii engages in phagotrophy, which, beyond serving as a supplementary source of carbon and energy, may also facilitate the indirect assimilation of inorganic nutrients.

Abstract Image

固氮合藻 Braarudosphaera bigelowii 的吞噬作用。
生物固氮为生活在寡营养开阔海洋中的微生物提供固定氮。UCYN-A2 是以前已知的布拉鲁德磷藻(Braarudosphaera bigelowii)的共生体,现在认为它是布拉鲁德磷藻的一个早期细胞器,可以用固定氮交换固定碳。间接证据表明,B. bigelowii 可能是一种混养(噬食性)光养鞭毛虫。本研究的目的是通过几种独立的方法来确定大肠杆菌是否能吃细菌。结果表明,B. bigelowii 以 5-7 cells/h/B. bigelowii 的速度捕食共生细菌,夜间的总体捕食率明显高于白天。通过 16S rRNA 基因扩增片段测序分析评估细菌丰度的变化,可能表明 B. bigelowii 会优先捕食特定的细菌基因型。此外,Lysotracker™ 染色法也表明大叶榕有消化活动。碳和氮固定测量结果表明,仅靠光合作用无法满足大肠杆菌对碳的需求,这意味着大肠杆菌需要异养菌的补充。这些独立的证据共同揭示了大叶榕有吞噬作用,除了作为碳和能量的补充来源外,还可能促进无机营养物质的间接同化。
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来源期刊
Environmental Microbiology Reports
Environmental Microbiology Reports ENVIRONMENTAL SCIENCES-MICROBIOLOGY
CiteScore
6.00
自引率
3.00%
发文量
91
审稿时长
3.0 months
期刊介绍: The journal is identical in scope to Environmental Microbiology, shares the same editorial team and submission site, and will apply the same high level acceptance criteria. The two journals will be mutually supportive and evolve side-by-side. Environmental Microbiology Reports provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following: the structure, activities and communal behaviour of microbial communities microbial community genetics and evolutionary processes microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors microbes in the tree of life, microbial diversification and evolution population biology and clonal structure microbial metabolic and structural diversity microbial physiology, growth and survival microbes and surfaces, adhesion and biofouling responses to environmental signals and stress factors modelling and theory development pollution microbiology extremophiles and life in extreme and unusual little-explored habitats element cycles and biogeochemical processes, primary and secondary production microbes in a changing world, microbially-influenced global changes evolution and diversity of archaeal and bacterial viruses new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens.
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