日本亚热带冲绳岛周围不同沿海基质中沉积微生物群落的多样性、组成和潜在作用。

IF 6.2 2区 环境科学与生态学 Q1 GENETICS & HEREDITY Environmental Microbiome Pub Date : 2024-07-30 DOI:10.1186/s40793-024-00594-1
Kohei Hamamoto, Masaru Mizuyama, Miyuki Nishijima, Ayumi Maeda, Kodai Gibu, Angelo Poliseno, Akira Iguchi, James Davis Reimer
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引用次数: 0

摘要

背景:海洋底栖原核生物群落在包括珊瑚礁在内的沿海环境的物质循环中发挥着至关重要的作用。作为珊瑚礁环境中共生菌、有益菌和病原菌的潜在贮藏库,沿海沉积微生物群落尤为重要,因此可能在当地生态系统功能中发挥核心作用。然而,由于以往的研究主要集中在单个地点或特定的环境条件上,因此缺乏对岛屿尺度上多个地点的不同环境进行比较的研究,特别是侧重于原核生物群落的研究。在我们的研究中,我们从日本冲绳岛周围的七个地点采集了沿海沉积物,包括三种不同的底栖类型:沙质底部、海草草甸和有硬骨珊瑚的硬底层。然后,我们利用代谢编码来确定原核生物的组成,并估算基因编码的酶,以推断其功能:结果:结果表明,三种基质的原核生物组成明显不同。与沙质底层相比,海草草甸的原核生物α-多样性明显更高。ANCOM 分析表明,在每种基质中,多种细菌的数量都不同。在珊瑚礁地点,可能与疾病和热应力有关的机会性细菌(如Rhodobacterales、Verrucomicrobiales和Cytophagales)相对较多,而海草草甸地点则大量存在Desulfobacterales、Steroidobacterales和Chromatiales,这些都是海草草甸中常见的细菌种类。根据我们的基因编码酶分析,珊瑚礁地点的差异丰度酶数量最多。值得注意的是,超氧化物歧化酶是珊瑚组织中抗氧化压力的一种重要酶,在珊瑚礁区含量丰富。我们的研究结果提供了在每种基质中需要研究的原核生物清单,并进一步强调了考虑微生物组的重要性,尤其是在关注环境保护时:我们的研究结果证明,原核生物代谢编码能够捕捉三种不同环境中微生物群落的组成差异和多样性。结论:我们的研究结果证明,原核生物代谢编码能够捕捉到三种不同环境中微生物群落的组成差异和多样性。此外,一些类群在特定环境中的数量也有所不同,基因编码的酶组成也显示了生态功能的可能差异。进一步的研究,结合实地观察和时间取样,是更好地了解当地微生物群落与周围底栖生物群落之间相互作用的关键。
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Diversity, composition and potential roles of sedimentary microbial communities in different coastal substrates around subtropical Okinawa Island, Japan.

Background: Marine benthic prokaryotic communities play crucial roles in material recycling within coastal environments, including coral reefs. Coastal sedimentary microbiomes are particularly important as potential reservoirs of symbiotic, beneficial, and pathogenic bacteria in coral reef environments, and therefore presumably play a core role in local ecosystem functioning. However, there is a lack of studies comparing different environments with multiple sites on the island scale, particularly studies focusing on prokaryotic communities, as previous investigations have focused mainly on a single site or on specific environmental conditions. In our study, we collected coastal sediments from seven sites around Okinawa Island, Japan, including three different benthic types; sandy bottoms, seagrass meadows, and hard substratum with living scleractinian corals. We then used metabarcoding to identify prokaryotic compositions and estimate enzymes encoded by genes to infer their functions.

Results: The results showed that the three substrata had significantly different prokaryotic compositions. Seagrass meadow sites exhibited significantly higher prokaryotic alpha-diversity compared to sandy bottom sites. ANCOM analysis revealed that multiple bacterial orders were differentially abundant within each substratum. At coral reef sites, putative disease- and thermal stress-related opportunistic bacteria such as Rhodobacterales, Verrucomicrobiales, and Cytophagales were comparatively abundant, while seagrass meadow sites abundantly harbored Desulfobacterales, Steroidobacterales and Chromatiales, which are common bacterial orders in seagrass meadows. According to our gene-coded enzyme analyses the numbers of differentially abundant enzymes were highest in coral reef sites. Notably, superoxide dismutase, an important enzyme for anti-oxidative stress in coral tissue, was abundant at coral sites. Our results provide a list of prokaryotes to look into in each substrate, and further emphasize the importance of considering the microbiome, especially when focusing on environmental conservation.

Conclusion: Our findings prove that prokaryotic metabarcoding is capable of capturing compositional differences and the diversity of microbial communities in three different environments. Furthermore, several taxa were suggested to be differentially more abundant in specific environments, and gene-coded enzymic compositions also showed possible differences in ecological functions. Further study, in combination with field observations and temporal sampling, is key to achieving a better understanding of the interactions between the local microbiome and the surrounding benthic community.

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来源期刊
Environmental Microbiome
Environmental Microbiome Immunology and Microbiology-Microbiology
CiteScore
7.40
自引率
2.50%
发文量
55
审稿时长
13 weeks
期刊介绍: Microorganisms, omnipresent across Earth's diverse environments, play a crucial role in adapting to external changes, influencing Earth's systems and cycles, and contributing significantly to agricultural practices. Through applied microbiology, they offer solutions to various everyday needs. Environmental Microbiome recognizes the universal presence and significance of microorganisms, inviting submissions that explore the diverse facets of environmental and applied microbiological research.
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