根瘤微生物组与海草物种密切相关:对三种沿海海草的比较研究。

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Applied and Environmental Microbiology Pub Date : 2024-12-18 Epub Date: 2024-11-06 DOI:10.1128/aem.01754-24
Hao Sun, Xuerui Liu, Tianyu Wang, Shuai Liu, Rui Zhang, Xiangrui Guo, Zhen Yu, Ye Zhao, Pingping Shen, Yanying Zhang
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引用次数: 0

摘要

海草草甸是沿海地区重要的海洋生态系统,为人类提供生态和经济服务。然而,由于气候变化和人类活动,这些生态系统正面临衰退。根圈相关微生物群在海草的生存和适应过程中发挥着至关重要的作用。之前的研究探讨了海草草甸中的一般微生物群落及其作用,但对不同海草物种的特定根瘤微生物群落及其相互依存关系的了解还存在差距。我们的研究利用高通量和元基因组测序技术,分析了中国山东沿海地区的中华绒毯草(Ruppia sinensis,RS)、日本藻(Zostera japonica,ZJ)和滨海藻(Zostera marina,ZM)根瘤菌群中的微生物群落组成及其新陈代谢。我们发现,与其他两种海草相比,RS、ZJ和ZM样品中分别富集了Rhodobacteraceae、Desulfocapsaceae和Sulfurovaceae,而从RS到ZM和ZJ样品中的细菌连接则有所减少。介导反硝化作用的 nirKS 和 norBC 在 RS 样品中的丰度较高,分别为 2.38% ± 0.59% 和 2.14% ± 0.24%。RS 样品还显示出较高水平的硫酸盐同化还原基因,但较低水平的硫酸盐异化还原和氧化基因,将硫化物转化为 L-半胱氨酸和乙酸的能力较强。从 RS 根圈元基因组中组装的元基因组具有更高的多样性,并被归入八个门。我们的研究可为分析不同海草根瘤微生物组的细菌群落结构和代谢功能提供一个典型项目:海草在海洋生态系统中不可或缺,提供了许多重要服务,其健康状况受到相关根瘤微生物组的显著影响。虽然已有研究调查了海草草甸中的微生物群落及其生态作用,但特定地理区域的根瘤微生物组与海草物种之间的相关性却很有限。一些研究集中于各种海草根圈中的细菌组成,但这些微生物组的功能方面仍未得到探索。我们的研究填补了这一空白,揭示了 Ruppia sinensis、Zostera japonica 和 Zostera marina 所寄生的细菌群落在组成、连接、功能和代谢(如氮和硫代谢)方面的多样性。我们的研究揭示了海草物种在等效环境中塑造根圈微生物群落的重要作用,强调了海草物种在塑造根圈微生物群落中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rhizosphere microbiomes are closely linked to seagrass species: a comparative study of three coastal seagrasses.

Seagrass meadows are important marine ecosystems in coastal areas, offering ecological and economic services to the mankind. However, these ecosystems are facing declines due to climate changes and human activities. Rhizosphere-associated microbiomes play critical roles in the survival and adaptation of seagrasses. While prior studies have explored the general microbial communities and their roles in seagrass meadows, there is a gap in understanding the specific rhizosphere microbiomes of different seagrass species and their interdependent relationships. Our study analyzed the microbial community composition and their metabolism in the rhizosphere of Ruppia sinensis (RS), Zostera japonica (ZJ), and Zostera marina (ZM) obtained from the coastal area of Shandong, China, using high throughput and metagenome sequencing. We found that Rhodobacteraceae, Desulfocapsaceae, and Sulfurovaceae were enriched in RS, ZJ, and ZM samples, respectively, compared with the other two seagrass species, and the bacterial connections were decreased from RS to ZM and ZJ samples. The abundances of nirKS and norBC, mediating denitrification, were higher in RS samples with 2.38% ± 0.59% and 2.14% ± 0.24%, respectively. RS samples also showed a higher level of genes in assimilatory sulfate reduction but lower levels in dissimilatory sulfate reduction and oxidation, with a greater ability to convert sulfide into L-cysteine and acetate. Metagenome-assembled genomes from metagenome of RS rhizosphere had a higher diversity and were assigned to eight phyla. Our study could provide a typical project to analyze the bacterial community structures and metabolic functions in the rhizosphere microbiomes of different seagrasses.

Importance: Seagrasses are indispensable in marine ecosystems, offering numerous critical services, with their health significantly influenced by associated rhizosphere microbiomes. Although studies have investigated the microbial communities and their ecological roles in seagrass meadows, the correlations between rhizosphere microbiome and seagrass species from a particular geographic region are limited. Some studies concentrated on the bacterial composition within the rhizosphere of various seagrasses, but the functional aspects of these microbiomes remain unexplored. Our research delves into this void, revealing that Ruppia sinensis, Zostera japonica, and Zostera marina host diverse bacterial community in the composition, connections, functions, and metabolism, such as nitrogen and sulfur metabolism. Our study revealed that seagrass species play an important role in shaping the rhizosphere microbiomes in an equivalent environment, emphasizing the importance of seagrass species in shaping the rhizosphere microbial communities.

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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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