Multi-omics reveals the inhibition of asexual reproduction in the jellyfish Aurelia coerulea polyp by Bacillus pacificus.

IF 5.4 2区 环境科学与生态学 Q1 GENETICS & HEREDITY
Hao Sun, Xuerui Liu, Manzoor Ahmad, Xiangrui Guo, Zhen Yu, Ye Zhao, Pingping Shen, Yanying Zhang, Zhijun Dong
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引用次数: 0

Abstract

Background: Jellyfish blooms pose a serious threat to marine ecosystems and coastal socio-economic activities, requiring urgent development of control technologies to manage harmful jellyfish. Associated bacteria hold considerable importance in the growth and development of marine invertebrates. We isolated Bacillus pacificus SG15 from the seagrass rhizosphere and observed that this strain could inhibit the asexual reproduction of the jellyfish Aurelia coerulea polyp. However, the precise interaction processes underlying this inhibition remain unclear. Therefore, we aimed to elucidate these processes by performing a coculture experiment coupled with analyses utilizing high-throughput sequencing, transcriptomics, metabolomics, and fluorescence in situ hybridization.

Results: Our findings indicate that the transcription of genes involved in the absorption of vitamins B5, B11, B12, C and biotin was inhibited with SG15 treatment despite relatively high concentrations of vitamins and their derivatives in the culture medium. SG15 treatment increased the levels of carbohydrate metabolism genes, including those involved in pyruvate metabolism, glycolysis/gluconeogenesis, pentose phosphate pathways, and citrate cycle metabolites. Furthermore, SG15 influenced both endodermal and ectodermal polyp cells.

Conclusions: Collectively, our findings helped elucidate the interactions between associated bacteria and polyps and the process by which B. pacificus SG15 inhibits polyp asexual reproduction, providing novel insights into the role of bacteria in the development of marine invertebrates. This study could provide a theoretical framework and empirical evidence for the biological control of jellyfish blooms in the marine aquaculture area, which may help develop strategies aimed at mitigating the impacts of jellyfish blooms on marine ecosystems and coastal communities.

多组学揭示了太平洋芽孢杆菌对水母蓝纹水母无性繁殖的抑制作用。
背景:水母大量繁殖对海洋生态系统和沿海社会经济活动构成严重威胁,迫切需要开发控制有害水母的技术。相关细菌在海洋无脊椎动物的生长发育中具有相当重要的作用。从海草根际分离到太平洋芽孢杆菌SG15,发现该菌株能抑制水母蓝纹水母的无性繁殖。然而,这种抑制作用背后的确切相互作用过程仍不清楚。因此,我们旨在通过进行共培养实验,结合高通量测序、转录组学、代谢组学和荧光原位杂交分析来阐明这些过程。结果:我们的研究结果表明,尽管培养基中含有相对高浓度的维生素及其衍生物,但SG15处理抑制了参与维生素B5、B11、B12、C和生物素吸收的基因的转录。SG15处理增加了碳水化合物代谢基因的水平,包括涉及丙酮酸代谢、糖酵解/糖异生、戊糖磷酸盐途径和柠檬酸循环代谢产物的基因。此外,SG15对内胚层和外胚层息肉细胞均有影响。结论:总的来说,我们的发现有助于阐明相关细菌与水螅之间的相互作用以及B. pacificus SG15抑制水螅无性繁殖的过程,为细菌在海洋无脊椎动物发育中的作用提供了新的见解。本研究可为海洋养殖区水母华的生物防治提供理论框架和实证依据,有助于制定减轻水母华对海洋生态系统和沿海群落影响的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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