通过益生菌-肠道微生物群-免疫轴合理设计益生菌预防虾白粪综合征

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY npj Biofilms and Microbiomes Pub Date : 2024-04-11 DOI:10.1038/s41522-024-00509-5
Haonan Sha, Jiaqi Lu, Jiong Chen, Jinbo Xiong
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摘要

越来越多的证据表明,一些复杂的疾病可归因于多种病原体的共同感染,例如对虾白粪综合症(WFS);然而,目前缺乏实验证据来验证这种因果关系。这一缺陷进一步阻碍了益生菌的合理设计,使其无法为对虾抵抗 WFS 带来预期的益处。在此,我们验证了弗氏弧菌、珊瑚弧菌和管氏弧菌(比例为 7:2:1)在对虾 WFS 病因中的因果关系,完全符合科赫假说。相应地,我们精确地设计了四种拮抗菌株:相应地,我们精确设计了四种拮抗菌株:Ruegeria lacuscaerulensis、Nioella nitratireducens、Bacillus subtilis 和 Streptomyces euryhalinus,其比例为 4:3:2:1,可有效防止 WFS 的发生。膳食中补充益生菌可刺激肠道有益菌群、链霉素、短链脂肪酸、牛磺酸代谢潜能、网络稳定性、紧密连接和宿主选择,同时降低肠道微生物群的更替率和平均变异度,从而促进生态和机械屏障对病原体的抵御。此外,补充益生菌还激活了虾的免疫通路,如 Fcγ R 介导的吞噬作用、Toll 样受体和 RIG-I 样受体信号通路,从而赋予免疫屏障。总之,我们建立了一个更新的框架,用于精确验证多种病原体的共同感染,并合理设计拮抗益生菌。此外,我们的研究结果还从益生菌-肠道微生物组-宿主免疫轴揭示了设计益生菌的潜在有益机制。
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Rationally designed probiotics prevent shrimp white feces syndrome via the probiotics–gut microbiome–immunity axis

Increasing evidence infers that some complex diseases are attributed to co-infection with multiple pathogens, such as shrimp white feces syndrome (WFS); however, there is a lack of experimental evidence to validate such causal link. This deficiency further impedes rational design of probiotics to elicit desired benefits to shrimp WFS resistance. Herein, we validated the causal roles of Vibrio fluvialis, V. coralliilyticus and V. tubiashii (in a ratio of 7:2:1) in shrimp WFS etiology, which fully satisfied Koch’s postulates. Correspondingly, we precisely designed four antagonistic strains: Ruegeria lacuscaerulensis, Nioella nitratireducens, Bacillus subtilis and Streptomyces euryhalinus in a ratio of 4:3:2:1, which efficiently guarded against WFS. Dietary supplementation of the probiotics stimulated beneficial gut populations, streptomycin, short chain fatty acids, taurine metabolism potentials, network stability, tight junction, and host selection, while reducing turnover rate and average variation degree of gut microbiota, thereby facilitating ecological and mechanical barriers against pathogens. Additionally, shrimp immune pathways, such as Fcγ R-mediated phagocytosis, Toll-like receptor and RIG-I-like receptor signaling pathways conferring immune barrier, were activated by probiotics supplementation. Collectively, we establish an updated framework for precisely validating co-infection with multiple pathogens and rationally designing antagonistic probiotics. Furthermore, our findings uncover the underlying beneficial mechanisms of designed probiotics from the probiotics–gut microbiome–host immunity axis.

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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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