低张力胁迫下海鳉渗透调节器官(鳃和肠道)中微生物群的作用和出现。

IF 2.2 2区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Comparative Biochemistry and Physiology D-Genomics & Proteomics Pub Date : 2024-07-02 DOI:10.1016/j.cbd.2024.101285
Keng Po Lai , Delbert Almerick T. Boncan , Xian Qin , Ting Fung Chan , William Ka Fai Tse
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引用次数: 0

摘要

鳃和肠道是鱼类的两个主要渗透调节器官。最近,研究已从这些器官的渗透调节机制扩展到对栖息于其中的微生物群落的探索。现在已经知道,这两个器官中的微生物群落会随着渗透压的变化而变化。然而,在海水和淡水转移条件下,确定这两个器官中这些微生物群落的主要贡献者和共存情况的研究却很有限。目前的数据挖掘报告对我们小组之前发表的两个数据集进行了生物信息学分析,旨在深入了解渗透压条件下宿主与细菌之间的关系。我们将样本分为四组:对照海水鳃(LSW)、对照海水肠道(TSW)、淡水转移鳃(LFW)和淡水转移肠道(TFW)。结果表明,LSW 与 TSW 相比,具有更高的多样性、丰富度和均匀度。然而,LFW和LSW在淡水转移实验后并没有表现出明显的差异。我们进一步应用共生网络分析,首次报道了影响这两个器官群落结构的类群相互作用。此外,我们还在海水样本中发现了丰富的外氨酸生物合成,表明其在海水环境中的潜在作用。经过 6 小时的埃克托因处理后,在鳃中观察到 Na+/K+-atpase 和 cftr 的 mRNA 表达水平升高。这些发现为今后研究渗透压胁迫下宿主与细菌之间的相互作用奠定了基础。
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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Roles and occurrences of microbiota in the osmoregulatory organs, gills and gut, in marine medaka upon hypotonic stress

Gills and gut are the two primary osmoregulatory organs in fish. Recently, studies have expanded beyond the osmoregulatory mechanisms of these organs to explore the microbiota communities inhabiting them. It is now known that microbial communities in both organs shift in response to osmotic stress. However, there are limited studies identifying the major contributors and co-occurrence among these microbiota in both organs under seawater and freshwater transfer conditions. The current data mining report applied the bioinformatics analysis on two previous published datasets from our group, aiming to provide insights into host-bacteria relationships under osmotic stress. We divided the samples into four groups: control seawater gills (LSW); control seawater gut (TSW); freshwater transfer gills (LFW); and freshwater transfer gut (TFW). Our results showed that LSW had higher diversities, richness, and evenness compared to TSW. However, both the LFW and LSW did not show any significant differences after the freshwater transfer experiment. We further applied co-occurrence network analysis and, for the first time, reported on the interactions of taxa shaping the community structure in these two organs. Moreover, we identified enriched ectoine biosynthesis in seawater samples, suggesting its potential role in seawater environments. Increased mRNA expression levels of Na+/K+-atpase, and cftr, were observed in gills after 6 h of ectoine treatment. These findings provide a foundation for future studies on host-bacteria interactions under osmotic stress.

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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
69
审稿时长
33 days
期刊介绍: Comparative Biochemistry & Physiology (CBP) publishes papers in comparative, environmental and evolutionary physiology. Part D: Genomics and Proteomics (CBPD), focuses on “omics” approaches to physiology, including comparative and functional genomics, metagenomics, transcriptomics, proteomics, metabolomics, and lipidomics. Most studies employ “omics” and/or system biology to test specific hypotheses about molecular and biochemical mechanisms underlying physiological responses to the environment. We encourage papers that address fundamental questions in comparative physiology and biochemistry rather than studies with a focus that is purely technical, methodological or descriptive in nature.
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