<p><i>Vibrio harveyi</i> infection causes significant economic losses in <i>Sebastes schlegelii</i> aquaculture. The gut microbiota plays a crucial role in immune modulation and metabolic balance. This study investigated the dynamic changes and interactions between gut microbiota, metabolites, and immune gene expression at 24, 48, and 72 h post-infection. The results revealed that <i>V. harveyi</i> infection notably altered the gut microbiota composition, with an increase in pathogenic bacteria such as <i>Vibrio</i> and <i>Pseudoalteromonas</i>, while beneficial bacteria like <i>Sphingomonas</i> and <i>Methylobacterium</i>/<i>Methylorubrum</i> decreased. Metabolomic profiling showed significant changes in metabolites, particularly organic acids, lipids, and amino acids, especially at 48 and 72 h. Additionally, two key metabolites, Trans-Cinnamic acid and Dioctyl succinate, were significantly correlated with both gut microbiota composition and immune regulation. qPCR analysis indicated that pro-inflammatory cytokines <i>TNF-α</i>, <i>IL-1β</i>, and <i>IL-6</i> peaked at 48 h and then declined, while gut barrier-related genes, including occludin, <i>ZO-1</i>, and <i>claudin-1</i>, showed continuous downregulation.</p>

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Gut microbiota-metabolite dynamics in Sebastes schlegelii following Vibrio harveyi infection

  • Yindong Gu,
  • Yongxiang Yu,
  • Chunyuan Wang,
  • Yingeng Wang,
  • Zhiqi Zhang,
  • Xiaojun Rong,
  • Meijie Liao,
  • Lei Qin,
  • Bin Li,
  • Zheng Zhang

摘要

Vibrio harveyi infection causes significant economic losses in Sebastes schlegelii aquaculture. The gut microbiota plays a crucial role in immune modulation and metabolic balance. This study investigated the dynamic changes and interactions between gut microbiota, metabolites, and immune gene expression at 24, 48, and 72 h post-infection. The results revealed that V. harveyi infection notably altered the gut microbiota composition, with an increase in pathogenic bacteria such as Vibrio and Pseudoalteromonas, while beneficial bacteria like Sphingomonas and Methylobacterium/Methylorubrum decreased. Metabolomic profiling showed significant changes in metabolites, particularly organic acids, lipids, and amino acids, especially at 48 and 72 h. Additionally, two key metabolites, Trans-Cinnamic acid and Dioctyl succinate, were significantly correlated with both gut microbiota composition and immune regulation. qPCR analysis indicated that pro-inflammatory cytokines TNF-α, IL-1β, and IL-6 peaked at 48 h and then declined, while gut barrier-related genes, including occludin, ZO-1, and claudin-1, showed continuous downregulation.