ArticleCurrent research in microbial sciences2025
Shifting seas and first feeds: gut microbiome dynamics in juvenile chum salmon (
Article in Current research in microbial sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- The variation profile of associated microbiota in juvenile whelkFrontiers in microbiology · 2026Article
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Authors and funding
4 authors.
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No grant is acknowledged in the PubMed record.
Abstract
Background: The early development of host-associated microbiota is crucial for host health and resilience. In migratory fish like chum salmon, the transition from freshwater to seawater and the onset of feeding are critical life stages that may be susceptible to environmental stressors, including those related to climate change. However, the relative influence of diet versus environment on microbiome stabilization remains unclear under ecologically relevant conditions. This study investigated the dynamics of gut bacterial communities in juvenile chum salmon during the first 90 days post-hatching, exploring how first feeding and freshwater-to-seawater transition shape the gut microbiota, with implications for climate sensitivity. Results: High-throughput 16S rRNA gene amplicon sequencing revealed highly dynamic gut/body microbiota. Prior to feeding, bacterial communities exhibited considerable fluctuations and lacked compositional stability. However, following the onset of feeding at 35 days post-hatching (DPH), the gut microbiota rapidly stabilized, indicating a strong influence of dietary microbes. Dominant taxa in freshwater stages included Conclusions: This study demonstrates that the gut microbiota in juvenile chum salmon is assembled by both environmental microbial input from diet and water, and is ultimately filtered by the host. This selective process highlights potential vulnerabilities of chum salmon to shifts in feed and ambient microbial communities, both of which are sensitive to environmental changes. Our findings underscore the importance of understanding host-microbe-environment triads for predicting climate-related vulnerabilities in wild salmon and for guiding future microbiome-based aquaculture strategies.
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