Journal
AQUACULTURE
Volume 534, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.aquaculture.2020.736227
Keywords
Digesta microbiome; Chinook salmon; RAS; Diet; Next generation sequencing; 16S rRNA gene; King salmon
Categories
Funding
- New Zealand Ministry of Business, Innovation and Employment (MBIE), Efficient Salmon research program [CAWX1606]
- Seafood Innovations Ltd. [1501]
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The intestinal microbiome of Chinook salmon consists mainly of Firmicutes, Bacteroidetes, Proteobacteria, and Actinobacteria, which are partially shared among feces, surrounding water, and feed. Some bacterial taxa are only present in feces, indicating possible acquisition or growth in the gut rather than the surrounding environment. Inter-individual variation suggests host-specific variability that needs further investigation.
The intestinal microbiome has recently been described for a variety of fish species and has been shown to influence host biology, including physiology, health and behavior. Knowledge of the intestinal microbiome of a species and how it can favorably be modulated to enhance production in different rearing systems is therefore of benefit for farmed fish. Here we describe the microbiome of the digesta (feces) of Chinook salmon (Oncorhynchus tshawytscha) reared in a seawater recirculation aquaculture system (RAS) and compare it to the microbiome found in the surrounding water and feed. The effects of varying lipid levels in three different diets were also investigated. We used high-throughput sequencing of the V3/V4 region of the 16S rRNA gene to determine the microbial community in the different samples. The dominant phyla in Chinook salmon feces were Firmicutes, Bacteroidetes, Proteobacteria and Actinobacteria. Most of the taxa dominating feces samples were also present in the surrounding water or feed, suggesting that the microbiome is partially shared with the ambient environment. About 40% of all taxa were only present in feces, indicating that these bacterial taxa were either acquired previously and could belong to the attached, rather than transient, microbiome or were at levels below detection in the surrounding environment but grew well in the gut. Differences among individuals were detected and could suggest host-specific variability, which requires further investigation. Variation in dietary lipid levels did not alter the microbiome among cohorts. Identifying the key bacterial communities in the Chinook salmon gut microbiome will help establish strategies to reliably attain and maintain a healthy gut microbiome in fish reared in RAS systems.
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