孵化场类型会影响大西洋养殖鲑鱼(Salmo salar)转移到海洋后的鳃微生物组。

IF 4.9 Q1 MICROBIOLOGY Animal microbiome Pub Date : 2024-11-08 DOI:10.1186/s42523-024-00347-y
Kelly J Stewart, Annette S Boerlage, William Barr, Umer Z Ijaz, Cindy J Smith
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引用次数: 0

摘要

背景:三文鱼养殖涉及淡水和海水阶段。最近,海水阶段多因素鳃健康挑战的增加导致人们迫切需要了解鳃微生物组。人们对鳃微生物群组成的驱动因素以及淡水阶段对其长期组成的影响还缺乏了解。我们在两个不同的投入季节(S0(2018 年)和 S1(2019 年))对在六种不同的淡水运行系统--循环水养殖系统(RAS)、穿流式养殖系统(FT)和基于湖泊的系统--中养殖的七组大西洋鲑鱼在转移到七个海水养殖场之前和之后的鳃微生物组进行了表征:利用 16S rRNA 基因的 V1-V2 区域,我们生成了没有宿主污染的扩增子文库。结果表明,孵化系统对鳃微生物组有影响(PERMAOVA R2 = 0.226,P 2 = 0.528,P 结论:孵化系统与鳃微生物组之间存在着明显的差异:我们发现孵化系统、湖泊、FT 或 RAS 对鳃微生物组有显著影响。转入海洋后,微生物组发生了变化,变得更加相似。转运后,鱼类转运到的各个地点对微生物组的组成有很大影响,但孵化系统仍然存在一些有趣的聚类。未来以增强鳃部微生物组为目标的鳃病缓解方法可能在淡水阶段最有效,因为与在海上相比,在孵化场的水和鳃之间有更多的共享ASV。
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Hatchery type influences the gill microbiome of Atlantic farmed salmon (Salmo salar) after transfer to sea.

Background: Salmon aquaculture involves freshwater and seawater phases. Recently there has been an increase in multifactorial gill health challenges during the seawater phase which has led to an urgent need to understand the gill microbiome. There is a lack of understanding on what drives the composition of the gill microbiome, and the influence the freshwater stage has on its long-term composition. We characterise the gill microbiome from seven cohorts of Atlantic salmon raised in six different freshwater operational systems-recirculating aquaculture system (RAS), flowthrough (FT) and loch-based system, prior to and after transfer to seven seawater farms, over two different input seasons, S0 (2018) and S1 (2019).

Results: Using the V1-V2 region of the 16S rRNA gene, we produced amplicon libraries absent of host contamination. We showed that hatchery system influenced the gill microbiome (PERMAOVA R2 = 0.226, p < 0.001). Loch and FT systems were more similar to each other than the three RAS systems, which clustered together. On transfer to sea, the gill microbiomes of all fish changed and became more similar irrespective of the initial hatchery system, seawater farm location or season of input. Even though the gill microbiome among seawater farm locations were different between locations (PERMAOVA R2 = 0.528, p < 0.001), a clustering of the gill microbiomes by hatchery system of origin was still observed 7-25 days after transfer (PERMAOVA R = 0.164, p < 0.001). Core microbiomes at genera level were observed among all fish in addition to freshwater only, and seawater only. At ASV level core microbiomes were observed among FT and loch freshwater systems only and among all seawater salmon. The gill microbiome and surrounding water at each hatchery had more shared ASVs than seawater farms.

Conclusion: We showed hatchery system, loch, FT or RAS, significantly impacted the gill microbiome. On transfer to sea, the microbiomes changed and became more similar. After transfer, the individual sites to which the fish were transferred has a significant influence on microbiome composition, but interesting some clustering by hatchery system remained. Future gill disease mitigation methods that target enhancing the gill microbiome may be most effective in the freshwater stage, as there were more shared ASVs between water and gill at hatchery, compared to at sea.

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