Skin-Mucus Prokaryote Community of Atlantic Salmon (Salmo salar) in Response to Bath Challenge With Tenacibaculum dicentrarchi.

IF 2.2 3区 农林科学 Q2 FISHERIES
Ruben Avendaño-Herrera, Linette Tralma, Hernán Wicki, Fernanda Barrios-Henríquez, Héctor A Levipan
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Abstract

Fish skin mucus is continuously replaced by epidermal cells, making it a highly dynamic microenvironment and an effective barrier against waterborne pathogens. The objective of this study was to understand the effects of tenacibaculosis, caused by the bacterium Tenacibaculum dicentrarchi, on the skin-associated microbiome of Atlantic salmon (Salmo salar). We used a vector-free and waterborne infection model of T. dicentrarchi strain TdCh05 in Atlantic salmon smolts for 21 days. Skin swab samples were collected at 2 h and 21 days post-infection (hpi and dpi, respectively) for 16S rRNA gene amplicon sequencing using DNA or complementary DNA (cDNA) as templates. Non-metric multidimensional scaling analysis grouped the samples into distinct clusters depending on the treatment and template. Similarity-Percentage (SIMPER) analysis indicated that between ~42% and 43% of the total amplicon sequence variants (ASVs) across all samples accounted for 90% of the compositional differences among all treatments and the two templates, highlighting the contribution of Tenacibaculum ASVs. Comparisons (by SIMPER) between non-infected and TdCh05-challenged fish at 2 hpi indicated that Tenacibaculum ASVs contributed to between ~52% and 58% of the differences in compositional clustering between samples. A significant drop in skin-mucus alpha diversity in TdCh05-challenged fish was also detected, followed by alpha diversity recovery at 21 dpi. In turn, at 21 dpi, microbiome changes were related to higher interaction complexity among taxa and community instability. Furthermore, 16S cDNA-based sequencing indicated that the potential activity of the Atlantic salmon skin-associated microbiome during disease progression was primarily driven by Tenacibaculum spp. Further research is needed to elucidate the role of other potentially active components (e.g., Pseudomonadales) of the skin-associated microbiome for the onset and/or progression of tenacibaculosis.

大西洋大马哈鱼皮肤黏液原核生物群落对双中心腱藻浴挑战的响应。
鱼的皮肤粘液不断被表皮细胞所取代,使其成为一个高度动态的微环境,是抵御水传播病原体的有效屏障。本研究的目的是了解由二叉腱杆菌引起的腱杆菌病对大西洋鲑鱼(Salmo salar)皮肤相关微生物群的影响。本研究采用大西洋鲑鱼幼鱼无媒介水传感染TdCh05模型,持续21天。分别于感染后2 h和21 d(分别为hpi和dpi)采集皮肤拭子样本,以DNA或互补DNA (cDNA)为模板进行16S rRNA基因扩增子测序。非度量多维尺度分析将样本根据处理方法和模板分成不同的簇。相似性-百分比(SIMPER)分析表明,所有样品中扩增子序列变异(asv)总量的42% ~ 43%占所有处理和两个模板之间组成差异的90%,突出了Tenacibaculum asv的贡献。在2 hpi时,对未感染和tdch05攻毒的鱼进行SIMPER比较表明,tenacbaculum asv对样本间组成聚类差异的贡献在52% ~ 58%之间。tdch05致毒鱼的皮肤粘液α多样性也显著下降,随后在21 dpi时恢复。反过来,在21 dpi时,微生物组的变化与分类群之间更高的相互作用复杂性和群落不稳定性有关。此外,基于16S dna的测序表明,大西洋鲑鱼皮肤相关微生物组在疾病进展过程中的潜在活性主要是由Tenacibaculum spp驱动的,需要进一步的研究来阐明皮肤相关微生物组的其他潜在活性成分(例如假单胞菌)在tenacibaculosis的发病和/或进展中的作用。
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来源期刊
Journal of fish diseases
Journal of fish diseases 农林科学-海洋与淡水生物学
CiteScore
4.60
自引率
12.00%
发文量
170
审稿时长
6 months
期刊介绍: Journal of Fish Diseases enjoys an international reputation as the medium for the exchange of information on original research into all aspects of disease in both wild and cultured fish and shellfish. Areas of interest regularly covered by the journal include: -host-pathogen relationships- studies of fish pathogens- pathophysiology- diagnostic methods- therapy- epidemiology- descriptions of new diseases
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