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Transcriptome Analysis of Greenfin Horse-Faced Filefish (Thamnaconus septentrionalis) Gills in Response to Amyloodinium ocellatum (AO) Infection

文献类型： 外文期刊

作者： Yang, Li-Guo 1 ; Wang, Yue 2 ; Xu, Wen-Bin 3 ; Qin, Bo 1 ; Ying, Na 1 ; Song, Xue-Feng 1 ; Yue, Yan-Feng 1 ; Wang, Xiao-Shan 1 ; Zhang, Bian-Bian 1 ; Wu, Yan-Qing 1 ;

作者机构： 1.Chinese Acad Fishery Sci, East China Sea Fisheries Res Inst, Shanghai 200090, Peoples R China

2.Zhejiang Ocean Univ, Marine Sci & Technol Coll, Zhoushan 316022, Peoples R China

3.Zhejiang Univ, Coll Anim Sci, Hangzhou 310058, Peoples R China

关键词： aquaculture; disease control; tetraodontiformes; RNA-seq; pathway analysis

期刊名称：FISHES （ 影响因子：3.17； 五年影响因子：3.098 ）

ISSN：

年卷期： 2022 年 7 卷 5 期

页码：

收录情况： SCI

摘要： The greenfin horse-faced filefish (Thamnaconus septentrionalis) is susceptible to recurrent Amyloodinium ocellatum (AO) infestation over the grow-out production cycle. This parasite breeds mainly on the gills, causing hypoxia in the fish body, and leading to many deaths. The host-parasite response drives a complex immune reaction, which is poorly understood. To generate a model for host-parasite interaction and the pathogenesis of AO in greenfin horse-faced filefish, an RNA-seq approach, differential gene expression, GO, and KEGG analyses were employed. Overall, 624 new genes and 2076 differentially expressed genes (DEGs) were detected, including 942 upregulated and 1134 downregulated genes in the gills. Compared with the control group, the expression of leptin a, GTPase IMAP family member 4, and NLR family CARD domain-containing protein 3 was significantly higher in the AO-infected group. Conversely, cell wall integrity and stress response component 1-like, and hepcidin-like were significantly downregulated in the gills of AO-infected fish. GO and KEGG enrichment analysis indicated that DEGs were significantly enriched in signaling pathways associated with viral protein interaction with cytokine and cytokine receptor and cytokine-cytokine receptor interaction. Collectively, this transcriptomic study provides novel molecular insights into the pathology caused by AO infestation and alternative theories for future research implementing strategies to control and manage AO.

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