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IHNV Infection Induces Strong Mucosal Immunity and Changes of Microbiota in Trout Intestine

生物 传染性造血坏死病毒 免疫系统 粘液 失调 微生物群 微生物学 免疫 虹鳟 先天免疫系统 免疫学 鳟鱼 肠粘膜 肠道菌群 病毒学 生态学 医学 生物信息学 渔业 内科学
作者
Zhenyu Huang,Mengting Zhan,Gaofeng Cheng,Ruiqi Lin,Xue Zhai,Haiou Zheng,Qingchao Wang,Yongyao Yu,Zhen Xu
出处
期刊:Viruses [MDPI AG]
卷期号:14 (8): 1838-1838 被引量:22
标识
DOI:10.3390/v14081838
摘要

The fish intestinal mucosa is among the main sites through which environmental microorganisms interact with the host. Therefore, this tissue not only constitutes the first line of defense against pathogenic microorganisms but also plays a crucial role in commensal colonization. The interaction between the mucosal immune system, commensal microbiota, and viral pathogens has been extensively described in the mammalian intestine. However, very few studies have characterized these interactions in early vertebrates such as teleosts. In this study, rainbow trout (Oncorhynchus mykiss) was infected with infectious hematopoietic necrosis virus (IHNV) via a recently developed immersion method to explore the effects of viral infection on gut immunity and microbial community structure. IHNV successfully invaded the gut mucosa of trout, resulting in severe tissue damage, inflammation, and an increase in gut mucus. Moreover, viral infection triggered a strong innate and adaptive immune response in the gut, and RNA−seq analysis indicated that both antiviral and antibacterial immune pathways were induced, suggesting that the viral infection was accompanied by secondary bacterial infection. Furthermore, 16S rRNA sequencing also revealed that IHNV infection induced severe dysbiosis, which was characterized by large increases in the abundance of Bacteroidetes and pathobiont proliferation. Moreover, the fish that survived viral infection exhibited a reversal of tissue damage and inflammation, and their microbiome was restored to its pre−infection state. Our findings thus demonstrated that the relationships between the microbiota and gut immune system are highly sensitive to the physiological changes triggered by viral infection. Therefore, opportunistic bacterial infection must also be considered when developing strategies to control viral infection.

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