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

Viruses 2022 30 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 40 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Zhenyu Huang, Xue Zhai, Mengting Zhan, Gaofeng Cheng, Gaofeng Cheng, Ruiqi Lin, Ruiqi Lin, Xue Zhai, Xue Zhai, Haiou Zheng, Haiou Zheng, Qingchao Wang, Yongyao Yu, Zhen Xu

Summary

Researchers found that infectious hematopoietic necrosis virus (IHNV) infection in trout induced strong mucosal immune responses in the intestine while simultaneously altering gut microbiota composition, highlighting the complex interplay between viral pathogens, commensal bacteria, and mucosal immunity in fish.

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 (<i>Oncorhynchus mykiss</i>) 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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