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

Viruses. 2022 Aug 22;14(8):1838. doi: 10.3390/v14081838.

Abstract

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.

Keywords: 16S rRNA sequencing; RNA−seq; commensal microbiota; mucosal immune system; viral pathogens.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Fish Diseases*
  • Immunity, Mucosal
  • Infectious hematopoietic necrosis virus*
  • Inflammation
  • Intestinal Mucosa
  • Mammals
  • Microbiota*
  • Oncorhynchus mykiss*
  • RNA, Ribosomal, 16S / genetics
  • Rhabdoviridae Infections*

Substances

  • RNA, Ribosomal, 16S

Grants and funding

This work was supported by the National Natural Science Foundation of China (32225050, 32073001) to Z.X., the National Natural Science Foundation of China (3210210315) to Y.Y., the National Natural Science Foundation of China (31802317) to Q.W.