# Overwinter Syndrome in Grass Carp (Ctenopharyngodon idellus) Links Enteric Viral Proliferation to Mucosal Disruption via Multiomics Investigation

## TL;DR

Overwinter Syndrome in grass carp causes intestinal barrier failure linked to viral proliferation and disrupted host immunity.

## Contribution

This study reveals a triple-barrier failure in grass carp intestines during Overwinter Syndrome via multiomics analysis.

## Key findings

- OWS causes physical, microbial, and immune barrier failure in grass carp intestines.
- Caudoviricetes phages expand and correlate with host gene dysregulation in OWS.
- Gut microbiota richness increases without diversity changes, indicating viral-driven dysbiosis.

## Abstract

What are the main findings?
OWS involves triple-barrier failure: physical, microbial, and immune disruption in grass carp intestine.Caudoviricetes phages expand and correlate with host gene dysregulation.

OWS involves triple-barrier failure: physical, microbial, and immune disruption in grass carp intestine.

Caudoviricetes phages expand and correlate with host gene dysregulation.

What are the implications of the main findings?
Viral proliferation is linked to disrupted nucleotide metabolism and mucosal immunity.Gut microbiota shows elevated richness but stable diversity, reflecting viral-driven dysbiosis without a dominant bacterial pathogen.

Viral proliferation is linked to disrupted nucleotide metabolism and mucosal immunity.

Gut microbiota shows elevated richness but stable diversity, reflecting viral-driven dysbiosis without a dominant bacterial pathogen.

Overwinter Syndrome (OWS) affects grass carp (Ctenopharyngodon idellus) aquaculture in China, causing high mortality and economic losses under low temperatures. Failure of antibiotic therapies shows limits of the ‘low–temperature–pathogen’ model and shifts focus to mucosal barrier dysfunction and host–microbiome interactions in OWS. We compared healthy and diseased grass carp collected from the same pond using histopathology, transcriptomics, proteomics, and metagenomics. This integrated approach was used to characterize intestinal structure, microbial composition, and host molecular responses at both taxonomic and functional levels. Results revealed a three-layer barrier failure in OWS fish: the physical barrier was compromised, with structural damage and reduced mucosal index; microbial dysbiosis featured increased richness without changes in diversity or evenness, and expansion of the virobiota, notably uncultured Caudovirales phage; and mucosal immune dysregulation indicated loss of local immune balance. Multi-omics integration identified downregulation of lysosome-related and glycosphingolipid biosynthesis pathways at transcript and protein levels, with disrupted nucleotide metabolism. Overall gut microbial richness, rather than individual taxa abundance, correlated most strongly with host gene changes linked to immunity, metabolism, and epithelial integrity. Although biological replicates were limited by natural outbreak sampling, matched high-depth multi-omics datasets provide exploratory insights into OWS-associated intestinal dysfunction. In summary, OWS entails a cold-triggered breakdown of intestinal barrier integrity and immune homeostasis. This breakdown is driven by a global restructuring of the gut microbiome, which is marked by increased richness, viral expansion, and functional shifts, ultimately resulting in altered host–microbe crosstalk. This ecological perspective informs future mechanistic and applied studies for disease prevention.