# Comprehensive analysis of lncRNAs and mRNAs revealed potential participants in the process of avian reovirus infection

**Authors:** Shaqiu Zhang, Jinkang Li, Mingshu Wang, Renyong Jia, Shun Chen, Mafeng Liu, Dekang Zhu, Xinxin Zhao, Ying Wu, Qiao Yang, Juan Huang, Xumin Ou, Di Sun, Bin Tian, Yu He, Zhen Wu, Anchun Cheng

PMC · DOI: 10.3389/fmicb.2025.1539903 · Frontiers in Microbiology · 2025-02-05

## TL;DR

This study identifies key genes and a new lncRNA involved in avian reovirus infection in ducks, offering insights for prevention and treatment.

## Contribution

Discovery of a novel lncRNA, linc000889, that inhibits avian reovirus replication.

## Key findings

- 3,818 mRNAs were up-regulated and 4,573 mRNAs were down-regulated in ARV-infected duck cells.
- The lncRNA linc000889 was found to inhibit ARV replication at multiple levels.
- Genes like PARP9, TLR7, TRIM33, and ATG5 were significantly upregulated during ARV infection.

## Abstract

Avian reovirus (ARV), a double-stranded RNA virus, frequently induces immunosuppression in poultry, leading to symptoms such as irregular bleeding and spleen necrosis in infected ducks. Since 2017, the morbidity and mortality rates associated with ARV infection in poultry have been on the rise, progressively emerging as a significant viral disease impacting the duck farming industry in China. In our study, we collected duck embryo fibroblasts 18 h post-infection with ARV and conducted transcriptome sequencing analysis. The analysis revealed that 3,818 mRNA expressions were up-regulated, 4,573 mRNA expressions were down-regulated, 472 long noncoding RNAs (LncRNAs) were up-regulated, and 345 lncRNAs were down-regulated. We employed qRT-PCR to validate the sequencing results, confirming their accuracy. The transcriptome data indicated significant upregulation of the PARP9, TLR7, TRIM33, and ATG5 genes, suggesting their potential involvement in ARV infection. Notably, our study identified a novel functional lncRNA, MSTRG.9284.1 (It was named linc000889 in the present study), which inhibits the replication of ARV at the transcriptional, translational levels and viral titer. Overall, this study has identified numerous ARV-induced differentially expressed mRNAs and lncRNAs, including the functional lncRNA linc000889 that inhibits ARV replication. This discovery provides new insights into the mechanisms of ARV infection and may contribute to the development of new prevention and treatment strategies.

## Linked entities

- **Genes:** PARP9 (poly(ADP-ribose) polymerase family member 9) [NCBI Gene 83666], TLR7 (toll like receptor 7) [NCBI Gene 51284], TRIM33 (tripartite motif containing 33) [NCBI Gene 51592], ATG5 (autophagy related 5) [NCBI Gene 9474]

## Full-text entities

- **Genes:** PARP9 (poly(ADP-ribose) polymerase family member 9) [NCBI Gene 83666] {aka ARTD9, BAL, BAL1, MGC:7868}, TLR7 (toll like receptor 7) [NCBI Gene 51284] {aka IMD74, SLEB17, TLR7-like}, TRIM33 (tripartite motif containing 33) [NCBI Gene 51592] {aka DDH4, ECTO, PTC7, RFG7, TF1G, TIF1G}, ATG5 (autophagy related 5) [NCBI Gene 9474] {aka APG5, APG5-LIKE, APG5L, ASP, SCAR25, hAPG5}
- **Diseases:** viral disease (MESH:D014777), ARV infection (MESH:D012088), infected (MESH:D007239), spleen necrosis (MESH:D013160), bleeding (MESH:D006470)
- **Species:** Avian orthoreovirus (no rank) [taxon 38170]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11835999/full.md

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11835999/full.md

## References

62 references — full list in the complete paper: https://tomesphere.com/paper/PMC11835999/full.md

---
Source: https://tomesphere.com/paper/PMC11835999