Transcriptomic Analysis of Metformin's Effect on Bovine Viral Diarrhea Virus Infection.

RNA-seq bovine viral diarrhea virus transcriptome analysis

Journal

Veterinary sciences
ISSN: 2306-7381
Titre abrégé: Vet Sci
Pays: Switzerland
ID NLM: 101680127

Informations de publication

Date de publication:
15 Aug 2024
Historique:
received: 24 06 2024
revised: 10 08 2024
accepted: 13 08 2024
medline: 28 8 2024
pubmed: 28 8 2024
entrez: 28 8 2024
Statut: epublish

Résumé

(1) Background: Bovine viral diarrhea virus (BVDV) causes calf diarrhea, bovine respiratory syndrome, and cow abortion, resulting in substantial economic losses in the cattle industry. Owing to its persistent infection mechanism, BVDV is a major challenge in the treatment of cattle. (2) Methods: To determine how metformin (Met) inhibits the interaction between BVDV and host cells, we treated BVDV-infected cells with Met. We then performed an RNA sequencing (RNA-seq) analysis of Met-treated cells infected with BVDV to identify differentially expressed genes (DEGs). Consequently, the RNA-seq results were validated through real-time quantitative PCR (qPCR). (3) Results: Our analysis revealed 3169 DEGs in the Met-treated cells (Met group) vs. the negative controls (NC group) and 2510 DEGs in the BVDV-infected cells after pretreatment with Met (MetBVDV group) vs. the BVDV-infected cells (BVDV group). The DEGs were involved in MDBK interactions during BVDV infection, as indicated by Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses. The potential interactions of the DEGs were confirmed via a protein-protein interaction (PPI) network. Met treatment induced autophagy signaling activity and the expression of the autophagy-related genes ATG2A, ATG4B, ATG10, and ATG12 in BVDV-infected Met-pretreated cells. (4) Conclusions: We found that the host transcriptomic profile was affected by BVDV infection and Met pretreatment. These findings offer valuable new insights and provide support for future studies on the inhibition of BVDV replication by Met.

Identifiants

pubmed: 39195830
pii: vetsci11080376
doi: 10.3390/vetsci11080376
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Natural Science Foundation of Xinjiang Uygur Autonomous Region
ID : 2022D01E15
Organisme : Tianshan Talents Project of Xinjiang Uygur autonomous region
ID : 2022TSYCCX0049

Auteurs

Zeyu Li (Z)

College of Veterinary Medicine, Xinjiang Agricultural University, Urumqi 830052, China.
Xinjiajng Key Laboratory of New Drug Study and Creation for Herbivorous Animals, Urumqi 830052, China.

Yuanxiu He (Y)

College of Veterinary Medicine, Xinjiang Agricultural University, Urumqi 830052, China.
Xinjiajng Key Laboratory of New Drug Study and Creation for Herbivorous Animals, Urumqi 830052, China.

Junzhen Chen (J)

College of Veterinary Medicine, Xinjiang Agricultural University, Urumqi 830052, China.
Xinjiajng Key Laboratory of New Drug Study and Creation for Herbivorous Animals, Urumqi 830052, China.

Duoliang Ran (D)

College of Veterinary Medicine, Xinjiang Agricultural University, Urumqi 830052, China.
Xinjiajng Key Laboratory of New Drug Study and Creation for Herbivorous Animals, Urumqi 830052, China.

Jianbo Yue (J)

Division of Natural and Applied Science, Duke Kunshan University, Kunshan 215316, China.

Qiang Fu (Q)

College of Veterinary Medicine, Xinjiang Agricultural University, Urumqi 830052, China.
Xinjiajng Key Laboratory of New Drug Study and Creation for Herbivorous Animals, Urumqi 830052, China.

Huijun Shi (H)

College of Veterinary Medicine, Xinjiang Agricultural University, Urumqi 830052, China.
Xinjiajng Key Laboratory of New Drug Study and Creation for Herbivorous Animals, Urumqi 830052, China.

Classifications MeSH