Evidence map›Paper›PMID 39272286›Full record

ArticleAnimals : an open access journal from MDPI2024

RNA-Seq Analysis of Glycolysis Regulation of Avian Leukosis Virus Subgroup J Replication.

Ting Yang, Lingling Qiu, Shihao Chen, Zhixiu Wang, Yong Jiang, Hao Bai, Yulin Bi, Guobin Chang

Abstract read
In one paragraph

Article in Animals : an open access journal from MDPI, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Ting YangCollege of Animal Science and Technology, Yangzhou University, Yangzhou 225009, China.
Lingling QiuCollege of Animal Science and Technology, Yangzhou University, Yangzhou 225009, China.
Shihao ChenCollege of Animal Science and Technology, Yangzhou University, Yangzhou 225009, China.
Zhixiu WangCollege of Animal Science and Technology, Yangzhou University, Yangzhou 225009, China.
Yong JiangCollege of Animal Science and Technology, Yangzhou University, Yangzhou 225009, China.
Hao BaiInstitutes of Agricultural Science and Technology Development, Yangzhou University, Yangzhou 225009, China.ORCID 0000-0002-5738-4186
Yulin BiCollege of Animal Science and Technology, Yangzhou University, Yangzhou 225009, China.
Guobin ChangCollege of Animal Science and Technology, Yangzhou University, Yangzhou 225009, China.ORCID 0000-0001-5712-626X

Funding

This work was supported by the Major Project of Agricultural Biological Breeding Grant (2023ZD04053), the Earmarked Fund for CARS (CARS-41), and the Postgraduate Research & Practice Innovation Program of Jiangsu Province (KYCX23_3595). 2023ZD04053,CARS-41,KYCX23_3595
6 · The paper itself

Abstract

Avian Leukosis virus (ALV) is a widely spread virus that causes major economic losses to the global poultry industry. This study aims to investigate the effect of glycolysis on the replication of the ALV-J virus and identify the key circular RNAs that regulate the replication of the ALV-J virus. We found that glucose uptake, pyruvate content, and lactate content in DF1 cells were increased after ALV-J infection. Moreover, inhibiting the glycolysis of ALV-J-infected DF1 cells reduced the replication of the ALV-J virus. To further study the mechanism of glycolysis in the replication of the ALV-J virus, we performed RNA-seq on ALV-J-infected and ALV-J-infected cells treated with glycolysis inhibition. RNA-seq results show that a total of 10,375 circular RNAs (circRNAs) were identified, of which the main types were exonic circular RNAs, and 28 circRNAs were differentially expressed between ALV-J-infected and ALV-J-infected cells treated with glycolysis inhibition. Then, we performed functional enrichment analysis of differentially expressed circRNA source and target genes. Functional enrichment analysis indicated that some circRNAs might be involved in regulating the replication of the ALV-J virus by influencing some pathways like glycolysis/gluconeogenesis, the NOD-like receptor signaling pathway, MAPK signaling pathway, p53 signaling pathway, Toll-like receptor signaling pathway, Insulin signaling pathway, and Apoptosis. This study revealed the effect of glycolysis on the replication of the ALV-J virus in DF1 cells and its possible regulatory mechanism, which provided a basis for understanding the factors influencing the replication of the ALV-J virus and reducing the rate of infection of the ALV-J virus in poultry.

Indexed as

ALV-JCircRNAglycolysisvirus replication

Identifiers

PMID39272286
PMCPMC11394362

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