Virus Details


VHFID9650

Host Factor Information

Gene Name OLIG2
HF Protein Name Oligodendrocyte Transcription Factor 2
HF Function Present in Oligodendrocyte precursor cells
Uniprot ID Q13516
Protein Sequence View Fasta Sequence
NCBI Gene ID 10215
Host Factor (HF) Name in Paper Olig2
Gene synonyms BHLHB1 BHLHE19 PRKCBP2 RACK17
Ensemble Gene ID ENSG00000205927
Ensemble Transcript ENST00000333337.3;ENST00000382357.4
KEGG ID Go to KEGG Database
Gene Ontology ID(s) GO:0000122, GO:0000785, GO:0000981, GO:0005634, GO:0005737, GO:0007423, GO:0021522, GO:0021530, GO:0021794, GO:0042552, GO:0042802, GO:0045665, GO:0045944, GO:0046983, GO:0048663, GO:0048714, GO:0061564, GO:0070888, GO:0071837, GO:1990837,
MINT ID N.A.
STRING Click to see interaction map
GWAS Analysis Click to see gwas analysis
OMIM ID 606386
PANTHER ID PTHR19290;PTHR19290:SF32
PDB ID(s) N.A.,
pfam ID PF00010,
Drug Bank ID N.A.,
ChEMBL ID N.A.
Organism Homo sapiens (Human)

Pathogen Information

Virus Name Japanese encephalitis virus
Virus Short Name JEV
Order Amarillovirales
Virus Family flaviviridae
Virus Subfamily N.A
Genus Flavivirus
Species Japanese encephalitis Virus
Host Vertebrates
Cell Tropism Neurons
Associated Disease Japanese Encephalitis
Mode of Transmission Sexual contact, blood, breast feeding
VIPR DB link https://www.viprbrc.org/brc/vipr_search.do?species=Japanese_encephalitis_virus
ICTV DB link https://ictv.global/report/183/flaviviridae
Virus Host DB link

Publication Information

Paper Title Single-cell RNA sequencing reveals the immune features and viral tropism in the central nervous system of mice infected with Japanese encephalitis virus
Author's Name Ling’en Yang, Junyao Xiong, Yixin Liu, Yinguang Liu, Xugang Wang, Youhui, Bibo Zhu, Huanchun Chen, Shengbo Cao and Jing Ye.
Journal Name Jounrnal of Neuroinflammation
Pubmed ID 38532383
Abstract Japanese encephalitis virus (JEV) is a neurotropic pathogen that causes lethal encephalitis. The high susceptibility and massive proliferation of JEV in neurons lead to extensive neuronal damage and inflammation within the central nervous system. Despite extensive research on JEV pathogenesis, the effect of JEV on the cellular composition and viral tropism towards distinct neuronal subtypes in the brain is still not well comprehended. To address these issues, we performed single-cell RNA sequencing (scRNA-seq) on cells isolated from the JEV-highly infected regions of mouse brain. We obtained 88,000 single cells and identified 34 clusters representing 10 major cell types. The scRNA-seq results revealed an increasing amount of activated microglia cells and infiltrating immune cells, including monocytes & macrophages, T cells, and natural killer cells, which were associated with the severity of symptoms. Additionally, we observed enhanced communication between individual cells and significant ligand-receptor pairs related to tight junctions, chemokines and antigen-presenting molecules upon JEV infection, suggesting an upregulation of endothelial permeability, inflammation and antiviral response. Moreover, we identified that Baiap2-positive neurons were highly susceptible to JEV. Our findings provide valuable clues for understanding the mechanism of JEV induced neuro-damage and inflammation as well as developing therapies for Japanese encephalitis.
Used Model
DOI 10.1186/s12974-024-03071-18