Virus Details


VHFID11054

Host Factor Information

Gene Name HNRNPK
HF Protein Name Heterogeneous Nuclear Ribonucleoprotein K
HF Function Essential for virus replication
Uniprot ID P61978
Protein Sequence View Fasta Sequence
NCBI Gene ID 3190
Host Factor (HF) Name in Paper HNRNPK
Gene synonyms HNRPK
Ensemble Gene ID ENSG00000165119
Ensemble Transcript ENST00000351839.7 [P61978-1];ENST00000360384.9 [P61978-1];ENST00000376263.8 [P61978-2];ENST00000376281.8 [P61978-2];ENST00000457156.6 [P61978-3];ENST00000704004.1 [P61978-3];ENST00000704005.1 [P61978-2];ENST00000704006.1 [P61978-1];ENST00000704011.1 [P61978-2];ENST00000704051.1 [P61978-1];ENST00000704052.1 [P61978-1];ENST00000704053.1 [P61978-1];ENST00000704057.1 [P61978-2];ENST00000704058.1 [P61978-1];ENST00000704059.1 [P61978-2]
KEGG ID Go to KEGG Database
Gene Ontology ID(s) GO:0000398, GO:0000785, GO:0002102, GO:0003677, GO:0003723, GO:0003729, GO:0005634, GO:0005654, GO:0005737, GO:0005925, GO:0006357, GO:0006396, GO:0007165, GO:0010494, GO:0010988, GO:0016020, GO:0019904, GO:0031048, GO:0042802, GO:0042995, GO:0043066, GO:0045296, GO:0045892, GO:0045944, GO:0048024, GO:0048025, GO:0048260, GO:0060816, GO:0070062, GO:0071013, GO:1902165, GO:1905599, GO:1990904,
MINT ID P61978
STRING Click to see interaction map
GWAS Analysis Click to see gwas analysis
OMIM ID 600712;616580
PANTHER ID PTHR10288
PDB ID(s) 1J5K, 1KHM, 1ZZI, 1ZZJ, 1ZZK, 7CRE, 7CRU, 7RJK, 7RJO,
pfam ID PF00013, PF08067,
Drug Bank ID DB11638, DB12695,
ChEMBL ID N.A.
Organism Homo sapiens (Human)

Pathogen Information

Virus Name Nipah virus
Virus Short Name NiV
Order Mononegavirales
Virus Family Paramyxoviridae
Virus Subfamily N.A.
Genus Henipavirus
Species Nipah henipavirus
Host Vertebrates
Cell Tropism N.A.
Associated Disease Fever and headache
Mode of Transmission Sexual contact, blood, breast feeding
VIPR DB link https://www.viprbrc.org/brc/vipr_search.do?species=Nipah_virus
ICTV DB link https://ictv.global/report/152/paramyxoviridae
Virus Host DB link

Publication Information

Paper Title Analysis of Nipah Virus Replication and Host Proteome Response Patterns in Differentiated Porcine Airway Epithelial Cells Cultured at the Air-Liquid Interface
Author's Name Martin Müller 1, Kerstin Fischer 2, Elisabeth Woehnke 1, Luca M Zaeck 1, Christoph Prönnecke 3, Michael R Knittler 4, Axel Karger 1, Sandra Diederich 2, Stefan Finke 18
Journal Name Viruses
Pubmed ID 37112941
Abstract Respiratory tract epithelium infection plays a primary role in Nipah virus (NiV) pathogenesis and transmission. Knowledge about infection dynamics and host responses to NiV infection in respiratory tract epithelia is scarce. Studies in non-differentiated primary respiratory tract cells or cell lines indicate insufficient interferon (IFN) responses. However, studies are lacking in the determination of complex host response patterns in differentiated respiratory tract epithelia for the understanding of NiV replication and spread in swine. Here we characterized infection and spread of NiV in differentiated primary porcine bronchial epithelial cells (PBEC) cultivated at the air-liquid interface (ALI). After the initial infection of only a few apical cells, lateral spread for 12 days with epithelium disruption was observed without releasing substantial amounts of infectious virus from the apical or basal sides. Deep time course proteomics revealed pronounced upregulation of genes related to type I/II IFN, immunoproteasomal subunits, transporter associated with antigen processing (TAP)-mediated peptide transport, and major histocompatibility complex (MHC) I antigen presentation. Spliceosomal factors were downregulated. We propose a model in which NiV replication in PBEC is slowed by a potent and broad type I/II IFN host response with conversion from 26S proteasomes to immunoproteasomal antigen processing and improved MHC I presentation for adaptive immunity priming. NiV induced cytopathic effects could reflect the focal release of cell-associated NiV, which may contribute to efficient airborne viral spread between pigs.
Used Model PBEC-ALI
DOI 10.3390/v15040961