RRC ID 79147
著者 Sagou K, Sato Y, Okuno Y, Watanabe T, Inagaki T, Motooka Y, Toyokuni S, Murata T, Kiyoi H, Kimura H.
タイトル Epstein-Barr virus lytic gene BNRF1 promotes B-cell lymphomagenesis via IFI27 upregulation.
ジャーナル PLoS Pathog
Abstract Epstein-Barr virus (EBV) is a ubiquitous human lymphotropic herpesvirus that is causally associated with several malignancies. In addition to latent factors, lytic replication contributes to cancer development. In this study, we examined whether the lytic gene BNRF1, which is conserved among gamma-herpesviruses, has an important role in lymphomagenesis. We found that lymphoblastoid cell lines (LCLs) established by BNRF1-knockout EBV exhibited remarkably lower pathogenicity in a mice xenograft model than LCLs produced by wild-type EBV (LCLs-WT). RNA-seq analyses revealed that BNRF1 elicited the expression of interferon-inducible protein 27 (IFI27), which promotes cell proliferation. IFI27 knockdown in LCLs-WT resulted in excessive production of reactive oxygen species, leading to cell death and significantly decreased their pathogenicity in vivo. We also confirmed that IFI27 was upregulated during primary infection in B-cells. Our findings revealed that BNRF1 promoted robust proliferation of the B-cells that were transformed by EBV latent infection via IFI27 upregulation both in vitro and in vivo.
巻・号 20(2)
ページ e1011954
公開日 2024-2-1
DOI 10.1371/journal.ppat.1011954
PII PPATHOGENS-D-23-01470
PMID 38300891
PMC PMC10833513
MeSH Animals Epstein-Barr Virus Infections* Herpesviridae* / metabolism Herpesvirus 4, Human Humans Interferons / metabolism Membrane Proteins / metabolism Mice Up-Regulation Virus Latency
リソース情報
遺伝子材料 CSII-CMV-MCS-IRES2-Bsd (RDB04385)