Indoleamine 2,3-Dioxygenase Is Involved in Interferon Gamma's Anti-BKPyV Activity in Renal Cells.
Animals
BK Virus
/ drug effects
Cell Line
Cell Line, Tumor
Chlorocebus aethiops
Humans
Indoleamine-Pyrrole 2,3,-Dioxygenase
/ antagonists & inhibitors
Interferon-alpha
/ immunology
Interferon-gamma
/ immunology
Interferons
/ immunology
Kidney Tubules, Proximal
Signal Transduction
Vero Cells
Viral Structural Proteins
/ genetics
Virus Replication
/ drug effects
BK virus
immunity
indoleamine-2,3-dioxygenase
interferon
Journal
Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722
Informations de publication
Date de publication:
07 08 2020
07 08 2020
Historique:
received:
10
07
2020
revised:
31
07
2020
accepted:
05
08
2020
entrez:
14
8
2020
pubmed:
14
8
2020
medline:
24
2
2021
Statut:
epublish
Résumé
Reactivation of BK polyomavirus (BKPyV) infection is frequently increasing in transplant recipients treated with potent immunosuppressants and highlights the importance of immune system components in controlling viral reactivation. However, the immune response to BKPyV in general and the role of antiviral cytokines in infection control in particular are poorly understood. Here, we investigated the efficacy of interferons (IFN) alpha, lambda and gamma with regard to the BKPyV multiplication in Vero cells. Treatment with IFN-gamma inhibited the expression of the viral protein VP1 in a dose-dependent manner and decreased the expression of early and late viral transcripts. Viral inhibition by IFN-gamma was confirmed in human cells (Caki-1 cells and renal proximal tubular epithelial cells). One of the IFN-stimulated genes most strongly induced by IFN-gamma was the coding for the enzyme indoleamine 2,3 dioxygenase (IDO), which is known to limit viral replication and regulates the host immune system. The antiviral activity induced by IFN-gamma could be reversed by the addition of an IDO inhibitor, indicating that IDO has a specific role in anti-BKPyV activity. A better understanding of the action mechanism of these IFN-gamma-induced antiviral proteins might facilitate the development of novel therapeutic strategies.
Identifiants
pubmed: 32784805
pii: v12080865
doi: 10.3390/v12080865
pmc: PMC7472348
pii:
doi:
Substances chimiques
IDO1 protein, human
0
Indoleamine-Pyrrole 2,3,-Dioxygenase
0
Interferon-alpha
0
Viral Structural Proteins
0
Interferon-gamma
82115-62-6
Interferons
9008-11-1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
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