Unknown

Dataset Information

0

Human Cytomegalovirus UL23 Antagonizes the Antiviral Effect of Interferon-γ by Restraining the Expression of Specific IFN-Stimulated Genes.


ABSTRACT: Interferon-γ (IFN-γ) is a critical component of innate immune responses in humans to combat infection by many viruses, including human cytomegalovirus (HCMV). IFN-γ exerts its biological effects by inducing hundreds of IFN-stimulated genes (ISGs). In this study, RNA-seq analyses revealed that HCMV tegument protein UL23 could regulate the expression of many ISGs under IFN-γ treatment or HCMV infection. We further confirmed that among these IFN-γ stimulated genes, individual APOL1 (Apolipoprotein-L1), CMPK2 (Cytidine/uridine monophosphate kinase 2), and LGALS9 (Galectin-9) could inhibit HCMV replication. Moreover, these three proteins exhibited a synergistic effect on HCMV replication. UL23-deficient HCMV mutants induced higher expression of APOL1, CMPK2, and LGALS9, and exhibited lower viral titers in IFN-γ treated cells compared with parental viruses expressing full functional UL23. Thus, UL23 appears to resist the antiviral effect of IFN-γ by downregulating the expression of APOL1, CMPK2, and LGALS9. This study highlights the roles of HCMV UL23 in facilitating viral immune escape from IFN-γ responses by specifically downregulating these ISGs.

SUBMITTER: Wang H 

PROVIDER: S-EPMC10145438 | biostudies-literature | 2023 Apr

REPOSITORIES: biostudies-literature

altmetric image

Publications

Human Cytomegalovirus UL23 Antagonizes the Antiviral Effect of Interferon-γ by Restraining the Expression of Specific IFN-Stimulated Genes.

Wang Hankun H   Peng Weijian W   Wang Jialin J   Zhang Chunling C   Zhao Wangchun W   Ran Yanhong Y   Yang Xiaoping X   Chen Jun J   Li Hongjian H  

Viruses 20230420 4


Interferon-γ (IFN-γ) is a critical component of innate immune responses in humans to combat infection by many viruses, including human cytomegalovirus (HCMV). IFN-γ exerts its biological effects by inducing hundreds of IFN-stimulated genes (ISGs). In this study, RNA-seq analyses revealed that HCMV tegument protein UL23 could regulate the expression of many ISGs under IFN-γ treatment or HCMV infection. We further confirmed that among these IFN-γ stimulated genes, individual APOL1 (Apolipoprotein-  ...[more]

Similar Datasets

| S-EPMC5805366 | biostudies-literature
| S-EPMC7109688 | biostudies-literature
| S-EPMC2573374 | biostudies-literature
| S-EPMC3196417 | biostudies-literature
| S-EPMC3417313 | biostudies-literature
| S-EPMC2193580 | biostudies-literature
| S-EPMC10340457 | biostudies-literature
| S-EPMC2195910 | biostudies-literature
| S-EPMC6527189 | biostudies-literature
| S-EPMC4858707 | biostudies-literature