Transcriptomic analysis of KSHV-infected primary oral fibroblasts: The role of interferon-induced genes in the latency of oncogenic virus.

Lu Dai,Jovanny Zabaleta,Lihua Bai,Liang Yang,Jing Qiao,Erik K Flemington,Zhen Lin,Zhiqiang Qin

doi:10.18632/oncotarget.9720

Abstract

The Kaposi sarcoma-associated herpesvirus (KSHV) is the causative agent of Kaposi sarcoma (KS), the most common HIV/AIDS-associated tumor worldwide. Involvement of the oral cavity portends a poor prognosis for patients with KS, but the mechanisms for KSHV regulation of the oral tumor microenvironment are largely unknown. Infiltrating fibroblasts are found within KS lesions, and KSHV can establish latent infection within human primary fibroblasts in vitro and in vivo, but contributions for KSHV-infected fibroblasts to the KS microenvironment have not been previously characterized. In the present study, we used Illumina microarray to determine global gene expression changes in KSHV-infected primary human oral fibroblasts (PDLF and HGF). Among significantly altered candidates, we found that a series of interferon-induced genes were strongly up-regulated in these KSHV-infected oral cells. Interestingly, some of these genes in particular ISG15 and ISG20 are required for maintenance of virus latency through regulation of specific KSHV microRNAs. Our data indicate that oral fibroblasts may represent one important host cellular defense component against viral infection, as well as acting as a reservoir for herpesvirus lifelong infection in the oral cavity.

Highlights

Kaposi sarcoma-associated herpesvirus (KSHV) is one of the most common etiologic agents for cancers arising in the setting of immune suppression, including Kaposi sarcoma (KS)—the most common HIV/AIDSassociated tumor worldwide and a leading cause of morbidity and mortality in this population [1]
We recently reported that KSHV successfully established latent infection in primary human gingival fibroblasts (HGF) or periodontal ligament fibroblasts (PDLF) in vitro, and virus de novo infection induced a tumor-associated fibroblast (TAF)-like phenotype within these cells [10]
KSHV de novo infection strongly up-regulates a series of interferon-induced gene in these oral cells, which are closely related to the maintenancy of virus latency

Summary

Introduction

Kaposi sarcoma-associated herpesvirus (KSHV) is one of the most common etiologic agents for cancers arising in the setting of immune suppression, including Kaposi sarcoma (KS)—the most common HIV/AIDSassociated tumor worldwide and a leading cause of morbidity and mortality in this population [1]. We used Illumina microarray to assess the altered gene profile in KSHV-infected PDLF and HGF relative to unifected mock cells. KSHV de novo infection strongly up-regulates a series of interferon-induced gene in these oral cells, which are closely related to the maintenancy of virus latency.

Results

Conclusion