Warren Cody J, Griffin Laura M, Little Alexander S, Huang I-Chueh, Farzan Michael, Pyeon Dohun
Department of Microbiology, University of Colorado School of Medicine, Aurora, Colorado, United States of America.
Department of Cell Biology and Neuroscience, University of California Riverside, Riverside, California, United States of America.
PLoS One. 2014 May 14;9(5):e96579. doi: 10.1371/journal.pone.0096579. eCollection 2014.
Type I interferons (IFN-α and β) induce dynamic host defense mechanisms to inhibit viral infections. It has been recently recognized that the interferon-inducible transmembrane proteins (IFITM) 1, 2 and 3 can block entry of a broad spectrum of RNA viruses. However, no study to date has focused on the role of IFITM proteins in DNA virus restriction. Here, we demonstrate that IFN-α or -β treatment of keratinocytes substantially decreases human papillomavirus 16 (HPV16) infection while robustly inducing IFITM1, 2 and 3 expression. However, IFITM1, 2 and 3 overexpression did not inhibit HPV16 infection; rather, IFITM1 and IFITM3 modestly enhanced HPV16 infection in various cell types including primary keratinocytes. Moreover, IFITM1, 2 and 3 did not inhibit infection by two other DNA viruses, human cytomegalovirus (HCMV) and adenovirus type 5 (Ad5). Taken together, we reveal that the entry of several DNA viruses, including HPV, HCMV, and Ad5 is not affected by IFITM1, 2 and 3 expression. These results imply that HPV, and other DNA viruses, may bypass IFITM restriction during intracellular trafficking.
I型干扰素(IFN-α和β)诱导动态宿主防御机制以抑制病毒感染。最近人们认识到,干扰素诱导跨膜蛋白(IFITM)1、2和3可阻断多种RNA病毒的进入。然而,迄今为止尚无研究聚焦于IFITM蛋白在DNA病毒限制中的作用。在此,我们证明,用IFN-α或 -β处理角质形成细胞可显著降低人乳头瘤病毒16型(HPV16)感染,同时强力诱导IFITM1、2和3的表达。然而,IFITM1、2和3的过表达并未抑制HPV16感染;相反,IFITM1和IFITM3在包括原代角质形成细胞在内的多种细胞类型中适度增强了HPV16感染。此外,IFITM1、2和3并未抑制另外两种DNA病毒,即人巨细胞病毒(HCMV)和5型腺病毒(Ad5)的感染。综上所述,我们揭示包括HPV、HCMV和Ad5在内的几种DNA病毒的进入不受IFITM1、2和3表达的影响。这些结果表明,HPV及其他DNA病毒在细胞内运输过程中可能绕过IFITM限制。