Guanylate-binding protein 1 participates in cellular antiviral response to dengue virus

Mouse macrophage cell line RAW264.7 can be readily infected by DENV, and served as an in vitro model for the study of host innate immune response to DENV. By using a quantitative RT-PCR (qRT-PCR) based small cDNA array (SABiosciences, Frederick, MD), we measured the expression profile of genes from Jak-Stat signaling pathway in DENV (DENV 2, New Guinea C strain) infected RAW264.7 cells. A number of genes were found up- or down-regulated upon DENV infection, as reported in our previous work (Additional file 1of Ref. [22]). Among them, Gbp1 was upregulated 3.97-fold in DENV infected cells in comparison to uninfected controls. Independent qRT-PCR and Western blotting further confirmed the upregulation of GBP1 (mRNA and protein) upon DENV infection (Figure 1, A and B). Recent studies have identified host genes that upregulated in human patients with acute DENV infection [23, 24]. GBP1 was one of the genes most highly induced in patients’ blood cells during early DENV infection [23], and this is consistent with our result here shown in in vitro study.

To study the specific role of GBP1 during DENV infection, an siRNA based RNA interference study was performed in RAW264.7 cells. siRNAs specific for Gbp1 or scrambled control (N.C.) were delivered into RAW264.7 cells respectively via electroporation. 24hrs after siRNA transfection, cells were challenged by DENV (MOI=1.0) for another 24hrs. Cells were then harvested and total RNA and cDNA were made according to standard protocols. Gbp1 was silenced efficiently as analyzed by qRT-PCR (Figure 2A) using gene specific primers (Table 1) and by Western blot (Figure 2B). The intracellular viral loads, in terms of the transcript levels of the envelop gene (E), were quantified by qRT-PCR and normalized to mouse beta-actin gene. As shown in Figure 2C, the DENV viral load was increased 5.0-fold (p<0.05) in Gbp1 silenced cells compared with control cells. To measure the production of infectious virus from these cells, a plaque assay was performed in 293T cells. The titers of virus in supernatants from Gbp1 silenced cells were about 10- fold higher compared with that from control cells (Figure 2D). These data suggested that Gbp1 has an anti-viral activity against DENV in RAW264.7 cells.

In order to examine whether the silencing of Gbp1 would affect the expression of cytokines, the expressions of some representative cytokines and chemokines were measured in Gbp1 siRNA or scrambled siRNA treated cells after DENV infection. Total of six genes were chosen for the study, including type I interferon (Ifnβ1), Interleukin-6 (Il6), Chemokine (C-X-C motif) ligand 1 (Cxcl1), Chemokine (C-X-C motif) ligand 2(Cxcl2), Chemokine (C-C motif) ligand 5(Ccl5) and C-C chemokine receptor type 5(Ccr5). Gene specific primers and probe sets were purchased from Applied Biosystems (Carlsbad, CA). After DENV infection, the transcription levels of Ifnβ1, Il6, and Ccl5 in Gbp1 silenced groups were decreased 2 to 3-fold comparing with controls (p<0.05). However, transcription levels of Cxcl1/2 and Ccr5 were not significantly affected (Figure 3, A-F). Consistent with the mRNA expression, the protein secretion of IFNβ and IL6 were decreased in Gbp1 silenced cells (Figure 3, G and H). These data suggested that antiviral role of Gbp1 is associated with its ability to modulate some antiviral or pro-inflammatory cytokines during DENV infection.

NF-κ B (nuclear factor- kappa B) and AP1 (activator protein 1) play crucial roles in antiviral innate immune response through promoting the transcription of numerous antiviral or pro-inflammatory genes [25, 26]. Since the expression levels of some cytokines were decreased in Gbp1 silenced cells after DENV infection, we further measured the activities of NF-κB and AP1 upon GBP1 silencing. 293 cells can be robustly infected by DENV[27], and are the most common system to measure the transcriptional factor activity using dual luciferase reporter assay. Reporter plasmids pGL- NF-κB, pGL-AP1 and pRL-TK (internal control) (Promega, Madison, MI) in together with siRNAs specific for human GBP1 or scrambled control (N.C.), were delivered into 293T cells respectively by transfection using Lipofectamine® LTX & PLUS (Invitrogen, Grand Island, NY). 24hrs after transfection, cells were challenged by DENV (MOI=1.0) for another 24hrs, respectively. RNAi efficiency was confirmed by Western blot (Figure 4A). Cells were then harvested and lysed for dual luciferase reporter assay (Promega, Madison, MI). The relative activity of NF-κB was decreased by 40% in GBP1 knockdown cells in comparison with controls; while the AP1 activity was not significantly impaired in this case (Figure 4, B and C). These data suggested that GBP1 may influence activity of NF-κB, thereby contribute to the production of anti-viral or pro-inflammatory cytokines/chemokines. This could also partially address the mechanisms of how GBP1 inhibits DENV replication in cell culture.

More and more attention has been focused on the roles of large GTPase family in immune response [12‐14]. GBP1 can be induced by IFNγ as well as IFNα/β, and its induction can be augmented by TNF-α, IL-1 or LPS[12]. The inhibitory roles of GBP1 to different pathogens have been reported [17‐19, 21]. Itsui and his colleague showed that HCV replication was suppressed significantly by overexpression of GBP1, while binding of the HCV-NS5B protein to GBP1 countered the antiviral effect through inhibition of GTPase activity [21]. MacMicking speculated that GBP1 might help to limit the cell-to-cell spread of progeny virus through its anti-cell proliferative activity [13, 28]. GBP1 has modest antiviral activity against the negative strand RNA viruses (such as Rhabdovirus, vesicular stomatitis virus), as well as the positive strand RNA viruses (Picornovirus and encephalomyocarditis virus) in cultured cells [19]. In both anti- chlamydia and antiviral study, the GTPase domain of GBP1 was suggested to be critical for its inhibitory activity [18, 21]. A recent in vivo study further suggested that GBPs can solicit host defense proteins, including the phagocyte oxidase, antimicrobial peptides, and autophagy effectors, to kill intracellular bacteria [17]. While, more work are still needed to address the role and mechanisms of GBP1 in different infection models especially for viruses.

In this study, we confirmed that GBP1 shows inhibitory effect on DENV infection, influences the activity of NF-κB and further contributes to the production of anti-viral and pro-inflammatory cytokine/chemokines. This could be a novel mechanism for GBP1 to exert its antiviral activity in cellular level. Since NF-κB can be activated upon a broad range of pathogen infection, this could be a common action for GBP1 to play its role in different infection models. Further experiments will address the detail mechanisms of GBP1 on influencing NF-κB pathway in various models.