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* Antiviral Innate Immunity Project, Tokyo Metropolitan Institute of Medical Science, Tokyo Metropolitan Organization for Medical Research, Tokyo, Japan;
Department of Vascular Biology, Hirosaki University School of Medicine, Hirosaki, Aomori, Japan;
21st Century Center of Excellence Program, Graduate School of Medicine, University of Tokyo, Tokyo, Japan;
National Institute of Advanced Industrial Science and Technology, Gene Function Research Center, Tsukuba Science City, Japan;
¶ Department of Chemistry and Biotechnology, School of Engineering, University of Tokyo, Tokyo, Japan;
|| Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390;
# Department of Host Defense, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan;
** Department of Animal Development and Physiology, Graduate School of Biostudies, Kyoto University, Kyoto, Japan; and
Department of Virology III, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan
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Abstract |
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 Top Abstract IntroductionMaterials and MethodsResultsDiscussionDisclosuresReferences |
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Introduction |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionDisclosuresReferences |
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B, and activating transcription factor-2/c-Jun (3). Among them, IRF-3 is essential for the primary activation of IFN genes (4). IRF-3 is phosphorylated at specific serine residues (5, 6) by two members of the IB kinase (IKK) family, TANK-binding kinase 1 (TBK1) and IKKi/IKK
(7, 8), and forms an active DNA-binding holocomplex with a transcriptional coactivator, p300 or the CREB-binding protein, in the nucleus (9). The analysis of knockout mice for tbk1 and ikki genes demonstrated the essential and redundant role of these genes in the activation of IRF-3 (10, 11). IRF-7 is also regulated by these kinases and involved in the secondary induction of IFN genes (8, 12, 13).
Recently, we have identified a DExD/H-box-containing RNA helicase, retinoic acid-inducible gene I (RIG-I), as an essential component of the sensor of intracellular dsRNA (14). RIG-I encodes a caspase recruitment domain (CARD) at the N terminus, in addition to an RNA helicase domain. The helicase domain recognizes dsRNA and regulates signal transduction in an ATPase-dependent manner. Although the CARD of RIG-I directly transmits a signal leading to the activation of both IRF-3 and NF-B, the precise machinery for the activation remains unknown. In the mammalian database, we found two other DExD/H-box-containing RNA helicases that are closely related to RIG-I. Melanoma differentiation-associated gene 5 (MDA5) is the closest relative of RIG-I, exhibiting 23 and 35% aa identities in the N-terminal CARD and C-terminal helicase domain, respectively. MDA5 has been implicated in the regulation of the growth and differentiation of melanoma cells (15). MDA5 was independently identified as a binding target for V proteins of paramyxoviruses (16). Although the precise mechanism is unclarified, these V proteins inhibit the dsRNA-induced activation of the IFN-
gene through MDA5. Another helicase, LGP2 (17), shows 31 and 41% aa identities to the helicase domains of RIG-I and MDA5, respectively, but completely lacks CARD. In this report, we show that MDA5 acts as a positive regulator in the virus-induced activation of type I IFN genes. We provide evidence that RIG-I and MDA5 transmit an identical signal leading to the activation of IRF-3, IRF-7, and NF-B. Many virus-encoded proteins specifically target these helicases to escape from antiviral detection by the host cells. The other family member LGP2 functions as a dominant-negative regulator of RIG-I/MDA5-mediated signaling, suggesting its role in negative feedback.
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Materials and Methods |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionDisclosuresReferences |
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L929 cells were maintained in MEM with 5% FBS and penicillin/streptomycin. 293T cells, Huh7 cells, and mouse embryonic fibroblasts (MEFs) were maintained in DMEM with 10% FBS and penicillin/streptomycin. The transient transfection of the L929 and 293T cells was performed as described previously (14). The 293T cells in Fig. 1C, Huh7 and MEFs, were transfected by FuGENE6 (Roche). The stable transformants of the L929 cells were established by the transfection of a linearized empty vector (pEF-BOS) or an expression plasmid for RIG-I (pEF-flagRIG-Ifull), RIG-IC (pEF-flagRIG-IC), MDA5 (pEF-flagMDA5full), or LGP2 (pEF-flagLGP2) with pCDM8neo, followed by selection with G418 (1 mg/ml). Virus infection, poly(rI):poly(rC) (poly(I:C)) transfection, and preparation of cell extracts were performed as reported previously (14). Luciferase assay was performed with a dual-luciferase reporter assay system (Promega). As the internal control for the dual-luciferase assay, pRL-TK (Promega) was used.
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p-55C1BLuc, p-55UASGLuc, p-55A2Luc, p-125Luc, pEFGal4/IRF-3, pEFGal4/IRF-7, pEF-flagRIG-I, pEF-flagRIG-IC, pEF-flagRIG-IKA, pEF-flageIF4A, pcDNA3.1-nonstructural protein 3/4A (NS3/4A), pKS336-Sv-V, and pKS336-Sv-Vu were described previously (14, 18, 19). The pEF-flagRIG-IN, which contains the N-terminal 229 aa of RIG-I, was obtained by the insertion of oligonucleotides at the EcoRI sites of RIG-I cDNA. The cDNA of MDA5 was isolated by the RT-PCR technique, and inserted into the XbaI/ClaI sites of pEF-BOS+ with oligonucleotides for the N-terminal flag tag (pEF-flagMDA5). The nucleotide sequence of the cDNA was confirmed with a BigDye DNA-sequencing kit (Applied Biosystems). The cDNA of LGP2 (GenBank accession no. AK021416) was purchased from the Biological Resource Center of National Institute of Technology and Evaluation, and inserted into the XbaI sites of pEF-BOS with oligonucleotides for the N-terminal flag tag (pEF-flagLGP2). The deleted and site-directed mutants of MDA5 were obtained by the insertion of the appropriate oligonucleotides and the Kunkel method (20), respectively (pEF-flagMDA5N, pEF-flagMDA5C, and pEF-flagMDA5KA).
EMSA
EMSA was performed as described previously (14).
Abs, ELISA, immunoprecipitation, and immunoblotting
Anti-murine IRF-3, anti-p50-tag, and anti-V protein Abs were described in our previous reports (14, 19). The anti-flag (M2; Sigma-Aldrich) Ab and anti-actin Ab (Chemicon) are commercial products. The anti-LGP2 antiserum was obtained by immunizing the rabbits with synthetic peptides (IQAKKWSRVPFSVC) of LGP2 conjugated to bovine thyroglobulin. The Ab was affinity-purified by using immobilized Ag peptide. We confirmed that this anti-LGP2 antiserum specifically recognized recombinant LGP2 expressed in 293T cells. ELISA, SDS-PAGE, native-PAGE, and immunoblotting were performed as described previously (14). Immunoprecipitation was performed as shown in previous report using anti-flag M2 affinity gel (Sigma-Aldrich) (5).
Poly(I:C)-pulldown assay
Poly(I:C)-pulldown assay was performed as described previously (14).
RNA interference
The vector for small interfering RNA (siRNA), piGENE hU6, and constructs for control or RIG-I siRNA were described previously (14). The sequences for the siRNA targeting murine MDA5 and LGP2 mRNA are 5'-GTCATTAGTAAATTTCGCACT-3' and 5'-GGATGGAGTTGGAAGATGA-3', respectively. For the reporter assay, the L929 cells were transiently transfected with p-55C1BLuc and pRL-TK as reporters, together with the siRNA vectors. The cells were mock-infected or Newcastle disease virus (NDV)-infected, and subjected to dual-luciferase assay. The quantitative assay for endogenous mRNA was performed as described previously (14).
Virus yield titration
Stable L929-derived transformants were mock-infected or infected with vesicular stomatitis virus (VSV) or encephalomyocarditis virus (EMCV). The virus yield in culture supernatants was determined by plaque assay as described previously (14).
Mouse IFN titration
MEFs were stimulated by NDV infection or poly(I:C)/DEAE dextran transfection. After 24 h, culture media were collected, ultracentrifuged to remove viruses and poly(I:C) (436,000 x g, 10 min), and subjected to IFN assay. The mouse IFN was titrated using the L929 cells in a 96-well plate and EMCV as a challenge virus. The IFN titer was normalized using an international standard.
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Results |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionDisclosuresReferences |
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RIG-I and MDA5 share a limited homology in their overall primary structure (Fig. 1A). Notably, the two proteins contain tandem CARD-like regions at their N-termini as well as C-terminal DExD/H-box helicase domains. The previous observation that the CARD of RIG-I and those of Nod1 and Nod2 target a distinct set of downstream molecules (14) prompted us to compare the functions of the CARDs of RIG-I and MDA5. The overexpression of the CARD of either RIG-I (RIG-IN) or MDA5 (MDA5N) resulted in the constitutive activation of the reporter p-55C1BLuc, which is essentially regulated by multimerized IRF binding sites (Fig. 1B). Furthermore, these CARDs activated the endogenous IFN- gene, resulting in the secretion of the IFN- protein without exogenous stimuli, such as viral infection (Fig. 1C). The fusion transcription factor containing the DNA-binding domain of Gal4 and the C-terminal regulatory domain of IRF-3 (Gal4-IRF-3) was activated by the expression of RIG-IN or MDA5N (Fig. 1D), showing that IRF-3 is a downstream target. Consistent with this, RIG-IN and MDA5N induced the IRF-3 holocomplex (Fig. 1E) and IRF-3 dimer (Fig. 1F). These results show that the CARD of MDA5 is capable of activating IRF-3 similarly to that of RIG-I. Interestingly, tbk1–/– cells are defective in IRF-3 dimer formation induced by RIG-IN or MDA5N, suggesting that these CARDs signal through the protein kinase TBK1 (Fig. 1F). This is consistent with our observation that RIG-IN and MDA5N result in the phosphorylation of Ser 386 of IRF-3 (6) (Fig. 1G). It has been reported that the NS3/4A of the hepatitis C virus blocks RIG-I-mediated signaling through its protease activity (18). Although the target of the NS3/4A protease has not yet been identified, this hypothetical molecule functions downstream of MDA5N and RIG-IN, because the activation of IRF-3 was blocked by NS3/4A (Fig. 1, G and H). Moreover, Gal4-IRF-7 and NF-B were activated by RIG-IN and MDA5N (Fig. 1, I and J). In summary, these results strongly suggest that the CARDs of RIG-I and MDA5 activate the overlapping cascade.
Positive and negative signalings by the full-length RIG-I, MDA5, and LGP2
The overexpression of the full-length RIG-I and MDA5 failed to activate the reporter genes, p-55C1BLuc and pIFNLuc; however, considerable activation was observed after stimulation by virus infection or dsRNA transfection (Fig. 2A). Similarly, the dimerization of IRF-3 induced by dsRNA was increased by the overexpression of RIG-I or MDA5 without significant basal activation (Fig. 2B). These results show that RIG-I and MDA5 act as positive regulators of virus-induced signaling and are under strict negative regulation in the absence of stimuli.
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, similarly to RIG-I and MDA5 (14, 21), whereas the house keeping actin expression was unaffected (Fig. 3B). To explore the functions of these proteins, we generated mutants of RIG-I and MDA5 lacking CARD (RIG-IC and MDA5C) as well as having an inactivated Walker’s ATP binding motif by the Lys-to-Arg substitution of the respective helicases (RIG-IKA and MDA5KA). For comparison, a distantly related DExD/H helicase, eukaryotic initiation factor 4A (eIF4A), was used. Under these conditions, full-length RIG-I and MDA5 enhanced the virus-induced gene induction (Fig. 3C). eIF4A did not affect the virus-induced activation of the reporter; however, as reported earlier, RIG-IC and RIG-IKA strongly inhibited the virus-induced gene activation (14). In contrast, MDA5C and MDA5KA neither augmented nor suppressed the gene activation by the virus. In either case, the helicase domain alone is incapable of transducing positive signaling. Moreover, the results show that ATPase activity is critical to the functioning of RIG-I and MDA5 as positive regulators. LGP2 strongly inhibited the gene activation, similarly to RIG-IC. In cells stably expressing RIG-IC or LGP2, virus-induced dimerization of endogenous IRF-3 was severely impaired (Fig. 3D). These results suggest that LGP2 functions as a physiological negative feedback regulator. Consistent with this, knockdown of LGP2 markedly enhanced gene activation induced by NDV infection (Fig. 3E). The binding of these helicases to dsRNA was investigated by pulldown assay (Fig. 3F). All of the tested helicases bound to poly(I:C)-agarose, except eIF4A with a relative affinity of LGP2>>RIG-I>MDA5, confirming that the RIG-I family recognizes dsRNA.
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In our previous work, we showed that the stable expression of the RIG-I protein in cultured cells severely inhibits viral replication (14). We compared the antiviral activity of the RIG-I family by the same assay using EMCV and VSV as infecting viruses (Fig. 4). These viruses cause a severe "shutoff" of the host RNA and protein syntheses; thus, they are fully competent to induce lytic infection in L929 cells. RIG-I and MDA5 significantly reduced the viral yield 100- to 1000-fold, whereas LGP2 did not affect the viral yield. Likewise, the artificial inhibitor RIG-IC did not affect the viral yield (our unpublished observations).
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The above-mentioned results using mutant proteins indicate that, in addition to their structural homology, RIG-I and MDA5 share functional similarities. To explore the loss-of-function phenotype of these proteins, we performed knockdown of RIG-I and MDA5 using siRNA. We used luciferase reporter (Fig. 5A) and quantification of endogenous target gene expression (Fig. 5B) as readout. Vector and control siRNAs did not affect the virus-induced activation of the reporter p-55C1BLuc and endogenous IFN gene expression. The siRNA targeting endogenous mouse RIG-I or MDA5 blocked the gene induction in a dose-dependent manner (Fig. 5A). Furthermore, the expression of endogenous IFN mRNA was specifically inhibited by siRNA for either RIG-I or MDA5 (Fig. 5B). These results indicate the requirement of endogenous RIG-I and MDA5 in the signaling.
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30%) suppression of the NDV-induced reporter gene expression, suggesting that the NDV-induced signal is largely insensitive to the V-protein-mediated inhibition. The expression of RIG-I resulted in a marked augmentation of the NDV-induced reporter gene activation; however, it was not notably affected by the V protein expression. In contrast, the enhancement of the virus-induced gene activation by MDA5 was completely abrogated by the V protein as reported (16). A Vu protein exhibited an activity indistinguishable from that of the V protein, indicating that the C-terminal region is sufficient for the inhibition. The selective inhibition of MDA5 by V protein is likely due to selective physical interaction as revealed by coprecipitation experiment (Fig. 6B), in which RIG-I did not interact with V protein.
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Discussion |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionDisclosuresReferences |
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B. We do not know the direct target of RIG-I and MDA5 at present. FADD is unlikely the hypothetical target because it is dispensable in the signaling triggered by NDV. Its requirement in poly(I:C)-induced signaling suggests its role during or after the cytoplasmic uptake of extracellular dsRNA.
The following observations suggest that RIG-I and MDA5 function in parallel rather than in series. First, the knockdown of either proteins partially blocked the signaling (Fig. 5). Second, the SeV V protein, which is a potent and selective inhibitor of MDA5, did not completely abrogate the signaling (Fig. 6). Third, the expression of RIG-I and MDA5 did not exhibit a marked synergy in reporter assays (our unpublished observations). Finally, the Fugu genome contains a single gene encoding the CARD-containing helicase related to RIG-I and MDA5. RIG-I and MDA5 are ubiquitously expressed in various mouse tissues, except in the brain and spinal cord (24). Our analyses revealed that these proteins function similarly, except some details. Overexpression of CARD of RIG-I activated endogenous IFN- gene more efficiently than that of MDA5 (Fig. 1C), although these proteins activated IRF-3, IRF-7, and NF-B efficiently (Fig. 1). Therefore, we do not exclude a possibility of differential activation of unidentified transcription factor(s) by RIG-I and MDA5. A more clear distinction between these proteins is selective inhibition of MDA5 by V protein, due to specific physical interaction (Fig. 6). Thus, having two genes with overlapping functions may be beneficial in avoiding the viral inhibitors.
In cytokine signaling, negative regulators have been identified, which provide a negative feedback loop for avoiding uncontrolled signaling (25). Defects in these negative regulators often result in pathological conditions due to excessive reaction. LGP2 belongs to the RIG-I family, but lacks CARD. Similarly to the artificial RIG-IC and RIG-IKA, LGP2 acts as a strong inhibitor of virus-induced signaling, whereas MDA5C and MDA5KA do not. The observations that MDA5 binds to dsRNA with a lower affinity than RIG-I and LGP2 (Fig. 3F), and that RIG-IC and LGP2 are incapable of blocking the signaling induced by the overexpression of RIG-IN (our unpublished observations), indicate that the sequestration of dsRNA from wild-type RIG-I and MDA5 is the mechanism of the inhibition. It is worth noting that, although the binding affinity of MDA5 is significantly low, MDA5 efficiently transmits signals by poly(I:C) (Fig. 2A), suggesting that the binding affinity per se does not determine downstream signaling. Therefore, it is tempting to speculate that transient formation of MDA5/dsRNA complex is sufficient to trigger downstream signaling ("hit-and-run model"), however to inhibit the signaling, persistent "sequestration" by stable complex formation is required. Alternatively, involvement of additional regulatory factor(s) in the recognition of dsRNA by RIG-I and MDA5 is a possibility. Interestingly, proteins with unrelated dsRNA binding motifs, including a dsRNA-dependent protein kinase, an RNA-specific adenosine deaminase, and a protein activator of dsRNA-dependent protein kinase, do not inhibit the virus-induced signaling (26), suggesting that LGP2 specifically masks the target RNA from recognition by RIG-I and MDA5. LGP2 is strongly induced by type I IFN (Fig. 3B), and knockdown of LGP2 results in enhanced gene induction (Fig. 3E); thus, it is likely responsible for the negative feedback of IFN gene activation.
Figure 7 shows the signaling cascade triggered by virus infection. Because RIG-I and MDA5 are IFN-inducible (14, 21), once the signal is triggered by the virus, this innate antiviral loop initiates autoamplification until the triggering molecule dsRNA is removed and/or the natural inhibitor LGP2 is induced. The viral genome also undergoes autoamplification through the expression of the viral proteins. Apparently, the two amplifications are mutually inhibitory through virus-encoded inhibitory peptides and host antiviral proteins. Particularly, an increasing number of studies suggest that viruses encode numerous inhibitory proteins for the molecules of the innate antiviral loop (27). In summary, the outcome of an infection is determined by the equilibrium between viral replication and innate antiviral responses, concretely by the viral load, the activities of viral inhibitors, and the host signaling molecules including RIG-I and MDA5. This principle may be useful in designing antiviral drugs and therapies. Particularly, the agonist of RIG-I and MDA5 is expected to enable the potentiation of host antiviral innate immunity.
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Acknowledgments |
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Disclosures |
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Footnotes |
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1 This work is supported by Japan Society for the Promotion of Science, Ministry of Education, Culture, Sports, Science and Technology of Japan, Nippon Boehringer Ingelheim, and Toray Industries. 
2 Address correspondence and reprint requests to Dr. Takashi Fujita, Antiviral Innate Immunity Project, Tokyo Metropolitan Institute of Medical Science, Tokyo Metropolitan Organization for Medical Research, 3-18-22 Honkomagome, Bunkyo-ku, Tokyo 113-8613, Japan. E-mail address: fujita{at}rinshoken.or.jp
3 Abbreviations used in this paper: IRF, IFN regulatory factor; IKK, IB kinase; TBK1, TANK-binding kinase 1; RIG-I, retinoic acid-inducible gene I; CARD, caspase recruitment domain; MDA5, melanoma differentiation associated gene 5; MEF, mouse embryonic fibroblast; poly(I:C), poly(rI):poly(rC); NS3/4A, nonstructural protein 3/4A; siRNA, small interfering RNA; NDV, Newcastle disease virus; VSV, vesicular stomatitis virus; EMCV, encephalomyocarditis virus; eIF4A, eukaryotic initiation factor 4A; SeV, Sendai virus; FADD, Fas-associated protein with death domain.
Received for publication March 11, 2005. Accepted for publication June 16, 2005.
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J.-P. Parisien, D. Bamming, A. Komuro, A. Ramachandran, J. J. Rodriguez, G. Barber, R. D. Wojahn, and C. M. Horvath A Shared Interface Mediates Paramyxovirus Interference with Antiviral RNA Helicases MDA5 and LGP2 J. Virol., July 15, 2009; 83(14): 7252 - 7260. [Abstract] [Full Text] [PDF]
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V. Fensterl, C. L. White, M. Yamashita, and G. C. Sen Novel Characteristics of the Function and Induction of Murine p56 Family Proteins J. Virol., November 15, 2008; 82(22): 11045 - 11053. [Abstract] [Full Text] [PDF]
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M.-J. Kim and J.-Y. Yoo Active Caspase-1-Mediated Secretion of Retinoic Acid Inducible Gene-I J. Immunol., November 15, 2008; 181(10): 7324 - 7331. [Abstract] [Full Text] [PDF]
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D. Sarkar, R. DeSalle, and P. B. Fisher Evolution of MDA-5/RIG-I-dependent innate immunity: Independent evolution by domain grafting PNAS, November 4, 2008; 105(44): 17040 - 17045. [Abstract] [Full Text] [PDF]
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N. Tamassia, V. Le Moigne, M. Rossato, M. Donini, S. McCartney, F. Calzetti, M. Colonna, F. Bazzoni, and M. A. Cassatella Activation of an Immunoregulatory and Antiviral Gene Expression Program in Poly(I:C)-Transfected Human Neutrophils J. Immunol., November 1, 2008; 181(9): 6563 - 6573. [Abstract] [Full Text] [PDF]
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J. K. Roth-Cross, S. J. Bender, and S. R. Weiss Murine Coronavirus Mouse Hepatitis Virus Is Recognized by MDA5 and Induces Type I Interferon in Brain Macrophages/Microglia J. Virol., October 15, 2008; 82(20): 9829 - 9838. [Abstract] [Full Text] [PDF]
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V. Bitko, A. Musiyenko, M. A. Bayfield, R. J. Maraia, and S. Barik Cellular La Protein Shields Nonsegmented Negative-Strand RNA Viral Leader RNA from RIG-I and Enhances Virus Growth by Diverse Mechanisms J. Virol., August 15, 2008; 82(16): 7977 - 7987. [Abstract] [Full Text] [PDF]
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B. N. Kalali, G. Kollisch, J. Mages, T. Muller, S. Bauer, H. Wagner, J. Ring, R. Lang, M. Mempel, and M. Ollert Double-Stranded RNA Induces an Antiviral Defense Status in Epidermal Keratinocytes through TLR3-, PKR-, and MDA5/RIG-I-Mediated Differential Signaling J. Immunol., August 15, 2008; 181(4): 2694 - 2704. [Abstract] [Full Text] [PDF]
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T. Saito and M. Gale Jr. Differential recognition of double-stranded RNA by RIG-I-like receptors in antiviral immunity J. Exp. Med., July 7, 2008; 205(7): 1523 - 1527. [Abstract] [Full Text] [PDF]
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J. Wang, S. Wu, X. Jin, M. Li, S. Chen, J. L. Teeling, V. H. Perry, and J. Gu Retinoic Acid-Inducible Gene-I Mediates Late Phase Induction of TNF-{alpha} by Lipopolysaccharide J. Immunol., June 15, 2008; 180(12): 8011 - 8019. [Abstract] [Full Text] [PDF]
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A. Murali, X. Li, C. T. Ranjith-Kumar, K. Bhardwaj, A. Holzenburg, P. Li, and C. C. Kao Structure and Function of LGP2, a DEX(D/H) Helicase That Regulates the Innate Immunity Response J. Biol. Chem., June 6, 2008; 283(23): 15825 - 15833. [Abstract] [Full Text] [PDF]
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S. L. Day, I. A. Ramshaw, A. J. Ramsay, and C. Ranasinghe Differential Effects of the Type I Interferons {alpha}4, {beta}, and {epsilon} on Antiviral Activity and Vaccine Efficacy J. Immunol., June 1, 2008; 180(11): 7158 - 7166. [Abstract] [Full Text] [PDF]
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A. Paun, J. T. Reinert, Z. Jiang, C. Medin, M. Y. Balkhi, K. A. Fitzgerald, and P. M. Pitha Functional Characterization of Murine Interferon Regulatory Factor 5 (IRF-5) and Its Role in the Innate Antiviral Response J. Biol. Chem., May 23, 2008; 283(21): 14295 - 14308. [Abstract] [Full Text] [PDF]
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Z. Wang, M. K. Choi, T. Ban, H. Yanai, H. Negishi, Y. Lu, T. Tamura, A. Takaoka, K. Nishikura, and T. Taniguchi Regulation of innate immune responses by DAI (DLM-1/ZBP1) and other DNA-sensing molecules PNAS, April 8, 2008; 105(14): 5477 - 5482. [Abstract] [Full Text] [PDF]
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P. Gee, P. K. Chua, J. Gevorkyan, K. Klumpp, I. Najera, D. C. Swinney, and J. Deval Essential Role of the N-terminal Domain in the Regulation of RIG-I ATPase Activity J. Biol. Chem., April 4, 2008; 283(14): 9488 - 9496. [Abstract] [Full Text] [PDF]
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J. S. Yount, L. Gitlin, T. M. Moran, and C. B. Lopez MDA5 Participates in the Detection of Paramyxovirus Infection and Is Essential for the Early Activation of Dendritic Cells in Response to Sendai Virus Defective Interfering Particles J. Immunol., April 1, 2008; 180(7): 4910 - 4918. [Abstract] [Full Text] [PDF]
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M. Kramer, B. M. Schulte, L. W. J. Toonen, P. M. Barral, P. B. Fisher, K. H. W. Lanke, J. M. D. Galama, F. J. M. van Kuppeveld, and G. J. Adema Phagocytosis of Picornavirus-Infected Cells Induces an RNA-Dependent Antiviral State in Human Dendritic Cells J. Virol., March 15, 2008; 82(6): 2930 - 2937. [Abstract] [Full Text] [PDF]
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M.-J. Kim, S.-Y. Hwang, T. Imaizumi, and J.-Y. Yoo Negative Feedback Regulation of RIG-I-Mediated Antiviral Signaling by Interferon-Induced ISG15 Conjugation J. Virol., February 1, 2008; 82(3): 1474 - 1483. [Abstract] [Full Text] [PDF]
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B. L. Fredericksen, B. C. Keller, J. Fornek, M. G. Katze, and M. Gale Jr. Establishment and Maintenance of the Innate Antiviral Response to West Nile Virus Involves both RIG-I and MDA5 Signaling through IPS-1 J. Virol., January 15, 2008; 82(2): 609 - 616. [Abstract] [Full Text] [PDF]
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Y.-M. Loo, J. Fornek, N. Crochet, G. Bajwa, O. Perwitasari, L. Martinez-Sobrido, S. Akira, M. A. Gill, A. Garcia-Sastre, M. G. Katze, et al. Distinct RIG-I and MDA5 Signaling by RNA Viruses in Innate Immunity J. Virol., January 1, 2008; 82(1): 335 - 345. [Abstract] [Full Text] [PDF]
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A. Jung, H. Kato, Y. Kumagai, H. Kumar, T. Kawai, O. Takeuchi, and S. Akira Lymphocytoid Choriomeningitis Virus Activates Plasmacytoid Dendritic Cells and Induces a Cytotoxic T-Cell Response via MyD88 J. Virol., January 1, 2008; 82(1): 196 - 206. [Abstract] [Full Text] [PDF]
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M. Tasaka, N. Sakamoto, Y. Itakura, M. Nakagawa, Y. Itsui, Y. Sekine-Osajima, Y. Nishimura-Sakurai, C.-H. Chen, M. Yoneyama, T. Fujita, et al. Hepatitis C virus non-structural proteins responsible for suppression of the RIG-I/Cardif-induced interferon response J. Gen. Virol., December 1, 2007; 88(12): 3323 - 3333. [Abstract] [Full Text] [PDF]
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T. Kanda, R. Steele, R. Ray, and R. B. Ray Hepatitis C Virus Infection Induces the Beta Interferon Signaling Pathway in Immortalized Human Hepatocytes J. Virol., November 15, 2007; 81(22): 12375 - 12381. [Abstract] [Full Text] [PDF]
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J. Seago, L. Hilton, E. Reid, V. Doceul, J. Jeyatheesan, K. Moganeradj, J. McCauley, B. Charleston, and S. Goodbourn The Npro product of classical swine fever virus and bovine viral diarrhea virus uses a conserved mechanism to target interferon regulatory factor-3 J. Gen. Virol., November 1, 2007; 88(11): 3002 - 3006. [Abstract] [Full Text] [PDF]
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Y. Hirata, A. H. Broquet, L. Menchen, and M. F. Kagnoff Activation of Innate Immune Defense Mechanisms by Signaling through RIG-I/IPS-1 in Intestinal Epithelial Cells J. Immunol., October 15, 2007; 179(8): 5425 - 5432. [Abstract] [Full Text] [PDF]
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M. Gong, S. Hay, K. R. Marshall, A. W. Munro, and N. S. Scrutton DNA Binding Suppresses Human AIF-M2 Activity and Provides a Connection between Redox Chemistry, Reactive Oxygen Species, and Apoptosis J. Biol. Chem., October 12, 2007; 282(41): 30331 - 30340. [Abstract] [Full Text] [PDF]
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T. Matsumiya, S. M. Prescott, and D. M. Stafforini IFN-{epsilon} Mediates TNF-{alpha}-Induced STAT1 Phosphorylation and Induction of Retinoic Acid-Inducible Gene-I in Human Cervical Cancer Cells J. Immunol., October 1, 2007; 179(7): 4542 - 4549. [Abstract] [Full Text] [PDF]
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T. Abe, Y. Kaname, I. Hamamoto, Y. Tsuda, X. Wen, S. Taguwa, K. Moriishi, O. Takeuchi, T. Kawai, T. Kanto, et al. Hepatitis C Virus Nonstructural Protein 5A Modulates the Toll-Like Receptor-MyD88-Dependent Signaling Pathway in Macrophage Cell Lines J. Virol., September 1, 2007; 81(17): 8953 - 8966. [Abstract] [Full Text] [PDF]
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N. Jounai, F. Takeshita, K. Kobiyama, A. Sawano, A. Miyawaki, K.-Q. Xin, K. J. Ishii, T. Kawai, S. Akira, K. Suzuki, et al. The Atg5 Atg12 conjugate associates with innate antiviral immune responses PNAS, August 28, 2007; 104(35): 14050 - 14055. [Abstract] [Full Text] [PDF]
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F. Terenzi, C. White, S. Pal, B. R. G. Williams, and G. C. Sen Tissue-Specific and Inducer-Specific Differential Induction of ISG56 and ISG54 in Mice J. Virol., August 15, 2007; 81(16): 8656 - 8665. [Abstract] [Full Text] [PDF]
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J. B. Prescott, P. R. Hall, V. S. Bondu-Hawkins, C. Ye, and B. Hjelle Early Innate Immune Responses to Sin Nombre Hantavirus Occur Independently of IFN Regulatory Factor 3, Characterized Pattern Recognition Receptors, and Viral Entry J. Immunol., August 1, 2007; 179(3): 1796 - 1802. [Abstract] [Full Text] [PDF]
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F. Diao, S. Li, Y. Tian, M. Zhang, L.-G. Xu, Y. Zhang, R.-P. Wang, D. Chen, Z. Zhai, B. Zhong, et al. Negative regulation of MDA5- but not RIG-I-mediated innate antiviral signaling by the dihydroxyacetone kinase PNAS, July 10, 2007; 104(28): 11706 - 11711. [Abstract] [Full Text] [PDF]
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J. S. Yount, T. M. Moran, and C. B. Lopez Cytokine-Independent Upregulation of MDA5 in Viral Infection J. Virol., July 1, 2007; 81(13): 7316 - 7319. [Abstract] [Full Text] [PDF]
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K. Yasuda, C. Richez, J. W. Maciaszek, N. Agrawal, S. Akira, A. Marshak-Rothstein, and I. R. Rifkin Murine Dendritic Cell Type I IFN Production Induced by Human IgG-RNA Immune Complexes Is IFN Regulatory Factor (IRF)5 and IRF7 Dependent and Is Required for IL-6 Production J. Immunol., June 1, 2007; 178(11): 6876 - 6885. [Abstract] [Full Text] [PDF]
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J. Hiscott Triggering the Innate Antiviral Response through IRF-3 Activation J. Biol. Chem., May 25, 2007; 282(21): 15325 - 15329. [Abstract] [Full Text] [PDF]
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M. Yoneyama and T. Fujita Function of RIG-I-like Receptors in Antiviral Innate Immunity J. Biol. Chem., May 25, 2007; 282(21): 15315 - 15318. [Full Text] [PDF]
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G. Cheng, J. Zhong, J. Chung, and F. V. Chisari Double-stranded DNA and double-stranded RNA induce a common antiviral signaling pathway in human cells PNAS, May 22, 2007; 104(21): 9035 - 9040. [Abstract] [Full Text] [PDF]
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J. Johnson, V. Albarani, M. Nguyen, M. Goldman, F. Willems, and E. Aksoy Protein Kinase C{alpha} Is Involved in Interferon Regulatory Factor 3 Activation and Type I Interferon-beta Synthesis J. Biol. Chem., May 18, 2007; 282(20): 15022 - 15032. [Abstract] [Full Text] [PDF]
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T. Venkataraman, M. Valdes, R. Elsby, S. Kakuta, G. Caceres, S. Saijo, Y. Iwakura, and G. N. Barber Loss of DExD/H Box RNA Helicase LGP2 Manifests Disparate Antiviral Responses J. Immunol., May 15, 2007; 178(10): 6444 - 6455. [Abstract] [Full Text] [PDF]
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Y. Yang, Y. Liang, L. Qu, Z. Chen, M. Yi, K. Li, and S. M. Lemon Disruption of innate immunity due to mitochondrial targeting of a picornaviral protease precursor PNAS, April 24, 2007; 104(17): 7253 - 7258. [Abstract] [Full Text] [PDF]
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C. L. Johnson, D. M. Owen, and M. Gale Jr. Functional and Therapeutic Analysis of Hepatitis C Virus NS3{middle dot}4A Protease Control of Antiviral Immune Defense J. Biol. Chem., April 6, 2007; 282(14): 10792 - 10803. [Abstract] [Full Text] [PDF]
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K. Onoguchi, M. Yoneyama, A. Takemura, S. Akira, T. Taniguchi, H. Namiki, and T. Fujita Viral Infections Activate Types I and III Interferon Genes through a Common Mechanism J. Biol. Chem., March 9, 2007; 282(10): 7576 - 7581. [Abstract] [Full Text] [PDF]
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S. Balachandran, T. Venkataraman, P. B. Fisher, and G. N. Barber Fas-Associated Death Domain-Containing Protein-Mediated Antiviral Innate Immune Signaling Involves the Regulation of Irf7 J. Immunol., February 15, 2007; 178(4): 2429 - 2439. [Abstract] [Full Text] [PDF]
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H. Zhou and S. Perlman Mouse Hepatitis Virus Does Not Induce Beta Interferon Synthesis and Does Not Inhibit Its Induction by Double-Stranded RNA J. Virol., January 15, 2007; 81(2): 568 - 574. [Abstract] [Full Text] [PDF]
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T. Saito, R. Hirai, Y.-M. Loo, D. Owen, C. L. Johnson, S. C. Sinha, S. Akira, T. Fujita, and M. Gale Jr. Regulation of innate antiviral defenses through a shared repressor domain in RIG-I and LGP2 PNAS, January 9, 2007; 104(2): 582 - 587. [Abstract] [Full Text] [PDF]
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Z. Feng, M. Cerveny, Z. Yan, and B. He The VP35 Protein of Ebola Virus Inhibits the Antiviral Effect Mediated by Double-Stranded RNA-Dependent Protein Kinase PKR J. Virol., January 1, 2007; 81(1): 182 - 192. [Abstract] [Full Text] [PDF]
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A. Komuro and C. M. Horvath RNA- and Virus-Independent Inhibition of Antiviral Signaling by RNA Helicase LGP2 J. Virol., December 15, 2006; 80(24): 12332 - 12342. [Abstract] [Full Text] [PDF]
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M. Sasai, M. Shingai, K. Funami, M. Yoneyama, T. Fujita, M. Matsumoto, and T. Seya NAK-Associated Protein 1 Participates in Both the TLR3 and the Cytoplasmic Pathways in Type I IFN Induction J. Immunol., December 15, 2006; 177(12): 8676 - 8683. [Abstract] [Full Text] [PDF]
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L. Hilton, K. Moganeradj, G. Zhang, Y.-H. Chen, R. E. Randall, J. W. McCauley, and S. Goodbourn The NPro Product of Bovine Viral Diarrhea Virus Inhibits DNA Binding by Interferon Regulatory Factor 3 and Targets It for Proteasomal Degradation J. Virol., December 1, 2006; 80(23): 11723 - 11732. [Abstract] [Full Text] [PDF]
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P. Paladino, D. T. Cummings, R. S. Noyce, and K. L. Mossman The IFN-Independent Response to Virus Particle Entry Provides a First Line of Antiviral Defense That Is Independent of TLRs and Retinoic Acid-Inducible Gene I J. Immunol., December 1, 2006; 177(11): 8008 - 8016. [Abstract] [Full Text] [PDF]
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K. Matsui, Y. Kumagai, H. Kato, S. Sato, T. Kawagoe, S. Uematsu, O. Takeuchi, and S. Akira Cutting Edge: Role of TANK-Binding Kinase 1 and Inducible I{kappa}B Kinase in IFN Responses against Viruses in Innate Immune Cells J. Immunol., November 1, 2006; 177(9): 5785 - 5789. [Abstract] [Full Text] [PDF]
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A. Audige, M. Urosevic, E. Schlaepfer, R. Walker, D. Powell, S. Hallenberger, H. Joller, H.-U. Simon, R. Dummer, and R. F. Speck Anti-HIV State but Not Apoptosis Depends on IFN Signature in CD4+ T Cells J. Immunol., November 1, 2006; 177(9): 6227 - 6237. [Abstract] [Full Text] [PDF]
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M. A. Samuel and M. S. Diamond Pathogenesis of West Nile Virus Infection: a Balance between Virulence, Innate and Adaptive Immunity, and Viral Evasion J. Virol., October 1, 2006; 80(19): 9349 - 9360. [Full Text] [PDF]
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M. Severa, E. M. Coccia, and K. A. Fitzgerald Toll-like Receptor-dependent and -independent Viperin Gene Expression and Counter-regulation by PRDI-binding Factor-1/BLIMP1 J. Biol. Chem., September 8, 2006; 281(36): 26188 - 26195. [Abstract] [Full Text] [PDF]
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H. Kumar, T. Kawai, H. Kato, S. Sato, K. Takahashi, C. Coban, M. Yamamoto, S. Uematsu, K. J. Ishii, O. Takeuchi, et al. Essential role of IPS-1 in innate immune responses against RNA viruses J. Exp. Med., July 10, 2006; 203(7): 1795 - 1803. [Abstract] [Full Text] [PDF]
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W. B. Cardenas, Y.-M. Loo, M. Gale Jr., A. L. Hartman, C. R. Kimberlin, L. Martinez-Sobrido, E. O. Saphire, and C. F. Basler Ebola Virus VP35 Protein Binds Double-Stranded RNA and Inhibits Alpha/Beta Interferon Production Induced by RIG-I Signaling. J. Virol., June 1, 2006; 80(11): 5168 - 5178. [Abstract] [Full Text] [PDF]
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L. Gitlin, W. Barchet, S. Gilfillan, M. Cella, B. Beutler, R. A. Flavell, M. S. Diamond, and M. Colonna Essential role of mda-5 in type I IFN responses to polyriboinosinic:polyribocytidylic acid and encephalomyocarditis picornavirus PNAS, May 30, 2006; 103(22): 8459 - 8464. [Abstract] [Full Text] [PDF]
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T. Yoshikawa, T. Iwasaki, M. Ida-Hosonuma, M. Yoneyama, T. Fujita, H. Horie, M. Miyazawa, S. Abe, B. Simizu, and S. Koike Role of the Alpha/Beta Interferon Response in the Acquisition of Susceptibility to Poliovirus by Kidney Cells in Culture J. Virol., May 1, 2006; 80(9): 4313 - 4325. [Abstract] [Full Text] [PDF]
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F. Weber, V. Wagner, S. B. Rasmussen, R. Hartmann, and S. R. Paludan Double-stranded RNA is produced by positive-strand RNA viruses and DNA viruses but not in detectable amounts by negative-strand RNA viruses. J. Virol., May 1, 2006; 80(10): 5059 - 5064. [Abstract] [Full Text] [PDF]
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K. Takahashi, T. Kawai, H. Kumar, S. Sato, S. Yonehara, and S. Akira Cutting edge: roles of caspase-8 and caspase-10 in innate immune responses to double-stranded RNA. J. Immunol., April 15, 2006; 176(8): 4520 - 4524. [Abstract] [Full Text] [PDF]
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Y.-M. Loo, D. M. Owen, K. Li, A. K. Erickson, C. L. Johnson, P. M. Fish, D. S. Carney, T. Wang, H. Ishida, M. Yoneyama, et al. Viral and therapeutic control of IFN-beta promoter stimulator 1 during hepatitis C virus infection PNAS, April 11, 2006; 103(15): 6001 - 6006. [Abstract] [Full Text] [PDF]
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B. L. Fredericksen and M. Gale Jr. West Nile Virus Evades Activation of Interferon Regulatory Factor 3 through RIG-I-Dependent and -Independent Pathways without Antagonizing Host Defense Signaling J. Virol., March 15, 2006; 80(6): 2913 - 2923. [Abstract] [Full Text] [PDF]
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