Viral suppressors of the RIG-I-mediated interferon response are pre-packaged in influenza virions

Liedmann, Swantje; Hrincius, Eike R.; Guy, Cliff; Anhlan, Darisuren; Dierkes, Rüdiger; Carter, Robert; Wu, Gang; Staeheli, Peter; Green, Douglas R.; Wolff, Thorsten; McCullers, Jonathan A.; Ludwig, Stephan; Ehrhardt, Christina

doi:10.1038/ncomms6645

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Published: 09 December 2014

Viral suppressors of the RIG-I-mediated interferon response are pre-packaged in influenza virions

Swantje Liedmann¹,
Eike R. Hrincius²,
Cliff Guy³,
Darisuren Anhlan¹,
Rüdiger Dierkes¹,
Robert Carter⁴,
Gang Wu⁴,
Peter Staeheli⁵,
Douglas R. Green³,
Thorsten Wolff⁶,
Jonathan A. McCullers^2,7,
Stephan Ludwig^1,8 &
…
Christina Ehrhardt^1,8

Nature Communications volume 5, Article number: 5645 (2014) Cite this article

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Abstract

The type I interferon (IFN) response represents the first line of defence to invading pathogens. Internalized viral ribonucleoproteins (vRNPs) of negative-strand RNA viruses induce an early IFN response by interacting with retinoic acid inducible gene I (RIG-I) and its recruitment to mitochondria. Here we employ three-dimensional stochastic optical reconstruction microscopy (STORM) to visualize incoming influenza A virus (IAV) vRNPs as helical-like structures associated with mitochondria. Unexpectedly, an early IFN induction in response to vRNPs is not detected. A distinct amino-acid motif in the viral polymerases, PB1/PA, suppresses early IFN induction. Mutation of this motif leads to reduced pathogenicity in vivo, whereas restoration increases it. Evolutionary dynamics in these sequences suggest that completion of the motif, combined with viral reassortment can contribute to pandemic risks. In summary, inhibition of the immediate anti-viral response is ‘pre-packaged’ in IAV in the sequences of vRNP-associated polymerase proteins.

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Introduction

The type I interferon (IFN) system is a central host defence mechanism that recognizes invading pathogens and rapidly establishes an anti-microbial state to restrict viral and bacterial infections. To ensure efficient replication, pathogens have faced an evolutionary challenge to develop strategies to circumvent, resist or counteract activation of the type I IFN response.

During negative-strand RNA virus infection, the RNA helicase retinoic acid inducible gene I (RIG-I) detects viral ribonucleoprotein complexes (vRNPs) as one pathogen-associated molecular pattern among others by combined recognition of RNA secondary base-pairing structures and 5′-triphospate termini^1,2. Following detection of vRNPs, RIG-I interacts with TRIM25 and is recruited to mitochondria by the scaffold protein MAVS, finally leading to the activation of the TBK-1/IRF-3 IFNβ induction pathway^3,4. Previous studies of this process have focused on the role of newly synthesized vRNPs accumulating in the cell hours after initial infection. One recent report, focusing on the bunyaviruses Rift Valley fever virus and La Crosse virus, suggested that incoming, encapsidated RNA virus genomes in the early stages of infection may induce the type I IFN response independent of replication². In contrast, very recently it was reported that induction of type I IFN by influenza viruses requires viral RNA synthesis and nuclear export. Incoming vRNPs were potentially ruled out as predominant inducer⁵.

Taking into account that viruses must attenuate the type I IFN response to establish efficient replication, the question arises if and how RNA viruses control early recognition of internalized vRNPs. For influenza A viruses (IAVs), the most prominent type I IFN antagonist is the nonstructural protein 1 (NS1). NS1 suppresses the type I IFN response by interacting with RIG-I^6,7 and TRIM25 (ref. 8). Very recently, first evidence arose that NS1 is maybe present in the virion⁹. Overall functionality of incorporated NS1 and the impact on the type I IFN response still need to be explored, but as the number of NS1 proteins per virion is very low (mean=4.2, s.d.=3.2), it might not be sufficient for inhibition of the early type I IFN response potentially activated by internalized vRNPs⁹. This would imply the existence of an additional NS1-independent mechanism of type I IFN antagonism specifically targeting the earliest type I IFN response.

Here we visualize IAV vRNPs in three-dimensional, high-resolution light microscopy as helical-like structures associated with the mitochondrial outer membrane. We identify the polymerase proteins PB1 and PA as part of the type I IFN inhibitory strategy evolved by IAV and suggest a specific amino-acid motif to interact with RIG-I and subsequently inhibit RIG-I-mediated type I IFN signalling. We suggest PB1/PA-mediated type I IFN inhibition to be targeted towards the early induction of type I IFN as PB1 and PA are already present when internalized vRNPs are sensed by RIG-I and are located in close proximity to the site of RIG-I activation.

Results and Discussion

STORM revealed vRNPs as helical structures at mitochondria

Using spinning disk laser scanning confocal microscopy, we visualized vRNPs localized in the mitochondrial network at 3 h post infection (h.p.i.). At this time point, vRNPs were not imported into the nucleus of human lung epithelial cells yet, whereas nuclear import was completed at 5 h.p.i. (Supplementary Fig. 1a). Therefore, we chose the 3 h.p.i. time point to investigate initial immune responses independent of viral replication in a physiological infection situation. In three-dimensional stochastic optical reconstruction microscopy (STORM), internalized vRNPs appeared as elongated, spiral structures (helical-like) of about 100–200 nm in length associated with the mitochondrial outer membrane (Fig. 1a–e, Supplementary Fig. 1b–f and Supplementary Movie 1), supporting previous structural determination of helical vRNPs by cryo-EM^10,11. At the same time RIG-I and the type I IFN signalling integrator MAVS are localized to the outer surface of the mitochondria and are distinctly positioned next to the vRNPs (Fig. 1d,e), suggesting trafficking of RIG-I-bound vRNPs to the mitochondria followed by interaction with MAVS (hypothesized model shown in Fig. 1f).

**Figure 1: High-resolution visualization of internalized IAV vRNPs revealed helical-like structure in close proximity to RIG-I and MAVS at the mitochondrial membrane.**

Although the apparent close proximity of either RIG-I or MAVS with vRNPs would suggest activation of the type I IFN-inducing pathway, we were not able to detect induction of the pathway at this time point (Supplementary Fig. 2). This emphasized the idea that before the expression of IAV genes, proteins of the vRNPs must inhibit RIG-I-mediated type I IFN induction.

Incoming vRNPs prevent type I IFN induction via PB1/PA

We identified an amino-acid signature in the polymerase proteins PB1 (398E/524S/563I) and PA (351E)—referred to as ESIE-motif—that determines type I IFN inhibitory properties, as previously observed¹². Disruption of the motif resulted in an enhanced type I IFN response upon viral infection as indicated by a stronger phosphorylation of STAT1 in human lung and bronchial epithelia (Fig. 2a, Supplementary Figs 3a,b, 4a,b) and elevated mRNA levels of IFN-related genes (Supplementary Fig. 3c) independent of any detectable changes in polymerase activity (Fig. 2b). Elevated mRNA levels of IFN-β were observed even in the presence of the translational elongation inhibitor cycloheximide that prevents viral protein synthesis and thereby viral replication (Fig. 2c, Supplementary Fig. 4c). Also, analysis of the oligomeric state of IRF3 revealed activation of the protein even upon blocking primary viral transcription with actinomycin D, confirming internalized vRNPs as one stimulus of the RIG-I-mediated type I IFN response (Fig. 2d, Supplementary Fig. 4d). Differences to a recent study by Killip and co-workers that seemingly ruled out internalized vRNPs as inducer of the type I IFN response⁵ are likely due to the type I IFN antagonistic properties of the polymerase proteins expressed by the analysed virus strains. The respective PB1 and PA proteins harbour amino acids in the ESIE-motif expected to antagonize IFN induction sufficiently, which might explain the lack in an early type I IFN response.

**Figure 2: The ESIE-motif within PB1 and PA mediates type I IFN response.**

The IFN antagonism of PB1/PA enhances virulence in vivo

To explore the functionality of the ESIE-motif in the context of complex immune regulatory processes within an organism, we infected mice and monitored survival, viral lung load and expression of IFN-β in mouse lungs. A mouse strain-independent reduction in morbidity and mortality was accompanied by diminished viral lung titres and elevated IFN-β mRNA levels attributable to abrogation of the domain (Fig. 2e–j, Supplementary Fig. 3d,e), suggesting a central immune regulatory function of the ESIE-motif for viral fitness. The functional link between the type I IFN antagonistic function of the ESIE motif and virulence was verified in mice lacking functional receptors for both type I and type III IFN (Ifnar1^−/−Ifnlr1^−/−). In such mice, pathogenicity and replication behaviour of wild-type and mutant virus were indistinguishable (Fig. 2h–j). Comparable results were seen in Stat1^−/− mice (data not shown). The type I IFN antagonistic function of the ESIE-motif is independent of the IAV subtype, as also in highly pathogenic H5N1 and H7N7 viruses the complete disruption of the motif caused an enhanced type I IFN response (Fig. 2k, Supplementary Fig. 3f,g and 4e,f).

PB1/PA-mediated IFN antagonism complements the action of NS1

We next generated a recombinant NS1 mutant virus (H1N1-NS1 96/97) lacking the ability to inhibit the type I IFN response via interaction with TRIM25 (ref. 8). Disruption of either the TRIM25-mediated type I IFN antagonistic properties of NS1 or of the ESIE-motif within PB1/PA separately caused a similar reduction in mortality and viral lung load, whereas the combination of both alterations had an additive effect (Supplementary Fig. 5a,b). This argues for an autonomous IFN antagonistic function of PB1/PA with a contribution to viral fitness similar to that of NS1-mediated TRIM25 inhibition. Further, the putative temporal differences in utility of the two systems suggest complementary functions in inhibition of the early and late activities of type I IFN.

Recruitment of vRNPs to mitochondria is affected by PB1/PA

To further analyse the mechanism of disruption of the type I IFN pathway, we used spinning disk laser scanning confocal microscopy to visualize internalized vRNPs and analysed the distance of vRNPs to mitochondria. Numbers of vRNPs associated to mitochondria were normalized to total numbers of vRNPs. We found that disruption of the ESIE-motif caused enhanced recruitment (1.5-fold) of incoming vRNPs to mitochondria (Fig. 3a,b) resulting in elevated IFN-β mRNA levels (1.5-fold) 3 h.p.i. (Fig. 3c). This indicates a spatial-temporal interplay of vRNP-RIG-I recruitment to mitochondria and type I IFN induction. The interaction with mitochondria-associated MAVS is a consequence of RIG-I activation as early step in the type I IFN signalling pathway. These results suggest that the type I IFN antagonistic properties of PB1/PA are targeted especially to the early induction phase via internalized vRNPs. The polymerase proteins bind to the 5′end of the viral genome, suggesting close proximity to interacting RIG-I. Co-immunoprecipitation (IP) of overexpressed proteins revealed complex formation of RIG-I and PB1/PA, indicating a direct interaction of these proteins, independent of the basal interaction of RIG-I with vRNPs mediated by the RNA 5′-triphosphate termini. This interaction was dependent on a functional ESIE-motif (Fig. 3d, Supplementary Fig. 4g). Based on these data, we suggest interaction of PB1/PA with RIG-I as potential mechanism to interfere with RIG-recruitment to mitochondria.

**Figure 3: Disruption of the ESIE-motif results in enhanced recruitment of incoming vRNPs to mitochondria.**

Insufficient structural data are available to determine the precise positions of the amino-acid residues forming the ESIE-motif in the secondary structure. A suggested model of the IAV polymerase heterotrimer predicts the E351 of PA to be on the protein surface and in proximity to PB1 (ref. 13). Based on this, we suggest the ESIE-motif as functional motif formed through the tertiary structure of the influenza polymerase heterotrimer that directly interacts with RIG-I and subsequently inhibits RIG-I-mediated type I IFN signalling, completing the picture of the type I IFN inhibitory capacity of the polymerase proteins^{12,13,14,15,16}. PB1 and PA are already present when internalized vRNPs are sensed by RIG-I and are located in close proximity to the site of RIG-I activation. First evidence for the presents of NS1 in influenza virions⁹ give rise to the assumption that co-evolution of several type I IFN counteracting strategies has taken place.

Amino-acid 398 in PB1 is evolutionary dynamic

Phylogenetic analysis to explore the occurrence of the ESIE-motif in IAV lineages revealed evolutionary variability of the position 398 in the PB1 protein, whereas the other three amino acids of the motif were highly conserved. Multiple swine and avian IAV lineages with a sustained D to E change at position 398 in the PB1 protein suggest selection of a fully intact ESIE-motif (Supplementary Fig. 6a,b). Focusing on swine IAV lineages, a D to E change occurred in the North America ‘classical’ swine lineage in the mid-1970s and persists in circulating strains until today (Supplementary Fig. 7). The 2009 pandemic H1N1 virus derived its genes from a reassortment event of the triple reassortant swine H1N2 lineage and the Eurasian swine H1N1 lineage^17,18,19,20 (Supplementary Fig. 8). Factors that dictate reassortment efficiency between allelic influenza virus gene segments are poorly characterized²¹. Nevertheless, as internal genes like the PB1 gene evolve slowly and do not show a high degree of host-specific evolution, they are frequently replaced during reassortment²². Thus, it remains possible that a novel pandemic virus may derive the PB1 segment from the North American ‘classical’ swine lineage or certain avian IAV populations encoding for PB1 398E resulting in completion of the ESIE-motif and potentially enhanced virulence.

Restoration of the ESIE-motif increases virulence of pdmH1N1

As an experimentally proof of this hypothesis, we introduced the functional ESIE-motif into the 2009 pandemic H1N1 virus, a strain usually lacking the complete motif by carrying PB1 398D. We observed enhanced antagonism of the type I IFN response (Fig. 4a, Supplementary Fig. 9a) independent of significant changes in polymerase activity (Fig. 4b) and even independent of viral replication (Fig. 4c). Increased morbidity and mortality were accompanied by enhanced viral load and diminished IFN-β mRNA levels in the lung of mice (Fig. 4d–f). This suggests the risk of multiple host lineage reassortant viruses—like foregone the 2009 pandemic H1N1 virus—with increased virulence mediated by the ESIE-motif.

**Figure 4: Introduction of the ESIE-motif in a pandemic H1N1 virus increases pathogenicity.**

Of note, a recombinant 2009 pandemic H1N1 virus mutant with PB1 398G—an amino acid change that disrupts the motif similar to the virus mutants H1N1-hIFN, H5N1-hIFN and H7N7-hIFN presented here—was highly attenuated (data not shown), suggesting the type I IFN antagonistic properties mediated by PB1 398D as sufficient for viral fitness, but PB1 398E as even more potent variant. In contrast to glycine (G), aspartic acid (D) and glutamic acid (E) both are negatively charged amino acids of related structure, suggesting a vital role of the position 398 in the PB1 protein.

In summary, we visualized IAV vRNPs in three-dimensional high-resolution light microscopy as helical-like structures associated with the mitochondrial outer membrane, despite the absence of an early type I IFN response. We identified PB1 and PA as new players in the type I IFN inhibitory strategy evolved by IAV, filling the gap in knowledge regarding early suppression of antiviral immune responses. The functional plasticity of IAV polymerase proteins emphasizes the evolutionary pressure for viruses with small genomes to evolve multifunctional proteins with temporally and spatially separated functions.

Methods

Viruses, cells, infection conditions and inhibitors

The following viruses were used: A/Puerto-Rico/8/34 (H1N1), A/Thailand/1(KAN-1)/2004 (H5N1), mouse-adapted A/Seal/Massachusetts/1/80 (H7N7)²³ and the pandemic H1N1 strain A/Hamburg/04/2009 (pdmH1N1). Recombinant viruses were generated using the pHW2000-based reverse genetic system (a kind gift of Dr Robert G. Webster, Memphis, TN, USA)²⁴. The following mutations were introduced by site-directed mutagenesis and confirmed by sequencing: H1N1-hIFN PB1 E398G PB1 S524G PB1 I563R PA E351K; H5N1-hIFN PB1 D398G PB1 S524G PA E351K; H7N7-hIFN PB1 D398G PB1 S524G PA E351K; pdmH1N1-lowIFN PB1 D398E PB1 R563I and H1N1-NS1 E96A NS1 E97A⁸. Primer sequences are provided in Supplementary Table 1. For generation of recombinant viruses, HEK293 were transfected with 1 μg of each of the eight plasmids using Trans-IT LT1 (Mirus) according to the manufacturer’s protocol. Cells were cultivated in DMEM supplemented with 0.2% bovine serum albumin. 6 h post transfection, medium was changed to DMEM supplemented with 0.2% bovine serum albumin, 1 mM MgCl₂, 0.9 mM CaCl₂, 100 U ml⁻¹ penicillin, 0.1 mg ml⁻¹ streptomycin and 0.3 μg ml⁻¹ TPCK-trypsin. 48 h post transfection, the supernatant was used for infection of Madin–Darby canine kidney cells (MDCK). All viruses were propagated in MDCK cells and handled under biosafety level 2 or 3 conditions. Virus titres were determined by plaque assay and haemagglutinin titration assay²⁵.

The human lung epithelial cell line A549 (American Type Culture Collection (ATCC)) was cultivated in DMEM (Lonza), whereas MDCK cells (ATCC) were cultivated in MEM (Lonza), both supplemented with 10% heat-inactivated fetal calf serum. NHBE cells (Lonza) were cultivated following the manufacturer’s protocol. U937 (ATCC) were cultivated in RPMI media (Lonza) supplemented with 10% fetal calf serum upon differentiation with 200 nM phorbol-12-myristate-13-actete (Sigma).

For infection, cells were inoculated with IAV at the indicated multiplicities of infection in PBS supplemented with 0.2% bovine serum albumin, 1 mM MgCl₂, 0.9 mM CaCl₂, 100 U ml⁻¹ penicillin and 0.1 mg ml⁻¹ streptomycin for 30 min at 37 °C following incubation with either DMEM or MEM supplemented with 0.2% BSA, 100 U ml⁻¹ penicillin and 0.1 mg ml⁻¹ streptomycin. Infections were performed in technical duplicates (western blot analysis) or triplicates (quantitative real-time PCR analysis).

Cycloheximide (Sigma) was used at 50 μg ml⁻¹ and actinomycin D (Sigma) at 1 μg ml⁻¹. Both were added to the medium 30 min before infection and throughout the infection period.

Minireplicon luciferase assay and transient transfection

Cells were transfected with Trans-IT LT1 (Mirus) according to the manufacturer’s protocol. To generate pcDNA3-H1N1-PB1-WT, pcDNA3-H1N1-PA-WT, pcDNA3-H1N1-PB1-hIFN and pcDNA3-H1N1-PA-hIFN, H1N1-WT- and H1N1-hIFN-derived PB1 and PA open reading frames were amplified from pHW2000-H1N1-PB1 or pHW2000-H1N1-PA and linked to a NotI and XbaI restriction site using the primer sets 5NotPB1 (5′-ATAAGAATGCGGCCGCTATGGATGTCAATCCG-3′) and 3XbaPB1 (5´-GTGTCTAGACTATTTTTGCCGTCTGAGCTCT-3′), and 5NotPA (5′-ATAAGAATGCGGCCGCTATGGAAGATTTTGTG-3′) and 3XbaPA (5′-GTGTCTAGACTAACTCAATGCATGTGTAAGG-3′) and inserted into pcDNA3. The generated plasmids together with pcAGGS-RIG-I-FLAG²⁶ were used for overexpression of the corresponding proteins and empty vectors served as control.

For the minireplicon luciferase assay, cells were transfected with plasmids encoding an antisense luciferase reporter gene flanked by the influenza promoters of the M-segment (pHW72-luc-vector; 0.5 μg) and the polymerase subunits PB2, PB1, PA (0.25 μg each) and NP (0.5 μg) of A/Puerto-Rico/8/34 (H1N1; pHW2000-vector) or A/Hamburg/04/2009 (pdmH1N1; pHW2000-vector). As negative control, cells were transfected with the same set of plasmids but leaving out the PB1 expression construct. 24 h post transfection, cells were harvested and measurement of luminescence was performed as described earlier²⁷.

Microscopy

A549 cells were grown on #1.5 chambered cover glasses. 3 h.p.i., cells were fixed for 10 min with 4% (v/v) paraformaldehyde and 0.1% (v/v) glutaraldehyde in PBS. Cells were briefly washed before quenching of reactive groups with 0.1% (w/v) sodium borohydride for 10 min and rinsed with TBS, before permeabilization with TBS containing 0.1% (v/v) Triton X-100 for 3 min. Cells were rinsed with TBS and blocked with TBS containing 2% bovine serum albumin before labelling of vRNPs with antibodies specific for viral NP (1:1,000; AbD serotec; MCA400), the outer mitochondrial membrane (1:1,000; Tom20; SCBT; sc-11415), RIG-I (1:500; Cell Signaling; #4520) and MAVS (1:200; Pierce; PA5-17256). Nuclear stain was performed using Hoechst 33258 (Life Technologies; H3569). Following incubation, cells were rinsed with TBS, and primary antibodies were detected using goat anti-mouse AF568 (1:2,000; Life Technologies; A11031), goat anti-rabbit AF647 (1:2,000; Life Technologies; A21245) goat anti-mouse ATTO488 (1:2,000; Labome; 610152121) secondary antibodies. Biotinylation was performed using EZ-Link Sulfo-NHS-LC-Biotin and Biotinylation Kits according to the manufacturer’s protocol (Pierce; 21435). Three-dimensional spinning-disc confocal images were acquired with a step size of 0.4 μm, and analysed using Imaris 7.6.5 software (Bitplane). Surfaces were created to segment mitochondria and vRNPs. The distance from each vRNP to the closest mitochondrial surface was measured via an intensity to distance transform. At least seven images were analysed per experiment (n=3) with at least 40 cells analysed per group.

Samples were similarly prepared for analysis of viral NP, RIG-I, MAVS and mitochondrial proteins using STORM²⁸. In brief, samples prepared as above were imaged using the N-STORM system built on a Nikon-Ti-E inverted microscope with a CFI SR Apo 100X TIRF objective having an numerical aperture of 1.49. Illumination was provided using an Agilent laser launch containing four laser lines, which were combined into a single optical fiber and collimated onto the back focal plane of the objective. Nominal output was measured as 20 mW for 405 nm, 80 mW for 488 and 561 nm, and 125 mW for 647 nm. Fluorescence emission was collected using an iXon DU897 Ultra EMCCD camera running at frame rate of 109 f.p.s. with EM Gain 17 mHz at 16-bit. 3D STORM was accomplished by insertion of an astigmatic lens into the light path before detection by a high-speed camera²⁹. Calibration of z data was performed using 100 nm fluorescent beads and a z-stepping range of 800 nm (ref. 29). To facilitate STORM using AF568 and AF647 fluorescent probes, samples were imaged for 40,000 frames in buffer comprised of 50 mM Tris-HCl, pH 7.0, 50 mM NaCl and 10% glucose, and containing freshly prepared 10 mM cysteamine, 0.2 mg ml⁻¹ catalase and 0.5 mg ml⁻¹ glucose oxidase. The reconstructed 3D STORM image was created using algorithms for molecule identification and drift correction as previously described²⁹ and employed by Nikon Instruments.

Electrophoresis, western blotting and IP

After infection, cells were lysed on ice with RIPA lysis buffer (25 mM Tris-HCl, pH 8.0, 137 mM NaCl, 10% glycerol, 0.1% SDS, 0.5% deoxycholic acid (DOC), 1% NP40, 2 mM EDTA pH 8.0, 5 μg ml⁻¹ leupeptin, 5 μg ml⁻¹ aprotinin, 0.2 mM Pefabloc, 1 mM sodium vanadate and 5 mM benzamidine) for 30 min and cleared from debris by centrifugation at 14,000 r.p.m. for 10 min at 4 °C. Protein concentrations were determined by Bradford assay. For SDS–polyacrylamide gel electrophoresis (PAGE) samples were prepared with 5 × denaturing sample buffer (312 mM Tris-HCl, pH 6.8, 10% SDS, 50% glycerol, 25% β-mercaptoethanol and 0.01% bromphenol blue), heated for 10 min at 95 °C, loaded on a SDS–polyacrylamide gel with a 4% stacking over a 10% resolving gel and separated at 15 mA per gel using electrophoresis buffer (25 mM Tris, 250 mM glycine, 0.1% SDS). Proteins were transferred to a nitrocellulose membrane using a wet blotting system at 400 mA for 60 min in transfer buffer (25 mM Tris, 192 mM glycin, 20% methanol). Blocking and probing with antibodies were performed following manufacturer’s protocols. STAT1 phosphorylation was analysed with a phospho-specific anti-STAT1 [pY701] rabbit mAb (1:1,000; Cell Signaling; #9171). Viral proteins were detected in western blot (WB) analysis by using an anti-NS1 mouse mAb (1:500; clone NS1-23-1; developed at the IMV, Muenster, Germany) and anti-M1 mouse mAb (1:1,000; Serotec; MCA401). Anti-ERK2 (C-14) rabbit pAb (1:1,000; Santa Cruz; sc-154) and anti-STAT1 rabbit pAb (1:1,000; Cell signaling; #9172) were used in WB analysis for loading controls. The oligomeric active state of IRF3 was analysed in native PAGE³⁰ followed by WB probing for IRF3 with an anti-IRF3 rabbit mAb (1:1000, Santa Cruz; sc-9082). Protein bands were visualized by standard enhanced chemiluminescence reaction. WBs were quantified using ImageJ 1.48v. pSTAT1 bands were normalized to STAT1 bands. NS1 and M1 bands were normalized to ERK2 bands. Depicted are the fold changes of band intensities of mutant viruses compared with wild-type viruses.

For IP cells were processed as described elsewhere³¹. Briefly, cells were lysed on ice with triton lysis buffer (20 mM Tris-HCl, pH 7.4, 137 mM NaCl, 10% glycerol, 1% Triton X-100, 2 mM EDTA, 50 mM sodium glycerophosphate, 20 mM sodium pyrophosphate, 5 μg ml⁻¹ leupeptin, 5 μg ml⁻¹ aprotinin, 0.2 mM Pefabloc, 1 mM sodium vanadate and 5 mM benzamidine) for 30 min and cleared by centrifugation at 14,000 r.p.m. for 10 min at 4 °C following incubation with protein A agarose for 1 h in an overhead shaker to minimize unspecific precipitation. Anti-RIG-I rabbit mAb (2 μg; Cell Signaling; #3743) was coupled to protein A agarose by incubation at 300 r.p.m. for 3 h at 4 °C before samples were added and incubated in an overhead shaker over night at 4 °C. Samples were washed three times with triton lysis buffer, prepared with 5 × denaturating sample buffer, heated for 10 min at 95 °C and subjected to SDS–PAGE. As IP-input controls, lysates were directly subjected to SDS–PAGE and WB analysis. RIG-I was visualized by the RIG-I antibody mentioned above. PB1 was detected by anti-PB1 rabbit Ab (1:1,000; GenScript; A01467). Anti-Tubulin rabbit mAb (1:1,000; Cell Signaling; #2128) was used for loading controls.

Quantitative real-time PCR (qRT–PCR)

Total RNA was isolated with the RNeasy mini kit (Qiagen) according to the manufacturer’s protocol. For cDNA synthesis, a total of 1 μg RNA and M-MLV Reverse Transciptase (Promega) were used. PCR was performed with QuantiFast SYBR Green PCR Kit (Qiagen) and carried out on a 7300 Real-Time PCR System (Applied Biosystem). Human IFN-β mRNA was detected with a specific QuantiTect primer assay (Qiagen; Hs_IFNB1_1_SG) and normalized against HPRT (Qiagen; Hs_HPRT_1_1_SG) using the 2^−ΔΔCT method³². Upregulation is depicted in relation to non-infected cells. Transcriptome analysis for type I IFN-related genes in U937 cells was performed by using the RT² Profiler PCR Array Human Interferons and Receptors (Qiagen, PAHS-064) according to the manufacturer’s instructions. Upregulation in PR8-hIFN-infected cells is depicted in relation to PR8-WT-infected cells.

Ethics statement

The Animal Care and Use Committee at St. Jude Children’s Research Hospital approved all mouse studies with wild-type mice. Experiments with IFN receptor-deficient mice were approved by the local animal welfare authority (Regierungspräsidium Freiburg) according to the local law and animal ethics regulations.

Mouse experiments

Eight-week-old female BALB/c, C57Bl/6, DBA/J2, Stat1^−/− mice (Jackson Laboratory) and Ifnar1^−/−Ifnlr1^−/− mice (male and female in mixed groups)³³ were used for the mouse studies. For infection, mice were anaesthetized either by intraperitoneal injection of 100 mg ketamine (Ceva) and 5 mg of xylazine (Ceva) per kg of body weight or by inhalation of 2.5% isoflurane (Baxter Healthcare Corporation). Mice were infected intra nasally (i.n.) with the indicated viruses and plaque-forming units (PFUs) in a 50 μl volume and monitored daily for disease symptoms, body weight and survival. Owing to animal welfare restrictions, mice were euthanatized upon a body weight loss of 25%.

Virus titres and cytokine levels in mouse lungs

For quantification of infectious virus particles in infected mouse lungs, mice were euthanatized on day 3 p.i. and lungs were collected in PBS. The lungs were homogenized using a FastPrep-24 homogenisator with Lysing Matrix D (MP Biomedical). PBS was added to obtain 10% tissue homogenates. The samples were centrifuged and the supernatants were used for determination of virus titres in standard plaque titration as described elsewhere²⁴. For analysing cytokine levels in total mouse lungs, animals were euthanatized on day 2 p.i. and lungs were collected in Trizol. For isolation of RNA, a modification of the RNAzol method was used³⁴. Reverse transcription and qRT–PCR reactions were conducted as described above. Murine IFN-β mRNA was detected with a specific QuantiTect primer assay (Qiagen; ifb1_1_SG mouse) and normalized against GAPDH (Qiagen; gapdh_3_SG mouse).

Phylogenetic analysis

All complete avian, human and swine PB1-coding sequences were acquired from FLUDB and translated into proteins. They were clustered at 98% identity to remove redundancy using USEARCH and aligned using MUSCLE with default options^35,36. Phylogenetic tree construction was performed using BEAST with the FLU substitution model and allowing gamma-distributed rates across sites^37,38. A relaxed molecular clock was assumed, with log-normally distributed branch rates. Default priors were used in all cases except for ucld.mean (exponential with mean 0.005) and ucld.stdev (exponential with mean 0.333). Fifty million generations of MCMC were performed. Phylogenetic analysis of representative viruses of the North American swine lineage and Eurasian swine lineage was conducted using MEGA5 (ref. 39).

Additional information

How to cite this article: Liedmann, S. et al. Viral suppressors of the RIG-I-mediated interferon response are pre-packaged in influenza virions. Nat. Commun. 5:5645 doi: 10.1038/ncomms6645 (2014).

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Acknowledgements

We thank Dr Richard Webby and Dr Stephen White for reviewing the manuscript, Dr Jennifer Peters for technical support with image analysis, Michaela Weber and Dr Friedemann Weber for support regarding analysis of IRF3 activation and Joshua Stokes for graphic support. This work was supported by grants of the Deutsche Forschungsgemeinschaft (DFG EH 235 1-2, DFG Lu477/16-1, DFG Graduate School 1409, SFB1009), the FluResearchNet, a nationwide research network to study zoonotic influenza sponsored by the Federal Ministry of Education and Research (BMBF) and the American Lebanese Syrian Associated Charities. E.R.H. was supported by the DFG.

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Authors and Affiliations

Institute of Molecular Virology (IMV), Center for Molecular Biology of Inflammation (ZMBE), University of Muenster, Von-Esmarch-Street 56, Muenster, D-48149, Germany
Swantje Liedmann, Darisuren Anhlan, Rüdiger Dierkes, Stephan Ludwig & Christina Ehrhardt
Department of Infectious Diseases, St. Jude Children’s Research Hospital, 262 Danny Thomas Place, Memphis, 38105-3678, Tennessee, USA
Eike R. Hrincius & Jonathan A. McCullers
Department of Immunology, St. Jude Children’s Research Hospital, 262 Danny Thomas Place, Memphis, 38105-3678, Tennessee, USA
Cliff Guy & Douglas R. Green
Department of Computational Biology, St. Jude Children’s Research Hospital, 262 Danny Thomas Place, Memphis, 38105-3678, Tennessee, USA
Robert Carter & Gang Wu
Institute of Virology, University Medical Center Freiburg, Hermann-Herder-Street 11, Freiburg, D-79104, Germany
Peter Staeheli
Division of Influenza and Other Respiratory Viruses, Seestraβe 10, Robert Koch-Institut, Berlin, D-13353, Germany
Thorsten Wolff
Department of Pediatrics, University of Tennessee Health Sciences Center, 50 N. Dunlap, Memphis, 38103, Tennessee, USA
Jonathan A. McCullers
Cluster of Excellence Cells in Motion, University of Muenster, Muenster, Germany
Stephan Ludwig & Christina Ehrhardt

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Swantje Liedmann
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Eike R. Hrincius
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Cliff Guy
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Darisuren Anhlan
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Rüdiger Dierkes
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Robert Carter
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Gang Wu
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Peter Staeheli
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Douglas R. Green
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Thorsten Wolff
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Jonathan A. McCullers
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Stephan Ludwig
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Christina Ehrhardt
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Contributions

Sw.L. designed the study, collected and analysed data and wrote the paper; E.R.H. collected data and was involved in study design and manuscript preparation; C.G. performed spinning disc microcopy and STORM analysis; D.A., R.D. and P.S. collected data; G.W. and R.C. performed bioinformatical sequence analysis; D.R.G. and T.W. were involved in study design, J.A.M., St.L. and C.E. were involved in study design and manuscript preparation.

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Correspondence to Stephan Ludwig.

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Supplementary Information

Supplementary Figures 1-9, Supplementary Table 1 and Supplementary References (PDF 8630 kb)

Video - Supplementary Movie1

High-resolution visualization of internalized IAV vRNPs revealed helical-like structure. (MOV 1060 kb)

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Liedmann, S., Hrincius, E., Guy, C. et al. Viral suppressors of the RIG-I-mediated interferon response are pre-packaged in influenza virions. Nat Commun 5, 5645 (2014). https://doi.org/10.1038/ncomms6645

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Received: 01 April 2014
Accepted: 23 October 2014
Published: 09 December 2014
DOI: https://doi.org/10.1038/ncomms6645

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