Generation of a variety of stable Influenza A reporter viruses by genetic engineering of the NS gene segment

Reuther, Peter; Göpfert, Kristina; Dudek, Alexandra H.; Heiner, Monika; Herold, Susanne; Schwemmle, Martin

doi:10.1038/srep11346

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Published: 12 June 2015

Generation of a variety of stable Influenza A reporter viruses by genetic engineering of the NS gene segment

Peter Reuther^1,2^na1,
Kristina Göpfert¹^na1,
Alexandra H. Dudek^1,2,3^na1,
Monika Heiner⁴^na1,
Susanne Herold⁴^na1 &
…
Martin Schwemmle¹^na1

Scientific Reports volume 5, Article number: 11346 (2015) Cite this article

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Abstract

Influenza A viruses (IAV) pose a constant threat to the human population and therefore a better understanding of their fundamental biology and identification of novel therapeutics is of upmost importance. Various reporter-encoding IAV were generated to achieve these goals, however, one recurring difficulty was the genetic instability especially of larger reporter genes. We employed the viral NS segment coding for the non-structural protein 1 (NS1) and nuclear export protein (NEP) for stable expression of diverse reporter proteins. This was achieved by converting the NS segment into a single open reading frame (ORF) coding for NS1, the respective reporter and NEP. To allow expression of individual proteins, the reporter genes were flanked by two porcine Teschovirus-1 2A peptide (PTV-1 2A)-coding sequences. The resulting viruses encoding luciferases, fluorescent proteins or a Cre recombinase are characterized by a high genetic stability in vitro and in mice and can be readily employed for antiviral compound screenings, visualization of infected cells or cells that survived acute infection.

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Introduction

Influenza A viruses (IAV) cause severe respiratory illness in humans and account for 250,000–500,000 annual deaths worldwide¹. Especially zoonotic transmission of IAV from avian reservoirs poses a constant threat to the human population², as exemplified recently by several fatal human cases upon H5N1 or H7N9 infections^3,4. Albeit infrequently, avian IAV can also establish new, aerosol-transmissible virus lineages in humans, resulting in devastating pandemics with high morbidity and mortality². The development of effective countermeasures, such as vaccines or therapeutics has been complicated by the ability of the viruses to rapidly mutate antigenic determinants or antiviral target structures^5,6,7. Improved vaccine approaches, identification of new antivirals and in general a better understanding of the fundamental biology of IAV infection is required to efficiently antagonize these human pathogens in future^8,9.

To achieve these tasks, a number of IAV encoding luciferases^{10,11,12,13,14,15} or fluorescent proteins^15,16,17,18 have been recently generated. The genome of IAV consists of 8 RNA segments with negative polarity¹⁹. These segments are numbered according to their size ranging from 2.3 kb (segment 1) to 0.9 kb (segment 8). Segments 1–3 encoding the polymerase subunits PB2, PB1 and PA respectively, segment 6 coding for the neuraminidase (NA) and segment 8 (NS) encoding both the non-structural protein 1 (NS1) and the nuclear export protein (NEP) have been shown to tolerate insertion of foreign genes, including that for the green fluorescence protein (GFP) with a length of around 0.7 kb^{11,12,13,14,15,16,17,18}. However, the integration of a reporter gene of this size represents a substantial increase of the overall segment length and is accompanied by substantial attenuation of viral replication^11,14,15,16. As a consequence, especially viruses comprising the GFP gene were shown to lose reporter activity after passage in cell culture or mice^15,16,20, which could render them unfavorable for many experimental approaches, such as multicycle growth experiments, long-term infection of model organisms or transmission studies.

The NS-segment comprises two overlapping ORFs coding for NS1 and NEP. While NS1 is translated from an intron-containing mRNA transcript, the NEP mRNA is generated by exploitation of the cellular splicing machinery (Fig. 1A)²¹. Manicassamy et al. were the first to utilize the NS-segment as vector for transgene expression in influenza A virus infected cells¹⁶. There, an NS1-GFP fusion protein and NEP are encoded by two non-overlapping genes, which are separated by the porcine Teschovirus-1 2A peptide (PTV-1 2A) coding sequence. PTV-1 2A mediates co-translational separation of NS1-GFP and NEP by a mechanism termed “stop-carry on” recoding²². The NS1-GFP expressing virus was found to be attenuated in cell culture and mice and it was proposed that this attenuation is based on an imbalance of NS1 and NEP protein levels, as the coordinated expression of both proteins is no longer regulated by splicing²³. In contrast to the NS1-GFP-expressing virus, however, we could recently show that processing of NS1 and NEP from two non-overlapping genes separated by PTV-1 2A does not result in detectable impairment of viral replication in cell culture and mice²⁴. Based on this favorable property of PTV-1 2A, we engineered influenza A viruses harboring an NS segment encoding reporter genes flanked by two genetically distinct PTV-1 2A-encoding sequences. These viruses are genetically stable in cell culture and mice and express a variety of luminescent and fluorescent reporters as well as a Cre recombinase.

Results

PTV-1 2A-mediated co-translational separation of NS1 and NEP does not interfere with viral replication

To confirm that the NS-segment of the mouse-adapted IAV A/SC35M (H7N7)²⁵ allows satisfying co-translational separation of NS1 and NEP, we generated a pHW2000 based²⁶ rescue plasmid (NS1_2A_NEP) that encodes NS1 and NEP in a single ORF (Fig. 1A). Here, the splice donor and acceptor sites of the NS1 gene were silenced by site-directed mutagenesis without affecting the amino acid sequence. A PTV-1 2A-coding sequence was introduced to mediate co-translational separation of NS1 and NEP. As expected from our previous work²⁴, a recombinant virus carrying this modified NS-segment (SC35M_{NS1_2A_NEP}) replicates as efficiently as wild type SC35M (SC35M_WT) in mammalian MDCK-II cells (Fig. 1B). To analyze whether this modified NS-segment causes an altered NS1:NEP protein ratio during infection, we determined the levels of these proteins in the lysates of MDCK-II cells infected with SC35M_WT or SC35M_{NS1_2A_NEP} at a multiplicity of infection (MOI) of 0.1. As shown in Fig. 1C, NS1 (26 kDa) and NEP (14.5 kDa) protein levels were comparable between the two viruses 24 hours post infection (h.p.i.). However, we also detected a 40 kDa band corresponding to an NS1-2A-NEP polyprotein with both an NS1- and an NEP-specific antibody in the cell lysate of SC35M_{NS1_2A_NEP}-infected cells, indicating that the 2A-mediated “stop-carry on” recoding is not completely efficient.

Fusion of a GFP to the nuclear export protein (NEP) results in compromised viral growth

Based on recent observation that N-terminally GFP-tagged NEP (GFP-NEP) retains its nuclear export and polymerase co-factor function in vitro^27,28, we reasoned that reporter genes might be introduced into the viral genome as NEP-fusion constructs. To demonstrate this, we generated a pHW2000-based NS segment rescue plasmid coding for NS1, 2A and a GFP-NEP fusion protein (Fig. 2A). Using this plasmid, we could indeed successfully generate a recombinant GFP-encoding virus (SC35M_{NS1_2A_GFP-NEP}). SC35M_{NS1_2A_GFP-NEP} is characterized by severe attenuation in MDCK-II cells, which was most obvious at 24 and 36 h.p.i., when viral titers in the cell supernatant were reduced by several log₁₀ relative to cells infected with SC35M_WT (Fig. 2A). In contrast to SC35M_{NS1_2A_NEP} (Fig. 1C), we observed highly elevated levels of NEP in lysates of cells infected with SC35M_{NS1_2A_GFP-NEP} (Fig. 2B). This is consistent with earlier observations that fusion of GFP increases the stability of NEP²⁷ and that higher levels of NEP impair viral growth²³. Although there is an increasing body of evidence that NEP is a multifunctional protein crucial for vRNP nuclear export, polymerase activity and viral budding^29,30, little is known about the spatiotemporal regulation of these diverse functions. As we hardly detected any NS1-2A-GFP-NEP polyprotein in the lysate of SC35M_{NS1_2A_GFP-NEP}-infected cells (Fig. 2B), this virus might serve as a valuable tool for the visualization of changes in the subcellular localization of NEP or its interaction with host factors in the course of an infection.

Introduction of a second PTV-1 2A peptide permits the generation of stable reporter viruses

The fusion of GFP to NEP substantially compromised viral growth (Fig. 2A). Since this represents a major drawback for many experimental approaches, we set out to generate rescue plasmids allowing the expression of a gene of interest without its fusion to NS1 or NEP. To achieve this, we introduced a second PTV-1 2A-coding sequence between the transgene and NEP (Fig. 3A). This sequence was genetically modified to the highest possible extent to prevent homologous recombination with the non-modified PTV-1 2A nucleotide sequence (see Material and Methods). Using this approach, we were able to rescue viruses encoding three different fluorescent reporter genes: GFP (SC35M_{NS1_2A_GFP_2A_NEP}), its blue fluorescent derivate Azurite (SC35M_{NS1_2A_Azurite_2A_NEP})³¹ and the red fluorescent protein dsRed (SC35M_{NS1_2A_dsRed_2A_NEP}). All reporter viruses replicated to similar high viral titers of 10⁸ PFU/ml 36 h.p.i., which represents an attenuation of approximately one log₁₀ relative to SC35M_WT (Fig. 3A). Replication of SC35M_{NS1_2A_dsRed_2A_NEP} was particularly delayed, as indicated by the low viral titer 24 hours post infection (Fig. 3A). As expected, infection of A549 cells with the reporter viruses resulted in well detectable fluorescence signals performing live cell imaging microscopy (Fig. 3B). To analyze the genetic stability of the modified NS segments, viruses were passaged four times in A549 cells and the proportion of reporter-expressing infectious viral particles was determined by plaque assay and subsequent fluorescent microscopy. As shown in table 1, all viruses retained their reporter gene after passaging in human cells, indicating a favorable stability of the reporter gene at least over 4 rounds of passaging. To analyze the recoding efficiency of the two PTV-1 2A peptides, NS1, GFP and NEP protein levels were determined in lysates of cells infected with SC35M_{NS1_2A_GFP_2A_NEP} (Fig. 3C). Besides detection of the three individual proteins, we observed with both GFP- and NEP-specific antibodies a protein band of approximately 40 kDa corresponding to a GFP-2A-NEP fusion protein (Fig. 3C). A faint signal, which is visible above this GFP-2A-NEP band in the GFP-immunoblot might indicate the presence of low levels of an NS1-2A-GFP construct. Interestingly, we could not visualize a high molecular weight band corresponding to an NS1-2A-GFP-2A-NEP polyprotein. Consistently, we observed high levels of unprocessed reporter proteins fused to NEP in the lysates of cells infected with SC35M_{NS1_2A_dsRed_2A_NEP} and SC35M_{NS1_2A_Azurite_2A_NEP} (Fig. S1). To further characterize the fluorescent reporter viruses in vivo, BALB/c mice were infected intranasally with 1,000 PFU of the respective viruses and viral lung titers were determined 48 h.p.i. All reporter viruses replicated to significant titers between 5 × 10⁵ and 5 × 10⁶ PFU/lung (Fig. 3D). This also included SC35M_{NS1_2A_dsRed_2A_NEP}, which showed delayed replication properties in cell culture compared to both SC35M_{NS1_2A_GFP_2A_NEP} and SC35M_{NS1_2A_Azurite_2A_NEP} (Fig. 3A). However, viral lung titers of all reporter viruses were substantially lower than the titers observed after infection of BALB/c mice with SC35M_WT. Accordingly, the LD₅₀ of the fluorescent reporter viruses is increased compared to SC35M_WT³² (Table 2). To monitor the genetic stability of the three reporter viruses in vivo, plaque assays were performed on the lung homogenates of the infected BALB/c mice and screened for reporter expression by fluorescent microscopy. This revealed that in all analyzed plaques (100/reporter virus) reporter expression was maintained, again demonstrating the high genetic stability of the here presented viruses (Table 1). To visualize spread of the reporter viruses in lungs of infected animals, BALB/c mice were infected intranasally with 10,000 PFU of SC35M_{NS1_2A_GFP_2A_NEP} or SC35M_{NS1_2A_dsRed_2A_NEP}. 48 hours post infection lungs were collected and subjected to microscopic analysis. Virus replication, as monitored by green or red fluorescence, could be observed in the epithelial layer of the bronchiolar tube (Fig. 3E, filled arrow heads) as well a in the distal lung tissues (Fig. 3E, transparent arrow heads). Taking together, these data indicate that our fluorescent reporter viruses are genetically stable and allow tracing of different virus-infected lung cells in mice.

Table 1

Full size table

Table 2 LD₅₀ of fluorescent reporter viruses.

Full size table

Generation of luciferase-encoding viruses for screening approaches

Luciferases have been proven to be valuable tools in screening approaches for the identification of novel antiviral substances or host factors^33,34,35,36. To generate a stable, luciferase-encoding virus, the gene for the Renilla luciferase (RenLuc) (~0.9 kB) was introduced into the NS-segment. MDCK-II cells infected with the resulting virus (SC35M_{NS1_2A_RenLuc_2A_NEP}) at an MOI of 0.001 released 10⁸ PFU/ml into the cell supernatant after 48 hours (Fig. 4A). However, compared to SC35M_WT-infected cultures, SC35M_{NS1_2A_RenLuc_2A_NEP} revealed impaired viral growth. To prove stable expression of luciferase, SC35M_{NS1_2A_RenLuc_2A_NEP} was passaged 4 times in human A549 cells. Reporter analysis of ten plaque-purified viruses revealed no loss of luciferase activity (Tab. 1), indicating stable expression of the RenLuc gene. To analyze whether SC35M_{NS1_2A_RenLuc_2A_NEP} could be employed for antiviral compound screenings, we treated infected MDCK-II cells with increasing concentrations of the viral polymerase inhibitor ribavirin and determined luciferase activity 24 hours post infection. As shown in Fig. 4B, RenLuc activity decreased in a dose-dependent manner reaching a baseline at approximately 100 μM of ribavirin. The classic approach to analyze the antiviral activity in cell culture is the determination of viral titers. There, effects at an early stage within the first 6 hours of infection, prior to efficient particle formation, cannot be visualized. As the expression of virus-encoded luciferase is dependent on viral RNA synthesis and not particle release, we reasoned that SC35M_{NS1_2A_RenLuc_2A_NEP} would allow quantification of antiviral activity of the viral polymerase inhibitor ribavirin at early time points post infection. To show this, SC35M_{NS1_2A_RenLuc_2A_NEP}-infected MDCK-II cells were cultured in the presence of 0, 30 or 60 μM of ribavirin and analyzed at different time points post infection for viral titers in the supernatant and luciferase activity in the cell lysate (Fig. 4C). Already at 3 h.p.i., we observed a substantial dose dependent difference in luciferase activity, whereas a first reduction of viral titers was detected at 12 hours post infection. Furthermore, we could not resolve differences in the antiviral efficacy between cells treated with 30 μM or 60 μM ribavirin by determination of viral titers, while this was possible as soon as 6 hours post infection by measuring luciferase activity.

The Gaussia luciferase (GLuc) represents an attractive luminescent reporter for many experimental approaches, not least due to its small size and its secretion from mammalian cells^37,38. Indeed, insertion of the GLuc-coding sequence into the viral NS segment revealed a recombinant virus (SC35M_{NS1_2A_GLuc_2A_NEP}), which was only partially attenuated but highly stable in cell culture (Fig. 4D, Tab.1). As expected, the supernatant of MDCK-II cells infected with this virus contained significant levels of secreted GLuc (Fig. 4E). To evaluate whether this extracellular reporter activity could be exploited as a measure for viral replication, we infected MDCK-II cells in the presence of ribavirin and determined luciferase activity and virus titers from the supernatant at different time points post infection. As anticipated, luciferase activity differed dependent on the concentration of ribavirin (Fig. 4F). However, especially at 24 hours post infection, differences in luciferase activity were not proportional to differences in virus titers determined from the same supernatants, most probably due to extracellular accumulation of the highly stable GLuc³⁸. As for the fluorescent reporter viruses, we detected high levels of unprocessed, luciferase-NEP fusion proteins in lysates of cells infected with SC35M_{NS1_2A_GLuc_2A_NEP} and SC35M_{NS1_2A_RenLuc_2A_NEP} (Fig. S1).

A Cre recombinase-encoding virus allows visualization of cells that are infected or survived acute infection

The Cre-Lox recombination is a widely used method to control gene expression in cell culture or animal models^39,40. To generate a genetically stable virus that would allow activation or deactivation of genes specifically in infected cells, we introduced a Cre recombinase gene into the NS segment (SC35M_{NS1_2A_Cre_2A_NEP}). Infection of MDCK-II cells revealed a high viral titer of 10⁸ PFU/ml cell culture supernatant 48 h post infection (Fig. 5A). However, SC35M_{NS1_2A_Cre_2A_NEP} showed a delayed viral growth especially at 12 and 24 hours post infection compared to SC35M_WT (Fig. 5A). To functionally monitor expression of Cre, we established a human airway derived Calu-3 cell line harboring a loxP-flanked dsRed gene followed by a silenced eGFP gene⁴¹ (Fig. 5B). Upon Cre-mediated recombination, the dsRed gene is eliminated and cells express eGFP, resulting in a switch from red to green fluorescence and consequently constitutive GFP expression is inherited to progeny cells after proliferation. As IAV suppress host protein synthesis and induce apoptosis^42,43,44, we expected that viral infection would complicate identification and analysis of reporter cells upon virus-induced recombination. Indeed, as judged by live cell imaging, infected Calu-3 cells only showed faint green fluorescence 24 hours post infection and were almost completely eliminated at later time points (Fig. 5C, infected). To prevent virus-induced cell death and allow limited viral replication, we treated virus-infected cells with ribavirin (0.1 mM) 3 hours post infection and kept them under treatment to abrogate further replication. We anticipated that this would allow sufficient expression of Cre recombinase and the associated switch to GFP expression as well as prolonged cell survival (Fig. 5B). Indeed, increasing number of GFP-positive Calu-3 reporter cells were observed in a time dependent manner upon infection at an MOI of 1 with SC35M_{NS1_2A_Cre_2A_NEP} and subsequent ribavirin treatment (Fig. 5C, infected + ribavirin). As we could show in cell culture that SC35M_{NS1_2A_Cre_2A_NEP} allows the visualization of cells that survived IAV infection, we hypothesized that we could also trace and identify such cells in vivo using a suitable mouse model. For this reason, rosa^mT/mG mice⁴⁵ were infected intranasally with a sublethal dose of SC35M_{NS1_2A_Cre_2A_NEP}. These transgenic animals comprise a loxP-flanked tdTomato ORF upstream of an eGFP gene integrated into the Rosa26 locus. Analogous to the earlier described cell culture system, Cre-mediated recombination results in a switch from red to green fluorescence in virtually all cell types. Infected animals were sacrificed at 2, 7 or 21 days post infection to collect their lungs for microscopic examination. Two and 7 days after infection, green fluorescent cells could be detected within the epithelial layer of bronchioles (Fig. 5D, filled arrow heads) as well as in distal lung tissues (Fig. 5D, transparent arrow heads). A similar distribution of GFP-positive cells was observed 21 days post infection, a time point where infection was already cleared (data not shown), indicating that diverse populations of epithelial cells survived the virus infection. Interestingly, while 2 days post infection only individual cells in alveolar tissues showed green fluorescence, clusters of adjacent GFP-positive cells could be visualized already 7 days p.i., which might derive from progenitor cells that survived acute infection. To reveal the identity of the GFP-positive cells found in the distal lung compartment, we subjected lung cells from rosa^mT/mG mice infected with SC35M_{NS1_2A_Cre_2A_NEP} to flow cytometric analysis at days 2, 7 and 21 post infection. We could identify recombined, GFP-positive cells within lung epithelial cell populations (EpCam⁺), including alveolar epithelial cells type 1 (AEC I, EpCam^lowT1α⁺), alveolar epithelial cells type 2 (AEC II, EpCam^lowT1α^–), stem and/or progenitor cells (EpCam^highCD24^low) and small airway epithelial cells (EpCam^highCD24^high) (Fig. 6 A and B). Of note, all infectious viruses isolated from the lungs of infected animals by plaque purification 2 days post infection encoded a functional Cre recombinase as judged by GFP expression in the Calu-3 reporter cells, highlighting the genetic stability of SC35M_{NS1_2A_Cre_2A_NEP} in mice (Table 1). Taken together, this reporter virus in combination with flow cytometric analysis represents a powerful tool to identify and quantify acutely infected lung cells as well as cells that survived acute infection.

Stable introduction of transgenes into the PB2-segment of SC35M is at the cost of viral replication capacity

As for the NS-segment, it was shown that the PB2-segment tolerates the integration of foreign genes downstream of the PB2 ORF^11,12,46. Since this approach represents an alternative to the NS segment as a vector for transgene expression, we generated pHW2000-based rescue plasmids encoding GFP or GLuc separated from the PB2 ORF by a PTV-1 2A-coding sequence (Fig. 7A). To guarantee packaging of the modified segment into viral particles, a terminal stretch of the segment was duplicated and fused downstream to the reporter gene as described by others⁴⁷. Both viruses, encoding GFP (SC35M_{PB2_2A_GFP}) or GLuc (SC35M_{PB2_2A_GLuc}) could be successfully generated. Specific fluorescent signals were observed upon infection of A549 cells with SC35M_{PB2_2A_GFP} by live cell imaging microscopy (Fig. 7A) and significant levels of luciferase could be detected in the supernatant of MDCK-II cells infected with SC35M_{PB2_2A_GLuc} (Fig. 7B). Analysis of the replication efficiency of these viruses in MDCK-II cells, revealed a substantial attenuation of SC35M_{PB2_2A_GLuc} compared to SC35M (Fig. 7A). In sharp contrast, viral growth of SC35M_{PB2_2A_GFP} was, to our surprise, as efficient as wild type virus (Fig. 7A). However, analysis of viral plaques obtained with SC35M_{PB2_2A_GFP} revealed that only 1 out of 123 plaques was GFP positive (Tab. 1), indicating that the vast majority of these viruses lost the intact reporter gene after a single passage on human cells. Indeed, sequencing of the RNA extracted from six GFP-negative plaques revealed that the GFP gene was deleted, most likely by homologous recombination at the duplicated packaging signals. Interestingly, SC35M_{PB2_2A_GLuc} did not lose its reporter activity after 4 passages (Tab. 1), suggesting that smaller genes might be tolerated on the expense of viral fitness.

To improve the genetic stability of the GFP-encoding PB2 segment, the highest possible number of silent mutations was introduced into the last 129 nucleotides of the PB2 ORF to prevent homologous recombination at the duplicated packaging signals (Fig. 7C). This modification resulted in a virus, designated SC35M_{PB2mod_2A_GFP}, which was strongly attenuated in cell culture but genetically stable over four passages in A549 cells (Tab. 1). To rule out the possibility that this attenuation resulted from mutation of the PB2 ORF rather than from insertion of the transgene, we deleted the GFP-coding sequence from the PB2 segment (Fig. 7D). This virus (SC35M_PB2mod) replicated in cell culture almost as efficiently as SC35M_WT. In summary, this suggests that stable integration of a transgene into the PB2-segment of SC35M is possible but associated with severe attenuation.

Discussion

Influenza A reporter viruses are important tools to study the biology of IAV and screening approaches. However, these viruses show in general impaired viral replication efficiencies, probably resulting in an unfavorable selective pressure towards loss of the reporter gene. Especially the latter may cause difficulties in the interpretation of the results observed with reporter viruses. In this study, we developed a strategy that allows the stable integration of reporter genes into the NS-segment of IAV. We achieved this by converting the NS segment into a single ORF encoding NS1, the respective gene of interest and NEP. The reporter gene was flanked by two sequences coding for the porcine Teschovirus-1 2A peptide (PTV-1 2A), thereby allowing co-translational separation of NS1, the reporter protein and NEP. The feasibility of this method was demonstrated by the successful generation of recombinant IAV, encoding a variety of fluorescent reporter proteins or catalytically active enzymes. Dependent on the gene inserted into the NS segment, we observed various degrees of attenuation. Most importantly, these genetically modified viruses displayed a high genetic stability over 4 passages in cell culture as well as over a single passage in mice and can be readily used for a broad range of in vitro and in vivo applications.

The levels of viral mRNA transcripts coding for NS1 or NEP in influenza A virus-infected cells is regulated by splicing, resulting in defined protein ratios of NEP and NS1. This is of special importance with respect to recent findings suggesting that the relative amount of NEP coordinates the intracellular timing of an infection and that an aberrant NS1 to NEP ratio results in inhibition of viral replication²³. Intriguingly, the co-translational processing by PTV-1 2A seems rather inefficient, resulting in a substantial proportion of uncleaved polyprotein in cells infected with the recombinant viruses (Fig. 1C). As a consequence, the level of free NEP is comparable to that detected in cells infected with wild type virus preventing significant attenuation as exemplified best with the recombinant virus SC35M_{NS1_2A_NEP} harboring no additional reporter gene (Fig. 1C). Interestingly, cells infected with SC35M_{NS1_2A_GFP_2A_NEP} expressed high levels of a GFP-2A-NEP fusion protein, while NS1-2A-GFP was almost not detectable (Fig. 3C and Fig. S1). This might be the result of context-specific differences in 2A-mediated recoding efficiency or could be explained by a higher stability of GFP-2A-NEP compared to NS1-2A-GFP.

Integration of foreign genes into the NS segment using the method presented in this study, can lead to impaired viral fitness. This might be a result of (I) low levels of NEP due to inefficient PTV-1 2A activity (Fig. 3C), (II) an intrinsic feature of the inserted reporter gene or (III) increased overall length of the NS segment. Indeed, integration of larger genes into the viral genome including firefly luciferase (~2 kb) or β-galactosidase (~3 kb) failed, suggesting a particular length restriction.

We could show for SC35M that insertion of the GFP gene into the PB2-segment results in the rapid loss of reporter activity due to homologous recombination of the duplicated packaging sequences (Fig. 7A and Tab.1). Loss of the reporter gene could be prevented by extensive modification of these sequences but was associated with significantly impaired viral growth (Fig. 7C and Tab.1). In contrast to the NS segment, introduction of reporter genes into the PB2 segment of SC35M did not result in viruses that are suited for further in vitro and in vivo studies. However, we cannot exclude the possibility that this might be different for other influenza A virus strains.

Importantly, the recombinant viruses described in this study harboring reporter genes in the NS segment are genetically stable in cell culture and mice. This includes fluorescent protein-encoding genes shown to be readily eliminated in cell culture or mice when present as NS1-fusion genes^15,16,20. Genetically stable reporter viruses offer several advantages, including the reliable identification and determination of the relative abundance of virus-infected cells by microscopic tracing of these cells in a model organism. Because of their genetic stability, luciferase-encoding viruses might be robust tools for high throughput screening approaches. Here, SC35M_{NS1_2A_RenLuc_2A_NEP} might be superior, as the activity of the virus-encoded RenLuc allows measurements already early upon infection and parallels with viral titers at later time points (Fig. 4C).

Sublethal infection of mice with influenza A virus is cleared by day 10–14 and no infectious particles can be isolated from the lung of these animals there upon⁴⁸. Using the Cre recombinase-encoding virus, we could trace cells that survived viral infection in the lungs of infected rosa^mT/mG mice 21 days after viral challenge. GFP-positive cells were found in various lung tissues including the epithelial layers lining the larger and also smaller airways (alveoli and bronchioles) of the respiratory tract. The fact that we could only observe the formation of GFP-positive cell clusters at later time points post infection (Fig. 5D) suggests that a proportion of these cells represents progeny of formerly infected and surviving cells, as GFP expression is inherited. Consistently, flow cytometry revealed the presence of GFP-positive cells among the stem and/or progenitor population 2, 7 and also 21 days post infection (Fig. 6B). Intriguingly, similar experiments were recently performed with an engineered H1N1 virus (A/Puerto Rico/8/1934) encoding a Cre recombinase within the PB2 segment⁴⁶. In this case the authors could identify recombined cells exclusively in the larger airways of the respiratory tract. The reason for this discrepancy is unclear but could be related to differences in the segment used as vector for Cre recombinase-expression or might result from the different subtype of hemagglutinin (HA) of both mouse-adapted virus strains. While HA of PR/8 (H1N1) possesses a monobasic cleavage site, HA of SC35M (H7N7) harbors a multibasic cleavage site, which might facilitate infection of a broader spectrum of lung cells. Of note, influenza virus replication is known to be accompanied by the production of defective interfering particles (DIs) as well as semi-infectious particles (SIs)^49,50,51,52. We cannot exclude the possibility that recombination events observed in cells of infected rosa^mT/mG mice were caused by the incorporation of such particles, which might not have the capacity to induce cell death. Importantly, the in vivo prevalence of DIs and SIs remains to be elucidated⁵³.

Taken together, we present a strategy that permits the introduction of foreign genes into the NS genome segment of Influenza A viruses. This was achieved by conversion of the intron-containing NS segment into a segment that allows the expression of reporter genes by two porcine Teschovirus-1 2A peptide (PTV-1 2A)-coding sequences. Such engineered viruses were shown to be genetically stable over at least 4 passages in cell culture and a single passage in mice and thus represent attractive tools to study influenza A viruses in vitro and in vivo.

Methods

Plasmid construction

The Azurite gene was amplified from pGEMHE-X-Azurite, which was kindly provided by Max Ulbrich. The template used to amplify the Cre recombinase gene (pMIG-Cre) was a gift from Hassan Jumaa. The Gaussia Luciferase gene sequences derived from pT7-NYMVmg-Gluc⁵⁴ and the Renilla luciferase-coding sequence was obtained from pRL-SV40 (Promega). The eGFP gene was amplified from pCAGGS-GFP-P²⁷. pHW2000-based²⁶ rescue plasmids to generate SC35M were described by others³². The NS1_2A_NEP plasmid was generated by deletion of the Flag-tag sequence of NS1_2A_Flag-NEP²⁴ by performing overlapping fusion PCR. The same plasmid served as template to create NS1_2A_GFP-NEP where the Flag-tag sequence was replaced by an eGFP gene. NS1_2A_GFP_2A_NEP was obtained by insertion of a second genetically altered PTV-1 2A encoding sequence (GCCACAAATT TCTCTCTCCT CAAGCAAGCC GGGGACGTCG AGGAGAATCC CGGGCCC) between the genes for eGFP and NEP by overlapping fusion PCR. Furthermore, a SacII and a KpnI restriction site upstream and downstream of the eGFP gene respectively were introduced. NS1_2A_Renilla_2A_NEP and NS1_2A_Cre_2A_NEP were generated by overlapping fusion PCR using NS1_2A_GFP_2A_NEP as template. All other transgene-encoding NS-segment rescue plasmids were generated by PCR amplification of the transgene and SacII/KpnI-digestion-ligation into NS1_2A_GFP_2A_NEP. The PB2_2A_GFP and PB2_2A_GLuc plasmids were generated in two steps. First, a PB2_2A_GFP_2A_NEP and a PB2_2A_GLuc_2A_NEP intermediate was generated by PCR amplification of PB2 and digestion-ligation into NS1_2A_GFP_2A_NEP and NS1_2A_GLuc_2A_NEP. In a second step, the 2A_NEP sequence was replaced by 166 nucleotides of the 3’ end of the PB2 segment by overlapping fusion PCR. To obtain PB2mod_2A_GFP, silent mutations within the last 129 nucleotides of the 3’ end of the PB2 ORF (GCcAAaGGcG AaAAaGCcAA cGTcCTgATc GGcCAgGGcG AtGTcGTccT GGTcATGAAa aGaAaaGaGA tagctccATc CTgACcGAtt ccCAaACaGC cACaAAgAGg ATcaGaATGG CtATtAAc) were introduced into PB2_2A_GFP by annealing of two synthetic DNA oligonucleotides and subsequent overlapping fusion PCR. PB2mod was generated by removal of the 2A_GFP sequence from PB2mod_2A_GFP via PCR amplification and digestion-ligation.

Cells and retroviral transduction

HEK293T, A549, Calu-3 and MDCK-II cells were grown in Dulbecco’s modified Eagle’s medium supplemented with 10% fetal calf serum, 2 mM L-glutamine and 1% penicillin/streptomycin. All cells were cultured at 37 °C and 5% CO₂. Calu-3 cells harboring the loxp-dsRed-loxp-eGFP expression cassette were generated by retroviral transduction and subsequent selection in puromycine-containing media as described by the manufacturer (Stratgene). Pseudotyped retroviurses were produced in HEK293T cells upon transfection with pMSCV-loxp-dsRed-loxp-eGFP-Puro-WPRE (Addgene plasmid 32702, kindly provided by Hans Clevers), pVPack-GP and pVPack-VSV-G as decribed (Stratagene).

Virus rescue

To generate recombinant influenza viruses, HEK293T cells were transfected in a 6 well format with 8 bidirectional pHW2000 rescue plasmids²⁶ encoding the respective viral genome segments (300 ng of plasmid DNA/segment). 24 hours post transfection, 200 μl of supernatant was transferred to MDCK-II cells (6 well format). Recombinant viruses were plaque-purified upon the observation of cytopathic effects.

Determination of viral growth kinetics

MDCK-II cells were infected at an MOI of 0.001 and cultured in infection medium (Dulbecco’s modified Eagle medium supplemented with 0.2% bovine serum albumin [BSA], 2 mM l-glutamine and 1% penicillin-streptomycin). At 12, 24, 36 and 48 hours post infection 150 μl of supernatant was collected and subjected to plaque assay for determination of virus titer.

Passaging and analysis of reporter stability

For each passage of fluorescent and luminescent reporter viruses, A549 cells were infected at an MOI of 0.01 and cultured in infection medium (see preceding chapter). 48 hours post infection, supernatant was collected and virus titer was determined by plaque assay. After 4 passages, plaques induced by fluorescent reporter viruses were analyzed and counted using a fluorescent microscope. To determine the reporter expression of passaged, luciferase-encoding viruses, 10 plaques were randomly picked and used for infection of MDCK-II cells and 24 hours post infection luciferase activity was measured. SC35M_{NS1_2A_Cre_2A_NEP} was passaged on MDCK-II cells. After 4 passages and subsequent plaque assay, Calu-3 cells containing the loxp-dsRed-loxp-eGFP expression cassette were infected with plaque-purified viruses. After 3 hours, medium was replaced by Ribavirin-containing (100 μM) medium. Recombination events resulting in a switch from red to green fluorescence were analyzed with a fluorescent microscope.

Determination of luciferase activity

Luciferase activity in whole cell lysates or in 5 μl of supernatant of MDCK-cells cultured in 6-well plates was determined using a luciferase assay system (Promega) according to the manufacturer’s instructions.

Immunoblot analysis

Virus infected cells were incubated with lysis buffer (20 mM Tris, pH 7.5, 100 mM NaCl, 0.5 mM EDTA, 0.5% NP-40, 1% protease inhibitor mix G [Serva, Heidelberg, Germany], 1 mM dithiothreitol [DTT]) for 15 min on ice. After centrifugation at 13,000 rpm at 4 °C, supernatants were complemented with SDS page sample buffer⁵⁵ and incubated at 95 °C. Proteins were separated in SDS-PAGE gels (15%) and transferred to nitrocellulose membranes. Antibodies for detection of NEP and NS1 were a gift from Thorsten Wolff and Christina Ehrhardt respectively. The commercial antibodies for detection of GFP and tubulin were purchased from Santa Cruz Biotechnology (GFP) and Sigma-Aldrich (tubulin).

Animal experiments

All animal experiments were performed in accordance with the relevant guidelines (German animal protection law (TierSchG)) and approved by the welfare committees of the University of Freiburg, as well as the local authorities. Six-to-eight-week-old mice were anaesthetized with a mixture of ketamin (100 μg per gram body weight) and xylazine (5 μg per gram) administered intraperitoneally and inoculated intranasally with the indicated doses of viruses in 40 μl PBS containing 0.3% bovine serum albumin (BSA). Animals were sacrificed, if severe symptoms developed, or body weight loss approached 25% of the initial value. Lung homogenates were prepared using the FastPrep24 system (MP Biomedicals). Briefly, after addition of 800 μl of PBS containing 0.2% BSA, lungs were subjected to two rounds of mechanical treatment for 10 s each at 6.5 ms⁻¹. Tissue debris was removed by low-speed centrifugation. The LD₅₀ values were calculated based on the infectious dose (PFU). BALB/c mice were obtained from Janvier (Strasbourg). Rosa^mT/mG mice (Gt(ROSA)26Sor^{tm4(ACTB-tdTomato,-EGFP)Luo}) (Jackson laboratory) contain the two-color fluorescent rosa^mT/mG allele from which the cell membrane localized red fluorescent tdTomato is expressed. Upon Cre-Lox recombination directed by lox-P sites flanking the tdTomato gene, eGFP expression is induced.

Tissue histology

At appropriate time points, mice were sacrificed and lungs were transcardially perfused with 0.9% NaCl prior to fixation in 4% paraformaldehyde (PFA) in 0.1 M phosphate buffer at 4 °C overnight. After washing in ddH₂O the lungs were first transferred into a 15% sucrose solution in 0.1 M phosphate buffer (w/v) for 4 h and thereafter in a 30% sucrose solution in 0.1 M phosphate buffer (w/v) overnight (4 °C). For cryosection, lungs were embedded within Tissue-Tek O.C.T. compound, solidified on dry ice and cut to 15 μm thickness using a cryotome (Leica Microsystems, Germany). The sections were mounted onto gelatine-coated slides and dried at room temperature overnight in the dark. The slides were washed twice in phosphate buffer, DAPI (Invitrogen) stained at an end concentration of 300 nM in 0.1 M phosphate buffer for 7 min and again washed 3 times in 0.1 M phosphate buffer. Dried slides were embedded within IMMU-Mount™ (ThermoShandon), coverslipped and stored in the dark at 4 °C until further use.

Isolation of murine distal lung cells

Mouse lungs were perfused with HBSS (Gibco) followed by instillation of dispase (BD Biosciences) into the lung through the trachea and incubation in dispase for 40 minutes as previously described⁵⁶. Trachea and large airways were dissected and the remaining distal lung tissue was homogenized (GentleMACS, MACS Miltenyi Biotech) in DMEM/2.5% HEPES with 0.01% DNase (Serva) and filtered through 100 μm and 40 μm nylon filters. Cell suspensions were incubated with biotinylated rat anti-mouse CD45, CD16/32 and CD31 mAb (BD Biosciences) for 30 minutes at 37 °C followed by incubation with biotin-binding magnetic beads and magnetic separation to deplete leukocytes and endothelial cells prior to flow cytometric analysis.

Flow cytometry

The following antibodies were used for flow cytometric analyses: CD326 (EpCam) APC-Cy7 (clone G8.8), CD24 PE-Cy7 (clone: M1/69), T1α/podoplanin APC (clone: 8.1.1.), CD31 Pacific Blue (clone 390), all Biolegend. CD45 V450 (clone 30-F11, BD Biosciences). Multicolor flow cytometry was performed with an LSR Fortessa® using DIVA software (BD Bioscience). For analytical measurements 0.5–1 × 10⁶ cells were freshly stained with fluorochrome-labeled antibodies for 15 minutes at 4 °C in MACS buffer. The stained cells were washed and fixed in 4% paraformaldehyde and resuspended in MACS buffer.

Fluorescence microscopy

Fluorescence images of cultured cells seeded in black, clear bottom 96 well microplates (Greiner) were acquired on a Zeiss Observer.Z1 inverted epifluorescence microscope (Carl Zeiss, Jena) equipped with an AxioCamMR3 camera using a 40x objective. Fluorescence microscopy of lung sections was performed on a Zeiss Axioplan 2 epifluorescence microscope (Carl Zeiss, Jena) equipped with an ApoTome optical sectioning module using a 10x objective. Images were recorded with an AxioCamMR camera (Carl Zeiss, Jena).

Additional Information

How to cite this article: Reuther, P. et al. Generation of a variety of stable Influenza A reporter viruses by genetic engineering of the NS gene segment. Sci. Rep.5, 11346; doi: 10.1038/srep11346 (2015).

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Acknowledgements

This study was funded by the Deutsche Forschungsgesellschaft (SCHW 632/11-2) and the Excellence Initiative of the German Research Foundation (GSC-4, Spemann Graduate School, to A.D.). P.R. was recipient of a Studienstiftung des deutschen Volkes fellowship. We thank Veronika Götz, Sebastian Giese and Linda Brunotte for critical reading of the manuscript. We are grateful to Max Ulbrich, Hassan Jumaa and Hans Clevers for kindly providing us with plasmid DNA.

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Reuther Peter and Göpfert Kristina contributed equally to this work

Authors and Affiliations

Institute for Virology, University of Freiburg, 79104, Freiburg, Germany
Peter Reuther, Kristina Göpfert, Alexandra H. Dudek & Martin Schwemmle
Faculty of Biology, University of Freiburg, 79104, Freiburg, Germany
Peter Reuther & Alexandra H. Dudek
Spemann Graduate School of Biology and Medicine (SGBM), University of Freiburg, 79104, Freiburg, Germany
Alexandra H. Dudek
Department of Internal Medicine (Pulmonology), University of Giessen and Marburg Lung Center, German Center for Lung Research, D-35392, Giessen, Germany
Monika Heiner & Susanne Herold

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Peter Reuther
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P.R., S.H. and M.S. conceived and designed the experiments. P.R., K.G., A.D., M.H., S.H. and M.S. performed the experiments and analyzed the data. P.R. and M.S. wrote the manuscript.

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Reuther, P., Göpfert, K., Dudek, A. et al. Generation of a variety of stable Influenza A reporter viruses by genetic engineering of the NS gene segment. Sci Rep 5, 11346 (2015). https://doi.org/10.1038/srep11346

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Received: 21 January 2015
Accepted: 21 May 2015
Published: 12 June 2015
DOI: https://doi.org/10.1038/srep11346

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