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Int J Med Sci 2011; 8(2):88-96. doi:10.7150/ijms.8.88 This issue Cite

Research Paper

Parvovirus B19 Nonstructural Protein-Induced Damage of Cellular DNA and Resultant Apoptosis

Brian D. Poole^1,2, Violetta Kivovich^1,3,4,5, Leona Gilbert^4,5, Stanley J. Naides^{1, 5,6}

1. Huck Institute for Life Sciences, Pennsylvania State University College of Medicine/Milton S. Hershey Medical Center, Hershey, PA, USA
2. Current: Department of Microbiology and Molecular Biology, Brigham Young University, Provo, UT, USA
3. MD/PhD Program, Pennsylvania State University College of Medicine/Milton S. Hershey Medical Center, Hershey, PA, USA
4. Chemical Biology Division, Department of Biological and Environmental Science, University of Jyväskylä, Jyväskylä, Finland
5. Division of Rheumatology, Department of Medicine, Pennsylvania State University College of Medicine/Milton S. Hershey Medical Center, Hershey, PA, USA
6. Current: Quest Diagnostics Nichols Institute, San Juan Capistrano, CA, USA

✉ Corresponding author: Stanley J. Naides, MD, Immunology, Quest Diagnostics Nichols Institute, 33608 Ortega Highway, San Juan Capistrano, CA 92690. Tel. 949 728-4578; fax 949 728-7852; email: stanley.j.naidescom

Abstract

Parvovirus B19 is a widespread virus with diverse clinical presentations. The viral nonstructural protein, NS1, binds to and cleaves the viral genome, and induces apoptosis when transfected into nonpermissive cells, such as hepatocytes. We hypothesized that the cytotoxicity of NS1 in such cells results from chromosomal DNA damage caused by the DNA-nicking and DNA-attaching activities of NS1. Upon testing this hypothesis, we found that NS1 covalently binds to cellular DNA and is modified by PARP, an enzyme involved in repairing single-stranded DNA nicks. We furthermore discovered that the DNA nick repair pathway initiated by poly(ADPribose)polymerase and the DNA repair pathways initiated by ATM/ATR are necessary for efficient apoptosis resulting from NS1 expression.

Keywords: Parvovirus B19, DNA damage and repair, fulminant liver failure, apoptosis, autoantibody, systemic lupus erythematosus

Introduction

Parvovirus B19 (B19) is a common virus with multiple clinical presentations. Infection in children is typically seen as erythema infectiosum, or fifth disease (1), while adults often experience arthropathy lasting up to several months (2). Autoantibodies are often found subsequent to B19 infection, and are associated with arthropathy (3-5). In patients with chronic hemolytic anemias, such as sickle cell disease or hereditary spherocytosis, the destruction of the erythroid precursor pool by B19 leads to aplastic crisis (6). B19 infection is implicated in hepatitis non-A-E acute fulminant liver failure (7-16). Although these are the best-described clinical illnesses caused by B19, the virus has been implicated in a wide spectrum of other illnesses (17).

B19 infects a variety of cell types, but predominantly replicates in erythroid precursors (18). Infection of other cell types results in a limited, non-replicative state with overexpression of the viral nonstructural protein, NS1, and little expression of genes for the structural proteins VP1 and VP2 (19). Previous work in our laboratory showed that B19 is capable of infecting liver cells, and that the resulting restricted infection induces apoptosis, most likely through the action of NS1 (19, 20). NS1 is cytotoxic when transfected into erythroid cells (21), COS-7 cells (22) and liver-derived cells (20). In cell types which are non-productive for viral infection, NS1-induced apoptosis proceeds in a caspase 9-dependent manner, indicative of internal apoptotic stimuli (20, 22).

The NS1 protein of parvovirus B19 exhibits multiple functions, with NTP binding, helicase, nickase, and transcription factor activities (23-25). Because of these DNA-modifying activities, we hypothesized that NS1 induces apoptosis by damaging cellular DNA. Apoptosis resulting from DNA damage would be consistent with the caspase-9-dependent apoptotic pathway (20, 22).

This hypothesis is supported by the action of NS1 proteins from similar parvoviruses. The nonstructural proteins from the parvoviruses minute virus of mouse (MVM) and H-1 parvovirus also utilize helicase and DNA binding activities to fulfill their functions in viral replication (26-29). NS1 from MVM binds covalently to the viral genome as part of the replication process (29, 30). In addition, NS1 from MVM and H-1 parvovirus colocalizes with the cellular DNA repair machinery (31-33). Covalent attachment to cellular DNA would cause a significant lesion, as would the introduction of multiple single-strand breaks. DNA damage due to the actions of NS1 would be expected to result in apoptosis in a portion of infected cells.

This study utilized cloned NS1 under the control of an inducible promoter to examine the mechanisms of NS1-induced apoptosis. The NS1 DNA sequence was fused to that of green fluorescent protein (GFP) (http://tools.invitrogen.com/content/sfs/vectors/pindsp1gfp.pdf) to allow visualization and purification of NS1 (GFP/NS1). Cellular expression of this vector has previously been shown to induce apoptosis in the same manner as infection with natural B19, while a mutant of NS1 with the NTP binding region deleted induced significantly less apoptosis (20). The GFP/NS1 vector was utilized in this study to investigate the role of the DNA-damaging activities of NS1 in NS1-induced apoptosis.

There are several mechanisms through which NS1 could cause DNA damage resulting in apoptosis. We hypothesized that NS1 could covalently attach to chromosomal DNA, in much the same way that the nonstructural proteins of MVM and H-1 parvovirus attach to the viral genome. Covalent attachment of NS1 to cellular DNA was investigated in this study using denaturing SDS-PAGE and autoradiography. Attachment of NS1 to DNA would be expected to initiate the DNA repair pathways that sense distortions in the DNA helix. These pathways were examined by inhibition of the key proteins ataxia telangiectasia related (ATR) and ataxia telangiectasia-mutated (ATM). The DNA-nicking activity that NS1 uses to separate viral genomes would be expected to activate the single-strand break DNA repair pathway if applied to host cell DNA. This pathway was investigated by studying the activity of Poly(ADP-ribose)Polymerase (PARP), the protein which detects nicks in DNA and activates the repair process.

Both the nick repair and ATR/ATM-mediated bulky adduct repair pathways can result in apoptosis if the damage is severe. Damage of chromosomal DNA by parvoviral proteins has not been directly demonstrated, except in the case of specific integration of AAV. We present here evidence suggesting that NS1 is attached to DNA in a covalent manner, and that both DNA-helix distorting and single strand nick forms of DNA damage are important pathways to apoptosis upon expression of NS1.

Materials and Methods

Transfection

A GFP/NS1 expression vector under the control of the ecdysone response element previously constructed in our laboratory was utilized for these experiments as previously described (20). Briefly, HepG2 cells were grown on glass coverslips in hepatocyte wash medium (Invitrogen, Carlsbad, CA) supplemented with 10% fetal calf serum. Either GFP/NS1 or the parental vector, pIND(GFP)SP1 (Invitrogen) was cotransfected with the ecdysone receptor plasmid pVGRXR (Invitrogen) into the cells using Lipofectamine (Invitrogen) and PLUS reagent (Invitrogen). Expression of GFP/NS1 or GFP was induced by the addition of 10 µg/ml ponasterone A (Invitrogen). Protein expression was monitored by fluorescence microscopy.

Immunoprecipitation and chromatin immunoprecipitation

Cells expressing either GFP/NS1 or GFP were lysed with 1% SDS in TE buffer. The lysate was centrifuged through a Qiashredder (Qiagen, Valencia CA) to shear DNA. Lysates were then mixed with 2 ml of 1% triton-X 100 (Fisher, Hampton, NH) in PBS containing protease inhibitors (Sigma protease inhibitor cocktail, Sigma-Aldrich, St. Louis, MO). 25 μl of anti-GFP polyclonal antibody (Rockland, Gilbertsville, PA) were added and the mixture was allowed to bind for 14 hours at 4^oC in an end-over end rotator. Immune complexes were bound to protein G-agarose beads (Pierce, Rockford, IL) for three hours at 4^oC. Immunoprecipitates were washed 5x with 1% triton-X 100 in PBS, and once with PBS alone, and boiled for 5 minutes under reducing conditions in 1% SDS, 4M urea and 0.7 M 2-mercaptoethanol. Immunoprecipitates were electrophoresed on a 7.5-14% polyacrylamide gel and used for autoradiography and Western blotting.

For chromatin immunoprecipitation, 10⁷ cells were cotransfected with pVGRXR and either GFP/NS1 or pIND(GFP)SP1. Protein expression was induced with ponasterone A 24 hours post-transfection and the cellular DNA was metabolically labeled with 10 µCui α³²P thymidine triphosphate (Perkin Elmer) in supplemented hepatocyte wash medium (Invitrogen). After immunoprecipitation, one aliquot of each immunoprecipitate was treated with 10 units DNase (Roche) for 1 hour at 37^oC. After SDS-PAGE, proteins were transferred to nitrocellulose and used to expose Kodak MS film to obtain an autoradiograph image. GFP antibodies were then used to identify the location of the transgenic protein by Western Blotting.

Western blotting

HepG2 cells were lysed in 1% (w/v) SDS, 4M urea and 0.7M 2-mercaptoethanol. Lysates were electrophoresed through 7.5-14% acrylamide gels (BioRad, Hercules, CA). Proteins were transferred to nitrocellulose membranes and bound with anti-GFP polyclonal rabbit antiserum (Invitrogen) or poly(ADP ribose) (PAR) monoclonal antibody (Pharmingen, San Diego, CA) at 1:5000 dilution. Species-specific secondary antibodies (Amersham, Piscataway, NJ) were used for detection with ECL+ chemiluminescence (Amersham).

Detection of apoptosis

Transfected HepG2 cells were grown on glass coverslips and stained with annexin-V-Alexa fluor 594 (Molecular Probes, Eugene, OR) as previously described (19, 20). Transfected cells were identified by green fluorescence and examined for apoptosis using a 528-553 nm excitation filter and a 600-660 nm barrier filter to allow for detection of the red-fluorescing apoptosis marker. Apoptotic cells also exhibited condensed nuclei when stained with Hoescht 33342 (Molecular Probes).

Treatment with pharmacologic agents

Transfected HepG2 cells were pretreated with 8 to 14 mM caffeine (Sigma) for 3 hours before induction of protein expression. Caffeine was maintained on the cells during expression of GFP or GFP/NS1. PARP was inhibited by incubating transfected cells with 5-aminoisoquinolinone (Calbiochem) at 250, 25, 2.5, and 0.25 μM concentrations 3 hours prior to transgene induction. The inhibitor was maintained on the cells throughout the experiment.

Statistical Analysis

The student's T test (2-tailed) was used to evaluate significant differences in the experiments involving inhibition of apoptosis, and the Pearson's correlation test was used to determine whether inhibition was dose-dependent. P values of less than 0.05 were considered significant.

Results

Covalent attachment of NS1 to chromosomal DNA

Association of NS1 with chromosomal DNA was detected using chromatin immunoprecipitation. HepG2 cells were transfected with the GFP/NS1 expression vector or GFP vector alone and metabolically labeled with ³²P-thymidine triphosphate during the protein expression phase of the experiment. Labeled DNA was detected by autoradiography and proteins were detected by Western blotting. Radioactivity was found in specific bands that perfectly overlapped with bands formed by GFP/NS1, but not GFP, as revealed by Western blotting (Figure 1). The colocalization of the radioactive signal with NS1 shows that DNA is bound to NS1 in the lysate. The harsh denaturing methods used both in the immunoprecipitation and in the preparation of the samples for SDS-PAGE strongly suggest that DNA could not have been present with the NS1 fusion protein unless covalently linked. Treatment of the immunoprecipitate with DNase before SDS-PAGE decreased the radiographic signal by 63%, indicating that the radioactive label is DNA, and not from another source such as phosphorylation of NS1 (Figure 1).

Involvement of the DNA damage repair pathway

DNA damage normally blocks progression through the cell cycle and, when severe, causes apoptosis through the intrinsic or mitochondrial pathway. Caffeine uncouples DNA damage from cell cycle progression and apoptosis, primarily through the inhibition of the DNA damage sensing protein ATM and ATR, (34, 35). The involvement of the DNA damage repair pathway in NS1-induced apoptosis was examined in GFP/NS1-transfected cells by treating the cells with caffeine. Incubation of GFP/NS1-transfected cells with caffeine inhibited apoptosis in a dose-dependent manner, reducing the percentage of apoptotic cells by nearly 70% at a concentration of 14 mM (Figure 2).

 Figure 1 

DNA is covalently bound to NS1 protein. A. Autoradiography of GFP-immunoprecipitated ³²P labeled cells shows radioactive DNA colocalizing with GFP/NS1 (100 kd), but not GFP alone (37 kd), after boiling in SDS with urea and β-mercaptoethanol. GFP and GFP/NS1 were detected by western blot. The blot shown is representative of 4 independent experiments. B. Incubation of immunoprecipitates with DNase before the denaturation step abrogates the radiographic signal by 63% (N=3 experiments, error bars indicate the range).

 Figure 2 

The ATM/ATR-mediated DNA repair pathways are necessary for efficient NS1-induced apoptosis. A. Caffeine treatment of GFP/NS1-transfected HepG2 cells led to a decrease in apoptosis of up to 63%, indicating the necessity for ATR-dependent activity in apoptosis. The decrease in apoptotic caffeine-treated cells compared to cells without caffeine treatment was significant by the student's t test for the three concentrations. Pearson correlation analysis comparing caffeine dose to apoptosis showed that the inhibition was dose-dependent (p<0.041). The data were derived from 3 independent experiments. Error bars indicate the standard error of the mean.

No difference was observed in apoptosis between the GFP-transfected cells and the untransfected cells upon treatment with caffeine. The decrease in apoptosis upon treatment with caffeine supports the finding that NS1 induces apoptosis through DNA damage that alters the chromatin structure.

Involvement of the DNA nick repair pathway

Although the ATM/ATR-dependent DNA repair pathway is important in optimal NS1-induced apoptosis, NS1 may also activate other DNA damage repair pathways that can lead to apoptosis. Single-strand nicks in genomic DNA would be expected to activate PARP and the nick repair pathway. Activated PARP transfers Poly(ADP ribose) (PAR) to neighboring proteins in response to DNA damage (36-38). As a method of investigating the involvement of PARP activation in NS1-induced apoptosis, the NS1 fusion protein was examined for the presence of activated PAR moieties, which would indicate the presence of NS1 in a DNA lesion that was sufficient to activate PARP, as well as demonstrating that the two molecules, NS1 and PARP were in physical contact. GFP/NS1 or GFP alone were immunoprecipitated from transfected cells, and western blotting was performed using an anti-PAR antibody. GFP/NS1 was poly(ADP ribose)ylated, while GFP was not (Figure 3A). Poly(ADP ribose)ylation of NS1 shows that NS1 exists in the cell in contact with activated PARP, and hence, in the presence of sufficient DNA nicks to activate this repair pathway. To study the importance of the PARP-initiated DNA repair pathway in NS1-induced apoptosis, the cell-permeable PARP inhibitor 5-aminoisoquinolinone (5AIQ) was added to GFP/NS1-transfected HepG2 cells. Inhibition of PARP significantly (p<0.003) reduced apoptosis in these cells compared to treatment with DMSO alone (Figure 3B). Inhibition of apoptosis was maximal at 57% at a concentration of 25 µM. This finding demonstrates that PARP activation, and therefore the PARP-induced DNA repair pathway, is an important mechanism of NS1-induced apoptosis.

 Figure 3 

PARP is active and necessary for efficient apoptosis in NS1-transfected cells. A. Immunoprecipitated GFP/NS1 protein was poly(ADP ribose)ylated, as shown by a band at 100 kd on the blot probed with anti-poly ADP ribose (PAR, left blot) antibodies. The blots were stripped and reprobed with anti-GFP (right), showing that PAR colocalizes with the GFP/NS1 fusion protein. GFP alone is not ribosylated, as evidenced by the lack of a PAR band corresponding to GFP at 37 kD. Blots shown are representative of three independent experiments. B. PARP activity is necessary for optimal NS1-induced apoptosis. Addition of the PARP inhibitor 5-aminoisoquinolinone (5AIQ) to GFP/NS1 expressing HepG2 cells reduced apoptosis by 57% (p<0.003). Addition of 5-aminoisoquinolinone had no effect on the GFP transfected cells. N=3, error bars indicate the range of values.

Discussion

This work identifies several lines of evidence indicating that NS1 damages cellular DNA, and that this damage leads to apoptosis. Upon detection of DNA damage, DNA damage response proteins inhibit the cell cycle and are capable of inducing apoptosis if the DNA lesion is not repaired. Several of these repair pathways involve the DNA damage sensing kinases ATR and ATM. Upon activation, ATR and ATM phosphorylate a variety of substrates, including CHK-1, p53, and p73, each of which further transduces signals that result in DNA repair or apoptosis (39, 40). Blockage of the cell cycle has been noted in B19 and other parvovirus infected cells (21, 33, 41, 42), and p53 was implicated in NS1-induced apoptosis of COS-7 cells (22). These earlier findings suggest that NS1 may induce these DNA repair mechanisms. The experiments in this study are consistent with ATR/ATM-mediated DNA repair being important for parvovirus B19 NS1 protein-induced apoptosis. Inhibition of ATR and ATM with caffeine (34) substantially decreased the amount of apoptosis observed in the NS1-expressing cells. Although there are limitations inherent in these methods, the results presented are suggestive of DNA damage as a cause of NS1-induced apoptosis. ATM principally binds to free DNA ends or DNA strand breaks (43), while ATR recognizes single-stranded regions of DNA common to multiple types of DNA lesions and that are often caused by collapsed replication forks (44). NS1 could easily cause double strand breaks through the simple mechanism of nicking both DNA strands a short distance apart. Nicking and binding to the DNA end would not only create broken strands, but adducts that would likely interrupt replication and activate ATR-dependent DNA damage repair and apoptosis.

The pathway responsible for the repair of single-strand nicks in DNA is also important for NS1-induced apoptosis. This pathway is mediated through PARP. Upon binding DNA nicks, PARP transfers poly(ADP ribose) (PAR) chains to many of the surrounding proteins, leading to DNA repair and a decrease in the ATP levels of the cell (37, 38). If the damage to the DNA is extensive, both the adduct repair and nick repair pathways may result in apoptosis (37, 38, 45-49). Activation of PARP has been demonstrated to induce apoptosis in neuronal cells, to interfere with the electron potential of the mitochondria, and to be required for the translocation of apoptosis inducing factor from the mitochondria to the nucleus (36-38, 45).

The finding that NS1 is directly (ADP ribose)ylated in transfected cells provides direct evidence for an interaction between NS1 and PARP. Since PARP is active at the site of single strand DNA breaks, and single-strand nicking is a known activity of NS1 protein, it is likely that NS1 is nicking the cellular DNA, thereby inducing DNA damage. This damage leads to apoptosis, as shown by decreased apoptosis after PARP activity was inhibited with 5-aminoisoquinolinone.

The importance of DNA damage to NS1-induced apoptosis is shown by the abrogation of apoptosis in the presence of inhibitors of DNA damage recognition enzymes. Both the single strand nick repair pathway, mediated by PARP, and the helix-distorting damage repair pathways, mediated by ATM or ATR, are necessary for optimal induction of apoptosis induced by NS1 expression, since inhibition of these pathways significantly decreases apoptosis in transfected cells. It is likely that NS1 additionally uses mechanisms other than the DNA damage repair pathways studied here to induce apoptosis, given that some level of apoptosis persists even under maximal inhibitory conditions. However, the degree of inhibition seen upon administration of these agents indicates that DNA damage is the primary mechanism for NS1-induced apoptosis in these cells. It is likely that NS1 causes cell death by at least two mechanisms, primarily DNA damage-induced apoptosis in non-permissive cells and through other mechanisms in permissive cells.

These dual pathways correlate with differential viral expression in these cell types. In permissive cells, all B19 genes are transcribed, while in nonpermissive cells NS1 expression predominates (19, 50). NS1 expression leads to DNA damage in nonpermissive cells, where NS1 is over expressed, while the productive infection in permissive cells may lead to cell death by other mechanisms. One such method of inducing cell death is through TNF-α induced signaling (51). TNF-α was not involved in NS1-induced apoptosis of transfected HepG2 cells studied in our previous work (20). Other mechanisms that are responsible for cell death in permissive parvovirus infection include MVM NS1 interactions with Casein Kinase II, resulting in cytoskeletal rearrangement and cell death (52, 53), or the generation of reactive oxygen species in response to DNA damage induced by H1 parvovirus NS1 protein (54). Such mechanisms may contribute albeit to a lesser degree than direct DNA damage to the apoptosis seen in these cells. The relatively small number of cells killed by NS1 expression or B19 infection (approximately 1/3-1/2) can be explained if those cells that die are those that are both replicating and unable to adequately repair their DNA, while cells that can repair the damage survive. If NS1 were directly acting on apoptosis-inducing factors, increased cytotoxicity would be anticipated.

Single strand nicks are the type of DNA damage that would be expected from a parvovirus nonstructural protein that functions to separate the DNA replicative form into individual genomes. The process of nicking by NS1 in MVM is highly regulated, depending on both cellular factors, such as RPA, and recognition by NS1 of a specific DNA sequence (30, 55). The involvement of single strand nicks in B19 NS1-induced apoptosis of hepatocytes suggests that either the DNA-nicking activity by NS1 protein of B19 is not as highly regulated as in MVM, and so is able to proceed on cellular DNA, or that there are sites suitable for NS1 nicking on the chromosomes. Future studies analyzing the site at which NS1 binds to the chromatin should demonstrate the NS1 binding sequence.

An appealing possibility suggested by the finding of NS1-DNA attachment concerns the development of autoantibodies after B19 infection. B19 infection often results in the production of anti-DNA autoantibodies (3, 4). A viral protein, such as NS1, with a covalently linked DNA strand could serve as a hapten-carrier system. In this model, autoreactive B cells recognizing DNA in a DNA-protein complex could internalize the complex, and present peptides derived from NS1 to virus-specific T cells. NS1-specific T cells, generated in the normal immune response to B19 (56), could then activate the DNA-reactive B-cells that present NS1 peptides on their MHC molecules, leading to the development of autoantibodies. DNA and histones do in fact become immunogenic when bound by the large T antigen of polyomaviruses (57-60), a similar situation to what we envision with B19. Antigen presenting cell (APC) uptake of apoptotic bodies or immune complexes containing NS1- modified DNA would allow APC presentation of NS1 peptides on their MHC and activation of NS1-specific T cells. Parvovirus B19 may be an example of a virus that naturally induces anti-DNA antibodies in this manner (Figure 4).

This testable model for the generation of autoantibodies in response to B19 infection is attractive in that it assumes the utilization of T cells that are specific for viral NS1 protein, avoiding the need for autoreactive T cells, which tend to be tightly regulated. T cells specific for NS1 that are activated in the immune response against B19 would be sufficient to activate B cells to initiate the production of autoantibodies. Clinically, it is interesting when considering this model that patients with high titers of anti-NS1 antibodies also are more likely to develop arthropathy, a condition which may be a result of autoantibody production (5, 61-63). In addition to NS1, it is possible that autoimmune responses may be generated to other nuclear proteins associated with nucleosomal DNA or NS1.

 Figure 4 

Model for B19 NS1 induction of anti-DNA antibodies. B19 induced apoptosis generates nucleosomes and apoptotic bodies containing NS1 modified DNA. Anergized anti-DNA B cells take up NS1 modified nucleosomal DNA through their anti-DNA immunoglobulin surface receptor and present NS1 peptides in the context of MHC to NS1-specific T cells. The NS1 specific T cells are activated by APC that express NS1 peptides in the context of surface MHC after uptake of apoptotic bodies or immune complexes containing NS1-modified DNA The NS1-specific T cells provide the helper signal required, in addition to the DNA signal, for the anergized B cell to break tolerance. vDNA, viral DNA; hDNA, human DNA; TCR, T cell receptor; PS receptor, phosphatidylserine receptor; FcR, Fc receptor.

Acknowledgements

We would like to thank Jing Zhou and Amy Grote for technical assistance. We would also like to thank Prof. Matti Vuento for his continuing support in this project. This work was supported in part by the Arthritis Foundation, Central Pennsylvania Chapter and the H. Thomas and Dorothy Willits Hallowell Endowment.

Conflict of Interest

The authors have declared that no conflict of interest exists.

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Author contact

Corresponding author: Stanley J. Naides, MD, Immunology, Quest Diagnostics Nichols Institute, 33608 Ortega Highway, San Juan Capistrano, CA 92690. Tel. 949 728-4578; fax 949 728-7852; email: stanley.j.naidescom

Received 2010-12-2
Accepted 2011-1-13
Published 2011-1-15

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