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. 2006 Jun 14;8:55–62. doi: 10.1251/bpo118

Direct application of plasmid DNA containing type I interferon transgenes to vaginal mucosa inhibits HSV-2 mediated mortality

Bobbie Ann Austin 1, Cassandra M James 2, Peter Härle 3, Daniel JJ Carr 4,✉
PMCID: PMC1489265  PMID: 16900260

Abstract

The application of naked DNA containing type I interferon (IFN) transgenes is a promising potential therapeutic approach for controlling chronic viral infections. Herein, we detail the application of this approach that has been extensively used to restrain ocular HSV-1 infection, for antagonizing vaginal HSV-2 infection. We show that application of IFN-α1, -α5, and –β transgenes to vaginal mouse lumen 24 hours prior to HSV-2 infection reduces HSV-2 mediated mortality by 2.5 to 3-fold. However, other type I IFN transgenes (IFN- α4, -α5, -α6, and –α9) are non effectual against HSV-2. We further show that the efficacy of IFN-α1 transgene treatment is independent of CD4+ T lymphocytes. However, in mice depleted of CD8+ T lymphocytes, the ability of IFN-α1 transgene treatment to antagonize HSV-2 was lost.

Keywords: Virus, Interferon, T-lymphocyte, Transgene

Introduction

Herpes simplex virus 2 (HSV-2) is a sexually transmitted disease that causes painful recurrent mucosal cutaneous ulcerations. The overall estimated seroprevalence among humans living in the United States is 21.9% (1). Being a disease process with a disparate distribution in populations, HSV-2 affects even a higher percentage of humans of female gender, low socioeconomic status, and African or Mexican heritage (1, 2). Other risk factors for HSV-2 infection include: use of contraceptives in women (3, 4), minimal education, and number of sexual patterns (5). The development of genital ulcerations also augments the risk of human immunodeficiency virus (HIV) transmission (6); reciprocally, the infectiousness of HIV also increases during periods of HSV-2 reactivation (6).

Like other herpes viruses humans are the predominate host for HSV-2, and the virus establishes a lifelong infection. HSV-2 spreads from one human host to another via transmission of infectious virus in mucosal secretions at epithelial surfaces. Virus initially replicates within epithelial tissue in the initial site of inoculation prior to entering associated sensory ganglia, such as the sacral ganglia. Within sensory ganglia neurons, HSV-2 establishes a latent infection, from which the virus periodically reactivates and re-infects the initial site of infection. Episodic reactivations transpire as many as 4-5 times per year. However, recrudescent viral shedding is also common (7-9).

While HSV-2 is most commonly coupled with urogenital tract lesions, the virus can also inoculate mucosal epithelium in the upper body and establish latent infection in associated sensory neurons. A number of ocular diseases originate from HSV-2 infection including: anterior uveitis, stromal keratitis, and retinal necrosis (10, 11). HSV-2 can further spread from sensory ganglia to the CNS causing potentially lethal meningitis and encephalitis (12). Substantial increases in the incidence of HSV-2 infections in recent years have prompted studies to develop vaccinations and anti-viral therapies to curb this epidemic (13, 14).

Naked DNA vaccines encoding viral antigens or immune system adjuvants, such as chemokines have been tested as experimental vaccines against herpes simplex viruses 1 and 2 (15-21) and other viruses. A number of advantages with DNA vaccination have been enumerated including: relatively inexpensive vaccine preparation and resistance to temperatures over 50°C, both of which are critical factors for vaccination in resource poor populations, where up to 69% of women have serological evidence of HSV-2 (22). To better understand mechanisms of endogenous anti-herpes pathways, our lab utilizes plasmid DNA encoding type I interferon (IFN) transgenes as a means to control virus replication and spread.

IFNs are endogenous anti-viral cytokines elicited in response to viral infection. Transfection of mice with type I IFN transgenes is an established approach to reduce HSV-1 mediated mortality (23). Furthermore, the ability of type I IFN transgenes to antagonize HSV-1 relies on OAS/RNase L pathway induction (23), a known downstream IFN effector, which inhibits viral infectivity via RNA degradation. Transfection of mice with IFN-α1 transgenes also enhances cumulative survival of mice vaginally infected with HSV-2 (24). However, the facility of IFN-α1 transgene treatment to antagonize HSV-2 does not require induction of the OAS/RNase L pathway. Conversely, the ability of IFN-α1 transgene to antagonize HSV-2 requires induction of protein kinase R, an IFN inducible anti-viral pathway that inhibits protein synthesis (25). Presently, we detail the methodology for utilizing type I IFN transgenes to manage vaginal HSV-2 infection in a mouse model. We further show that the effectiveness of IFN-α1 transgenes requires CD8+ T lymphocytes. Finally, we assess the significance of other type I IFN trangenes at preventing HSV-2 mediated mortality.

Materials and Methods

Treatment of mice

Animal treatment was consistent with the National Institutes of Health Guidelines on the Care and Use of Laboratory Animals. All procedures were approved by the University of Oklahoma Health Sciences Center and Dean A McGee Eye Institutional Animal Care and Use Committees. Female ICR mice (Sprague Dawley, from Harlan Sprague Dawley), ages 6-8 weeks were subcutaneously injected with 2 mg DepoProvera 5 d prior to infection, since progesterone facilitates vaginal HSV-2 infection (26, 27). Four days after administration of DepoProvera, mice were anesthetized by i.p. injection with xylazine (2mg/ml; 6.6 ml/kg) and ketamine (30 mg/ml; 100 mg/kg). Subsequently, vaginal mucous was removed with sterile calcium alginate fiber tipped swabs (Fisher Scientific) prior to vaginal transfection with IFN transgenes - local administration of 100 μg DNA in 20 μl TE buffer - 10 mM Tris, 1 mM ethylendiaminetetracetic acid (EDTA), pH 8.0. Five days after administration of DepoProvera, mice were anesthetized (as described previously) and vaginal mucous was again removed prior to infecting vaginal lumen with 2,400 plaque forming units (PFU) HSV-2. Mice were monitored over 30 d post-infection (p.i.), and mortality was recorded for each group of animals.

Virus and cells

All culture media reagents were from Life Technologies, Gaithersburg, MD. Vero cells (African green monkey kidney), obtained from the American Type Culture Collection (Manassas, VA) were cultured in RPMI 1640, supplemented with 5% FBS, 2 % antibiotic/antimycotic, and 0.2 % gentamicin. Cells cultures were incubated in an atmosphere of 37°C, 5% CO2, and 95% humidity.

A clinical isolate of HSV-2 was obtained from University Hospital (New Orleans, LA) and propagated on Vero cells (28). Specifically, confluent monolayers of Vero cells, grown in two T-175 culture flasks, were infected with 0.1 MOI HSV-2, diluted in 6 mls prepared RPMI media. After 1 hour, medium was replaced with 20 ml fresh complete medium. When 90% cytopathic effect was observed, cells were subjected to one freeze thaw cycle. Cells were collected and non viral cellular debris was pelleted away from virus by centrifugation for 15 minutes at 4,000 rpm. Supernatant was further clarified by one more centrifugation for 15 minutes at 4,000 rpm. HSV-2 was pelleted from the clarified supernatant by centrifugation at 20,000 g × 2 h. Viral pellets were washed two times with sterile 1x phosphate buffered saline (PBS) and viral suspensions were combined in 1 ml sterile 1× PBS. Aliquots (50 μl) were stored at -80°C. Viral titer in triplicate was determined by transferring logarithmic dilutions (10-5 to 10-9) of HSV-2, diluted in complete medium, onto confluent Vero cells in 24-well plates. After 1 hour, medium was replaced with 0.5 % methylcellulose, diluted in complete medium. Viral plaque formation was assessed after a 32 h incubation period and recorded as PFU/ml.

CD4+ and CD8+ T cell depletion

CD4+ and CD8+ T lymphocytes were depleted and the depletion of T lymphocyte populations was monitored as previously described (29).

Plasmid DNA construction

The plasmid backbone, pkCMV (vector) was obtained from Vical Inc., San Diego, CA. This vector consists of: a) plasmid double stranded DNA backbone, b) immediate early CMV promoter for expression in mammalian cells, c) intron with splice donor/splice acceptor where the murine IFN transgenes (575-626 bp) were inserted (30), d) ori sequence for replication in mammalian cells, e) SV40 polyadenlyation signal, f) pUC origin of replication for propagation in Escherichia coli g) kanamycin resistance gene for selection in E. Coli. Further details about the original source and cloning procedures (30-34) have been described. Plasmid constructs were transformed into E. coli strain INVαF’ (Invitrogen, Carlsbad, CA) and products were analyzed by agarose gel electrophoresis (30). More details about plasmid production and purification can be found in the protocols section.

Statistical analysis

Survival studies were analyzed for significance (p≤0.05) by the Mann-Whitney U rank sum test, using the GBSTAT program (Dynamic Microsystems, Gaithersburg, MD).

Results

In ICR mice, which are highly susceptible to the lethal effects of herpes (35), we previously showed that transfection of mouse corneas with IFN-α1 and –β transgenes, 24 hours prior to HSV-1 infection, enhanced the cumulative survival of mice by 3-fold (23). Other type I IFN transgene treatments (IFN-α5 and –α6) were not effective at preventing the lethal effects of HSV-1 infection (23). To further explore whether type I IFN transgene subtypes also provide diverse levels of protection against HSV-2 infection, survival studies with type I IFN transgene treatment of female ICR mice, vaginally infected with HSV-2 were initiated. The cumulative survival of mice treated with IFN-α1, -α5, and –β transgenes, 24 hours prior to vaginal HSV-2 infection was enhanced by 2.5 to 3-fold (Fig. 1) in comparison to mice treated with vector alone (plasmid DNA backbone without an IFN transgene). Other IFN transgenes (IFN-α4, -αand –α9) were not effective at reducing HSV-2 mediated mortality (Fig. 1).

Fig. 1. A comparison of cumulative survival of mice when treated with IFN-α1, -α5, and –β transgenes and with vector alone.

Fig. 1

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Previously, we showed that CD4+ and CD8+ T lymphocytes are required for the anti-HSV-1 activity of IFN-α1 transgene treatment (29). To determine whether both CD4+ and CD8+ T lymphocytes are also required for the anti-HSV-2 activity of IFN-α1 transgene treatment, CD4+ and CD8+ T lymphocytes were depleted in mice hormonally susceptible to HSV-2. In comparison to treatment with normal rat serum, the cumulative survival of HSV-2 infected mice decreased by 2 and 4-fold, respectively, following depletion of CD8+ and CD4+ T lymphocytes (Fig. 2A). While the absence of both types of T lymphocytes negatively affected the survival of HSV-2 infected mice, with IFN-α1 transgene treatment, the impact of CD4+ T lymphocyte depletion was reversible. Specifically, mortality rates at the end of 30 d with IFN-α1 transgene treatment in CD4+ T lymphocyte depleted mice as well as mice treated with normal rat serum were the same (Fig. 2B). In contrast to this observation, in mice depleted of CD8+ T lymphocytes, the effectiveness of IFN-α1 transgene treatment was lost. With IFN-α1 transgene treatment and CD8+ T lymphocyte depletion, survival following HSV-2 infection decreased 2-fold, in comparison to survival with IFN-α1 transgene treatment in mice treated with normal rat serum (Fig. 2B).

Fig. 2. The treatment of HSV-2 infected mice and cumulative survival and the impact of CD4+ T-lymphocyte depletion.

Fig. 2

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Discussion

Previous work from our lab has shown that IFN transgene treatment is effective at reducing herpes mediated mortality, inhibiting viral replication, reducing viral antigen expression, reducing viral protein synthesis, reducing inflammatory leukocyte infiltration, inducing interferon stimulated gene expression, and inhibiting herpes reactivation (23, 24, 30, 36-41). In applying this methodology to antagonize other viruses, it is noteworthy that we have found application of transgenes 24 hours before HSV-1 infection to be more effective than earlier time points before infection or transgene treatment post-infection (29, 37, 38), with a minimal effective dose of 50-100 μg DNA/mouse eye (HSV-1) or 100 μg DNA/mouse vagina (HSV-2). The usefulness of transgene treatment, with respect to time of infection, is likely related to the transient nature of transgene expression following transfection. With IFN-α1 transgene treatment, transgene expression is only detected 24-72 hours post-transfection (37). The short-term nature of transgene expression following transfection using a naked DNA approach is a known obstacle to DNA based vaccine strategies (42). Transgene inoculation intramuscularly provides longer term expression (43).

In addition to length of expression, efficiency of transfection is also challenging. Following plasmid DNA transfection, only a small fraction of DNA molecules actually transfect target cells (42). Thus, high plasmid doses are typically used in animal models (42, 44). In our system we have shown, using a LacZ reporter gene, evidence of gene expression in vaginal epithelium at 3 days following application of plasmid DNA (24). The plasmid DNA also trafficks to the spinal cord and lymphatic tissue, 24 hours post-transfection of HSV-2 infected tissue (24). Coupled with the efficiency of transfection, we have encountered difficulties measuring biologically active levels of IFN following transfection of vaginal epithelium. However, we are able to detect increased levels of interferon stimulated gene expression using real time PCR (25). Ongoing efforts to overcome obstacles related to length and efficiency of transfection include: improving transfection efficiency and protecting DNA from degradation (42).

Transient expression is considered advantageous in the respect that foreign DNA is less likely to insert into the host genome (45). Even so, it is a critical consideration to develop delivery systems that target gene delivery to appropriate tissues. Delivery of IFN-transgenes via a mucosal route is a useful approach to study immune response because mucosal surfaces are the most likely site for herpes to invade hosts, and application of plasmid DNA is known to induce local and systemic cellular and humoral immunity (45). Related to this, it is vital to use a vector (control) in each experiment to separate IFN-inducible effects from immune response elicited by CpG motifs in the plasmid DNA backbone. In our model following topical application of plasmid DNA to vagina, reporter gene expression is detected locally and also in lymph node and spinal cord (24). Likewise, following topical application of plasmid DNA to eye, reporter gene expression is detected locally, with the innervating sensory ganglia (i.e., trigeminal ganglia), and also in spleen (29). Stimulation of humoral and cellular immunity with plasmid DNA is considerably less harmful than utilizing attenuated virus (46), and the adjuvant effect of CpG DNA is considered beneficial for immune studies because a separate adjuvant is not required. Nevertheless, identification of critical sites of targeted delivery along with increased delivery efficiency would enable the smallest effective dose. Smaller doses targeted to specific cells both reduce random distribution of foreign genes and increase therapeutic cost effectiveness.

Attempts to control delivery of plasmid DNA include use of polymers that condense plasmid DNA and increase diffusion through plasmid membrane, and use of cell-specific targeting ligands (47). Cell-specific targeting has been achieved by conjugating peptide to proteins that function to condense plasmid DNA. Moreover, conjugation of certain antibodies to lipids has been shown to increase efficiency of cell uptake. For example, conjugation of anti-transferrin antibodies to liposome-DNA complexes has been shown to increase gene delivery to cornea (48). Conjugation of transferrin to polyethyleneimine has further been shown to enhance transfection efficiency, likely via enhanced endocytosis (48).

Other attempts to control transgene expression involve development of tissue and cell-specific expression systems. Our IFN transgenes are under the control of a promiscuous viral promoter, CMV. This factor combined with distribution of plasmid DNA both locally as well as to lymphatic system, potentially leads to more widespread distribution of IFN than required for controlling site-specific herpes pathogenesis. Systemic release of high levels of IFN is known to cause numerous unwanted side effects including: fever, chills, headaches, achy muscles, diarrhea, loss of appetite, anemia, increased bleeding and bruising, and birth defects. Development of a more site-specific IFN-based anti-viral therapy with controlled expression is a long term goal. Generally, non-viral based transfection agents are not effective for delivering genes to the nervous system. Use of replication defective herpes amplicons or other replication defective neurotropic viruses show promise as potential vectors for delivery of anti-viral genes specifically to sites of herpes infection.

Acknowledgments

This work was supported by USPHS grant AI053108 (DJJC) and additional support from an NEI core grant EY12190. The authors have no conflicts of interest to declare related to this publication.

Appendix

Protocols

Protocol for plasmid purification: A slightly modified protocol from that provided with the Quantum Prep Plasmid Maxiprep Kit (Bio-Rad Laboratories, Inc.) is listed below. Further details about plasmid purification have been described (49).

Re-suspension buffer: 50 mM d-glucose, 10 mM EDTA, 25 mM Tris HCl (pH 8.0), and 2 mg/ml lysozyme

Alkaline Lysis solution: 0.2 N NaOH and 1% SDS in sterile double distilled water

Wash buffer: 200 mM NaCl, 40 mM Tris HCl, 4 mM EDTA, adjust pH to 7.5, and add an equal volume of 100% ethanol

Neutralization buffer: 4 M potassium-acetate (pH 4.8)

Weigh 23.55 g potassium acetate. Add 66 ml sterile double distilled water and 28.5 ml glacial acetic acid. Titrate with approximately 1.5 ml concentrated HCl to pH 4.8. Adjust volume to 100 ml with sterile double distilled water.

TE buffer: 10 mM Tris, 1 mM EDTA, pH 8.0

  1. Grow bacteria containing each interferon transgene in 1L of sterile Terrific broth (Bio 101 Systems), containing 50 μg/ml kanamycin, by incubating overnight (14-16 h) at 37°C with shaking (200 rpm).

  2. Pellet bacteria by centrifugation (5 minutes at 5,000g) in 500 ml sterile centrifuge bottles. Cells may be frozen at this point.

  3. Thaw cells at room temperature. Re-suspend cells by adding 15 ml cell re-suspension buffer containing DNase free RNase A (40 units/ml) to the pellet obtained from each 500 ml of bacteria broth. Pipet up and down until the cells are completely re-suspended.

  4. Add alkaline lysis buffer, containing a high concentration of anionic detergent (23 ml/pellet obtained from 500 ml bacteria broth) to lyse cell membranes, denature chromosomal DNA and proteins, and release plasmid DNA into the supernatant. Make sure that SDS has not precipitated out of solution by making the solution fresh, or warm solution to 37°C prior to use to dissolve any visible precipitate. Mix by swirling the bottle. Avoid vortexing at any time in the procedure to avoid shearing DNA.

  5. Neutralize by addition of 15 ml neutralization solution to return the pH to normal and allow the 2 strands of plasmid DNA to return to the native state. Make sure there is no visible precipitate in the neutralization solution; if precipitate is visible, warm to 37°C prior to use.

  6. Centrifuge at 10,000 g × 30 minutes to remove precipitated membrane, SDS, protein, and chromosomal DNA. Pour supernatant, containing plasmid DNA into a new centrifuge bottle. Centrifuge a second time at 10,000g × 10 minutes to remove any remaining debris.

  7. Bind plasmid DNA to a diatomaceous earth based DNA binding matrix by addition of 20 ml re-suspended matrix to cleared lysate. Swirl gently for 30 seconds. Allow DNA to bind for 5 minutes, then centrifuge for 5 minutes at 3,000 g to pellet the matrix.

  8. Wash matrix 4 times with one volume of wash buffer by centrifugation for 5 min at 4,000 rpm.

  9. Elute DNA with 5 ml sterile water × 2 -3 washes. Collect separate fractions from each wash. Typically one of the fractions will be more pure than the others.

  10. Precipitate plasmid DNA by adding 1/18th volume of 5 M NaCl and 2 volumes of cold 95-100% ethanol. Precipitate DNA overnight in the fridge.

  11. Pellet DNA by centrifugation for 30 minutes at 10,000g.

  12. Wash pellet by addition of 1 ml 70% ethanol. Tap tube to re-suspend plasmid DNA. Decant into microcentrifuge tube and centrifuge at 10,000 rpm for 1 minute. Repeat 5 times.

  13. Dry the pellet before re-suspending in TE buffer.

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