Tara Keil
Dongmei Liu2
Megan Lloyd
Jennifer Moffat
Robert Visalli- 1Department of Biomedical Sciences, Mercer University School of Medicine, Savannah, GA, United States
- 2Department of Microbiology and Immunology, Upstate Medical University, Syracuse, NY, United States
Although there are effective nucleoside analogs to treat HSV, VZV, and HCMV disease, herpesvirus infections continue to contribute to significant morbidity and mortality. Acyclovir is the drug of choice for HSV encephalopathy, yet there is an estimated 6–19% mortality rate with half of the survivors experiencing moderate to severe chronic neurological deficits. For VZV, current treatments are inadequate to prevent acute and persistent pain due to zoster. Treatment of HCMV with GCV requires close monitoring particularly in patients with impaired renal function and there are no approved treatments for congenital HCMV infections. New therapeutic options to control cytomegalovirus reactivation in bone marrow and stem cell transplant patients are needed to improve patient outcome. No successful chemotherapeutic options are available for EBV, HHV-6, 7, and 8. Drug resistance is a concern for HCMV, HSV, and VZV since approved drugs share common mechanisms of action. Targeting DNA encapsidation or capsid assembly provide additional options for the development of non-nucleoside, small molecule anti-herpesviral drugs.
Human Herpesviral Diseases – Toward Reducing Worldwide Morbidity and Mortality
The enveloped, dsDNA human herpesviruses (Herpesviridae) are classified as either alpha, beta or gamma herpesviruses depending on their genetic relatedness, host range, replication cycle and latency properties (Arvin, 2007). The subfamily Alphaherpesvirinae includes three relatively ubiquitous pathogens, herpes simplex viruses type 1 (HSV-1) and type 2 (HSV-2), and varicella-zoster virus (VZV). All three infect mucosal epithelia and establish life-long latency in cells of neuronal origin.
Primary infection and reactivation of latent HSV-1 or 2 results in asymptomatic shedding from the originally infected mucosal surface and/or symptomatic disease in the form of herpes labialis (cold sores) or genital lesions. Worldwide, 3.7 billion people under age 50 (67%) and 417 million people aged 15–49 (11%) are estimated to be infected with HSV-1 and HSV-2, respectively (Looker et al., 2015a,b). Genital herpes caused by either HSV-1 or HSV-2 is estimated to affect >400 million persons worldwide (Groves, 2016). HSV-1 is primarily associated with herpes labialis and HSV-2 with epidemic sexually transmitted herpes genitalis (Whitley and Gnann, 1992), yet both viruses can cause serious systemic diseases including herpetic keratitis and viral encephalitis. These latter diseases are of major concern in immunocompromised patients, especially those undergoing transplant surgery and chemotherapy. Globally, neonatal HSV infection is estimated to occur in about ten cases per 100,000 live births and results in significant morbidity and mortality (Looker et al., 2017). Recent studies also suggest an increased risk for Alzheimer’s disease for patients with the apolipoprotein 4 (APOE-ε4) allele isoform whom are predisposed to an elevated HSV-1 viral load in neural tissue (Steel and Eslick, 2015; Olsson et al., 2016; Agostini et al., 2018; Ashraf et al., 2018; Fulop et al., 2018; Hogestyn et al., 2018; Kristen et al., 2018).
The genus Varicellovirus contains the species human alphaherpesvirus 3, commonly known as varicella zoster virus (VZV or HHV-3). VZV infection typically occurs at a young age resulting in varicella (chickenpox). Varicella occurs primarily in unvaccinated children and young adults and can lead to complications such as encephalitis, pneumonia, or bronchitis (Gershon et al., 2015). VZV can reactivate later in life to cause neurologic conditions, especially herpes zoster (shingles) and post-herpetic neuralgia (Gilden, 2015). In some individuals, pain remaining after resolution of zoster lesions may become a debilitating disease. Additionally, as one of the TORCH infections, primary VZV infection during pregnancy can cause congenital varicella syndrome consisting of fetal limb hypoplasia, cutaneous scarring, and blindness in the fetus (Ahn et al., 2016). VZV remains the only herpesvirus for which vaccines exist: Varivax (Merck) and ProQuad (Merck) for primary varicella (chickenpox), and Zostavax (Merck) and Shingrix (GlaxoSmithKline) for zoster (shingles). However, these vaccines are not approved for use in pregnant women, people with certain allergies, and those with immune suppression. The vaccine strain can also establish latency and reactivate. The overall disease burden has been significantly reduced as vaccination rates have increased. Breakthrough cases with mild symptoms are occasionally observed in vaccinated persons. Leung et al. (2019) reported in 2019 that “levels of varicella vaccination coverage with two or more doses and the proportion of adolescents with evidence of immunity increased from 2007 to 2014, though 16% lacked evidence of immunity in 2014.” Hence, suboptimal vaccination rates, shingles in the aging population, and the potential role of VZV in other serious diseases such as ocular involvement (Kedar et al., 2019) or vasculopathy (Nagel et al., 2017; Nagel and Bubak, 2018) warrant continued development of effective treatment options for VZV.
Within the Herpesviridae sub-family of Betaherpesvirinae are the species human cytomegalovirus (HCMV or HHV-5) and human herpesviruses type 6A (HHV-6A), 6B (HHV-6B), and 7 (HHV-7). Shared characteristics include infection and establishment of latency in lymphocytes and monocytes/macrophages. Like the other herpesviruses, most people are infected with the Betaherpesvirinae by adulthood, and many do not present with symptoms. Primary infections are typically asymptomatic in immunocompetent individuals, however, HCMV infection during pregnancy can significantly impair fetal development (Zavattoni et al., 2014). HCMV-associated disease pathologies seen in immunocompetent patients include mononucleosis syndrome, diabetes mellitus types 1 and 2, Guillain-Barré syndrome, and potential malignancies [i.e., glioblastoma (Rahman et al., 2019)]. Congenital HCMV is the leading infectious cause of intellectual disability and deafness in children. There are no approved treatments for the ∼0.7% of pregnant women who develop primary HCMV infection during pregnancy (Kenneson and Cannon, 2007; Leruez-Ville et al., 2016). However, there is some evidence that hyperimmune globulin may be beneficial for managing first-trimester infections (Nigro et al., 2019; Schleiss, 2019). Current best practice consists of counseling mothers to limit behaviors that increase risk for contracting a primary HCMV infection during pregnancy. In immunocompromised patients, HCMV is recognized to cause hepatitis, retinitis, colitis, pneumonitis, esophagitis, polyradiculopathy, transverse myelitis, and subacute encephalitis (Gupta and Shorman, 2019). Solid organ transplant recipients often take medications that suppress their T-cell mediated immune response long-term to prevent allograft rejection, and thus are particularly at risk for HCMV disease (Azevedo et al., 2015). The recent approval of letermovir offers a new treatment option for HCMV in allogeneic stem cell transplant patients (see below). Acute HHV-6b and HHV-7 infection, known as 6th disease or roseola infantum, can present as a high fever with accompanying rash in young infants and toddlers. Reactivation of betaherpesviruses is not uncommon in immunocompromised transplant, cancer and AIDS patients (Campadelli-Fiume et al., 1999; Nogalski et al., 2014).
The gammaherpesviruses include Epstein-Barr virus (EBV) and HHV-8. Infectious mononucleosis and Burkitt’s lymphoma result from infection of B-cells with EBV (Houldcroft and Kellam, 2015). The presence of HHV-8, a common opportunistic pathogen of AIDS, is strongly associated with the development of Kaposi’s sarcoma (KS) (Cesarman, 2014).
Viral Terminase Inhibitors for Treating Human Cytomegalovirus Infections
Toxicity is an issue among approved HCMV therapies including ganciclovir (GCV), foscarnet and cidofovir. These drugs have complex administration and monitoring requirements and are associated with several toxicities including myelosuppression. For example, GCV, the preferred drug of the three is not recommended for patients when the absolute neutrophil count is under 500 cells/ml or when the platelet count is under 25,000/ml (Grayson, 2010). Hematologic malignancies and advanced HIV/AIDS, as well as many of the pharmacotherapies used to treat them, often result in myelosuppression. Patients affected by these diseases are among the highest risk group for severe HCMV infection, yet treatments options are limited. Herpesvirus terminases are part of the molecular nano-motor that initiates viral DNA translocation into empty capsids (Rao and Feiss, 2015). Inhibition of terminase activity results in the accumulation of empty viral capsids and no infectious viral particles are assembled. Terminase has been recognized as a viable antiviral target and several compounds that block the terminase complex have been described including the naphthalenesulfonate BAY 38-4766 (Buerger et al., 2001), benzimidazoles (Underwood et al., 1998; Buerger et al., 2001; Hwang et al., 2007), hydroxypyridonecarboxylic acid compounds (Wang et al., 2017; Kankanala et al., 2018) and letermovir (Goldner et al., 2011; Foolad et al., 2018; Gentry et al., 2019). Letermovir is a dihydroquinazolinyl-acetic acid that represents a new class of HCMV inhibitors that was recently approved for clinical use (Table 1). Briefly, In 2011 Goldner et al. (2011) reported a small molecule compound (AIC246) that had potent in vitro activity against HCMV with novel mechanism of action. The compound was active against laboratory and clinical isolates (EC50 ∼4 nM with CC50 90 μM). Due to letermovir’s distinct mechanism of action, cross resistance to cidofovir, foscarnet and/or ganciclovir was absent.
Table 1. Drugs and compounds targeting herpesviral DNA encapsidation and viral capsid assembly.
In murine studies of HCMV infected xenografts, AIC246 had favorable toxicological and pharmacological profiles and proved more effective against HCMV than valganciclovir (Lischka et al., 2010). Phase I and II trials demonstrated that AIC246 had a favorable pharmacokinetic profile, was well tolerated and safe (Chemaly et al., 2014; Stoelben et al., 2014; Kropeit et al., 2017a,b, 2018). In a phase three study, letermovir reduced clinically significant HCMV infection in allogeneic stem cell transplant patients (Marty et al., 2017). Successful Phase II and III clinical trials resulted in approval of letermovir in the United States, Canada, Japan, Switzerland, and the European Commission for the prevention of HCMV infection and disease in adult HCMV-seropositive recipients of an allogeneic hematopoietic stem cell transplant (Maffini et al., 2016; Fuji et al., 2017; Chen et al., 2018; Cho et al., 2018; El Helou and Razonable, 2019; Katayama and Iwato, 2019; Ljungman et al., 2019; Mori, 2019).
The viral terminase complex has a low frequency of natural polymorphisms and thus pre-existing mutations associated with resistance in clinical isolates without prior exposure to letermovir seemed unlikely (Pilorge et al., 2014). Douglas et al. (2019) demonstrated that patients taking letermovir had no significant increase in genomic HCMV variants after 24 weeks compared to patients who had been taking a placebo, suggesting low rates of resistance development to letermovir. However, laboratory and clinical resistance to letermovir has been demonstrated and can be mediated by amino acid substitutions within the HCMV UL56 gene (Chou, 2015, 2017; Goldner et al., 2015; Chou et al., 2018; Douglas et al., 2019; Frietsch et al., 2019; Jo et al., 2019; Komatsu et al., 2019; Piret and Boivin, 2019). Studies comparing the development of resistance in vitro for GCV and letermovir showed that mutations conferring resistance to letermovir developed more rapidly than gangciclovir (Chou et al., 2018). An increasing number of letermovir resistant isolates have been documented in patients thus complicating clinical management (Razonable, 2018). The emergence of clinical resistance further emphasizes the need for additional anti-HCMV therapeutic options.
Small Molecule Compounds Targeting Alphaherpesvirus Capsids and DNA Encapsidation
Capsid Assembly Inhibitors
Numerous capsid assembly inhibitors have been described for dengue (Scaturro et al., 2014), Hepatitis C (Kota et al., 2012), and, a first-in-human trial of GSL4, a Hepatitis B virus capsid assembly inhibitor (Merlini et al., 2019). In 2012, the first herpesvirus capsid assembly inhibitor, 35B2, a pyrazolo [1,5-c]1,3,5-triazin-4-one derivative (35B2) (Table 1) was identified (Inoue et al., 2012). 35B2 showed in vitro activity against both ACV resistant and sensitive strains of VZV. Strains resistant to 35B2 were found to have mutations in ORF40, the VZV major capsid protein. Infected fibroblasts treated with 35B2 showed altered localization of MCP. Additionally, electron microscopic studies demonstrated the lack of capsid formation in the presence of 35B2 suggesting that the pyrazolo compound affected normal capsid assembly. No in vivo results have been reported to date. The data suggest that novel antivirals can be identified that target herpesviral M to inhibit normal capsid formation.
Portal Inhibitors
Herpesvirus DNA enters and exits the capsid through its portal. The portal protein, located at a single capsid vertex is required for DNA packaging in dsDNA bacteriophages and herpesviruses. Portal proteins of the human herpesviruses, although only modestly conserved at the primary amino acid level, share a conserved core structure.
In 2000, the thiourea compound its N-(4-[3-(5-Chloro-2,4-dimethoxyphenyl)-thioureido]-phenyl)-acetamide and its 2-fluoro-benzamide derivative (WAY-150183; Table 1), were found to inhibit HSV-1 replication in vitro (van Zeijl et al., 2000). Lack of a functional portal on the capsid vertex prevented both the cleavage of concatameric viral DNA into genome length progeny and the packaging of the DNA into capsids. In 2003, a class of non-nucleoside N-(α methylbenzyl-N′-arylthiourea analogues, termed Compounds 1, 2, and 3 demonstrated in vitro inhibition of VZV replication (Visalli et al., 2003). The isolation of resistant isolates to either the HSV-1 or VZV inhibitors suggested that the compounds targeted UL6 or ORF54 portal proteins, respectively, and prevented DNA encapsidation (Visalli and van Zeijl, 2003; Visalli et al., 2003, 2014; Di Grandi et al., 2004). The HSV-1 compounds had good in vitro activity (0.4–1.5 uM) but no in vivo studies were reported for the compound series. The VZV compound series had excellent in vitro activity (IC50 10 nM – 1 μM), showed no cellular cytotoxicity (CC50 > 37 μM) and was effective against a panel of clinical isolates and ACV-resistant VZV strains. Only empty capsids were observed in the nuclei of VZV infected cells In the presence of compound.
Combined, the results suggested that small molecular thiourea compounds targeting herpesvirus portal proteins represented a new class of anti-herpesvirus inhibitors. Portal proteins are cyclical multimers formed of 12 or 13 subunits that create a hollow empty core or channel. Hence, the thiourea compounds likely inhibit encapsidation by affecting portal structure, function, and/or protein-protein interaction(s). Below, we provide the first in vivo evidence that a small molecule compound targeting a viral portal is a viable drug candidate. The host of range of VZV is limited to humans, therefor the in vivo efficacy of a thiourea analog was tested in a previously described SCID-Hu VZV infection model (Rowe et al., 2010; De et al., 2014). The results presented here are the first for any compound targeting a viral portal in an animal model.
Comp 1 (Table 1), an α-methylbenzyl thiorurea compound that prevented VZV DNA encapsidation in vitro, was evaluated in a SCID-Hu thymus/liver VZV infection model (Figure 1). Both doses of Comp 1 significantly reduced the VZV growth rate compared to vehicle (p = 0.0037). The treatment phase was extended beyond the typical 7 days to observe any potential side effects of the compound. Only the vehicle group lost weight whereas the compound treatment groups showed positive weight gain and the mice appeared well-hydrated with smooth fur indicating that Comp 1 was well-tolerated. Previous studies showed that compounds from the α-methylbenzyl series were not toxic in multiple cell lines [(Visalli et al., 2003), data not shown] nor in murine, canine and primate pharmacokinetic studies (data not shown). The results presented here merit further investigation of α-methyl benzyl analogs, in particular, newer compounds that have been optimized for oral bioavailability and that have activity against other herpesvirus family members.
Figure 1. SCID-Hu mice with thymus/liver xenografts were inoculated with VZVLUC (firefly luciferase) and treated with vehicle or Comp 1 at 2.5 or 5 mg/kg in Cremaphor-DMSO-Saline s.c. daily from 2 h after infection to Day 7. Each mouse was weighed on the day before virus inoculation in order to calculate the drug concentration in the preparations. (A) Mice were injected with D-luciferin (150 mg/kg s.c.) and then VZV replication was measured by IVIS bioluminescence imaging daily from days 1–10. VZV yield was calculated as fold change for each mouse by dividing Total Flux values by the lowest value on Day 1. The lines are the average for the group (N = 7 Vehicle group, N = 8 treatment groups), the error bars are the standard deviation of the mean. Both doses of Comp 1 significantly reduced VZV yield compared to vehicle on Day 7 (p = 0.0037; 1-way ANOVA with Dunnett’s Multiple Comparison Test). (B) Mice were weighed on Day 10 and the net change for each mouse was calculated. Each symbol represents one mouse (some mice in the Vehicle group lost weight due aggressive activity). No mice died in any of the three groups.
In 2017, a 5-chlorobenzo[b]thiophen derivative (45B5) (Table 1) was characterized as a potential anti-VZV compound (EC50 16.9 μM) (Yasui et al., 2017). All 45B5 resistant laboratory strains were found to have at least one mutation in ORF54. Cells infected in the presence of compound had decreased viral DNA synthesis and did not appear to affect portal-scaffold protein interactions. Therefore, it was postulated that 45B5 inhibits viral DNA release from the capsid portal vertex at the nuclear pore.
Perspective on Future Directions
The Herpesviridae are known to contribute significantly to worldwide human and animal morbidity and mortality. The herpesviral double stranded DNA genome is encased in an icosahedral protein capsid that is tethered to a lipid bilayer envelope by viral tegument proteins. The family name is derived from the Greek word herpein meaning “to creep” in reference to the unifying feature of these viruses to establish latency. Herpesvirus pathogenesis and disease manifestations are determined by the cell and tissue types that can be infected by the different viral species.
Nucleoside analogs such as ACV have been indispensable prophylactic and therapeutic treatment options. Even with the availability of effective nucleoside analogs, human herpesviruses are associated with substantial morbidity and mortality. We and others have proposed the development of new agents with unique mechanisms of action such as targeting the viral helicase-primase, ribonucleotide reductase, protease, glycoprotein attachment and fusion, viral protein kinases, and DNA encapsidation (e.g., terminase and portal inhibitors). Although several candidates with novel targets advanced to phase II and III clinical trials, only one compound, letermovir, has been approved for human use since the antisense antiviral fomivirsen (HCMV retinitis) and famciclovir more than twenty years ago (1998). The recent FDA approval of the letermovir is proof of principle that targeting herpesvirus DNA encapsidation is a viable chemotherapeutic strategy. In Figure 1 we show for the first time that targeting the viral portal protein in vivo is a viable option. It is possible that new compounds can be identified that target any of the three herpesvirus terminase subunits and/or portal proteins. There are still no approved chemotherapeutic options for EBV or HHV-6, 7, and 8. The limitations of current therapies due to specificity, toxicity, bioavailability and resistance merit the continued discovery and research of novel herpesvirus antivirals.
Data Availability Statement
The datasets generated for this study are available on request to the corresponding author.
Ethics Statement
The animal study was reviewed and approved by the IACUC [formerly known as the Committee for the Humane Use of Animals (CHUA)] evaluates the animal care and use program at SUNY Upstate Medical University and facilitates the conduct of meaningful scientific research that: (1) avoids or minimizes discomfort, distress, and pain in experimental animals consistent with sound scientific practices, (2) uses the minimum number of animals necessary to obtain valid results, and (3) considers non-animal models wherever possible. OLAW PHS Assurance: D16-00318; USDA Certificate: 21-R-0037; NYSDOH Unit: A073; AAALAC: Full Accreditation (accredited since 7/31/1999).
Author Contributions
TK, JM, and RV wrote the manuscript. JM and RV designed the experiments and analyzed the data. DL, ML, WC, and JM performed the animal studies. All authors contributed to the article and approved the submitted version.
Funding
JM was supported by NIAID, Division of Microbiology and Infectious Diseases, contract HHSN272201000023I.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
The authors wish to thank Dr. David Goode (Department of Chemistry, Mercer University) for assistance in drawing the compound structures.
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Keywords: antiviral, herpesvirus, letermovir, portal, terminase, encapsidation
Citation: Keil T, Liu D, Lloyd M, Coombs W, Moffat J and Visalli R (2020) DNA Encapsidation and Capsid Assembly Are Underexploited Antiviral Targets for the Treatment of Herpesviruses. Front. Microbiol. 11:1862. doi: 10.3389/fmicb.2020.01862
Received: 07 January 2020; Accepted: 15 July 2020;
Published: 12 August 2020.
Edited by:
Jason Kindrachuk, University of Manitoba, CanadaReviewed by:
Jocelyne Piret, Research Center of the CHU de Québec, CanadaGualtiero Alvisi, University of Padua, Italy
Copyright © 2020 Keil, Liu, Lloyd, Coombs, Moffat and Visalli. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Robert Visalli, Visalli_RJ@mercer.edu