key: cord-0718712-9ktbr62c
authors: Nau, Jeffrey; Luthra, Priya; Lanzer, Kathleen; Szaba, Frank; Cookenham, Tres; Carlson, Eric
title: Varenicline Prevents SARS-CoV-2 Infection In Vitro and in Rhesus Macaques
date: 2021-06-30
journal: bioRxiv
DOI: 10.1101/2021.06.29.450426
sha: 4763aaa2c90bf9261467f76197ea1f6f7c3af177
doc_id: 718712
cord_uid: 9ktbr62c

Background SARS-CoV-2 infections have resulted in a global pandemic, but an antiviral therapy for this novel strain of coronavirus does not currently exist. The objective of our study was to investigate the antiviral potential of the nicotinic acetylcholine receptor (nACHR) agonist varenicline tartrate against SARS-CoV-2. Methods We assessed antiviral activity using in vitro human cell assays and we assessed in vivo efficacy in a rhesus macaque model. Results In vitro studies found that varenicline tartrate, over a range of concentrations, reduced the infectivity of SARS-CoV-2 wildtype, alpha, and beta variants in Calu-3 cells and Caco-2 cells, with maintenance of cell viability. In vivo studies found that varenicline tartrate, administered as a nasal spray to rhesus macaques, reduced SARS-CoV-2 wildtype viral load and inhibited viral replication in the nasal mucosa and upper airway. Conclusion Although the study reported here was exploratory, we have confirmed that the nAChR agonist varenicline has the potential to interact with and inhibit SARS-CoV-2 infection and replication.

ABSTRACT Background SARS-CoV-2 infections have resulted in a global pandemic, but an antiviral therapy for this novel strain of coronavirus does not currently exist. The objective of our study was to investigate the antiviral potential of the nicotinic acetylcholine receptor (nACHR) agonist varenicline tartrate against SARS-CoV-2.

We assessed antiviral activity using in vitro human cell assays and we assessed in vivo efficacy in a rhesus macaque model.

In vitro studies found that varenicline tartrate, over a range of concentrations, reduced the infectivity of SARS-CoV-2 wildtype, alpha, and beta variants in Calu-3 cells and Caco-2 cells, with maintenance of cell viability. In vivo studies found that varenicline tartrate, administered as a nasal spray to rhesus macaques, reduced SARS-CoV-2 wildtype viral load and inhibited viral replication in the nasal mucosa and upper airway.

Although the study reported here was exploratory, we have confirmed that the nAChR agonist varenicline has the potential to interact with and inhibit SARS-CoV-2 infection and replication.

The severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is a novel strain of coronavirus that was first identified as an infectious agent in humans in 2019. 1 The disease caused by the SARS-CoV-2 viral outbreak was termed coronavirus disease 2019 ; the major clinical manifestations include cough, shortness of breath or difficulty breathing, fever, chills, muscle pain, headache, sore throat and a new loss of taste or smell.

This viral outbreak was recognized as a pandemic threat by the World Health Organization and began to rapidly overload health care systems, causing substantial morbidity and mortality worldwide. 2, 3 Recent evidence reports from 600,000-900,000 deaths in the United States, and from 3.9-7.1 million deaths worldwide. 4,5 Importantly, an effective preventative antiviral treatment for SARS-CoV-2 has not yet emerged. 6 Compounding the urgency for an effective treatment is the emergence of mutations (with changes in the spike protein) with increased rates of transmission and mortality. 7, 8 For example, the beta variant (first identified in South Africa) has 50% increased transmission and reduced neutralization by postvaccination antibodies compared with wildtype virus, 9 and the alpha variant (first identified in the United Kingdom) is more transmissable than the wildtype and has a 62.8% increase in mortality after 28 days. 10 Many studies have shown one route that SARS-CoV-2 uses to enter the host cell is via binding to angiotensin-converting enzyme-2 (ACE2) and subsequent fusion with the cell membrane. [11] [12] [13] Additional studies have shown that SARS-CoV-2 enters host cells mainly through ACE2-positive and transmembrane serine protease 2-positive nasal epithelial cells, which are specific ciliated and mucous secreting cells of the nasal mucosa. 14,15 Therefore, the nasal cavity potentially represents the most susceptible mucosal surface for infection within the respiratory tree, although the ocular surface is also susceptible to infection. 16 Concurrently, based on early observations of low smoking prevalence among hospitalized COVID-19 patients in China and the USA, a role for the nicotinic cholinergic system in SARS-CoV-2 infection was postulated. 17, 18 However, more recent studies suggest the relationship between smoking and SARS-CoV-2 is complex, and that smoking may indeed be a risk factor for severe disease, 19 but the role of nicotine and the nicotinic cholinergic system remains pertinent, though unclear.

Farsalinos et al. have identified a "toxin-like" amino acid in the receptor binding domain of the spike glycoprotein of SARS-CoV-2, that is homologous to a sequence found in snake venom known to interact with nicotinic acetylcholine receptors (nAChRs). 20, 21 Further, binding simulation studies have shown that SARS-CoV-2 has the ability to directly bind to nAChRs via its spike protein. 22 Binding to the nAChRs may explain the immune-mediated flares or myasthenia gravis-like findings in patients with autoimmune disease infected with SARS-CoV-2, or those vaccinated with mRNA/DNA based vaccines. 23, 24 Receptor binding raises the possibility that cholinergic agonists may have the ability to block nAChR interaction with SARS-CoV-2, as well as other coronaviruses that share similar amino acid sequences in their receptor binding domain. To complicate this potential role, the nicotine cholinergic system may also interact with the ACE2 system. 19 Overall, it is possible that nAChR agonists may have therapeutic value in SARS-CoV-2 infected patients, making them worthy of study.

Varenicline tartrate is a highly selective small-molecule nAChR agonist with full agonist activity at the α 7 receptor and partial agonist activity at the α 3β4, α 3α5β4, α 4β2, and α 6β2 receptors. [25] [26] [27] [28] Varenicline tartrate is FDA approved and indicated for use as an aid to smoking cessation treatment in oral tablet form 29 and is currently under investigation as a preservative-free aqueous nasal spray formulation (OC-01) for dry eye disease. In this study, we hypothesized that varenicline may have antiviral activity against SARS-CoV-2 by inhibiting viral host cell entry and thereby disrupting the replication cycle. Of note, varenicline in particular has been shown, using computational strategies, to bind to the spike glycoprotein of SARS-CoV-2 at the hinge site with high affinity. 30 By administering as a topical formulation, OC-01 (varenicline) nasal spray of offers a unique opportunity to target SARS-CoV-2 at the primary site of infection, binding, amplification, and transmission. Topical administration of varenicline as an aqueous nasal spray allows for the delivery of a high localized concentration to the mucosa that is unlikely to be achieved with systemic delivery.

The aim of this initial exploratory study was to investigate the antiviral potential of varenicline against SARS-CoV-2 using in vitro cell assays and an in vivo rhesus macaque model. Prior studies with SARS-CoV-2 wildtype using rhesus macaque model have found that infection results in mild to moderate clinical signs and high titers of virus in the upper and lower respiratory tract with multifocal lung inflammation. 31 and was pre-treated with various concentrations of varenicline tartrate (control = DMSO) for 1 hour at 37º C and under 5% CO 2 . Following the pre-treatment period, cells were exposed to the pre-treated SARS-CoV-2/varenicline tartrate for 2 hours and the plates were shaken every 15 minutes. Following this 2 hour incubation, the culture medium was removed and the Cell viability was determined at 72 hours using the CellTiter-Glo Luminescent Cell Viability Assay kit (Promega) and luminescence was recorded using a POLARstar OPTIMA plate reader (BMG Labtech). The percent cell viability was calculated by normalizing against DMSO only controls.

All statistical analyses were performed using GraphPad Prism (version 9, GraphPad Software, Inc.). For the calculation of 50% inhibitory concentration (IC 50 ) and 50% cytotoxic concentration (CC 50 ) of the compound, which indicate the inhibitor concentration leading to 50% reduction of infection or cell viability respectively, non-linear fit regression models were used. 

Quantitative RT-PCR for SARS-CoV-2 genomic (g) RNA Samples were assayed for virus concentration by SARS-CoV-2-specific qRT-PCR, which estimated the number of RNA copies in the collected tissue samples. Viral RNA was isolated from collected tissue samples using the Qiagen MinElute virus spin kit and a control for the amplification reaction was isolated from the SARS-CoV-2 stock. qRT-PCR was performed with Applied Biosystems 7500 Sequence detector and amplified using the 

We assessed the antiviral activity of varenicline tartrate against SARS-CoV-2 in Calu- Figure 2D ). Importantly, these in vitro conditions were not toxic and cell viability was maintained.

We assessed the antiviral activity of varenicline against SARS-CoV-2 in rhesus macaques. During the study, there were only minor changes in body weight and rectal temperatures, and no changes in respiratory rate, respiratory effort, cough, and fecal consistency (data not shown). No adverse events were detected. Figure 3D ).

To our knowledge these are the first in vitro and in vivo studies to show that a nAChR agonist has antiviral activity against SARS-CoV-2. Our initial in vitro cell assays demonstrated that varenicline reduced viral titers over a range of doses, against wildtype, alpha, and beta variants, without a negative impact on cell viability. Our initial in vivo studies indicated that varenicline administered as an aqueous nasal spray (approximately 1mM at each administration based on airway surface liquid calculations) prevented SARS-CoV-2 infection and replication in the nasal cavity of rhesus macques less than 24 hours after virus challenge. The results suggest a sound rationale for the use of OC-01 (varenicline) nasal spray as a therapeutic for pre-exposure/post-exposure prophylaxis to prevent infection, to decrease viral load, and/or to lessen severity and transmission of SARS-CoV-2. Additionally, in vitro results suggest that the mechanism for viral inhibition is conserved with the SARS-CoV-2 alpha and SARS-CoV-2 beta variants. Moreover, the nasal spray formulation of varenicline enables administration of a therapeutic dose directly to the nasal mucosa, which represents the most likely route of virus entry, replication, and infection for SARS-CoV-2. 12, 22, [34] [35] [36] In addition , there is a significant population of nAChRs on the olfactory bulb within the nasal mucosa; 37 this may help to understand the chemo-sensitive disorders seen with SARS-CoV-2 infection, such as loss or decline of taste and smell (ageusia and anosmia, respectively), which have been reported as unique clinical features of COVID-19. 38, 39 Our results are consistent with data from in silico studies that suggested varenicline binds directly to the receptor binding domain of the spike glycoprotein of SARS-CoV-2 at the hinge site with high affinity. This binding may prevent a change in the spike protein to the "up-conformation" and inhibit subsequent binding by the ACE2 and/or nAChR binding site, 30 thus potentially preventing host cell infection. In addition, the spike glycoprotein of SARS-CoV-2 may also directly bind with nAChRs, and binding studies have suggested that the Y674-R685 region of the protein adopts particular confirmations when binding to the α 4β2 and α 7 nAChR subtypes, 22 which also have the same high affinity for varenicline. 25 Therefore, unlike anti-SARS-CoV-2 vaccines and antibody therapeutics, the antiviral activity of varenicline is likely to be conserved for different SARS-CoV-2 variants as varenicline's affinity for nAChRs or the Y674-R685 region of the spike protein is completely independent of virus mutations. [25] [26] [27] [28] 30 Although the studies reported here were exploratory, we have confirmed that the nAChR agonist varenicline, the active ingredient of OC-01 nasal spray, has the potential to interact with and inhibit SARS-CoV-2 infection and replication. Further, the nicotinic cholinergic system has been postulated to be involved in the pathophysiology of severe COVID-19 due to the immune dysregulation and cytokine storm, as the cholinergic antiinflammatory pathway may be an important regulator of the inflammatory response. 17, 40 Given the in vitro and in vivo effectiveness seen in the studies, varenicline nasal spray warrants further investigation as an antiviral agent for pre-exposure/post-exposure prophylaxis, and/or prevention of transmission of SARS-CoV-2 wildtype and variants.

This study was sponsored by Oyster Point Pharma, Inc., the manufacturer of investigational varenicline OC-01 nasal spray. The Viral Disease and Translational Science Program at Trudeau Institute (Saranac Lake, NY) was a vendor, paid to complete the in vitro work outlined in this manuscript. BIOQUAL Inc. (Rockville, MD) was a vendor, paid to complete the animal work outlined in this manuscript. Medical writing assistance was provided by Janelle Keys, PhD, CMPP of Envision Pharma Group, and was funded by Oyster Point Pharma, Inc. Envision's services complied with international guidelines for Good Publication Practice (GPP3).

Oyster Point Pharma, Inc., was involved in the study designs, data collection, data analysis, and preparation of the manuscript.

EC and JN participated in the study design, interpretation of study results, and drafting of the manuscript. All authors participated in the critical revision and approval of the final version of the manuscript. PL, KL, FS and TC were involved in the in vitro study execution, data collection, and data analysis.

The author(s) have made the following disclosure(s). PL: research grant support, Oyster 

Each animal (N = 2) was treated with varenicline OC-01 nasal spray into each nostril 4 times daily for 5 days. On Day 1, the first and second OC-01 doses were administered, then animals were challenged with 1x10 5 pfu of SARS-CoV-2 WA/1/2020 isolate, then the third and forth OC-01 doses were administered. On Days 2 to 5, 4 doses of OC-01 were given, and on Day 6, 2 doses of OC-01 were given, and then animals were euthanased. Nasal swabs were collected for viral load analysis by qRT-PCR. Control animals (N = 3) did not received OC-01 treatment.

The target cells, Calu-3 and Caco-2, as well as SARS-CoV-2 (wildtype, alpha, and beta variants) were preincubated with different concentrations of varenicline tartrate for 1h at 37°C. The cells were infected with pre-treated virus at an MOI of 3 and antiviral activity was assessed by using the cell supernatants 24h post-infection. Error bars represent mean and standard deviation of three independent replicates: the experiment was performed as two independent replicates. CC 50 50% cytotoxic concentration; IC 50, 50% inhibitory concentration. 

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