Broad-Spectrum In Vitro Activity and In Vivo Efficacy of the Antiviral Protein Griffithsin against Emerging Viruses of the Family Coronaviridae
Viruses of the family Coronaviridae have recently emerged through zoonotic transmission to become serious human pathogens. The pathogenic agent responsible for severe acute respiratory syndrome (SARS), the SARS coronavirus (SARS-CoV), is a member of this large family of positive-strand RNA viruses that cause a spectrum of disease in humans, other mammals, and birds. Since the publicized outbreaks of SARS in China and Canada in 2002-2003, significant efforts successfully identified the causative agent, host cell receptor(s), and many of the pathogenic mechanisms underlying SARS. With this greater understanding of SARS-CoV biology, many researchers have sought to identify agents for the treatment of SARS. Here we report the utility of the potent antiviral protein griffithsin (GRFT) in the prevention of SARS-CoV infection both in vitro and in vivo. We also show that GRFT specifically binds to the SARS-CoV spike glycoprotein and inhibits viral entry. In addition, we report the activity of GRFT against a variety of additional coronaviruses that infect humans, other mammals, and birds. Finally, we show that GRFT treatment has a positive effect on morbidity and mortality in a lethal infection model using a mouse-adapted SARS-CoV and also specifically inhibits deleterious aspects of the host immunological response to SARS infection in mammals.
The Coronaviridae are a group of enveloped positive-strand RNA viruses of the group Nidovirales. This group of viruses was not, until recently, of major concern as a matter of public health, although they were long recognized as important agents of serious disease in domestic and companion animals. The recent evidence of zoonotic transfer of this family of viruses from bats to animals such as palm civet cats and then to humans during the 2002-2003 outbreak greatly increased scientific interest in the Coronaviridae (7, 14,19). The best-known coronavirus (CoV) is the causative agent of severe acute respiratory syndrome (SARS), termed the SARS-related coronavirus (SARS-CoV) (7, 14, 19). The lethal SARS outbreaks in China and Canada in 2002-2003 first brought SARS-CoV to public attention. The subsequent identification of two new human coronaviruses associated with acute respiratory infections in humans further illuminated the continuing potential threat that coronaviruses present to public health (31, 36).
Infection with SARS-CoV results from the binding of SARS-CoV spike glycoprotein (S) to angiotensin-converting enzyme 2 (ACE2) on the surface of susceptible cells in the lung followed by viral fusion with host cell membranes and transfer of virion contents into the cell (12, 25, 27). The infection stimulates significant cytokine responses in lung tissue that, together with pathologies associated with rapidly replicating virus, cause damage to the airway epithelium and alveolar membranes resulting in edema, respiratory distress, and (in ∼10% of cases) death (5). Due to the proven threat from SARS-CoV infections and the possibility of future zoonotic transmission of coronaviruses, efforts have been initiated to identify agents that could either reduce infection or suppress the deleterious cytokine response to SARS-CoV infection (8, 29).
The molecular physiology of the SARS-CoV life cycle and the host response to infection have provided numerous potential targets for chemotherapeutic intervention. In addition to vaccine development strategies, various research groups have targeted the SARS-CoV-specific main protease or viral attachment, entry, and fusion for intervention. SARS-CoV protease inhibitors which inhibit the enzyme at concentrations from 0.5 to 7 μM have been reported (2). The SARS-CoV papain-like protease (PLP) has also been successfully developed as a target for small-molecule antivirals, some of which are active in the 100 nM range (22). Viral entry inhibitors include SARS-CoV S glycoprotein heptad repeat peptides identified as potential inhibitors of viral fusion (3). Another broad-spectrum antiviral approach involves targeting the high-mannose oligosaccharides that are commonly found on viral surface glycoproteins. For example, carbohydrate-binding lectins, including Urtica dioica agglutinin (UDA), have been reported to bind to the SARS-CoV S protein and inhibit viral fusion and entry (33).
The antiviral protein griffithsin (GRFT) was originally isolated from the red alga Griffithsia sp. based upon its activity against the human immunodeficiency virus (HIV) (17). This unique 12.7-kDa protein was shown to bind specifically to oligosaccharides on the surface of the HIV envelope glycoprotein gp120. GRFT was shown to possess three largely identical carbohydrate-binding domains orientated as an equatorial triangle and affording multivalent binding and thereby increasing potency (37) (Fig. (Fig.1).1). Due to GRFT's ability to bind to specific oligosaccharides on envelope glycoproteins and block viral entry, it was hypothesized that GRFT might show broad-spectrum antiviral activity against other viruses, including SARS-CoV (38). Here we report the testing of GRFT for antiviral activity against a spectrum of coronaviruses, including SARS-CoV. In addition we present data on the specific binding interactions between GRFT and the SARS-CoV S protein. Finally, we evaluate the in vivo efficacy of intranasal administration of GRFT against infection with SARS-CoV in a lethal mouse model of pulmonary infection and explore the effects that GRFT treatment has on the induction of host cytokine response to SARS-CoV infection.
MATERIALS AND METHODS
In vitro antiviral testing methods. (i) Compounds.
Ribavirin was obtained from ICN Pharmaceuticals (Costa Mesa, CA). Multiferon (multisubtype, human alpha interferon [IFN-α], consisting of a1, a2, a8, a10, a14, and a21 human IFN-α subtypes) was kindly provided by Douglas Lind (Viragen Inc., Plantation, FL), and the SARS-CoV protease inhibitor was provided by Sui Xiong Cai (Maxim Pharmaceuticals, San Diego, CA). GRFT was produced by recombinant production in Nicotiana benthamiana and purified for use as reported previously (18). SARS-CoV spike glycoprotein was obtained through the NIH Biodefense and Emerging Infections Research Resources Repository, NIAID, NIH (SARS-CoV spike [S] protein with histidine tag, recombinant from baculovirus, NR-686). ACE2 was purchased from R & D Systems (Minneapolis, MN). Recombinant HIV-1IIIB gp120, produced in a baculovirus expression system, was purchased from Immunodiagnostics Inc. (Woburn, MA).
(ii) Cells and virus.
Human ileocecal colorectal human adenocarcinoma cells (HRT-18G), mouse embryonic liver cells (BNL), and human diploid fibroblast cells (MRC-5) obtained from the American Type Culture Collection (ATCC, Manassas, VA) were grown in Dulbecco's modified essential medium (DMEM) supplemented with 10% fetal bovine serum (FBS; HyClone Laboratories, Thermo-Fisher Scientific, Logan, UT) and 0.37% NaHCO3. Chicken embryonic fibroblast cells (UMNSAH/DF-1, East Lansing line), pig testis fibroblast cells (ST), human ileocecal colorectal human adenocarcinoma cells (HCT-8), and African green monkey kidney cells (Vero 76), all from the ATCC, were grown in Eagle's formulation of minimal essential medium (MEM) supplemented with 10% FBS and 0.22% NaHCO3 and propagated at 37°C.
Calf diarrheal virus (bovine coronavirus [BCoV]) was obtained from the ATCC and passaged in HRT-18G cells. Infectious bronchitis virus strain Connecticut A5968 (IBV; ATCC) was routinely grown in DF-1 cells. Mouse hepatitis virus (MHV) strain JHM (ATCC) and porcine transmissible gastroenteritis virus strain Miller (PCoV; ATCC) were passaged in BNL cells and ST cells, respectively. Human coronavirus strain OC43 (HCoV-OC43; ATCC) was passaged in HCT-8 cells (ATCC), and human coronavirus strain 229E (HCoV-229E; ATCC) was passaged in MRC-5 cells. The following reagent was obtained through the NIH Biodefense and Emerging Infections Research Resources Repository, NIAID, NIH: human coronavirus, NL63 (Amsterdam 1), NR-470. NL63 was grown in rhesus monkey kidney cells (LLC-MK2 cells) in MEM supplemented with 5% FBS, later reduced to 2% FBS in antiviral assays Severe acute respiratory syndrome-associated coronavirus strain Urbani (SARS-CoV) was obtained from the Centers for Disease Control and Prevention (Atlanta, GA), the Tor-II strain was from Heinz Feldman (National Microbiology Laboratory, Winnipeg, Manitoba, Canada), the Frankfurt strain was from Jindrich Cinatl (Klinikum der J. W. Goethe Universität, Frankfurt am Mein, Germany), and the CuHK strain was from Paul K. S. Chan (Chinese University of Hong Kong, Hong Kong, People's Republic of China). They were all passaged in Vero 76 cells. When viruses were grown, the FBS in each medium used above was reduced to 2% and the NaHCO3 was reduced to 0.22% with the exception of BCoV. For BCoV, the growth and antiviral test media were MEM without serum, 0.18% NaHCO3, 20 IU trypsin/ml, 2.0 μg EDTA/ml. For all antiviral assays, 50 μg/ml gentamicin was also added to the antiviral test medium.
(iii) Preparation of compounds for testing.
Compounds in solution were diluted in test medium (MEM without serum) through a series of eight 1/2-log10 dilutions for evaluation. A positive-control drug was also included to ensure that an overwhelming amount of virus was not used in the assay. The latter compounds also were diluted in test medium as described above.
(iv) CPE inhibition assay.
Cells were seeded into 96-well flat-bottomed tissue culture plates (Corning Glass Works, Corning, NY), 0.2 ml/well, at the proper cell concentration, and incubated overnight at 37°C in order to establish a cell monolayer. When the monolayer was established, the growth medium was decanted and the various dilutions of test compound were added to each well (3 wells/dilution, 0.1 ml/well). Compound diluent medium was added to cell and virus control wells (0.1 ml/well). Virus (viral multiplicity of infection [MOI] = 0.01 to 0.001), diluted in test medium, was added to compound test wells (3 wells/dilution of compound) and to virus control wells at 0.1 ml/well. Virus was added approximately 5 min after compound. Test medium without virus was added to all toxicity control wells (2 wells/dilution of each test compound) and to cell control wells at 0.1 ml/well. The plates were incubated at 37°C or at 33°C (HCoV-OC43, HCoV-299E, and HCoV-NL63) in a humidified incubator with a 5% CO2-95% air atmosphere until virus control wells had adequate cytopathic effect (CPE) readings. This was achieved in 3 to 10 days after virus exposure to cells, depending on the virus. Cells were then examined microscopically for CPE, this being scored from 0 (normal cells) to 4 (maximal, 100% CPE). The cells in the toxicity control wells were observed microscopically for morphological changes attributed to cytotoxicity. This cytotoxicity was also graded as T (100% toxicity, complete cell sloughing from plate), PVH (80% cytotoxicity), PH (60% cytotoxicity), P (40% cytotoxicity), PSl (20% cytotoxicity), and 0 (normal cells). The 50% effective dose (EC50) and 50% cytotoxic dose (IC50) was calculated by regression analysis of the virus CPE data and the toxicity control data, respectively. The therapeutic index (SI) for each compound tested was calculated using the formula SI = IC50/EC50.
(v) NR uptake assay of CPE inhibition and compound cytotoxicity.
The neutral red (NR) uptake assay was done on the same CPE inhibition test plates as described above to verify the inhibitory activity and the cytotoxicity observed by visual observation. The NR assay was performed using a modified method of Cavanaugh et al. (4) as described by Barnard et al. (1). Medium was removed from each well of a plate, 0.034% NRF (0.34% neutral red in phosphate-buffered saline [PBS] supplemented with formalin at 10%) was added to each well of the plate, and the plate was incubated for 2 h at 37°C in the dark. The NR solution was then removed from the wells and rinsed, and the remaining dye was extracted using ethanol buffered with Sörenson's citrate buffer. Absorbances at 540 nm/405 nm were read with a microplate reader (Opsys MR; Dynex Technologies, Chantilly, VA). Absorbance values were expressed as percentages of untreated controls and EC50, IC50, and SI values were calculated as described above.
(vi) ELISA studies.
The binding of GRFT to SARS-CoV spike (S) glycoprotein was analyzed in enzyme-linked immunosorbent assay (ELISAs) with two different modalities. For standard ELISA, purified S protein was immobilized at 10 ng/well to a 96-well protein-binding plate (Nunc; Maxisorp) by incubation for 2 h at room temperature. After being rinsed twice with PBS containing 0.1% Tween (PBS-T) and three times with blocking buffer (Superblock buffer in PBS containing 0.05% Tween 20; Pierce, Rockford, IL), the plate was incubated with blocking buffer for 3 h at room temperature and rinsed again with PBS-T. The wells were then incubated with 0.5 log10 serial dilutions of GRFT, followed by anti-GRFT rabbit polyclonal antibodies for 1 h at room temperature. After washing with PBS-T, the amount of bound GRFT was determined by adding a 1:5,000 dilution of goat anti-rabbit-horseradish peroxidase (HRP; ImmunoPure). The plate was washed again, and horseradish peroxidase substrate (Kirkegaard & Perry Laboratories) was added. The reaction was stopped by the addition of 50 μl/well of 2 M H2SO4, and absorbance was measured at 450 nm. To measure the inhibition of binding of GRFT to S protein by mannose, increasing concentrations of mannose were added to 100-μl aliquots of GRFT (1 μM in PBS) or PBS alone and incubated at room temperature for 30 min on a rocker. The aliquots were then added to an S-protein-coated plate and incubated for 1 h at room temperature. Binding of GRFT was measured as described above.
In studies to measure the ability of GRFT to prevent the binding of S protein to the ACE2 cellular receptor, S protein was bound to the wells of a 96-well plate as above and then, after blocking and washing, was treated with increasing concentrations of GRFT (0.0003 to 100 pmol/well). Following incubation with GRFT (2 h), the plate was then incubated with 50 ng/well of recombinant ACE2 (R & D Systems) and incubated for 1 h prior to washing and visualization with primary polyclonal goat-anti-ACE2 antibodies followed by horseradish peroxidase-ligated mouse anti-goat secondary antibodies monitored by absorbance at 450 nm.
(vii) Isothermal titration calorimetry.
The calorimetric binding experiments were carried out on a VP-ITC microcalorimeter (MicroCal, Inc., Northampton, MA). In the experiments, 5-μl aliquots of a GRFT solution (289.3 μM) were injected from a 250-μl syringe into a rapidly mixing (300 rpm) solution of either SARS-CoV spike (1.8 μM) or HIV-1IIIB gp120 (2.5 μM) contained within the calorimetric cell (1.4426 ml). Both experiments were carried out at 25°C in 10 mM sodium phosphate buffer, 60 mM NaCl, 0.02% NaN3 (pH 7.0). The isotherms were corrected for dilution/buffer effects and fitted using the Origin ITC analysis software according to the manufacturer's protocols. Concentrations of all proteins were determined by amino acid analysis. A nonlinear least-square method was used to fit the titration data and to calculate the errors. From the binding curve, values for enthalpy, stoichiometry, and binding affinity were extracted. The other thermodynamic parameters (free energy of binding and entropy values) were calculated using ΔG = −RTlnKa, ΔG = ΔH − TΔS, and R = 1.985 cal/(mol·K), where R is the universal gas constant, T is temperature in Kelvin, and Ka is the reaction equilibrium constant.
In vivo mouse testing methods. (i) Animals.
Six- to eight-week-old BALB/c female mice were purchased from NCI. The animals were maintained in an approved animal care facility and transferred to a biosafety level 3 (BSL3) facility prior to infection. This study was approved by the University of Iowa Animal Care and Use Committee. The animals used for this study were part of a four-armed experiment including sham-treated, positive-control (SARS-CoV-infected), griffithsin-treated, and rhesus theta-defensin-treated animals. The results with rhesus theta-defensin-treated and some of the positive-control and sham-treated animals were previously published (34).
(ii) Griffithsin administration.
Recombinant GRFT protein was prepared as described previously (18). Mice were lightly anesthetized, and GRFT (5 mg/kg of body weight/day) was delivered intranasally 4 h prior to administration of MA15 SARS-CoV, followed by 2 doses daily (2.5 mg/kg/dose) for 4 days following infection. This dose was adopted from a previous study of a similar viral entry inhibitor, cyanovirin-N, with influenza virus (28).
(iii) MA15 Urbani SARS-CoV infection.
Mice were anesthetized and inoculated intranasally with 3 × 105 PFU of mouse-adapted Urbani SARS-CoV (MA15) (23) in 30 μl sterile 1× PBS in an approved BSL3 facility. Mice were weighed and examined daily. Animals were euthanized if they lost >25% of their body weight. To obtain specimens for lung histology, virus titers, lung homogenates, and serum collection, mice were euthanized at baseline and at day 2, day 4, and day 10 postinfection (p.i.). The left lung was fixed in zinc formalin, and the right lung was homogenized and stored at −80°C.
(iv) Plaque assay.
The right lung was excised aseptically, placed in sterile 1× PBS, and homogenized manually with a tissue homogenizer. The homogenates were centrifuged at 12,000 rpm for 10 min, and supernatant was removed. Lung homogenate supernatants were diluted and applied to Vero cells and incubated for 1 h, and an overlay medium containing agarose was added to cell surface. Three days postinfection, cells were fixed in 10% formaldehyde and stained with 0.1% crystal violet. Formed plaques were counted.
To detect SARS-CoV antigen, zinc formalin-fixed paraffin sections were incubated with a monoclonal antibody to the SARS-CoV N protein (gift of John Nicholls, University of Hong Kong, Hong Kong) and expression was detected using a biotin-avidin system. Sections were examined and photographed under light microscopy.
Fixed tissues were processed, paraffin embedded, sectioned (4 μm), and hematoxylin and eosin stained. All slides were screened by a veterinary pathologist to first identify the histopathologic parameters that were appreciably altered. Subsequently, the slides were scored in a blinded fashion for lesion severity. Edema scores included the following35).
(vii) Multiplex cytokine assay.
To identify changes in cytokine protein expression, we performed a multiplex bead-based immunoassay using the Bio-Plex cytokine assay (Bio-Rad Laboratories) as previously reported (35). Lung tissue homogenates were studied at baseline and day 2, day 4, and day 10 postinfection. The Bio-Plex cytokine 23-Plex kit measured mouse interleukin-1α (IL-1α), IL-1β, IL-2, IL-3, IL-4, IL-5, IL-6, IL-9, IL-10, IL-1(p40), IL-12(p70), IL-13, IL-17, eotaxin, granulocyte colony-stimulating factor (G-CSF), granulocyte/macrophage CSF (GM-CSF), IFN-α, KC, monocyte chemoattractant protein 1 (MCP-1), MIP-1α, MIP-1β, RANTES, and tumor necrosis factor alpha (TNF-α) expression patterns and was used following the manufacturer's instructions. Fifty microliters of each lung tissue homogenate specimen was transferred to appropriate microtiter wells containing diluted antibody-coated bead complexes and incubation buffer. Samples were incubated for 30 min at room temperature and 18 h (both in the dark) at 4°C, with continuous shaking. Following a rinse with wash buffer, 25 μl detection antibody was added to each well, incubated for 30 min at room temperature (in the dark), and washed as described above. Next 50 μl of streptavidin-phycoerythrin was added to all wells and incubated for 10 min at room temperature (in the dark). All microtiter wells received a final wash, and beads were resuspended in 125 μl assay buffer and analyzed on the Bio-Plex suspension array system using Bio-Plex Manager software. Cytokine concentrations were automatically calculated based on standard curve data. Data from the mice used in the negative-control (sham-treated) and positive-control (SARS-CoV without GRFT) groups were included in a previously published study (35).
(viii) Statistical analysis.
The indicated statistical tests were used in experimental analyses. Student's t test was applied at the 95% confidence level (P < 0.05) to each paired comparison at each of their respective time points using Excel. Analysis of variance (ANOVA) was applied with Bonferroni correction for multiple comparisons.
GRFT inhibits in vitro infection of Coronaviridae.
In initial studies of the effect of GRFT against SARS-CoV (Urbani strain), GRFT was shown to potently inhibit the cytopathic effect of SARS-CoV on Vero 76 cells (38). As can be seen in Fig. Fig.2,2, GRFT reduced the percentage of cells killed by SARS-CoV (Urbani) in a concentration-dependent manner (EC50 = 48 nM) while showing minimal toxicity to the control cells. The antiviral activity of GRFT against SARS-CoV was not limited to the Urbani strain of the virus, as three additional strains of SARS-CoV were also sensitive to GRFT at similarly low concentrations (Table (Table1).1). In addition, GRFT demonstrated activity against a broad spectrum of other coronaviruses that infect mammals and birds in testing using a variety of cell lines. Of the coronaviruses tested several were susceptible to inhibition by GRFT below the lowest dose utilized (∼1 nM) (Table (Table2).2). It is interesting that GRFT mutants, in which the carbohydrate-binding domains were altered to prevent carbohydrate binding, were largely inactive against coronaviruses (EC50 of >50 μg/ml) (data not shown). Though all of the human coronaviruses were sensitive to GRFT at nanomolar concentrations, two coronaviruses, infectious bronchitis virus (IBV) and HCoV (NL63), were the most sensitive to inhibition (EC50 of <2.5 nm="" and="" 0="" 25="" respectively="" it="" is="" interesting="" that="" these="" viruses="" belong="" to="" the="" group="" 1="" 3="" phylogenetic="" groups="" of="" em="">Coronaviridae, respectively. NL63 uses the ACE2 receptor for binding (21), but IBV uses a receptor possessing α-2,3-linked sialic acid residues (34). Thus, at the receptor level, the two viruses appear to have nothing in common, other than their susceptibility to inhibition by carbohydrate-binding agents such as GRFT (13, 32). In addition, GRFT was shown to be active against both group 1 and 2 Coronaviridae which utilize different mechanisms for proteolytic cleavage of the spike glycoprotein (9).
GRFT binds directly to the SARS-CoV spike glycoprotein.
To determine if the activity of GRFT against SARS-CoV was due to specific interactions with the spike glycoprotein, ELISA studies utilizing recombinant SARS-CoV spike glycoprotein were performed which showed that GRFT binds to this protein in a concentration-dependent manner (Fig. (Fig.3A).3A). Additional experiments showed that this binding interaction could be inhibited by the addition of excess mannose, thereby indicating that the association between GRFT and SARS-CoV spike glycoprotein is carbohydrate dependent (Fig. (Fig.3B).3B). It should be noted, however, that the expression of the SARS-CoV spike glycoprotein in a baculovirus expression system could alter its glycosylation. Finally, ELISA studies were performed to determine if the binding of GRFT to SARS-CoV S glycoprotein was sufficient to inhibit the subsequent binding of the host cell receptor human ACE2 to S. These studies indicated that GRFT was unable to significantly inhibit the binding of the SARS-CoV S glycoprotein to ACE2 (data not shown). The inability of GRFT to inhibit S binding to ACE2 is similar to previous results with HIV-1 in which GRFT did not significantly inhibit the binding of gp120 to CD4 (17).
GRFT binds to SARS-CoV spike glycoprotein at multiple sites with high affinity.
Since previous studies with carbohydrate-binding proteins and HIV gp120 have shown the importance of multiple binding interactions between these proteins and specific oligosaccharides on the envelope glycoprotein (26), we undertook isothermal titration calorimetric studies with recombinant SARS-CoV spike and GRFT. The results of this experiment provided the binding stoichiometry between these two proteins and also showed that GRFT interactions with spike are enthalpically driven (Fig. (Fig.4),4), resulting in a dissociation constant (Kd) of 24.9 nM (Table (Table3).3). The binding interaction of GRFT with SARS-CoV S was compared to that of GRFT with HIV-1 gp120. The results show that GRFT has an ∼10:1 binding stoichiometry with gp120 compared to a 3:1 binding stoichiometry with S, a finding which suggests a greater presence of high-mannose oligosaccharides on gp120 than on S. In line with the greater binding enthalpy (ΔH) for GRFT with gp120, the dissociation constant for gp120 was tighter (8.2 nM) than that seen with S.
GRFT pretreatment prevents lethal pulmonary infection in mice.
The mouse-adapted MA15 SARS-CoV causes a dose-dependent lung disease and significant morbidity and mortality in BALB/c mice (23). Groups of mice were inoculated with 3 × 105 PFU of virus, a dose previously shown to cause at least 75% mortality (35). One group of mice received concomitant treatment with intranasally administered GRFT peptide as described in Materials and Methods. As shown in Fig. Fig.5A,5A, MA15-infected mice began to lose weight within 2 to 3 days of inoculation, and this continued until they died from the infection or recovered. Figure Figure5B5B shows the survival curve for sham-treated, SARS-CoV-infected, and GRFT-treated mice. In contrast to the outcomes in untreated mice, animals that received GRFT 4 h before inoculation with MA15 followed by twice-daily treatment for 4 days did not lose weight and exhibited 100% survival. Animals receiving sham treatment or GRFT treatment alone survived and exhibited no weight loss. We evaluated MA15 titers in lung tissue 0, 2, and 4 days postinoculation. As shown in Fig. Fig.5C,5C, GRFT treatment significantly diminished the tissue virus titers on day 2 postinfection (mean virus titers [PFU/g tissue]: GRFT plus SARS-CoV, day 2, 4.2 × 106, and day 4, 2.9 × 106; SARS-CoV alone, day 2, 8.5 × 107, and day 4, 1.1 × 107). In agreement with this observation, GRFT-treated animals also had reduced pulmonary viral antigen load assessed by localization of the SARS-CoV N gene antigen by immunohistochemistry (Fig. (Fig.66).
GRFT treatment decreases pulmonary pathology during SARS-CoV infection.
In humans and animal models SARS-CoV causes significant pathological changes in pulmonary tissues, characterized by necrotizing bronchiolitis, perivascular cellular inflammation, and alveolar edema (7, 14, 23). We assessed pulmonary histopathology at 2, 4, and 10 days postinfection in untreated, sham-treated (no virus), and GRFT-treated animals. Mice receiving GRFT alone developed a modest level of perivascular infiltrate that was largely resolved by 10 days (6 days following the last dose of GRFT) (Fig. (Fig.7).7). In contrast, mice treated with SARS-CoV alone manifested necrotizing bronchiolitis, perivascular infiltrates, and alveolar edema that were resolving by 10 days postinfection (in surviving animals). While mice receiving GRFT treatment and SARS-CoV exhibited robust perivascular infiltrates at levels greater than those with SARS-CoV alone, possibly due to the increased immunogenicity of GRFT-aggregated viral particles, the GRFT-treated mice had reduced levels of pulmonary edema at both 2 and 4 days postinfection and reduced severity of necrotizing bronchiolitis at 2 days postinfection. The histopathology scores are presented graphically in Fig. Fig.88.
GRFT treatment modifies cytokine responses in infected lung tissue.
It has been hypothesized that the morbidity and mortality associated with SARS-CoV infection originate from maladaptive cytokine/chemokine responses or suppression of innate immune responses (6, 20). We measured cytokine levels in pulmonary tissue homogenates 2 and 4 days following MA15 inoculation. As shown in Fig. Fig.99 (top panels), mice treated with GRFT and exposed to SARS-CoV showed significantly reduced levels of MIP-1α at day 2 postinfection compared to SARS-CoV alone. IL-1α and -β, RANTES, MCP-1, IL-12(p40), IL-6, and G-CSF also showed downward trends in GRFT-treated mice compared to SARS-CoV at day 2 p.i., but the differences were not statistically significant. At 4 days p.i. (Fig. (Fig.9,9, bottom panels), several cytokines were significantly reduced in GRFT-treated animals compared to those infected with SARS-CoV alone, including IL-1α and -β, IL-6, G-CSF, MCP-1, and IL-12(p40).
The potent antiviral lectin GRFT displayed low nanomolar activity against SARS-CoV (Urbani strain) with an EC50 of 0.61 μg/ml (48 nM). Previously, we had speculated that GRFT would be likely to have activity against SARS-CoV due to its carbohydrate specificity and the known carbohydrate components of the SARS-CoV envelope glycoprotein S (17). Extending our previous work (38), here we detail the activity of GRFT against several strains of SARS-CoV and show consistent advantageous selectivity indices for all of the tested strains (Table (Table1).1). The carbohydrate-binding agent Urtica dioica agglutinin (UDA) has been reported by others to display anti-SARS-CoV activity (33), but the concentrations necessary for inhibition were significantly higher than those that we report here for GRFT. This difference in activity could be attributed to the multivalent interactions that the three independent carbohydrate-binding sites afford GRFT (Fig. (Fig.1).1). Other agents reported to show activity against SARS-CoV, including SARS-CoV protease inhibitors (2) and SARS-specific heptad repeat peptides (3), also show such activity only at significantly higher molar concentrations than GRFT. Though human recombinant alpha interferon (multiferon) and other host-targeted agents have demonstrated anti-SARS activity at low concentrations (Table (Table2),2), their potency does not sig