Antiviral Activities of Sulfated Polysaccharides Isolated from Sphaerococcus coronopifolius (Rhodophytha, Gigartinales) and Boergeseniella thuyoides (Rhodophyta, Ceramiales)

Water-soluble sulfated polysaccharides isolated from two red algae Sphaerococcus coronopifolius (Gigartinales, Sphaerococcaceae) and Boergeseniella thuyoides (Ceramiales, Rhodomelaceae) collected on the coast of Morocco inhibited in vitro replication of the Human Immunodeficiency Virus (HIV) at 12.5 μg/mL. In addition, polysaccharides were capable of inhibiting the in vitro replication of Herpes simplex virus type 1 (HSV-1) on Vero cells values of EC50 of 4.1 and 17.2 μg/mL, respectively. The adsorption step of HSV-1 to the host cell seems to be the specific target for polysaccharide action. While for HIV-1, these results suggest a direct inhibitory effect on HIV-1 replication by controlling the appearance of the new generations of virus and potential virucidal effect. The polysaccharides from S. coronopifolius (PSC) and B. thuyoides (PBT) were composed of galactose, 3,6-anhydrogalactose, uronics acids, sulfate in ratios of 33.1, 11.0, 7.7 and 24.0% (w/w) and 25.4, 16.0, 3.2, 7.6% (w/w), respectively.

Polysaccharides from red seaweeds include different sulfated galactans, sulfated rhamnans or mannans, carrageenans and agars [6,9,11,13,14]. The predominant types of polysaccharide from red algae are galactans with a backbone of alternating 3-linked β-D-galactopyranosyl and 4-linked α-galactopyranosyl units: agar-type polysaccharide if the 4-linked α-galactopyranosyl units are in the L-configuration, and a carrageenan-type polysaccharide, if the 4-linked α-galactopyranosyl units are in the D-configuration [15]. Agars are typically low in sulfate ester substitution, but those from numerous sources are rich in methyl ether or pyruvate acetal substitution. Conversely, carrageenans are comparatively rich in sulfate ester substitution but poor in methyl ether substitution, and rarely contain significant levels of pyruvate acetal substitution [16]. Their modes of action have been attributed to the blockage of some early stages of the virus replication cycle [17,18].
The Moroccan Coast is particularly rich in algal biodiversity and constitutes a reserve of species of considerable economic, social and ecologic potential. Except studies of Abourriche et al. [19], Etahiri et al. [20], Moujahidi et al. [21], and Souhaili et al. [22] concerning antibacterial activities, nothing is known about the antiviral activities of red seaweed extracts collected on the coast of Morocco.
The present study lead to elucidating the chemical composition and antiviral activities against two enveloped viruses HSV-1 and HIV of water-soluble polysaccharides extracted from Sphaerococcus coronopifolius (Gigartinales, Sphaerococcaceae) and Boergeseniella thuyoides (Ceramiales Rhodomelaceae) and the first approach in vitro of time of action.

Chemical Composition from the Polysaccharides
Extraction yields from Sphaerococcus coronopifolius and Boergeseniella thuyoides were 25.5% and 17.8% respectively.
The chemical compositions of water-soluble polysaccharides are shown in Table 1. The polysaccharide from S. coronopifolius contains more galactose, uronic acid and sulfates than that of B. thuyoides. The latter contains more 3,6-anhydrogalactose and proteins.

Determination of the Molecular Weight of Polysaccharides
The weight average molecular weight (Mw) of polysaccharides is about 308,700 Da and 360,300 Da for S. coronopifolius and B. thuyoides respectively. The number average molecular weight (Mn) is about 52,400 Da and 171,500 Da with an index of polydispersity (Mw/Mn) of 2.101 and 5.891 for S. coronopifolius and B. thuyoides respectively. The polysaccharide from S. coronopifolius is more homogeneous than that of B. thuyoides.

HSV/Vero Model
Low percentage of cell destruction was observed for the two polysaccharides on Vero cells line (CC 50 > 250.0 µg/mL) ( Figure 3). After three days of treatment, no microscopically visible alteration of normal cell morphology was observed and viability assay showed no destruction of cell layer.
When polysaccharides and the viral suspension (MOI 0.001 ID 50 /cells) are simultaneously added, 100% of cellular protection was obtained for 12.5 µg/mL of polysaccharide from S. coronopifolius (EC 50 = 4.1 µg/mL). For polysaccharide extracted from B. thuyoides, 100% of cellular protection was obtained for 50µg/mL (EC 50 = 17.2 µg/mL) ( Figure 3). Acyclovir used as positive controls conferred total protection (100%) against HSV-1 with a low percentage of cell destruction (8%). In comparison with Acyclovir (SI: >500), the selectivity index (SI: 61 for polysaccharide extracted from S. coronopifolius and SI 14.5 for polysaccharide extracted from B. thuyoides) are low, but this study highlights the presence of an antiviral activity of marine sulfated polysaccharides.  The marine sulfated polysaccharides belonging to the Gigartinales recognized for the production of carrageenans [46,50], were shown to be potent and selective inhibitors of HIV-1 and HSV-1 replication in culture [6,13,44,51]. The sulfated galactan from Schizymenia binderi exhibited highly selective antiviral activity against Herpes simplex virus type 1 and 2, with selectivity indices >1000. This compound was shown to interfere with the initial adsorption of viruses to cells [16]. The kappa/iota/nu carrageenan from Gymnogongrus griffithsiae (Phyllophphoraceae, Gigartinales), exhibited antiherpetic activity with inhibitory concentration 50% (EC 50 ) values in 0.5-5.6 µg/mL, as determined in a virus plaque reduction assay in Vero cells. The galactans lacked cytotoxic effects and showed a broad spectrum of antiviral activity against HSV-1 and HSV-2. No direct virus inactivation was observed after virions treatment with the galactans. The mode of action of these compounds could be mainly ascribed to an inhibitory effect on virus adsorption. Most importantly, a significant protection against a murine vaginal infection with HSV-2 was afforded by topical treatment with the sulfated galactans [52]. The carrageenan from Callophyllus variegata (Kallymeniaceae, Gigartinales) showed potent antiviral activity against Herpes simplex type 1 and 2 with values of IC 50 ranging from 0.16 to 2.19 µg/mL, and against dengue type 2 with values of IC 50 from 0.10 to 0.41 µg/mL. Polysaccharides from algae belonging to the Ceramiales, biosynthesized sulfated agarans [16,53]. The latter also showed antiviral activity, but less effective than carrageenan. Some agarans isolated from the red seaweed Acanthofora spicifera (Rhodomelaceae, Ceramiales) showed a very selective and potent antiviral activity against HSV-1 and HSV-2 with EC 50 in the range of 0.6 and >50 µg/mL [54]. Further investigations are in progress to examine and confirm the efficiency of marine polysaccharide with higher MOI 0.01 and 0.1 ID 50 /cells.

Effect before Infection
Vero cells were not protected from HSV-1 infection when polysaccharides were only present before virus infection ( Table 2). The polysaccharides did not induce a durable antiviral state in the target cells.

Virucidal Assay
The preincubation of the virus with polysaccharides from S. coronopifolius and B. thuyoides had a moderated protection. The values of effective concentration 50% were 53.2 and 73.9 µg/mL for S. coronopifolius and B. thuyoides, respectively.

Virus Adsorption Assay
With Treatment I, a moderated antiviral activity was reported. With Treatment II, a high percentage of cell protection was observed for two polysaccharides. With Treatment III, a higher percentage of protection than in Treatment II was noted with EC 50 = 3.6 µg/mL for PSC and EC 50 = 13.1 µg/mL for PBT. Vero cells were not protected from HSV-1 infection when polysaccharides were present before infection ( Table 2).

Effect of Polysaccharide Addition Time
Vero cells were optimally protected (87-100%) when polysaccharide was added at 0-2 h after infection ( Table 2). After 3 h post-infection, antiviral activity decreased dramatically. In comparison, the EC 50 of acyclovir increased from 0.5 to 4.1 µg/mL between 0 and 5 h ( Table 2).
In conclusion for the HSV-1 model: Vero cells were not protected from HSV-1 infection when the polysaccharides were present only before virus infection. Sulfated polysaccharides did not adsorb to the cellular receptorse. The results also revealed that polysaccharides did not exert an important virucidal effect. Indeed, the preincubation of the virus with the polysaccharide for (2 h at 37 °C) protected Vero cells less against HSV-1. The EC 50 obtained after two days of incubation at 37 °C were increased.
The lack of virucidal activity for the polysaccharides from S. coronopifolius and B. thuyoides is in accordance with previous studies that found most algal sulfated polysaccharides are not able to produce significant virion inactivation [9,12,13,55,56]. However, it is quite possible that sulfated polysaccharide could affect the virus-cell attachment by spreading a three-dimensional gel network over the whole of the cell surface. This structural modification would entail envelope alteration and concealing of virus-specific receptors sites. Such a mechanism prevents adsorption of the viruses to the cell surface and hence penetration and replication. Sulfated polysaccharides interact precisely with positively charged domains on these glycoproteins. This will result in a "shielding-off" of these domains and thus prevent the virus from binding to the negatively charged sulfated polysaccharide [14,18,[57][58][59]. Heparan sulfate proteoglycans are assumed to be common cell ligands in the initial interaction of HSV-1 with host cell and external viral glycoprotein [58]. To determine the stage of HSV-1 infection affected by polysaccharide, cells were treated with the polymers at various times during the cycle of viral replication. The two polysaccharides were very effective when added at the early stages of virus growth (simultaneously with virus 0H) or when added 1 h after HSV-1 infection. Previous reports demonstrated the antiviral activity of complex sulfated polysaccharides extracted from various species of marine algae and suggested that sulfated polysaccharides interfered with the attachment of virions to host cells [6,7,9,[12][13][14]24,54,59,60]. On the other hand, the assays of Harden et al. [14] and Carlucci et al. [55] showed that the polysaccharide from algae can have potent inactivating properties against HSV-1. Harden et al. [14] reported that polysaccharide from gametophyte from Gigartina atropurpurea and Plocamium cartilagineum had potent virucidal activity and were active at very low concentrations (0.2-0.4 µg/mL respectively). The λ-carrageenan from Gigartina skottsbergii [60] and the sulfated glucuronogalactan from Schizymenia dubyi [18], also have potent inactivation (EC 50 = 0.5 µg/mL and 30 µg/mL, respectively) against HSV-1. Since polysaccharides antiviral action seemed to be efficacious by interference with early stage of the HSV-1 replication cycle, the effect on the viral adsorption was examined. The two polysaccharides protected Vero cells against HSV-1, however only if present during the first two hours after viral infection. The results confirm that sulfated polysaccharides exert their anti-HSV-1 activity mainly by interference with a very early stage of HSV-1 replication cycle (since replication was blocked when the compound was present during the virus adsorption period. Direct interference with the virus particle or a combined action on the virus and the cell on receptor sites, could account for the inhibitory effect of sulfated polysaccharide on the virus attachment to the host cells.

HIV/MT4 Model
Water-soluble extracts from S. coronopifolius and B. thuyoides are not toxic on cells MT4, even with 300 µg/mL.
The antiviral activity of the products was tested on virus HIV-1 NDK with 2 dilutions (7.5 × 10 −4 and 5 × 10 −4 ) on cells MT4 (Tables 3 and 4). The inhibiting effect is analyzed by observing under the microscope the presence or absence of syncitium in the wells. Table 3. Inhibiting effect on the HIV-1 NDK strain of the polysaccharide of S. coronopifolius at two viral dilutions.
-: absence of syncitium in all the wells; (+): presence of 1 or 2 syncitium by field; + and ++: presence of many syncitium per field; T: cellular death due to the viral replication; D: Days.  The polysaccharide of S. coronopifolius appeared to be active against HIV-1 replication until the seventh day for each concentration tested ( Table 3). The polysaccharide of B. thuyoides also prevents HIV-induced syncytium formation but at the stronger concentration after the seventh day. However, at the lowest concentrations, syncitia formation was observed (Table 4). Otherwise no cytotoxicity on the MT4 cells was observed.
The marine sulfated polysaccharides were shown to be potent and selective inhibitors of HIV-1 replication in culture. For example, Galactan sulfate from Agardhiella tenera (Gigartinales, Areschongiaceae) [8] was examined for its inhibitory effect on the cytopathic effect of HIV-1 (HTLVIIIB) and HIV-2 (LAV-2ROD), the compounds were found to provide protection at a concentration 10-fold higher than the concentration at which dextran sulfate (Mw 5 kDa) protected the cells (50% inhibitory concentration IC 50 approximately 0.5 and 0.05 μg/mL, respectively). Witvrouw et al. [61] demonstrated that galactan sulfated and dextran sulfate block the binding of HIV-1 to the MT-4 cells (IC 50 approximately 40.0 μg/mL and <0.20 μg/mL, respectively). Bourgougnon et al. [18] described the annual variation in composition and in vitro anti-HIV-1 activity of the sulfated glucuronogalactan from Schizymenia dubyi. Evaluation of the anti-HIV-1 effect of this polysaccharide indicated that syncitia formation and HIV-associated reverse transcriptase in vitro were completely suppressed at 5 μg/mL by the glucuronogalactan extracted from algae collected during the spring/summer period. The syncitia formation was completely suppressed with 5 μg/mL of galactan extracted from S. dubyi collected from April to July. This high anti-HIV-1 activity corresponded with a decrease in L-galactose, viscosity and sulfate content of the polysaccharide.

First Approach to Determining the Mode of Action
The time of action of the polysaccharide from S. coronopifolius was studied by adding the compound at different times of the experiment (Table 5). Table 5. Time of action of the sulfated polysaccharide from S. coronopifolius: Inhibition of syncitium formation by the polysaccharide added at different times of the culture: Throughout the whole experiment (Treatment (d)); before and during infection (Treatment (a)); during infection (Treatment (b)); or after infection (Treatment (c)) of MT4 cells with HIV.  T  T  T  T  ++  ++  +  +/++  T  T  T  T  MT4  ---------: absence of syncitium in all the wells; (+): presence of 1 or 2 syncitium by field; + and ++: presence of many syncitium per field; T: cellular death due to the viral replication; D: days.
Incubation before and during (a), or presence of sulfated polysaccharide from S. coronopifolius only during infection (b) with cells, was ineffective to block viral infection and the viral production was comparable with virus control (Table 5). To achieve its optimal effect on syncitium formation, the polysaccharide must be present during the whole culture (treatment d) or after infection (treatment c).
The time of action of the polysaccharide from B. thuyoides was studied by adding the compound at different times of the experiment (Table 6).
Incubation before and during (a) or presence of sulfated polysaccharide from B. thuyoides during infection (b) with cells was ineffective to block viral infection and the viral production was comparable with virus control (Table 6). To achieve its optimal effect on syncitium formation, the polysaccharide must be present during all the culture (treatment d) or after infection (treatment c). Table 6. Time of action of the sulfated polysaccharide from B. thuyoides: Inhibition of syncitium formation by the polysaccharide added at different times of the culture: Throughout the whole experiment (Treatment (d)); before and during infection (Treatment (a)); during infection (Treatment (b)); or after infection (Treatment (c)) of MT4 cells with HIV.    +  +  +  T  T  T  T  ++  ++  +  +/++  T  T  T  T  MT4  ---------: absence of syncitium in all the well; (+): presence of 1 or 2 syncitium by field; + and ++: presence of many syncitium per field; T: cellular death due to the viral replication; D: days.

Virus Neutralization Assay
To check the direct action of the products on the virus, they were incubated directly with the virus before adding CEM (Human T-Lymphoblastoid) cells. Even on cells CEM, the sulfated polysaccharide of S. coronopifolius is active at 5 µg/mL (100% of neutralization on the viral dilution of 5 × 10 −6 ). The sulfated polysaccharide of B. thuyoides showed 42% of neutralization on highest amount of virus (7.5 × 10 −6 ) but 100% of neutralization on the 5 × 10 -6 viral dilution. These results suggest that polysaccharide had a virucidal effect.
Activity of the polysaccharide after infection demonstrates that the compound blocks the replication of HIV-1 and then the syncitium formation between uninfected and infected cells. Polysaccharides are active when they are in contact only after the infection or throughout, which is not due to entry of the virus into the cells, but on the viral replication itself (like witness AZT, inhibitor of the reverse transcriptase). These results suggest a direct inhibitory effect on HIV-1 replication by controlling the appearance of the new generations of virus and potential virucidal effect. The mechanism of anti-HIV action is generally attributed to the inhibition of virus attachment to the cell surface by ionic interactions between polysaccharides and cells. Preincubation of sulfated polysaccharides with cell rather than virus has generally been shown to be necessary for effective inhibition [62]. In this study, the polysaccharide of S. coronopifolius and B. thuyoides, also shows inhibition when the polysaccharide is added after infection. Direct antiviral action of sulfated polysaccharides has, however, also been described and confirms our findings [6,7,18]. Furthermore, antiviral activity increases with increasing molecular weight and degree of sulfation [18,35]. The polysaccharide of S. coronopifolius contains more galactose, uronic acid and sulfates than polysaccharide of B. thuyoides. However, the polysaccharide from S. coronopifolius presents a slightly lower molecular weight but is more homogeneous than polysaccharide of B. thuyoides.
Research on effective chemotherapeutic treatment against HIV infection led to the development of agents which aim at specific and critical events in the replicative cycle of HIV. The conjugates of κ-carrageenans and AZT (3′-azido-3′-deoxythymidine) exert synergistic effects on the reduction of the infection of the human immunodeficiency virus (HIV) [63].
In conclusion, marine polysaccharides prevent syncytium formation, and thus protect uninfected cells from being killed by the HIV-infected cells. With inexpensive, water-soluble and poorly absorbed properties, they are also endowed with activity against various viruses other than HIV, including viruses such as HSV and CMV that occur as opportunistic pathogens in immuno-suppressed (i.e., AIDS) patients. Sulfated polysaccharides constitute actually attractive candidate for a vaginal anti-HIV formulation. They can be prepared and made available in large quantities at reasonable cost.

Extraction Techniques and Chemical Analysis Methods
Water extraction: Samples of S. coronopifolius and B. thuyoides were collected in 2007 at Belyounech (Strait of Detroit Gibraltar, Morocco). The samples were rinsed with sterile seawater to remove associated debris and necrotic parts. Epiphytes were removed from the algae. The samples were shade dried, cut into small pieces and powdered in a mixer grinder. The powder obtained was preserved cold (−12 °C). The seaweed was depigmented with absolute ethanol and acetone. Polysaccharides from seaweed powder (20 g) were extracted in hot distilled water (1.5 L) at 80 °C for 4 h with magnetic stirring. Insoluble residues were eliminated by filtration and centrifugation (20 min, 30,000 g). The supernatant was poured into 2 volumes of absolute ethanol during one night at 4 °C. The precipitate were recovered and washed by absolute acetone, dried overnight at 50 °C, weighed and ground to a powder. The polysaccharide was redissolved in distilled water, dialyzed against distilled water and freeze-dried [26,57].

Chemical Composition
Total carbohydrate was estimated by the phenol-sulfuric acid method of Dubois [64], using galactose as standard. Uronic acids were determined by m-hydroxydiphenyl of method from Blumenkrantz and Asobe-Hansen [65], modified by Filisetti-Cozzi and Carpita [66], using glucuronic acid as standard. For the determination of sugar composition, the monosaccharide residues released by acid hydrolysis were converted into their alditol acetate [67,68] and analyzed by GLC. The 3,6-anhydrogalactose content (3,6-AG) was determined by the colorimetric method of Yaphe and Arsenault [69]. Sulphate content was measured turbedimetrically after hydrolyzing 20 mg of polysaccharide in a sealed tube with 2N HCl at 100 °C for 2 h [70]. Protein content was estimated according to the method Bicinchoninic Acid (BCA) Protein Assay [71]. Pyruvic acid was determined by the 2,4-dinitrophenylhydrazine colorimetric method of Sloneker and Orentas [72] after hydrolysis (1 N chlorydric acid, 100 °C, 3 h).

FT-IR Spectroscopy
Infrared spectra were recorded from a KBr pellet of the polysaccharide on a spectrometer IR-TF Nicolet.

Cytotoxicity Assays Based Upon Cell Viability
Using the Vero cell/HSV-1 model, cytotoxicity was evaluated by incubating cellular suspensions (3.5 × 10 5 cells/mL) with various dilutions (concentration from 2.5 to 250 µg/mL, 4 wells per concentration) of polysaccharide in 96-well plates (48 h, 37 °C, 5% CO 2 ) in Eagle's MEM containing 8% FCS. The cells were examined daily under a phase-contrast microscope to determine the minimum concentration of polysaccharide that induced alterations in cell morphology, including swelling, shrinkage, granularity and detachment. Cytotoxicity by cell viability was tested using the neutral red dye method from Le Contel [74]. Optical density (OD) was measured at 540 nm using a spectrophotometer (SpectraCountTM, France, Packard). The 50% cytotoxic concentration (CC 50 ) was defined as the concentration that reduced the OD of treated cells to 50% of that of untreated cells.
Using the MT4/HIV model, cytotoxicity was evaluated by incubating MT4 cells (3 × 10 5 cells/mL) with the polysaccharides (final concentration 100-300 µg/mL) in 96-well plates during 1 h at 37 °C with 5% CO 2 . The MT4 cells, which are highly susceptible to the HIV cytopathic effect, were then cultured at 3 × 10 5 cells/mL in 24-well microtiter plates containing various dilutions of polysaccharides. After 4 days, the cell viability was measured by the dead cells exclusion with trypan blue. The 50% cytotoxic concentration (CC 50 ) was defined as the dose of the compound causing 50% cell death after 96 h of incubation at 37 °C [75].

Antiviral Assays Based Upon Cell Viability
Using the Vero cell/HSV-1 model, 100 µL of cellular suspension (3.5 × 10 5 cells/mL) in Eagle's MEM containing 8% FCS were incubated with 50 µL of a dilution of filtered polysaccharide (concentration from 2.5 to 250 µg/mL) in 96 well-plates (48 h, 37 °C, 5% CO 2 ). Three replicates were infected using 50 µL of medium and a virus suspension at a MOI of 0.001 ID 50 /cells. After incubation, antiviral activity was evaluated by the neutral red dye method. The antiherpetic compound acyclovir [9-(2-hydroxyethoxymethyl) guanine] was used as reference inhibitor. The 50% effective antiviral concentration (EC 50 ) was expressed as the concentration that achieved 50% protection of virus-infected cells from virus-induced destruction. The OD was related directly to the percentage of viable cells, which was inversely related to the cytopathic effect (CPE). The linear regression was determined for each assay on the basis of cell controls (0% CPE) and virus controls (100% CPE). Data were expressed as a percentage of protection (%P): [((ODt) virus − (ODc) virus)/((ODc)MOCK − (ODc) virus)] × 100. (ODt) virus was the OD of the test sample, (ODc) virus was the OD of the virus control, and (ODc)MOCK was the OD of the mock-infected control [75].
Using the cells MT4/HIV model, MT4 cells were first pre-incubated during 1 h at 37 °C in 96-well microtiter plates in RPMI 1640 culture medium with 10% FCS and 1% PNS antibiotics, 1% glutamine and 2 µg/mL polybrene and containing various concentrations of polysaccharide (3 × 10 5 cells/mL for 100 µL of compound). Infection of MT4 cells was performed by adding into wells 100 µL of HIV-1 suspension (dilution 10 −3 ). One hour after incubation at 37 °C, infected cells were washed three times with RPMI and cultured at 3 × 10 5 cells/mL in 24-well microtiter plates in the presence of polysaccharide. Cultures were grown for 7 days at 37 °C, under 5% CO 2 atmosphere and re-fed at day 3 post-infection with cell culture medium. After 4 days, the appearance of syncitium was followed every day on an inverted optical microscope. Controls were HIV-1-infected MT4 cells cultured without polysaccharide (control MT4/HIV-1) and uninfected MT4 cells (control MT4). Positive control was HIV-1 infected MT4 cells cultured with a dose of 0.1 µM AZT known to give 100% inhibition of virus replication (control AZT). The virus dilution used in the assay allowed syncitium formation at day 4 post-infection. The 50% inhibitory concentration (IC 50 ) of the compounds was expressed as the dose that caused 50% inhibition of viral production without direct toxicity to cells at day 7 post-infection. The therapeutic index (T1) was defined as the ratio of the 50% cytotoxic concentration to the 50% inhibitory concentration (CC 50 /IC 50 ) [6].

Virus Neutralization Assay
In order to confirm the direct action or not on the virus, a test of neutralization was carried out on CEM cells. In this protocol, the products are put in contact firstly with the virus, and then CEM cells are added. HIV-1 suspension (50 µL) were pre-incubated during 1 h at 37 °C in 96-well microtiter plates in RPMI 1640 culture medium with 10% FCS and 1% PNS antibiotics, 1% glutamine and 2 µg/mL polybrene and containing various concentrations of polysaccharides (50 µL). Then, CEM cells are added (5 × 10 5 cells for 100 µL of virus-compound mixture). One hour after incubation at 37 °C, three washings are carried out then the pellets are resuspended in medium RPMI and transferred in a 24 well microtiter plate in 1 mL of polysaccharide or medium RPMI for the controls cells and virus. The plates are placed at 37 °C and 5% of CO 2 . From day 3 or 4, the activity of the reverse transcriptase is measured every 3 days; the cells are re-fed with new medium and the cellular concentration adjusted to 5 × 10 5 cellules/mL. To measure the reverse transcriptase activity, 1 mL samples of cell-free supernatant collected at day 3, 6, and 10 post-infection were centrifuged (95,000 rpm, 4 °C, 5 min). The viral pellet was resuspended in 10 µL of NTE buffer containing 0.1% Triton X-100. The enzymatic reaction was performed in 40 µL of a reaction mixture of composition: Tris 50 mM, pH 7.8, MgCl 2 20 mM, KCl 20 mM, dithiothreitol 2 mM, oligo (dT) 12-18 0.25 OD/mL, poly(rA) 0.25 OD/mL and 3 HdTTP 2.5 µCi. After 1 h at 37 °C, the reaction products were precipitated with 20% trichloroacetic acid, filtered on Millipore 0.45 µm and the β radioactivity was measured. Controls were HIV-1-infected CEM cells cultured without polysaccharide and uninfected CEM cells. Positive inhibitory control was HIV-1 infected CEM cells cultured with AZT [6].

First Approach of Mode of Antiviral Action
A first approach to determine the mode of action polysaccharides was initiated by carrying out different treatments in the two models: 3.5.5.1. HSV/Vero Model [17,53,57,76] Effect before Infection To determine whether a cellular antiviral state could be induced by polysaccharide, cells were incubated with polysaccharide (24 h, 37 °C, 5% CO 2 ) and were then washed with PBS. Cells were inoculated with virus and incubated for 48 h (37 °C, 5% CO 2 ). The effect on virus multiplication was determined by the neutral red dye method for HSV-1.

Virucidal Assay
A virus suspension containing 0.001 ID 50 /cell of HSV-1 was incubated with an equal volume of medium with or without polysaccharide dilutions (10-250 µg/mL) for 2 h at 37 °C for HSV-1. One hundred microliters of mixed suspension was then added to 100 µL of cellular suspension (3 × 10 5 Vero cells/mL) in culture medium. After incubation for 48 h, the virucidal effect was determined using the neutral red dye method for HSV-1.

Virus Adsorption Assay
The inhibitory effect of polysaccharide on virus adsorption was measured on confluent monolayers of Vero cells infected with HSV-1 at 0.001 ID 50 /cell, under different treatments. In Treatment I, cells were exposed to HSV-1 in the presence of various polysaccharide dilutions. After virus adsorption (1 h at 4 °C), cells were washed with PBS to remove both polysaccharide and unadsorbed virus and further incubated with medium. In Treatment II, cells were exposed to HSV-1 and after a virus adsorption period (1 h at 4 °C), unadsorbed virus was removed and cells were further incubated with the medium containing different concentrations of polysaccharide. In Treatment III, polysaccharide was present both during and after the adsorption period. The effect on HSV-1 adsorption was determined after 2 days by the neutral red dye method.

Effect of Polysaccharide Addition Time
Monolayers of Vero cells were inoculated with HSV-1 at 0.001 ID 50 /cell, and polysaccharide was added simultaneously or after 1, 2, 3 or 5 h following infection. After 48 h of incubation, effect on HSV-1 replication was determined by the neutral red dye method.

HIV/MT4 Model [7]
Before and during Infection The concentrations range shown was in between 12.5 µg/mL to 100 µg/mL. Cells were pre-incubated for 2 h on a 96-well microtiter plate in culture medium containing different concentration of polysaccharide. Cells were infected adding into wells 100 µL of HIV-1 suspension (dilution 7.5 × 10 −5 or 10 −4 ). One hour after incubation, infected cells were washed three times with RPMI, infected and cultured without the compound.

During Infection
The polysaccharide was added simultaneously with the virus, and after 1 h of incubation, infected cells were washed three times with RPMI and cultured without polysaccharide.

After Infection
The polysaccharide was present only after infection.