In vitro anti-HIV-1 activity of the bioactive compound extracted and purified from two different marine macroalgae (seaweeds) (Dictyota bartayesiana J.V.Lamouroux and Turbinaria decurrens Bory)

Highly active antiretroviral therapy (HAART) is the only available remedial measure to treat HIV infected patients, as recognized by the WHO. However, it is associated with toxicity (nephrotoxicity), high cost and most preferably drug resistance in the first-line treatment. Wherefore, potential and novel natural source is the only option for the modern world to challenge this global issue. In recent years, sulfated polysaccharide from marine macroalgae shown to be biologically active as anti-inflammatory, anticoagulant, antitumor, immunomodulatory and antiviral agents. As a direct inhibitor of HIV including other retroviruses, it is considered as a “new generation antiretroviral drug”. In our present study, Fucoidan, a sulfated polysaccharide has been extracted from two different macroalgae Dictyota bartayesiana (DD) and Turbinaria decurrens (TD) based on hot water extraction method and further confirmed by FT-IR and RP-HPLC methods. Both the crude and purified fucoidan samples were evaluated for anti-HIV activity after ion exchange chromatography purification. The maximum inhibitory activity of crude and purified fucoidan samples are 90.5% and 89% in the fucoidan extracts of DD. Whereas, it was 89.7% and 92% in the fucoidan extracts of TD. Simultaneously, the IC50 values were determined and recorded as 1.56 µg/ml and 57.6 ng/ml in both the crude and purified fucoidan extracts of DD respectively. Similarly, for TD, it was 3 µg/ml and 131.7 ng/ml in the fucoidan extracts of TD. Therefore, further extensive research work is the most needful to fill the gaps to develop this sulfated polysaccharide as a potential drug for the treatment of HIV patients.

in the Asian Scenario 7 . Liu et al. 8 have reported complex HIV-1 drug resistant mutations in first-line HAART in China and suggested more varieties of drugs for the therapy with timely monitoring of the viral load. Gregson et al. 9 also reported drug resistance in the first-line HAART treatment using tenofovir in the low socio-economic people. This tends us to carry out a research work on the search for some novel anti-HIV therapeutics from the potent natural resources.
Ocean is an enormous source for novel bioactive metabolites which are highly effective and easily available. Marine bioproducts are in huge demand procuring many biological activities including antifungal, antimicrobial, antithrombotic, anti-inflammatory, anticoagulant and antiviral properties 10 . Marine macroalgae or macroalgae are the wonderful gift of Mother Nature with wide range of pharmacological activities. Polysaccharides are the major component of macroalgae and may vary according to the classification of macroalgae such as Chlorophyta (Green algae), Rhodophyta (Red algae) and Phaeophyta (Brown algae). The sulfated polysaccharides have sulphate groups in their molecular structure, have attracted much attention in the field of pharmacology. Intriguingly, brown algae are recorded to accumulate high quantity of sulfated polysaccharides including laminarin, fucoidan and alginates which have anti-HIV activity with wide spectrum of action mechanism 11 . Fucoidan consists of α-L-fucose residue as sole monosaccharide unit of a long chain homopolymer with sulfate groups.
The first most report on the antiviral activity of polysaccharide from seaweed was reported by Gerber et al. 12 in the year 1958, where, the seaweed extracts prevented the chick embryos from the infection of mumps and influenza B viruses. Potentially, effective antiviral property of sulfated polysaccharide from macroalgae was reported against human cytomegalovirus and HSV-1 and HSV-2 (Herpes Simplex Virus) 13 . Since, due to heterogeneity in the structure of sulfated polysaccharide fucoidan, the exact biological reason for their inhibition of retroviral particles is not yet completely derived 14 . However, the sulfated polysaccharide from macroalgae were reported to hamper the replication of retrovirus such as HIV, HSV, respiratory syncytial virus, cytomegalovirus and even dengue virus [15][16][17] .
It has been reported that the antiviral activity of fucoidan is due to their interaction with the enveloped viral particles or the receptor present on the surface of the host's cell membrane or may be with the viral enzymes. The sulfated polysaccharide is considered to be rarely tend to alterations by the antigenic drift of the viruses and do not express frequent site of drug-induced resistant mutation. The antiviral activity of sulfated polysaccharide is due to their binding with the HIV particle and hampering the early step of viral infection. The sulfate group may neutralize the positively charged amino acid on the viral envelope glyprotein (gp120) with a strong sulphation motif 18 .
The sulfated polysaccharide is proven to inhibit HIV-1 and HIV-2 along with other enveloped viruses including Herpes Simplex Virus type-1, Influenza virus A and B, Measles virus and respiratory synctial virus. The sulfated polysaccharide inhibits the fusion of virus and the host cell and viral adsorption to the host cells 19 . These virucidal agents have significant potential to inhibit HIV replication 20 . The direct inhibition of HIV-1 replication by the sulfated polysaccharide tends to the availability of new generation potential antiviral drugs 21 . Similarly, the sulfated polysaccharides are antiviral agents against wide spectrum human pathogenic retroviruses by inhibiting the viral replication without toxic effects on the host cells 22 .
In our present investigation, the most commonly found brown macroalgae such as Turbinaria decurrens (TD) and Dictyota bartayesiana (DD) from the Mandapam Coastal region (Gulf of Mannar) of Rameswaram, Tamil Nadu, India were collected, and evaluated for their bioactive potential for anti-HIV activity.

Results
Collection of macroalgae. The marine macroalgae namely Dictyota bartayesiana (DD) and Turbinaria decurrens (TD) were collected during the month of December 2017 from the Mandapam Coastal region, Rameswaram, Tamil Nadu, India. The collected seaweed samples were washed with water to remove epiphytes, sand particles and dried under shade. The shade dried seaweed biomasses were grounded to fine powder and stored for the extraction of sulfated polysaccharide.
Extraction and partial purification of sulfated polysaccharide from macroalgae. The shade dried biomasses of two brown macroalgae DD and TD were grounded to fine powder using a mortar and pestle for the extraction of sulfated polysaccharide. Figure 1, showing flow chart exemplifies the methods involved in the extraction and partial purification of crude sulfated polysaccharides. Fine powdered brown algae biomasses in which, DD looks grey ash in color whereas TD looks light brown in color.
The sulfated polysaccharide extracted from brown algae DD and TD were partially purified by dialysis using a cellulose membrane (Fig. 1). Partially purified sulfated polysaccharide of two brown algae DD and TD were subjected to devoid of moisture content by freeze-thaw method to obtain fine powder and yield was calculated. Therefore, the total yield of partially purified sulfated polysaccharide content was 0.768 g and 2.292 g from DD and TD with percentage yield of 7.68% and 22.92% respectively. The crude sulfated polysaccharide was extracted from both the marine macroalgae, and the total sulfated polysaccharide content extracted in DD was comparatively lower when compared to TD.
Reverse phase -high performance liquid chromatography (RP-HPLC) analysis. The predominant monosaccharide unit found in the sulfated polysaccharide fucoidan is fucose. Hence, in this present study fucose was employed as a standard for RP-HPLC analysis to determine fucoidan content in the two marine seaweed extracts. The standard fucose was purchased from Sigma-Aldrich and the crude sulfated polysaccharide extracts of the two brown algae were predigested with trifluoroacetic acid to hydrolyze fucoidan to yield fucose.
Based on the RP-HPLC analysis, the retention time (RT) for standard fucose was 1.56 (Fig. 2). Consequently, the RT for the predigested samples of D. bartayesiana and T. decurrens were 1.60 and 1.59 respectively (Figs 3 and 4).
Similarly, the concentration of fucose content found in the extracts of two brown algae were determined as 314 ng/µl and 956 ng/µl in D. bartayesiana and T. decurrens respectively (Fig. 5). It was distinctly clear that T. decurrens was rich in fucose content than D. bartayesiana.
From the overall HPLC results, it is very clear that the fucose content indirectly represents the presence of sulfated polysaccharide, fucoidan and the concentration was comparatively higher in the case of T. decurrens than D. bartayesiana. Unique peaks were obtained for fucose in both the samples and standard reveals that the higher amount of fucoidan was extracted in both the brown algae D. bartayesiana and T. decurrens.  (Table 3) and was determined by both the estimation of carbohydrate and sulfate. The total carbohydrate and total sulfate content were 0.173 µg/ ml and 0.020 µg/ml in D. bartayesiana. Similarly, in T. decurrens which were 0.380 µg/ml and 0.053 µg/ml respectively (Fig. 8). The total sulfated polysaccharide content was determined as 0.194 µg/ml and 0.433 µg/ml for D. bartayesiana and T. decurrens respectively (Fig. 8) and which were about 3.89% and 8.67% of the total biomass.
Anti-HIV activity of crude and purified sulfated polysaccharide extracts. From the results obtained by this assay, it is obviously clear that the inhibition of the HIV proliferation rate was directly proportional to the concentration of the test samples (crude sulfated polysaccharide) of brown algae DD and TD (Figs 9 and 10). The maximum inhibitory activity of crude fucoidan of brown algae DD and TD against HIV were 90.5% and 89.7% at 5 mg/ml concentration respectively. The IC 50 values measured were 1.56 µg/ml and 3 µg/ml for the crude sulfated polysaccharide extract of DD and TD respectively.
The anti-HIV study was again performed with the purified sulfated polysaccharide samples and the maximum inhibition percentage was found to be 92% and 89% with mean IC 50 values 131.7 ng/ml and 57.6 ng/ml for TD and DD respectively. And thus, both the purified extracts of DD and TD were found to obtain highly active HIV-inhibitory activity (around 90% inhibitory activity) (Figs 11 and 12).

Discussion
Seaweed is one among the most valuable, abundant and cheap source of most diverse biologically active compounds. One intimate compound from the seaweed is sulfated polysaccharide which is found associated with the cell walls of the seaweed which gives toughness and flexibility 23 . For example, fucoidan from brown algae (Phaeophyceae), Carrageenan from red algae (Rhodophyceae) and Ulvan from green algae (Chlorophyceae). These diverse sulfated polysaccharides from different algae have different properties due to their uniqueness with respect to their genus or even species levels. Particularly, this organic compound has allured much recognition among scientific researchers pharmaceutically, rather than food and cosmetic industries 24 . Therefore, in our present study, two different macroalgae such as Dictyota bartayesiana (DD) and Turbinaria decurrens (TD) were collected from the Gulf of Mannar regions.
Due to the heterogeneity of different fucoidan structures from various seaweed sources, different extraction methods were exemplified by various reports 14 . Hot water extraction method discussed by Mohamed and Agilli 25 was followed in our study. In which, crude polysaccharide extract was partially purified by dialysis and ion exchange chromatography. The crude sulfated polysaccharide extracted was 7.68% and 22.92% from DD and TD respectively, and which was high when compared with the study previously held by Dinesh et al. 26 from Sargassum swartzii (5.96%). Recently, many numbers of studies have been reported regarding the antitumor activity 27 , anticoagulant activity 28 , anti-inflammatory activity 29 and antiviral activity 13 of fucoidan from different brown algal extracts. Effective immunomodulatory activity of the sulfated polysaccharide fucoidan, have been recorded for anti-metastasis and anti-lymphangiogenesis 30,31 .
Since, antiviral activity of sulfated polysaccharide from macroalgae have been illustrated in many scientific reports. For example, fucan, a complex structure of glucuronic acid and sulfated fucose units extracted from the seaweed Cladosiphon okamuranus exhibits anti-dengue activity on type 2 virus (DENV-2) 32 and other marine seaweed extracts inhibits HSV-1, HSV-2 [33][34][35] . One common feature among these polysaccharides are, the presence of sulfate molecules attached to the sugar molecules. Hidari et al. 32 exemplified that sulphation of fucan, is the most needful for this antiretroviral activity. But, the reduction of carbohydrate molecules into monosaccharide also hampers antiviral property of the compound. Adding to this, sulfated xylomannans extracted from a red alga Sebdenia polydactyla inhibits the proliferation of HSV-1 in vitro in Vero cells, whereas the antiviral activity of the compound was lost when desulfated and retrieved its potent antiviral activity when over-sulfated 34 .
The HAART involves reverse transcriptase inhibitors as the first-generation ARV drugs licensed and suggested by the WHO, whereas, emerging of drug resistant virulent strains and its side effects are the bottle neck issue 36 . Wherefore, search for novel potent bioactive compounds from natural resources is the most needful www.nature.com/scientificreports www.nature.com/scientificreports/ research for antiretroviral therapy 37 . Our study is also one of the solutions to this issue by evaluating the bioactivity of sulfated polysaccharide extracted from two different macroalgae DD and TD from the Gulf of Mannar region for its antiretroviral activity.
The FT-IR results confirmed the presence of sulfate content in the crude extracts of DD and TD by the occurrence of organic sulfate groups which coincides with the results reported previously by Sinha et al. 38 . Similarly, the occurrence of fucoidan was hereby confirmed by RP-HPLC method with standard L-fucose as reference in both the crude SP extracts. From the purified crude extract, the total sulfated polysaccharide content was estimated as 3.89% and 8.67% with respect to DD and TD.
The fucoidan inhibits the infection of HIV to the host cell surface and hence effective in virucidal activity 34 . However, in vitro inhibition of HIV through prevention of viral replication was reported from the sulfated polysaccharides extracted from two red macroalgae 21 at an IC 50 value of 12.5 µg/mL and HSV-1 at 4.1 µg/mL and  www.nature.com/scientificreports www.nature.com/scientificreports/ 17.2 µg/mL. Concurrently, the crude fucoidan extracts from DD and TD in this present study were subjected to the evaluation of anti-HIV activity and found inhibiting the propagation of HIV at an IC 50 value of 1.56 µg/ml and 3 µg/ml respectively. Similarly, the average anti-HIV and IC 50 value of three brown seaweed extracts including Sargassum polycystum, S. mcclurei and Turbinaria ornata were between 0.33 and 0.7 μg/ml 18 , which is low when compared with the present study.
Thuy et al. 18 also concluded that the fucoidan was effective when pre-incubated with the virus rather incubated with the host cells and was ineffective after infection. However, the anti-HIV and IC 50 value of sulfated polysaccharide extracts from macroalgae E. arborea and S. filiformis resp. were 0.275 g/ml and 0.985 g/ml 39 . Comparatively, Prokofjeva et al. 40 suggested that high molecular weight fucoidans from Saccharina cichorioides and S. japonica were the most effective retroviral inhibitors. As a result, all the natural source of fucoidans are considered to be a potent anti-HIV compounds with irrespective of their sugar backbone and degree of sulfation even at very low concentrations from 0.001-0.05 μg/ml. Therefore, the IC 50 value of the purified fucoidan extracts of TD and DD from our present investigation were 131.7 ng/ml and 57.6 ng/ml and inhibits about 92% and 89% at maximum concentration with highly active HIV-inhibitory activity.    Table 3. The ion exchange purified elution from two different marine macroalgae rich in sulfated polysaccharide.    Rameswaram, Tamil Nadu, India was chosen for the collection of macroalgae samples to carry out our present study. Brown macroalgae was given importance due to the bioavailability of sulfated polysaccharide, and hence two different macroalgae Turbinaria decurrens J.V.Lamouroux (TD) and Dictyota bartayesiana Bory (DD) belonging to the family Phaeophyceae were collected from the above-mentioned site.
Extraction and partial purification of sulfated polysaccharide from macroalgae. The extraction of sulfated polysaccharide (SP) from the two different macroalgae (TD and DD) was carried out based on the hot water extraction method described by Mohamed and Agilli 25 . About 10 g of finely grounded seaweed biomasses were taken individually for depigmentation using petroleum ether and incubated overnight, followed by acetone in the second phase. The depigmented and air-dried residual seaweed powders were subjected to acid treatment with 0.1 M HCl at room temperature under constant stirring for 1 hour and kept for overnight incubation, followed by alkali treatment with 2% Na 2 CO 3 at 90 °C for 2 hours.
The residual contents were subjected to hot water extraction at 90 °C for 2 hours and repeated twice. After hot water extraction, the whole content was filtered through Whatman No.1 filter paper. The filtrate was then treated with 1 g of CTAB (Cetyltrimethyl ammonium bromide) for 15 min., the obtained precipitate was filtered through Whatman No.1 filter paper, washed twice with Milli-Q water and followed by the treatment with 20% ethanolic potassium iodide (KI) (20 g of KI in 80 ml of water in 20 ml of ethanol) for 30 min. The resultant precipitate was again washed twice with Milli-Q water and stored in a refrigerator at 4 °C. Then, the obtained crude sulfated polysaccharide extracts from both the macroalgae were partially purified by dialysis using Dialysis membrane-70 from HiMedia against Milli-Q water at 15 °C for two days. Then the residual contents were subjected to drying by freeze-thaw method intermittently to obtain dry powder, weighed and stored for further processes.

Reverse phase -high performance liquid chromatography (RP-HPLC) analysis. Prior to
RP-HPLC analysis, the crude sulfated polysaccharide extracts were hydrolyzed with trifluoroacetic acid (TFA). About 10 mg of crude sulfated polysaccharide extracts of both the macroalgae were predigested with 2 ml of 2 M TFA at 121 °C for 1 hour. Then after hydrolysis, the reaction medium was dried with vacuum concentrator and dissolved using distilled water. Then the resultant solutions were neutralized at pH 7.0 with 1 N NaOH 41 .
The conditions for RP-HPLC are HPLC pump with C18 column, Water 2489 UV/Vis -274 nm detector, HPLC grade water as mobile phase at flow rate of 0.6 ml/min. with injection volume of 1 ml. The concentration of samples were 1 µg/µl and same for standard L-Fucose obtained from Sigma-Aldrich.
Fourier transform infrared spectrometry (FT-IR). About 1 mg of each crude sulfated polysaccharide extracts were mixed with 100 mg of potassium bromide (KBr) in a mortar and pestle separately and placed in a pellet die to compress up to 10,000 psi. Then, the obtained pellet was placed in the FT-IR sample holder for analysis. The samples were analyzed by FT-IR spectrometer in a frequency range between 600 and 4000 cm −1 .
Ion exchange purification of sulfated polysaccharide. The crude sulfated polysaccharide extracts of both the brown algae were further purified using anion exchange chromatography (DEAE (Diethylaminoethyl cellulose) Sepharose from Sigma-Aldrich, 15 × 2.5 cm column). The samples were eluted with 5 ml of different molar concentrations of NaCl ranging from 0 to 3.6 M with 0.4 M interval in 50 mM sodium acetate buffer with pH 5.0. Each fraction was collected, dialyzed (Dialysis membrane-70, HiMedia) against Milli-Q water to free the fractions from NaCl and conserved for further processes.
Determination of carbohydrate and sulfate content. The total carbohydrate and sulfate content were determined in all the fractions after ion exchange purification based on the Phenol sulphuric acid method 42 and sodium rhodizonate method 43 respectively.
Anti-HIV activity of crude and purified sulfated polysaccharide extract. For the determination of anti-HIV activity of crude and purified sulfated polysaccharide extract, HIV-1 (Clade C strain) was obtained from the National Aids Research Institute (NARI, Pune, India) and incubated on human PBMC (Peripheral blood mononuclear cells) as described by Jackson et al. 44 . HIV Gag p24 assay was performed on blasted PBMC for the determination of anti-HIV activity of the test compound 45 . All the assays were performed in the biosafety level 2 + (BSL). The test compounds and a positive control (Nonoxynol-9) were treated in a series of concentrations with 15 pg of HIV-1 virus and incubated for 1 hour at 37 °C. Then after incubation, blasted PBMC cells (0.3 × 10 6 concentrations) was added and incubated for 37 °C for 2 hours. The cells were washed and re-suspended in 2% RPMI (Rosewell Park Memorial Institute) medium and further incubated for 5 days at 37 °C.
Three different groups were segregated namely the drug-positive control group (Nonoxynol-9), drug-negative control group (treated with distilled water) and a test compound group. After five days of incubation, the supernatants were collected and analyzed for anti-HIV activity by HIV Gag p24 protein concentration using ELISA (Enzyme-linked immune sorbent assay) plate assay 46 . The absorbance values were measured at 450 nm by ELISA plate reader, inhibitory concentrations values were determined for the respective concentrations of the test compound and the results were interpreted.

Conclusion
Drug resistance and toxicity are the associated issues with HAART while treating HIV in patients. Hence, search for a novel and potent natural source is an audible solution for this major issue in the upcoming decades. As a result, from our present study, fucoidan is one among the potent natural sulfated polysaccharide extracted from two different macroalgae Dictyota bartayesiana (DD) and Turbinaria decurrens (TD) and evaluated for its