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Viruses 2013, 5(5), 1219-1230; doi:10.3390/v5051219
Abstract: The Hepatitis C virus causes chronic infections in humans, which can develop to liver cirrhosis and hepatocellular carcinoma. The Bovine viral diarrhea virus is used as a surrogate model for antiviral assays for the HCV. From marine invertebrates and microorganisms isolated from them, extracts were prepared for assessment of their possible antiviral activity. Of the 128 tested, 2 were considered active and 1 was considered promising. The best result was obtained from the extracts produced from the Bacillus sp. isolated from the sponge Petromica citrina. The extracts 555 (500 µg/mL, SI>18) and 584 (150 µg/mL, SI 27) showed a percentage of protection of 98% against BVDV, and the extract 616, 90% of protection. All of them showed activity during the viral adsorption. Thus, various substances are active on these studied organisms and may lead to the development of drugs which ensure an alternative therapy for the treatment of hepatitis C.
Viruses cause many important diseases, and viral-induced emerging and re-emerging infectious diseases representing a major health threat to the public. Effective control of viral infection has remained an unachieved goal, due to virus intracellular replicative nature and readily mutating genomes, as well as the limited availability of anti-viral drugs and measures .
Hepatitis C virus (HCV) infection is a serious global health problem, and the patients with chronic infection have risk of developing liver cirrhosis and hepatocellular carcinoma . HCV infects as many as 170 million people worldwide, representing 3% of the world’s population . The big problem is that, in general, people with chronic hepatitis C are relatively asymptomatic and have few if any clinical manifestations prior to the development of cirrhosis .
Currently, no vaccine exists for hepatitis C vírus . The treatment for HCV infection consists of pegylated interferon (IFN)-α in combination with the nucleoside analog ribavirin (1-β-D-ribofuranosyl-1,2,4-triaxole-3-carboxamide) . This therapy is expensive, effective in only a subset of patients and associated with many side effects  such as depression, flu-like symptoms, fatigue, and hemolytic anemia, and, due to this, many patients are forced to discontinue therapy .
Since the discovery of the HCV, its propagation in cell culture has been a major goal for virologists worldwide. All human hepatitis viruses are very difficult to grow in cell culture . Because of this, another virus is used as a surrogate model for studies regarding HCV.
The bovine viral diarrhea virus (BVDV), a member of the Flaviviridae family (genus Pestivirus), shares similarities with HCV (genus Hepacivirus, Flaviviridae family) in terms of their replication cycles, biology and genetic organization, and shows the functionally homologous nature of many of their gene products, which are considered to be major targets for the development of anti-HCV agents .
BVDV is easy to culture in vitro, molecular clones are available for genetic studies and the virus undergoes a complete replication cycle. Both BVDV and HCV utilize the LDL receptor to enter cells, use a functionally similar internal ribosome entry site for translation, have a mechanistically similar NS5B RNA-dependent RNA polymerase, and a seemingly equivalent mechanism of virion maturation, assembly and egress .
Because of the lack of available vaccines and treatments not being tolerated by some patients, new antiviral agents to treat HCV infection are desperately needed .
Natural products derived from terrestrial and marine kingdoms represent an inexhaustible source of compounds with promising antiviral action, mainly for the variety of synthesized metabolites. In relation to infectious diseases, the exploration of the marine environment represents a promising strategy in the search for active compounds. It is necessary due to the appearance of resistance to available treatments in many microorganisms .
In this study, extracts were tested against BVDV to evaluate their potential antiviral activity.
2. Materials and Methods
2.1. Crude Extracts
Extracts derived from the metabolism of the bacteria strain were obtained by the method of liquid-liquid separation. A pre-inoculum of the isolates were cultured in 7 mL of isolation medium and incubated at 30 °C for 24 h at 100 rpm. After growth of the culture, the total volume was transferred to an Erlenmeyer flask containing 50 mL of the same medium and kept at the same temperature and rotation for 24 h. Again, 50 mL of bacterial growth were transferred to a glass jar containing 500 mL of the same medium and kept in the same conditions mentioned for seven days. After this period, 500 mL of ethyl acetate were added and the mixture was triturated in a blender with high rotation. Then, the mixture was stirred at 100 rpm for 24 h.
Initially, the mixture was filtered on Buchner funnel containing a pad of celite and then the organic phase was recovered in an Erlenmeyer flask using a separatory funnel. In the aqueous phase, the cell debris and the culture medium were retained, and in the organic phase, the possible biologically active metabolites were recovered.
The organic phase was then filtered through cotton and transferred to a round bottom flask. Extracts contained in the organic phase were concentrated in rotaevaporador (BuchiRotavapor R-215) in vacuum at 37 °C until complete drying of the solvent. Then the extracts were suspended in methyl alcohol, filtered with cotton, and the volume transferred to new tubes glass using Pasteur pipette. These tubes were led to Savant vacuum centrifuge, model 210A Speedvac ® Plus SC for evaporation. After complete drying of the solvent, the extracts were dissolved in 10% DMSO in medium AMH and kept at 4 °C until use in the antiviral activity assays.
2.3. Statistical analysis
The results were expressed as mean ± s.e.m. The selectivity index (SI) was determined by the ratio of CC50 to EC50. The statistically different effects of tested extracts on the inhibition of virus replication were compared with the control group using the Student’s t-test with p≤0.05 for significant result.
2.4. Identification of bacteria by 16S rRNA gene sequencing analysis
One sample of each of the sponges Petromica citrina (PC), and Chelonaplysilla erecta (CE) were collected at Saco do Poço (23453S; 45158W), and Ilha de Serraria (23484S; 45134W) at Ilha Bela region, São Paulo State, Brazil, at depths between 5 and 15 m. The sponges were placed in sterilized polyethylene bags containing seawater and immediately transported to the Centro de Biologia Marinha (CEBIMar) of the Universidade de São Paulo. Sponge samples were washed twice with sterilized seawater, cut into pieces and then thoroughly homogenized in a sterile mortar with sterile seawater. Triturated samples were diluted in hundred-fold series (10-2, 10-4) and aliquots of 100 µL were inoculated into Petri dishes containing the media: TSA Agar (Difco, USA), Marine Agar (DifcoTM, USA) and M1 (soluble starch 10 g/L, yeast extract 4 g/L, peptone 2 g/L, agar 15 g/L). All media were prepared with artiﬁcial seawater (ASW): KBr 0.1 g/L, NaCl 23.48 g/L, MgCl2.6H2O 10.61 g/L ,CaCl2 .2H2O 1.47 g/L, KCl 0.66 g/L 1, SrCl2 .6H2O 0.04 g/L, Na2SO4 3.92 g/L, NaHCO3 0.19 g/L, H3BO3 0.03 g/L. Cycloheximide (50 µg.mL-1) and nalidixic acid (15 µg.mL-1) were added to inhibit fungal and many fast-growing Gram-negative bacteria, respectively. Agar plates were incubated at 25 ºC and different colonies were isolated from the 2nd to the 30th day of plating. Pure cultures were obtained after serial transfers to the same culture medium used to plate the sponge samples. The maintenance of the isolates was performed by cryopreservation at -80 ºC (10% glycerol).
The strains were cultured in Nutrient Broth (NB) (Difco) for 24-48 h at 28 °C and genomic DNA was extracted from each strain . From the genomic DNA, 16S rRNA gene sequences were ampliﬁed by polymerase chain reaction (PCR) using bacterial universal primers p27f e p1401r  and sequencing .
The antiviral activity of each extract was evaluated initially in a standard titer assay where the extracts at nontoxic concentrations were added at the same time as the virus. This initial analysis identified which among the many extracts tested have antiviral activity against the virus. The results were considered promising if they showed a protection percentage of at least 90% and active if the result was higher than 97%.
One hundred twenty-eight extracts were tested, of wich two were active against the virus. This represents 1,5% of the total. One of them was considered promising. The Table 1 summarizes the information about the best results.
|Extract||Sponge||Genbank Access number||Identification||Inhibition percentage (%)|
|B511||Chelonaplysilla erecta||HQ433229||Exiguobacterium sp.||33|
|B515||Chelonaplysilla erecta||HQ433231||Vibrio sp.||25|
|B555||Petromica citrina||Deposit number in process||Bacillus sp.||98|
|B565||Petromica citrina||Deposit number in process||Bacillus sp.||37|
|B584||Petromica citrina||Deposit number in process||Bacillus sp.||98|
|B616||Petromica citrina||Deposit number in process||Bacillus sp.||90|
Characteristics of the extracts evaluated for antiviral activity. Name of the each extract evaluated, sponge from which the microorganism was obtained, Genbank access number, identification of the microorganism from which the extract was obtained, and inhibition percentage obtained on antiviral assay
The exploration of the marine environment represents a promising strategy in the search for active compounds against infectious diseases . This environment is still underexplored in Brazil, despite its large size and enormous diversity of species.
Besides its peculiar structures, marine natural products have an extraordinary diversity of molecular targets with expressive selectivity. This greatly increases the pharmacological and therapeutic potential of these molecules .
Marine sponges are among the richest sources of pharmacologically active products derived from marine organisms by their secondary metabolites and also by substances produced by their associated microorganisms. There are already known more than 5300 products that represent possible alternatives against diseases of bacterial, viral, fungal and parasitic origin .
Bacteria that gave rise to extracts evaluated in this study were isolated from marine sponges Petromica citrina and Chelonaplysilla erecta. The marine sponge Petromica citrina is endemic in the country. Previously, antimicrobial activity against some resistant bacteria from aqueous extracts of this sponge has been demonstrated . However, here, we only isolated active extracts of microorganisms from this sponge.
From the sponges, bacteria were isolated, Vibrio sp. and Bacillus sp., and the extracts obtained from them were evaluated against BVDV. Three of these Bacillus generated two active extracts (B555 and B584, IP=98%) and one promising (B616, IP=90%) against BVDV. These microorganisms were identified as Bacillus sp. These extracts showed SI greater than 4, which ensures its viability on in vitro assays.
Several activities have been described in relation to Bacillus sp. Studies showed that bacteria of this genus can devote more than 3% of its genome to genes related to the biosynthesis of secondary metabolites .
The experimental study of antiviral activity of spore-forming bacterium Bacillus pumilus "Pashkov", carried out in 2010, showed for the first time effective antiviral activity of cultural fluid that opens perspectives for development of medications against enterovirus infections .
The Bacillus intermedius RNAse showed antiviral activity in guinea-pigs and rabbits infected with outdoor rabies virus. The intramuscular injection of RNAase failed to protect the infected animals . This Bacillus intermedius RNAse previously showed antiviral activity in experiments with mice preinfected with street rabies virus .
A ribonuclease (RNase) with tobacco mosaic virus inhibition was isolated and purified from Bacillus cereus. The inhibitory activity of the RNase in the purification process against tobacco mosaic virus was tested, and the percentage inhibition of the purified RNase reached 90% .
Besides antiviral activity, Bacillus species have had several other activities described.
One study shows the Antiplasmodial activity of bacilosarcin A isolated from the octocoral-associated bacterium Bacillus sp. collected in Panama. The antiplasmodial activity of the isolated compounds was evaluated in vitro against the chloroquine-resistant Plasmodium falciparum strain W2 and this study constitutes a new addition to the few existing antiplasmodial metabolites isolated from heterotrophic bacteria associated with corals, showing that bacteria associated with marine invertebrates represents a promising resource for antimalarial research .
Another study showed the antibacterial and anticancer activity of ε-poly-L-lysine (ε-PL) produced by a marine Bacillus subtilis. The bacterium produced an active compound against a number of gram negative bacteria .
Already been demonstrated, yet, antifungal activity of Bacillus coagulans against Fusarium sp. , the activity of Macrolactin S isolated from Bacillus sp. AT 28 that inhibited the growth of S. aureus, Bacillus subtilis, and Escherichia coli , and the antimicrobial activity of Bacillus sp. strain FAS1 isolated from soil was demonstrated on the standard indicator species .
Therefore, this genus represents a rich source of bioactive substances and, according to the obtained results, can lead to the development of a new treatment option against HCV infection.
The preliminary tests of mechanism of action showed that the active extracts (B555 and B584) and the promising extract (B616) acts by inhibiting virus adsorption to cell, thus interfering with the progression of infection. This may result from changes in proteins involved in the interaction between the viral envelope and endosomal membrane.
The results of the present study provide further evidence for the potential of microorganisms isolated from marine invertebrates, that represents a reservoir of pharmacologically active substances. From microorganisms isolated from marine sponges, compounds with potential to lead to the development of an alternative therapy against HCV infection were identified. Two of them provided 98% of protection to the cell and their selectivity index was satisfactory. This activity occurred during the adsorption of the virus to the cell. Thus, the extract was able to interfere with the progression of infection. Further studies are necessary to discover the substance responsible for this activity and this substance may lead to the development of an alternative therapy as needed for the population.
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