Phlorotannins, which have been found to exist within brown algae, are formed by the polymerization of phloroglucinol (1,3,5-tryhydroxybenzene) monomer units and biosynthesized through the acetatemalonate pathway [18,19]. The phlorotannins are highly hydrophilic components with a wide range of molecular sizes ranging between 126 Da–650 kDa [20]. Marine brown algae accumulate a variety of phloroglucinol-based polyphenols, as phlorotannins of low, intermediate and high molecular weight containing both phenyl and phenoxy units [21,22]. Furthermore, phlorotannins consist of phloroglucinol units linked to each other in various ways, and are of wide occurrence amongst marine organisms, especially brown and red algae [21]. Based on the means of linkage, phlorotannins can be classified into four subclasses: fuhalols and phlorethols (phlorotannins with an ether linkage), fucols (with a phenyl linkage), fucophloroethols (with an ether and phenyl linkage), and eckols (with a dibenzodioxin linkage) [23]. Brown algae, which have a high concentration of phlorotannins (Figure 1), have been reported to possess anti-HIV activity (Table 1).

For the first time, Ahn et al. [24] reported that 8,8′-bieckol and 8,4‴-dieckol, which were isolated from the brown algae Ecklonia cava KJELLMAN, show an inhibitory effect on HIV-1 reverse transcriptase and protease. The inhibition against reverse transcriptase of 8,8′-bieckol with a biaryl linkage (IC₅₀, 0.5 μM) was 10-fold higher than that of 8,4‴-dieckol with a diphenyl ether linkage (IC₅₀, 5.3 μM), although these two phlorotannis are dimers of eckol. The authors suggested that the steric hindrance of the hydroxyl and aryl groups near the biaryl linkage of 8,8′-bieckol caused the potent inhibitory activity. Moreover, 8,8′-bieckol selectively inhibited reverse transcriptase over protease, and the inhibitory effect was comparable to the positive control nevirapine (IC₅₀, 0.28 μM). It is clear that the 8,8′-bieckol possessed higher inhibitory activity than 8,4‴-dieckol. Therefore, they evaluated the molecular mechanisms of this compound against HIV-1 reverse transcriptase using a homopolymeric template/primer under steady-state condition. Kinetic study showed that 8,8′-bieckol inhibited the RNA-dependent DNA synthesis activity of HIV-1 reverse transcriptase noncompetitively against dUTP/dTTP with a Ki value of 0.78 μM. Meanwhile, this compound also exhibited a noncompetitive inhibition (Ki, 0.23 μM) with respect to a homopolymeric template/primer, (rA)_n(dT)₁₅. A possible suggestion for this phenomenon is that 8,8′-bieckol binds to HIV-1 reverse transcriptase only after the template/primer initially binds to the enzyme. The inhibitory effects of this compound shown in this kinetic model are consistent with non-nucleoside RT inhibitors, such as pyridinones [27], trovirdine [28]. As a result, 8,8′-bieckol might be considered as a new nonnucleoside HIV-1 RT inhibitor.

In the next report, Ahn et al. [25] showed that Ishige okamurae Yendo-derived diphlorethohydroxycarmalol also has an inhibitory effect on HIV-1. This compound exhibited inhibitory effects on the HIV-1 reverse transcriptase and integrase with IC₅₀ values of 9.1 μM and 25.2 μM, respectively. However, diphlorethohydroxycarmalol did not show inhibitory activity against the HIV-1 protease.

Furthermore, 6,6′-bieckol, one of the main phloroglucinol derivative naturally occurring in Ecklonia cava, has a potent inhibition against HIV-1 induced syncytia formation, lytic effects, and viral p24 antigen production [26]. Moreover, 6,6′-bieckol selectively inhibited the activity of HIV-1 reverse transcriptase enzyme with an IC₅₀ of 1.07 μM, as well as the inhibition of HIV-1 entry. In addition, it exhibited no cytotoxicity at a concentration where it inhibited HIV-1 replication almost completely. Therefore, 6,6′-bieckol can be employed for the development of new generation therapeutic agents against HIV.

Chitin, a long-chain polymer of N-acetylglucosamine, is widely distributed as the principle component of living organisms such as insects, fungi, crustacean and invertebrates [29]. It is one of the most abundant polysaccharides and is usually prepared from the shells of crabs and shrimps [30]. Chitosan, a partially deacetylated polymer of N-acetylglucosamine, is produced commercially by deacetylation of chitin [31]. Chemical modification of chitin and chitosan generate new biofunctional materials which provide desired biological activities and physicochemical properties [32–36]. The sulfated chitin and chitosan (Figure 2) have a variety of biological functions, including anti-HIV-1, anti-oxidant, anti-microbial, blood anti-coagulant and hemagglutination inhibition activities. Moreover, some of these sulfated chitin and chitosan derivatives function in drug delivery, adsorption of metal ions, prevention of cancer metastasis, or as elicitors of resistance to late blight in potato [37–40].

Sosa et al. [41] report that the N-carboxymethylchitosan N,O-sulfate (NCMCS), a polysaccharide derived from N-carboxymethyl chitosan by a random sulfation reaction, could inhibit the propagation of the human immunodeficiency virus type 1 (HIV-1) in human CD4⁺ cells. Furthermore, they suggested that this activity was due to blocking of the interactions of viral coat glycoprotein receptors to target proteins on lymphocytes and competitive inhibition of HIV-1 reverse transcriptase. Therefore, NCMCS is considered as a potent anti-infection agent, which prevents the invasion of HIV-1 through inhibiting viral adsorption to the CD4 receptor and reverse transcription of the viral genome. However, the inhibitory effect of chitin sulfates on HIV-1 infection depends significantly on the sites of sulfation (Table 2) [42]. A regioselective sulfation of C-2 (C-2S) and/or C-3 (C-3S) groups of chitin showed a much higher inhibitory effect on the infection of AIDS virus in vitro than the 6-O-sulfonated (C-6S) derivatives. Moreover, the product with sulfation at both 2 and 3 positions (C-2,3S) completely inhibited the infection of AIDS virus to T lymphocytes at a concentration of 0.28 μg/mL without significant cytotoxicity. These results indicate that biological activities of sulfated chitin are controllable by changing the position of the sulfate groups.

Recently, many studies have developed aminoderivatized chitosans, which possess numerous biological activities such as anti-oxidant, anti-hypertensive, enzyme inhibition, and anti-microbial properties [43]. Among aminoderivatized chitosans, aminoethyl-chitosan, prepared from 50% deacetylated chitosan, showed activity against HIV-1 with an IC₅₀ value of 17 μg/mL [44]. Thus, aminoethyl-chitosan can be used as new generation drug candidates against HIV.

To improve the water-solubility and biological activity, chitosan also can be converted to chitooligosaccharides (COSs) via either chemical or enzymatic hydrolysis [45–47]. COSs and their derivatives are not only water-soluble [48] and have higher absorption profiles [49], but also possess various biological activities, such as ACE enzyme inhibition [50], anti-oxidant [51], anti-microbial [52], anti-cancer [53,54], immuno-stimulant [55], anti-diabetic [56], hypocholesterolemic [57], hypoglycemic [58], anti-Alzheimer’s [59], anti-coagulant [60] and adipogenesis inhibition [61]. In addition, sulfated chitooligosaccharide (SCOS), which were synthesized by a random sulfation reaction, have reported to possess anti-HIV activity at low molecular weight (3–5 kDa) (Figure 2) [62]. At nontoxic concentrations, SCOS significantly inhibited HIV-1-induced syncytia formation and lytic effect at EC₅₀ values of 2.19 μg/mL and 1.43 μg/mL, respectively. As well, the production of p24 antigen was suppressed at EC₅₀ values of 4.33 μg/mL and 7.76 μg/mL for HIV-1_RF and HIV-1_Ba-L, respectively. Moreover, SCOS exhibited inhibitory activities on viral entry and virus-cell fusion via blocking the binding between HIV-1 gp120 and CD4 cell surface receptor. These observations indicate that SCOS might be useful as a novel candidate for the development of anti-HIV-1 agents.

Sulfated polysaccharides (SPs) comprise a complex group of macro-molecules with a wide range of important biological activities. These polymers are chemically anionic and distributed widely not only in marine algae but also in animals such as mammals and invertebrates [63,64]. Marine algae are the most important source of non-animal SPs and the chemical structure of the polymers varies according to the algae species [65]. The amount of SPs in algae varies according to the divisions of marine algae, such as Chlorophyta (green algae), Rhodophyta (red algae) and Phaeophyta (brown algae). In recent years, various SPs isolated from marine algae have attracted much attention in the fields of biochemistry and pharmacology. They exhibit beneficial biological activities such as anti-HIV-1 [9], anti-adhesive [66], anti-coagulant [67], anti-cancer [68] and anti-inflammatory [69].

Many species of marine algae contain significant quantities of complex structural SPs that have been shown to inhibit the replication of enveloped viruses including members of the flavivirus, togavirus, arenavirus, rhabdovirus, orthopoxvirus, and herpesvirus families [70]. The chemical structure, including the degree of sulfation, molecular weight, constituent sugars, conformation and dynamic stereochemistry, affect the antiviral activity of algal sulfated polysaccharides [71–73]. Moreover, SPs may inhibit the attachment of viruses with target molecules on the cell surface. The viral attachment peptides are highly conserved regions within rather variable scaffolds of viral surface glycoproteins. These peptides are poorly subject to alterations by the natural antigenic drift of viruses. Likewise, they are not expected to represent frequent sites of drug-induced resistant mutation. Therefore, SPs directed toward these target peptides are preferred candidates for antiviral drug development [71,74–76]. In this regard, marine-derived SPs are great sources for the development of a new generation of anti-HIV therapeutics, as reported by several studies (Table 3). A number of SPs from red algae have exhibited an appreciable HIV-1 inhibitory activity. The sulfated glucuronogalactan from red algae Schizymenia dubyi was reported to possess anti-HIV activity [77]. Bourgougnonl et al. [77] determined the antiviral activity with HIV-1 by measuring the protective effect of sulfated glucuronogalactan against the virus-induced cytopathogenicity in MT4 cells over eight days. As shown in their study, the syncitial formation was completely suppressed with 5 μg/mL of this polysaccharide. Furthermore, the HIV-1 reverse transcriptase was inhibited at concentrations as low as 5 μg/mL, without cytotoxicity to MT4 cells. They suggested that the mechanism of action of this polysaccharide in vitro can be been mainly attributed to the inhibition of virus-host cell attachment or an early step of HIV infection.

In addition, sulfated galactans GFP extracted from the red algae Grateloupia filicina and GLPE obtained from Grateloupia longifolia also have antiretroviral activity in vitro. The sulfated galactan GFP has sulfate ester groups at carbon 2 and at carbon 2 and 6 for GLPE. Wang et al. [83] investigated the antiretroviral activity of these sulfated galactans in a model based on a primary isolate of HIV-1 and human peripheral blood mononuclear cells. These results showed that both GFP and GLPE had potent anti-HIV-1 activity when added at the time of infection and 2 h post-infection (EC_50s, 0.010–0.003 μM and EC_90s, 0.87–0.33 μM, respectively) with low cytotoxicity.

Moreover, brown algae are also known to produce a variety of interesting SPs, which have been found to exhibit anti-HIV activity with different mechanisms of action. Sulfated polymannuroguluronate (SPMG), a new form of sulfated polysaccharide extracted from brown algae with an average molecular mass of 8.0 kDa, is rich in 1,4-linked b-D-mannuronate, with an average of 1.5 sulfates and 1.0 carboxyl groups per sugar residue [86]. The involution of marine sulfated polymannuroguluronate in inhibition of HIV-1 entry was reported by Meiyu et al. [80]. They indicated that binding of SPMG either to soluble oligomeric rgp120 or to complexed rgp120–sCD4 mainly resided in the V3 loop region. The V3 loop of gp120, considered as a positively charged region, was targeted by negatively charged polysaccharides. In addition, the pre-incubation of SPMG with rgp120 triggered partial suppression of rgp120 binding to sCD4. Thus, they suggested that SPMG either shares common binding sites on gp120 with sCD4 or masks the docking sites of gp120 for sCD4. Finally, SPMG was shown to be less accessible for sCD4 when sCD4 was pre-combined with rgp120, though SPMG multivalently bound to sCD4 with relatively low affinity. However, SPMG may suppress the multivalent binding of rgp120 to sCD4 receptor when SPMG is added either prior to or after the interaction of rgp120 with sCD4. These effective suppressions indicate that SPMG endows both preventive and therapeutic potential on HIV-1 entry.

Fucans are a class of high molecular weight sulfated polysaccharides. They are widely distributed in several species of brown algae and composed of a mainly repeating chain of fucose. The sulfated fucans from the seaweed species Dictyota mertensii, Lobophora variegata, Spatoglossum schroederi and Fucus vesiculosus were reported to inhibit HIV reverse transcriptase (RT) by Queiroz et al. [84]. They have indicated that the galactofucan fraction from L. variegate, which is rich in galactose, fucose and glucose with a lower sulfate content, had a marked inhibitory effect on reverse transcriptase, with 94% inhibition for synthetic polynucleotides at a concentration of 1.0 μg/mL. On the other hand, fucan A from S. schroederi and D. mertensii, which contains mainly fucose with a lower sulfate level, showed a high inhibitory effect on RT enzyme at 1.0 mg/mL, with 99.03 and 99.3% inhibition, respectively. Meanwhile, fucan B from S. schroederi, which contains galactose, fucose and high sulfate level, showed a lower inhibitory activity (53.9%) at the same concentration. Taking another approach, the authors purified a fucan fraction from F. vesiculosus, a homofucan containing only sulfated fucose with high sulfate content, which exhibited high inhibitory activity of HIV on RT. This fraction inhibited 98.1% of the reaction with poly(rA)-oligo(dT) at a concentration of 0.5 mg/mL. In addition, they modified SPs by carboxyreduction and desulfation to determine the structure-activity relationship. These modified conditions reduced the inhibitory activities of these polysaccharides for RT approximately four-fold. From these results, they have suggested that fucan activity is dependent on both the ionic changes and the sugar rings that act to spatially orientate the charges in a configuration and recognizes the enzyme, thus determining the specificity of the binding.

In the recent study, Trinchero et al. [85] have shown that galactofucan fractions from the brown algae Adenocystis utricularis exhibited anti-HIV-1 activity in vitro. Among five fractions, EA1-20 and EC2-20 had a strong inhibitory effect on HIV-1 replication in vitro with low IC₅₀ values (0.6 and 0.9 μg/mL, respectively). Additionally, EA1-20 and EC2-20 displayed this capacity against wild type and drug-resistant HIV-1 strains. For active fractions, it was also shown that the inhibitory effect was not due to an inactivating effect on the viral particles but rather to a blockade of early events of viral replication. Based on these results, seaweed-derived SPs are regarded as good candidates for further studies on prevention of HIV-1 infection.

Beside macroalgae, microalgae are also considered as sources of novel SPs. Navicula directa is a diatom often collected at a sluice gate of deep sea water. Naviculan, a sulfated polysaccharide isolated from N. directa as a novel antiviral agent, consisted of fucose, xylose, galactose, mannose, rhamnose, and other trace amounts of sugar moieties. Lee et al. [82] reported that naviculan possesses antiviral activity, including against herpes simplex viruses type 1 (HSV-1) and herpes simplex viruses type 2 (HSV-2), displaying IC₅₀ values of 14 μg/mL and 7.4 μg/mL, respectively. In addition, naviculan also showed an inhibitory effect on the formation of cell–cell fusion between HIV gp160- and CD4-expressing HeLa cells with an IC₅₀ value of 53 μg/mL. From these results, it is indicated that this polysaccharide might act as an inhibitor for HSV and HIV-1 infection.

For the first time, Amornrut et al. [79] isolated a new type of D-galactan sulfate from clam Meretrix petechialis and the anti-HIV activity of this polysaccharide has been evaluated by the inhibition of syncytia formation. Inhibition of νPE 16-induced syncytia formation in CD4 HeLa cells by d-galactan sulfate was 56% at 200 μg/mL and this inhibitory effect is comparable to the positive control dextran sulfate (95% at the same concentration). The inhibition of syncytia formation might be due to the interference of D-galactan sulfate on CD4-gp 120 binding.

Recent studies demonstrated that SPs could be used as a vaginal antiviral formulation without disturbing essential functions of the vaginal epithelial cells and normal bacterial flora. It will be a continuous challenge to select the most promising drug candidates among the wide array of available polysaccharide compounds. The numerous advantages over other classes of antiviral drugs, such as relatively low production costs, broad spectrum of antiviral properties, low cytotoxicity, safety, wide acceptability and novel modes of action, suggest that SPs are promising drug candidates in the near future.

Lectins or carbohydrate-binding proteins are found in a variety of different species, ranging from prokaryotes to corals, algae, fungi, plants, invertebrates and vertebrates. They are involved in many biological processes, including host-pathogen interactions, cell-cell communication, induction of apoptosis, cancer metastasis and differentiation, targeting of cells, as well as recognizing and binding carbohydrates. Interestingly, lectins have the potential to block the binding of HIV to target cells, preventing HIV infection and dissemination [87]. Obviously, HIV-1 envelope glycoprotein gp120 is extensively glycosylated and contains approximately 24 potential N-linked glycosylated sites. These glycosylation sites are occupied with glycans that form almost 50% of the gp120 molecular weight. The gp120 glycans represent high-mannose, hybrid and complex classes and serve as ligands for different lectins [88]. The importance of gp120 glycans for the many aspects of HIV-1 infection makes them suitable targets for anti-HIV-1 treatment or prophylaxis [89–91]. There are several types of marine lectins for which anti-HIV activity has been reported (Table 4). Griffithsin (GRFT), a lectin isolated from the red algae Griffithsia sp, displayed potent anti-HIV activity [92]. GRFT is a completely novel protein with a molecular weight of 12.7 kDa. It consists of 120 usual amino acids, including one unusual amino acid at position 31 (151 Da). There are no cysteine residues among its 121 amino acids and no homology to any of the proteins or translated nucleotide sequences. Most likely, GRFT molecule is formed as a domain-swapped dimer in solution [92]. Mori et al. [92] determined that both native and recombinant GRFT potently inhibited the cytopathic effects of laboratory strains and clinical primary isolates of HIV-1 on T-lymphoblastic cells at concentrations as low as 0.043 μM. It was also shown to be active against both T-cell tropic and macrophage- tropic strains of HIV-1 at the same concentrations. Furthermore, GRFT blocked cell-cell fusion between chronically infected and uninfected cells at sub-nanomolar concentrations. In addition, it aborted the binding of CD4-dependent glycoprotein gp120 to receptor-expressing cells in a glycosylation-dependent manner, and prevent gp120 binding to 2G12 and 48d monoclonal antibody. Interestingly, soluble gp120 binding to GRFT was inhibited by the monosaccharides glucose, mannose and Glc-NAc but not by galactose, xylose, fucose, GalNAc or sialic acid-containing glycoproteins. The Mori et al. [92] study also indicated that GRFT may present four carbohydrate-binding domains, separated by three linker sequences Gly-Gly-Ser-Gly-Gly. This organization for this lectin could explain its unusually potent activity due to the possibility of the formation of multivalent bonds between GRFT and oligosaccharides on gp120. These properties make GRFT a promising potential candidate for development as a future pharmaceutical agent.

In recent years, marine invertebrates are attractive as new sources of unusual lectins. CVL is a 30 kDa β-galactose-specific lectin isolated from the marine worm Chaetopterus variopedatus [93]. Wang et al. [93] indicated that CVL interacts with the hydroxyl group of C-2 and C-4 in the galactose molecule. They also demonstrated that hydroxyl group at C-6 failed to influence binding of the galactose residues of glycoproteins with CVL while the hydroxyl group at C-3 appeared to be very significant for binding glycoproteins with the lectin. Moreover, they investigated the anti-HIV activity of CVL in vitro. Results showed that CVL inhibited cytopathic effect induced by HIV-1 and the production of viral p24 antigen at the early stage of virus replication with EC₅₀ values of 0.0043 and 0.057 μM, respectively. They also found that CVL could block the cell-to-cell fusion process of HIV infected and uninfected cells with an EC₅₀ value of 0.073 μM. Finally, CVL was showed to abort 86% and 21% of HIV-1 entry into host cells at concentrations of 0.33 μM and 0.07 μM, respectively. It is clear that CVL isolated from the marine worm C. variopedatus could be a potential candidate to prevent HIV-1 entry into cells.

In addition, the marine worm Serpula vermicularis was also subject as a source of new lectins. SVL is a GlcNAc-specific lectin newly purified and characterized by Molchanova et al. [94]. This lectin is a homotetrameric glycoprotein in which two identical subunits are connected with disulfide bonds. It is mainly composed of aspartic and glutamic acids, glycine, valine and serine; with relatively lower content of basic amino acids and cysteine. The sequence of N-terminal amino acids of SVL was determined as ADTPCQMLGSRYGWR. SVL was proven to potently inhibit the production of viral p24 antigen and cytopathic effects induced by HIV-1 in host cells at EC₅₀ values of 0.23 and 0.15 μg/mL, respectively.

Furthermore, Luk’yanov et al. [95] evaluated the anti-HIV activity of lectins isolated from marine invertebrates Crenomytilus grayanus, Didemnum ternatanum and Serpula vermicularis. CGL, a lectin isolated from C. grayanus mussel, exhibits a very high affinity to the glycoproteins of mucin type. DTL and DTL-A are lectins isolated from the ascidium D. ternatanum. DTL, a GlcNAc-specific lectin with a shorter carbohydrate-binding site, recognizes only terminal residues of GlcNAc and does not recognize the chitobiose core. DTL reveals N-chains of hybrid type rather than the carbohydrate chains of complex and highly mannose type. DTL-A, a GlcNAc/GalNAc and heparin-binding lectin, can be used to detect glycoproteins containing α-bound residues of GlcNAc/GalNAc and some SPs due to the peculiarities of its carbohydrate specificity. SVL-1 and SVL-2 are Ca²⁺-independent lectins, revealed in the marine worm S. vermicularis. SVL-1 is a mannan-binding lectin with molecular mass of 65 kDa while SVL-2 is a GlcNAc-specific lectin with molecular mass of 50 kDa. Their composition consists of two subunits connected with each other by disulfide bonds forming a tetramer. These lectins were reported to exhibit anti HIV-1 activity in in vitro experiments. The DTL, DTL-A, SVL-2, and CGL inhibited the HIV-1 III_B-induced syncytium formation in C8166 cells with EC₅₀ values of 0.002, 0.36, 0.15 and 27.88 μg/mL, respectively. Moreover, these lectins were confirmed to effectively inhibit virus replication and p24 antigen production at EC₅₀ values as shown in Table 4. Among these lectins, DTL, DTL-A and CGL displayed activity against cellular fusion between the H9/HIV-1 chronically infected cells and the C8166 uninfected cells at the following concentrations (EC₅₀): 1.37, 6.97 and 35.12 μg/mL, respectively. According to their results, DTL may be regarded as a potential candidate for the development of novel antiviral agents.

Marine-derived bioactive peptides have been isolated widely by enzymatic hydrolysis of marine organisms [96–100]. Proteolytic enzymes derived from microbes, plants and animals can be used for the hydrolysis process of marine proteins to develop bioactive peptides [101]. Bioactive peptides are inactive within the sequence of their parent protein and can be released by enzymatic hydrolysis [102]. Moreover, bioactive peptides usually contain 3–20 amino acid residues, and their activities are based on the amino acid composition and sequence [103]. Marine-derived bioactive peptides have been shown to possess many physiological functions, including anti-hypertensive or angiotensin-I-converting enzyme inhibition [104], anti-oxidant [105,106], anti-coagulant [107,108], and anti-microbial [109,110] activities. Additionally, several studies have reported the anti-HIV activity of marine bioactive peptides (Table 5).

Lee and Maruyama [111] considered that oyster produces antiviral and antibacterial substances for preventing infectious diseases. Thus, they searched for HIV-1 protease-inhibiting substances from oyster Crassostrea gigas. They observed and isolated two peptides, Leu-Leu-Glu-Tyr-Ser-Ile (1) and Leu-Leu-Glu-Tyr-Ser-Leu (2), which inhibited HIV-1 protease in thermolysin hydrolysate of oyster protein. The peptide 1 and 2 showed strong inhibition of HIV-1 protease at IC₅₀ values of 20 and 15 nM, respectively. Moreover, these peptides behaved as competitive inhibitors for HIV-1 protease with Ki values of 13 and 10 nM, respectively. Lee and Maruyama [111] confirmed that the presence of C-, N-terminal hydrophobic amino acids and the length of the amino acid sequence in these peptides are important for their inhibitory activity.

Over the years, sponges have been known as a source of novel bioactive peptides. The novel and unique structural features of these peptidic metabolites have generated considerable interest. Cyclic depsipeptides isolated from a number of marine sponges have reported to be active as HIV inhibitors [119]. Callipeltin A, a novel antiviral cyclic depsidecapeptide from sponge of the genus Callipelta, contains four amino acids in the L configuration, alanine, leucine, threonine (two residues); one (arginine) in the D configuration; two N-methyl amino acids, N-methyl alanine and N-methyl glutamine; a methoxy tyrosine, a 3,4-dimethyl-L-glutamine; and a 4-amino-7-guanidino-2,3-dihydroxypentanoic acid (AGDHE), formally derived from L-arginine [112]. Callipeltin A exhibited the inhibition of cytopathic effects induced by HIV-1 in CEM4 lymphocytic cell lines at an ED₅₀ value of 0.01 μg/mL. The general structure of callipeltin A was identified to be similar to a family of potent antiviral, didemnins, which support that it possesses anti-HIV activity.

Likewise, Ford et al. [113] have isolated novel cyclic depsipeptides papuamides A and B from sponges Theonella mirabilis and Theonella swinhoei. These peptides contain not only unusual amino acids, including 3,4-dimethylglutamine, β-methoxytyrosine, 3-methoxyalanine, and 2,3-diaminobutanoic acid or 2-amino-2-butenoic acid residues, but also the first marine-derived peptides reported to contain 3-hydroxyleucine and homoproline residues. These peptides also contain a previously undescribed 2,3-dihydroxy-2,6,8-trimethyldeca-(4Z,6E)-dienoic acid moiety N-linked to a terminal glycine residue. Papuamides A and B were reported to block the infection of human T-lymphoblastoid cells by HIV-1 sub(RF) in vitro with an EC₅₀ of approximately 4 ng/mL. The inhibitory activity of papuamides A was due to blockage by this peptide at the initial stage of the viral life cycle, but was not HIV-1 envelope glycoprotein specific [120]. At a similar concentration to papuamide A, papuamide B also prevents viral entry via interaction of this peptide with phospholipid present on the viral membrane [120]. Another anti-HIV candidate from the sponge is the microspinosamide, a new cyclic depsipeptide isolated from Sidonops microspinosa. This peptide incorporates 13 amino acid residues, and it is the first naturally occurring peptide to contain a β-hydroxy-p bromophenylalanine residue [114]. Rashid et al. [114] demonstrated that microspinosamide is capable of inhibiting the cytopathic effect of HIV-1 infection in an XTT-based in vitro assay with an EC₅₀ value of approximately 0.2 μg/mL.

In another study, Oku et al. [115] isolated a new HIV-inhibitory depsipeptide, neamphamide A, from the marine sponge Neamphius huxleyi. Neamphamide A contains an amino acid sequence of l-Leu, l-NMeGln, d-Arg, d- and l-Asn, two residues of d-allo-Thr, l-homoproline, (3S,4R)-3,4-dimethyl- lglutamine, β-methoxytyrosine, 4-amino-7-guanidino-2,3-dihydroxyheptanoic acid and an amide-linked 3-hydroxy-2,4,6-trimethylheptanoic acid moiety. Neamphamide A was reported to have cytoprotective activity against HIV-1 infection (EC₅₀, 28 nM). Similar to neamphamide A, mirabamides obtained from the marine sponge Siliquariaspongia mirabilis also potently inhibit HIV-1 fusion [116]. Among mirabamides, mirabamide A was found to be powerful against HIV-1 in neutralization and fusion assays with respective IC₅₀ values of 40 and 140 nM, while mirabamides C and D were shown to be less effective (IC₅₀ values between 140 nM and 1.3 μM for mirabamide C and 190 nM and 3.9 μM for mirabamide D). Further, Plaza et al. [116] confirmed that mirabamides inhibit HIV-1 at the level of membrane fusion, presumably through interactions with HIV-1 envelope glycoproteins. Other novel peptides, celebesides A and theopapuamide B, were also isolated from sponges of the same previously mentioned S. mirabilis [117]. Celebesides A is cyclic depsipeptide that incorporates a polyketide moiety and five amino acid residues, among which are the unusual amino acids phosphoserine and 3-carbamoyl threonine. Theopapuamide B, a undecapeptide, comprise two previously unreported amino acids, 3-acetamido-2-aminopropanoic acid and 4-amino-2,3-dihydroxy-5-methylhexanoic acid. Celebesides A displayed an inhibition of HIV-1 entry with an IC₅₀ value of 1.9 μg/mL, while theopapuamide B was active in the neutralization assay with an IC₅₀ value of 0.8 μg/mL. Plaza et al. [117] indicated that the inhibitory activity of Celebesides A is due to the presence of a phosphoserine residue conserved in the above-mentioned anti-HIV peptides but absent in the inactive theopapuamide. However, this hypothesis was ruled out by evidence given in the study of Zampella and collaborators [118]. Zampella et al. [118] isolated a new anti-HIV cyclodepsipeptide, homophymine A, from the marine sponge Homophymia sp. This peptide contains an amide-linked 3-hydroxy-2,4,6-trimethyloctanoic acid moiety and 11 amino acid residues, including four unusual amino acid residues: (2S,3S,4R)-3,4-diMe-Gln, (2R,3R,4S)-4-amino-2,3-dihydroxy-1,7-heptandioic acid, l-ThrOMe, and (2R,3R,4R)-2-amino-3-hydroxy-4,5-dimethylhexanoic acid. Obviously, homophymine A lacks β-methoxytyrosine residue which is replaced by an O-methyl threonine residue. Nevertheless, homophymine A was reported to potentially exhibit cytoprotective activity against HIV-1 infection with an IC₅₀ value of 75 nM. The antiviral activity found in homophymine A ruled out the hypothesis that β-methoxytyrosine is essential for antiviral activity.