Introduction

Since viral diseases (such as HIV, H1N1, HSV, etc.) have always been seriously threatening human life and health, antiviral compounds are continuously special attention. Some existing viral diseases including AIDS, hepatitis B, influenza and other diseases that can cause millions of deaths every year have not been able to be eradicated completely. New viral diseases such as coronavirus are beginning to sweep the world, and related medical treatments are under investigation (Barlow et al. 2020; Li et al. 2020). Considering the importance of marine compounds in antiviral activity, the potency of some marine natural products to target SARS CoV-2 main protease (Mpro) (PDB ID 6MO3) was investigated (Khan et al. 2020) and reported the molecular docking analysis of 2019-nCoV inhibition by antiviral compounds from marine natural resources (Vijayaraj et al. 2020). Recent scientific studies triumphantly reported new antiviral agents, which generally inhibit the virus replication cycle through affecting the important host cell factor(s) for virus replication and/or viral elements (Lou et al. 2014). Despite the rapid development in antiviral pharmaceuticals over the past few decades, the emergence of recombinant viruses, drug resistance, and cell toxicity make it an urgent need to develop new antiviral agents with higher efficiency and lower toxicity (Moghadamtousi et al. 2015).

The oceans, with their unique aquatic environment and rich biodiversity, have proven to be a plentiful source of diverse natural products with significant antimicrobial, antiviral, antimalarial, antitumor, anti-inflammatory, and anti-oxidant activities (Hou et al. 2019). Since the exploration of marine microorganisms began in the 1960s, marine microorganisms have gradually become a new field of natural product research. Approximately 150 to 200 new compounds of alkaloids, sesquiterpenoids, polyketides, and others are obtained from marine fungi annually (Moghadamtousi et al. 2015). In recent years, with the popularity of genomic sequencing information and genome mining analysis, more and more drugs have been discovered from the marine environment, which will have a significant impact on the discovery of new natural products (Zhao 2011). With the continuous development of technologies for marine microbial research, synthetic biological approaches also provide a total of possible biological activities for the secondary metabolites of marine microbes (Seghal Kiran et al. 2018). All of these indicate that natural products derived from marine microorganisms will continue to play a pivotal role in drug discovery and development.

Marine microorganisms are known producers of antiviral agents and may provide unlimited biological resources for the production of therapeutic drugs for the treatment and control of viral diseases in humans, ever more novel compounds with potential as pharmaceuticals, which have strong potential market value (Bhadury et al. 2006). Currently, more than 200 natural products with promising levels of anti-HIV activity have been isolated from marine organisms, following bioassay-guided protocols (Yasuhara-Bell and Lu 2010). Halovirs A–E, isolated from the marine fungus Scytidium sp., exhibit potent antiviral activity against HSV-1 with ED50 values of 1.1, 3.5, 2.2, 2.0 and 3.1 µM, respectively (Rowley et al. 2003). Stachyflin, a novel terpenoid isolated from the fungus Stachybotrvs sp., shows significant antiviral activity against H1N1 with an IC50 value of 0.003 µM, which is much better than anti-H1N1 drugs amantadine and zanamivir (with IC50 values of 5.3 and 0.75 µM, respectively) (Minagawa et al. 2002a, b). This highlights the important role of marine natural products in the discovery of new antiviral agents.

In recent reviews on the same topic, some focused on specific compounds or compound categories (Goh et al. 2020), some were related to the biological activity of marine natural products (Deshmukh et al. 2017), some focused on biological or geographic regions (Pech-Puch et al. 2020), and others were more general. Since the marine antiviral natural products discovered recently have not been studied systematically in recent years, we summarize here the research progresses of these antiviral natural compounds from marine microorganisms published in the past five years and discuss the research status of marine microbial-derived antiviral compounds in this period including 89 compounds in 60 references. Compounds with effective antiviral activity will be described in detail.

Marine microbial-derived antiviral compounds

The following section describes antiviral compounds from marine microbial resources. The compounds are organized according to their chemical structural classes namely alkaloids, quinones, peptides, polyketones, pyrones, sterols, terpenoids, and others.

Alkaloids

Alkaloids are an important class of basic nitrogen-containing natural organic compounds that are abundant in animals and plants. In recent decades, tetramic acids have attracted researcher's attention, their chemical and biosynthetic methods have also been widely reported (Henning and Gelbin 1993; Schobert and Schlenk 2008). Even so, the natural products containing decalin ring that appear frequently in microorganisms also show different biological activities (Li et al. 2014). Recently, several tetramic acid derivatives containing a decalin ring with antiviral biological activity, trichobotrysins A (1), B (2) and D (3) (Sun et al. 2015), were obtained from a fermentation broth of the fungal strain Trichobotrys effuse derived from the deep-sea sediment collected from the South China Sea. These compounds were shown to have activity against HSV-1 with IC50 values of 3.08, 9.37 and 3.12 µM, respectively.

Neosartoryadins A (4) and B (5) (Yu et al. 2015), were isolated from the endophytic fungus Neosartorya udagawae. They have a common unique pyrido [2,1-b]-quinazoline framework and a tetrahydrofuran ring, and the quinazoline is conjugated with a pyridine ring. Such compounds were first isolated from Aspergillus fumigates in 1992 (Numata et al. 1992). Using the cytopathic effect (CPE) inhibition assay to evaluate their antiviral activity, both 4 and 5 exhibited antiviral activity against H1N1 with IC50 values of 66 and 58 µM, respectively (ribavirin as positive control, IC50 = 94 µM). Biosynthetically, these compounds may derive from an assembly by l-tryptophan, ATA, l-valine, and 2-aminoisobutyric acid (Aib).

Pyrazine heterocycle is an important pharmacophore present as a basic scaffold in various clinical drugs with a wide range of pharmacological and therapeutic activities, such as antitumor, anti-inflammatory, antithrombotic, anti-diabetic, and anti-tubercular (Dolezal and Zitko 2012; Miniyar et al. 2013). Trypilepyrazinol (6) (Li et al. 2019b) isolated from marine-derived fungus Penicillium sp. is characterized by a pyrazine motif and has a broad spectrum of antiviral activity against human immunodeficiency virus (HIV) and hepatitis C virus (HCV) with IC50 values of 4.6 and 7.7 µM, respectively.

Raistrickindole A (7) and raistrickin (8) (Li et al. 2019a) were isolated from the marine-derived fungus Penicillium raistrickii. Both 7 and 8 showed anti-HCV activity in vitro with EC50 values of 5.7 and 7.0 µM, respectively (as compared to 0.05 µM of the positive control VX-950). Compound 7 had an unusual pyrazino[1′,2′:2,3]-[1,2]oxazino[6,5-b]indole tetraheterocyclic ring system, and this novel structure provides more possibilities for the discovery of antiviral compounds.

9(10H)-Acridanone (9) (Manimaran et al. 2018) (Fig. 1) was extracted from Streptomyces fradiae strain VITMK2, isolated from marine soil sediment sample collected from the mangrove forest region of Pichavaram, Tamil Nadu, India. The shrimp infected with WSSV and treated with 9 (500 µg, 250 µg, and 125 µg) showed survival rates of 88.89%, 83.33% and 55.56%, respectively. Docking of the compound with VP26 and VP28 of WSSV drug target proteins showed the least binding energy of − 5.71 kcal/mol and − 5.21 kcal/mol, respectively, predicting the strong interaction of the compound with VP26 and VP28.

Fig. 1
figure 1

Chemical structures of 1–9

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Quinones

Quinones are a class of aromatic organic compounds with two double bonds and a six-carbon atom cyclic diketone structure. They are often found in nature as pigments in animals, plants, and microorganisms. Two anthraquinones, aspergilols H (10) and I (11) (Huang et al. 2017), were isolated from fungus Aspergillus versicolor derived from the deep-sea sediment sample collected from the South China Sea. In vitro antiviral assay indicated that these compounds showed significant anti-HSV-1 activity with EC50 values of 4.68, 6.25 µM and CC50 values of 108.6, 50.7 µM, respectively (The corresponding EC50 and CC50 values of positive control acyclovir were 3.0 and > 1000 µM, respectively).

A citrinin dimer, seco-penicitrinol A (12) (Yang et al. 2018) was isolated from the extracts of the coculture of two marine algal-derived endophytic fungal strains Aspergillus sydowii and Penicillium citrinum. Compound 12 showed inhibitory activity towards influenza neuraminidase in vitro with an IC50 value of 24.7 µM (oseltamivir as positive control, IC50 = 3.6 µM).

Two anthraquinone derivatives, (‒)-2′R-1-hydroxyisorhodoptilometrin (13) and methyl 6,8-dihydroxy-3-methyl-9-oxo-9H-xanthene-1-carboxylate (14) (Jin et al. 2017) (Fig. 2) were isolated from the acidic fermentation broth (pH 2.5) of Penicillium sp. OUCMDZ-4736 collected from the sediment around roots of mangrove (Acanthus ilicifolius). Low pH induced the fungus producing abundant and diverse secondary metabolites. Compared with the positive control lamivudine, 13 showed stronger anti-hepatitis B virus activity by inhibiting HBsAg and HBeAg secretion in HepG2.2.15 cells.

Fig. 2
figure 2

Chemical structures of 11–15

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Actinomycetes isolated from mangrove ecosystem plays an important role in protecting human health by having the antagonistic activity against disease causing microorganisms. A novel bioactive compound, (Z)-1-((1-hydroxypenta-2,4-dien-1-yl)oxy)anthracene-9,10-dione (15) (Avilala et al. 2018) extracted from Nocardia alba KC710971 showed antiviral activity against two poultry viruses NDV and IBDV.

Peptides

Peptides are short chains of between 2 and 50 amino acids, linked by peptide bonds. Chains of less than 10 or 15 amino acids are called oligopeptides, and include dipeptides, tripeptides, and tetrapeptides. A class of thiodiketopiperazine-type alkaloids, eutypellazines A–L (16–27) (Niu et al. 2017) (Fig. 3), were extracted from deep-sea derived fungus Eutypella sp. collected from the South Atlantic Ocean. In vitro antiviral experiments showed that these compounds have antiviral activities and low cytotoxicity (CC50 > 100 µM). Compound 20 showed the strongest inhibitory effect on HIV-1 with an IC50 value of 3.2 ± 0.4 µM and the rest (16–19 and 21–27) demonstrated IC50 values of anti-HIV activity 14.8 ± 1.2, 11.5 ± 0.8, 10.7 ± 1.3, 8.5 ± 0.5, 16.6 ± 0.5, 18.2 ± 1.3, 13.3 ± 0.6, 6.7 ± 2.1, 4.9 ± 1.1, 5.8 ± 0.7, and 5.9 ± 0.9 µM, respectively. Structure–activity relationships (SAR) indicated that these analogues with thiomethyl group at C-2/C-2′ (19 and 20) showed more active than those with sulfide bridge (16–18 and 21–23) in the pentacyclic thiodiketopiperazines. A comparison of the inhibitory effect between 19 and 20 revealed a double bond at C-6′/C-7′ in 20 enhancing the activity. In regard to 24–27, the analogues with thiomethyl group at C-2/C-2′ (25) showed stronger effect than those with hydroxyl substitution (25–26), whereas the analogue with methoxy/hydroxyl substitution at C-2/C-2′ dramatically reduced the activity. Another study indicated that 25 showed the reactivation on latent HIV-1 transcription with a dose-dependent manner, whereas the remaining compounds exerted inactive in a dose of 100 µM. Compound 25 had the reactivation activity at 80 µM, which is comparable to the positive control of prostratin (5 µM) and SAHA (2.5 µM).

Fig. 3
figure 3

Chemical structures of 16–27

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Rubrumlines A–O (28–42) (Chen et al. 2015) (Fig. 4) is a class of prenylated indole diketopiperazines isolated from marine-derived fungus Eurotium rubrum. Antiviral tests showed that they all have weak anti-influenza A/WSN/33 virus activity. Structure–activity relationships (SAR) indicated that 28–42 exhibited a variety of antiviral activities dependent on the substituent groups and the olefinic location at diketopiperazine unit. The analogues with a saturated C8–C9 bond (33–34, 37 and 40–42) exerted weak antiviral effects. For the analogues with a ∆8,9 bond, 31 with a ∆12,15 unit at the diketopiperazine moiety instead of alanine unit such as 28–30, 35 and 36 significantly enhanced the antiviral activity. The analogues with a hydroxy group at C-15 of alanine unit (37–38) and with a ketone at C-12 (39) exhibited weak antiviral effects. Rubrumline N (41) with a MeO group at C-8 increased antiviral effect in comparison with rubrumline M (40) in which an OH group was substituted at C-8. The analogues with an isoprenyl unit in indole ring displayed stronger cytotoxic effects than those linked by an oxygenated isoprenyl unit (28–29 and 35–36) at a dose of 100 µM.

Fig. 4
figure 4

Chemical structures of 28–42

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A pair of enantiomeric alkaloid dimers, (+)-and (−)-pestaloxazine A (43 and 44) (Jia et al. 2015b) (Fig. 5), with an unprecedented symmetric spiro-[oxazinane-piperazinedione] skeleton consisting of 22 carbons and 12 heteroatoms, were isolated from a fungus Pestalotiopsis sp., derived from a soft coral. Pestaloxazine A belongs to the mixed polyketide-cyclo-dipeptide class of natural products (often referred to as a PKS-NRPS hybrid). According to the anti-EV71 assay in vitro, 43, 44, and their enantiomeric mixtures showed antiviral biological activity with IC50 values of 14.2 ± 1.3, 69.1 ± 3.1, and 16.0 ± 0.8 µM, respectively. It is worth noting that the antiviral activity of 43 is about 18-fold higher than that of ribavirin (IC50 = 256.1 ± 15.1 µM). In addition, their selectivity index (SI) for anti-EV71 activity is different, indicating that the stereochemistry of the spiro center may contribute to the antiviral activity and selectivity indices. Pestaloxazine A has a unique structural skeleton including its symmetric spiro [oxazinane-piper-azinedione] skeleton and two unique hemiaminal and oxazinane groups, and 10 of the 22 carbon atoms are oxygenation or nitrification which also contributes to the special structure.

Fig. 5
figure 5

Chemical structures of 43–44

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Two linear peptides, namely aspergillipeptides D (45) and E (46) (Ma et al. 2017) (Fig. 6), were isolated from a culture broth of marine gorgonian-derived fungus Aspergillus sp. obtained from the China South Sea gorgonian Melitodes squamata. Compounds 45 and 46 showed evident antiviral activity against herpes simplex virus type 1 (HSV-1) with IC50 values of 9.5 and 19.8 µM under their non-cytotoxic concentrations against a Vero cell line, respectively. In addition, 45 had antiviral activity against acyclovir-resistant clinical isolates of HSV-1-106 and HSV-1-153 at concentration of 12.5 µM with about 50% inhibition rate.

Fig. 6
figure 6

Chemical structures of 45–46

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Polyketones

Polyketones are a class of secondary metabolites produced by bacteria, fungi, plants, and animals. These substances are not necessary for the growth and development of organisms, but can be used for defense or intercellular communication. Asteltoxins E (47) and F (48) (Tian et al. 2015) (Fig. 7) discovered from marine-derived fungus Aspergillus sp. Compounds 47 and 48 showed significant activity against H3N2 with the prominent IC50 values of 6.2 ± 0.08 and 8.9 ± 0.3 µM, respectively. In addition, asteltoxin E also exhibited inhibitory activity against H1N1 with an IC50 value of 3.5 ± 1.3 µM.

Fig. 7
figure 7

Chemical structures of 47–48

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Pestalotiolide A (49) (Jia et al. 2015a) was a phthalide derivative obtained from marine-derived fungus Pestalotiopsis sp. Compared to the positive control ribavirin (IC50 = 418.0 µM), 49 exhibited significant anti-EV71 activity in vitro with an IC50 value of 27.7 µM. Structure–activity relationships (SAR) indicated that the glycosidation of 7-OH significantly increased anti-EV71 activity and the acetylation of 6′-OH also increased anti-EV71 activity. The acetoxy group at C-6′ had a positive contribution to anti-EV71 activity as well.

Isoprenylated cyclohexanols, truncateol M (50) (Zhao et al. 2015), was isolated from the solid culture of the sponge-associated fungus Truncatella angustata obtained from a finger sponge Amphimedon sp. collected from the bay of Yongxing Island in the South China Sea was fermented. The potential mechanism for 50 to suppress influenza infection by targeting virion assembly/release step to exert an effective inhibitory effect. The inhibitory effect of 50 on the H1N1 virus was almost six-fold more potent than OSV with an IC50 value of 8.8 µM (oseltamivir (OSV) as positive control, IC50 = 46.5 µM).

A new chromone, coniochaetone J (51) (Liu et al. 2017a) (Fig. 8), was isolated from deep-sea derived sediment fungus Penicillium sp. Compound 51 exhibited weak anti-EV71 activity in vitro with an IC50 value of 81.6 µM (ribavirin as positive control, IC50 = 0.6 µM).

Fig. 8
figure 8

Chemical structures of 49–51

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A class of phenolic lactones, spiromastilactones B, D–G, I–J and L (52–59) (Niu et al. 2016) (Fig. 9), were isolated from a deep-sea derived fungus Spiromastix sp. An antiviral assay revealed that these compounds show inhibitory activity against WSN influenza virus with low cytotoxicity. Among them, 54 and 55 have strong antiviral activity, even higher than their positive control compounds (oseltamivir, 10.0 µM and amantadine, 13.0 µM) with IC50 values of 6.0 ± 0.2 and 11.4 ± 1.3 µM, respectively. The remaining compounds have weak antiviral activity against WSN influenza virus with IC50 values of 16.2 ± 0.6, 27.6 ± 0.4, 30.7 ± 1.7, 74.9 ± 4.9, 38.2 ± 2.1, and 22.6 ± 0.9 µM, respectively. In addition, spiromastilactone D displayed the most potent activity by inhibiting a panel of influenza A and B viruses. Mechanistic studies indicated that spiromastilactone D binds to the hemagglutinin protein (HA) and disrupts the interaction of HA-sialic acid receptor, which is essential for the attachment and entry of all influenza viruses. In addition, 54 also showed modest inhibition on viral genome replication. These findings, in association with the inhibitory effects against a panel of influenza virus strains and less induction of drug resistance, suggested that the spiromastilactone entity may be an attracting scaffold for development of a new class of influenza virus inhibitors. Structure–activity relationships indicated that chlorination at either 3′ or 5′ or methylation of the 2′-hydroxyl group all enhanced the antiviral activity significantly. Simultaneous methylation of the 2′-hydroxyl group and chlorination at either 3′ or 5′ further enhance their potency against the WSN virus. However, chlorination at both 3′ and 5′ with the 2′-hydroxyl group either methylated or not decreased substantially the antiviral activity. Further, methylation of the 2′-hydroxyl group seems likely to be critical since the methylated derivatives were all more potent than their parent compounds. In contrast, methylation of 4′-hydroxyl group seems detrimental to the antiviral activity. Clearly, mono-methylation and mono-chlorination rather than di-methylation and/or di-chlorination of spiromastilactone promoted the antiviral activity, 54 exerting the most potent.

Fig. 9
figure 9

Chemical structures of 52–59

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Two phenolic polyketides, wailupemycin J (60) and R-Wailupemycin K (61) were isolated and identified from the fermentation broth of Streptomyces sp. associated with the marine green algae, Enteromorpha prolifera (Liu et al. 2017b). Compounds 60 and 61 at a concentration of 50 µg/mL showed anti-H1N1 virus activity with 47.8% and 42.5% inhibitions, respectively (positive control ribavirin, 45.3% inhibition). Regrettably, the IC50 values of 60 and 61 were not obtained due to the lack of quantity.

Abyssomicin monomers designated neoabyssomicin D (62) (Huang et al. 2018) (Fig. 10) was discovered from the marine-derived Streptomyces koyangensis. Compound 62 exhibited mild antiviral activity against herpes simplex virus at a concentration of 10 µM, the percentage of virus replication is low (31 ± 10%). Structurally as a representative of a novel abyssomicin skeleton, 62 contains a unique 8/5/5/7 tetracyclic core. The biosynthetic pathway may be that the internal Michael addition reaction at C-16 of abyssomicin 4 with the enolate formed by deprotonation at C-8 would yield abyssomicin 5 (Leon et al. 2015). The hydroxy group at C-9 can be eliminated in tandem with the cleavage of the C-10/C-11 bond, leading to the generation of the intermediate with a C-9/C-10 double bond. An aldol reaction between a C-8 enolate and C-11 yields a new seven-membered ring to give this compound.

Fig. 10
figure 10

Chemical structures of 60–62

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Pyrones

Pyrones are a class of heterocyclic chemical compounds. They contain an unsaturated six-membered ring with one oxygen atom and a ketone functional group. There are two isomers denoted as 2-pyrone and 4-pyrone. Methyl-(2-chloro-l,6-dihydroxy-3-methylxanthone)-8-carboxylate (63), methyl-(4-chloro-l,6-dihydroxy-3-methylxanthone)-8-carboxylate (64), methyl-(4-chloro-6-hydroxy-1-methoxy-3-methylxanthone)-8-carboxylate (65), methyl-(6-hydroxy-1-methoxy-3-methylxanthone)-8-carboxylate (66), 4-chloro-1,6-dihydroxy-3-methylxanthone-8-carboxylic acid (67), and 2,4-dichloro-1,6-dihydroxy-3-methylxanthone-8-carboxylic acid (68) (Kang et al. 2018) (Fig. 11) were isolated from the coastal saline soil-derived Aspergillus iizukae by application of an OSMAC approach. Compound 64 exhibited strong antiviral activities against H1N1, HSV-1, and HSV-2 with IC50 values of 44.6, 21.4, and 76.7 µM, respectively (ribavirin as the positive controls of H1N1 and acyclovir as the positive control of HSV-1 and HSV-2). The preliminary structure-activity relationships of 63–68 showed that the hydroxy group at C-1 and the methyl carboxylate group at C-8 essentially contributed to the anti-H1N1, anti-HSV-1, and anti-HSV-2 activities, and the position of the chlorine atom in ring A would affect the antiviral activities. Additionally, it seemed that methylation of the hydroxy group at C-1 or replacement of methyl carboxylate at C-8 by carboxylic acid, to a large extent, lower the antiviral effect.

Fig. 11
figure 11

Chemical structures of 63–68

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Heterologous expression of the type III polyketide synthase (PKS) gene vioA in marine-derived Streptomyces youssoufiensis led to production of violapyrones (VLPs) Q–T (69–72) (Hou et al. 2018) (Fig. 12). Besides, 69–72 showed anti-H1N1 activity with IC50 values of 58.8, 64.9, 30.6, and 68.4 µM, respectively. Compounds 69–72 also revealed anti-H3N2 activity with IC50 values of 95.0, 63.9, 45.3, and 72.8 µM, respectively. Preliminary structure–activity relationships research demonstrated that all the methylated compounds displayed stronger anti-virus activity than their non-methylated counterparts, among which 71 showed the best activities. Methylation of 4-OH has a negative effect on the anti-MRSA (methicillin-resistant Staphylococcus aureus) activity, with methylated VLPs displaying decreased (70) or abolished (71 and 72) activities in comparison with each of their non-methylated counterparts. Results suggested that methylation at 4-OH of these compounds enhanced anti-virus activity but reduced anti-MRSA activity.

Fig. 12
figure 12

Chemical structures of 69–72

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Sterols

Sterols, also known as steroid alcohols, are a subgroup of the steroids and an important class of organic molecules. They occur naturally in plants, animals, and fungi, and can be also produced by some bacteria. A new pregnane, 3α-hydroxy-7-ene-6,20-dione (73) (Yu et al. 2017) was obtained from the fungus Cladosporium sp. cultured from a gorgonian Dichotella gemmacea collected from the South China Sea. This compound has a rare configuration of 3α-OH that is different from most of pregnanes. Compound 73 showed antiviral activity against the respiratory syncytial virus (RSV) with the IC50 value of 0.12 µM. Cladosporisteroid B (74) (Pang et al. 2018), a highly oxygenated sterol, was also isolated from the culture extracts of sponge-derived fungus Cladosporium sp. and exhibited weak inhibitory activity against H3N2 with an IC50 value of 16.2 µM.

A new ergostane analogue, 3β-hydroxyergosta-8,14,24(28)-trien-7-one (75) (Li et al. 2019b) (Fig. 13), was isolated and characterized from the marine-derived fungus Penicillium sp. IMB17-046. Compound 75 displayed broad-spectrum antiviral activities against different types of viruses, showed anti-HIV activity with an IC50 value of 3.5 µM and potent anti-IAV activity with an IC50 value of 0.5 µM, that is 300-fold stronger than ribavirin.

Fig. 13
figure 13

Chemical structures of 73–75

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Terpenoids

Terpenoids are volatile substances distributed in the animal and plant kingdom, especially in essential oils of plants, and are important chemical components of natural medicine. Talaromyolide D (76) (Cao et al. 2019) was isolated from a marine fungus Talaromyces sp. Compound 76 displayed potent antiviral activity against pseudorabies virus (PRV) with a CC50 value of 3.35 µM.

Two new meroterpenoids, chrodrimanins K (77) and N (78) (Kong et al. 2017) were discovered from the fermentation broth of Penicillium sp. collected from a marine worm of Haikou Bay, China. Compounds 77 and 78 displayed anti-H1N1 activity with IC50 values of 74 and 58 µM, respectively.

A new meroterpenoid, stachybonoid A (79) (Zhang et al. 2017), was discovered from the crinoid-derived fungus Stachybotrys chartarum, a crinoid (Himerometra magnipinna) isolated from Xuwen Coral Reef Nature Reserve, Zhanjiang city, Guangdong Province, China. Compound 79 displayed inhibitory activity against the replication of dengue virus (DENV). Biosynthetically, orsellinic acid and farnesyl diphosphate underwent addition to form the intermediate ilicicolin B. Then, the terminal olefin bond in the prenyl group of ilicicolin B was epoxidized to obtain another intermediate. When the aromatic hydroxyl group was connected to the C-3 of the prenyl group by electrophilic addition, 79 was obtained.

Stachybogrisephenone B (80) (Qin et al. 2014) (Fig. 14) was discovered from the cultures of sponge-derived fungus Stachybotry sp. Compound 80 showed activity against intestinal virus EV71 with an IC50 value of 30.1 µM (ribavirin as positive control, IC50 = 0.60 µM).

Fig. 14
figure 14

Chemical structures of 76–80

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Others

Isoprenylated cyclohexanols, truncateols C (81), E (82) (Zhao et al. 2015), O (83) and P (84) (Zhao et al. 2018), were isolated from the marine-derived fungus Truncatella angustata collected from the South China Sea. Compounds 81 and 82 showed anti-H1N1 activities with IC50 values of 55 and 63.5 µM, respectively (the IC50 value of the positive control, oseltamivir was 46.5 µM). Compound 83 exhibited significant inhibition toward both HIV-1 and H1N1 virus with IC50 values of 39.0 ± 1.2 and 30.4 ± 0.4 µM, respectively. Compound 84 showed anti-HIV-1 activity with an IC50 value of 16.1 ± 0.7 µM. Due to lower cytotoxicity (CC50 > 100 µM), these compounds could be considered as potential anti-HIV lead compounds in comparison with the positive control efavirenz (CC50 > 40.6 µM).

A hexahydrobenzopyran derivative, cytosporin L (85) (Liao et al. 2017), was isolated from the marine-derived fungus Eutypella sp. collected from the South China Sea. Compound 85 obviously inhibited the respiratory syncytial virus (RSV) with the IC50 value of 72.01 µM (ribavirin as positive control).

New salicyloid derivative, vaccinol J (86) (Wang et al. 2017), was discovered from Pestalotiopsis vaccinii endogenous with the mangrove plant Kandelia candel (L.) Druce (Rhizophoraceae). Compound 86 was a salicyloid derivative that containing 2-methylfuran moiety and showed anti-enterovirus 71 (EV71) activity in vitro with an IC50 value of 30.7 µM (ribavirin as positive control, IC50 = 177.0 µM).

A new citrinin monomer, namely penicitrinol L (87) (Yang et al. 2018), was discovered from the extracts of the coculture of two marine algal-derived endophytic fungal strains Aspergillus sydowii and Penicillium citrinum. Compound 87 has the influenza neuraminidase (H5N1) inhibitory activity in vitro with an IC50 value of 41.5 µM.

A new anthranilic acid, anthranoside C (88) (Che et al. 2018), was isolated from a marine sponge-derived actinomycete Streptomyces sp. Compound 88 possessed a unique indole-containing scaffold and showed anti-influenza H1N1 virus activity with an IC50 value of 171 µM (ribavirin as positive control, IC50 = 133 µM). Biosynthetically, the compound may derive from an assembly by ATA and d-glucose. Structurally, 88 was comprised of ATA moiety and polyol units.

A new butenolide derivative, (4S)-10-hydroxy-10-methyl-11-oxo-dodec-2-en-1,4-olide (89) (Huang et al. 2019) (Fig. 15), was isolated from marine-derived Streptomyces koyangensis. Compound 89 displayed mild antiviral activity against herpes simplex virus with an EC50 value of 25.4 µM, which was characterized by an octyl substitution on C-position.

Fig. 15
figure 15

Chemical structures of 81–89

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Conclusions and outlooks

The explosive growth of global drug resistance has prompted drug research and development institutions to actively seek new antiviral drugs, especially the recent global outbreak of new coronary pneumonia, which has promoted enthusiasm for antiviral drug research unprecedented. Although there are many challenges in the exploration and development of marine microorganisms, many significant antiviral activity compounds have been obtained from marine microorganisms, and it is expected that marine microorganisms will continue to be a good source of antiviral drugs, especially the novel, highly effective, low-toxic antiviral natural products.

This review surveys natural products systematically with antiviral activity derived from marine microorganisms, and clarifies the antiviral activities of these compounds and related research progresses. In the literature spanning 2015–2019, marine microbial-derived natural products have made important progress in the study of antiviral lead compounds. A total of 89 secondary metabolites have been found, of which more than 30 have potent antiviral activities. Two secondary metabolites, trypilepyrazinol (6) and 3β-hydroxyergosta-8,14,24(28)-trien-7-one (75) showed potent broad-spectrum (HIV, HCV) antiviral activities worthy of further study (Table 1). Many significant antiviral activity compounds have been obtained from marine microorganisms, and it is expected that marine microorganisms will continue to be a good source of antivirals. The biological profiles of these leads provide hope for the discovery of highly effective and low-toxicity agents.

Table 1 Recent progresses in marine-derived antiviral natural products
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The antiviral compounds derived from marine microorganisms described herein can be divided into 8 biosynthetic categories; alkaloids, quinones, peptides, polyketones, pyrones, sterols, terpenoids and others (Fig. 16). Among them, peptides are the most group of secondary metabolites with potentially useful activities. Figure 17 shows that 10 viruses including H1N1, HIV, HSV, H3N2, EV71, HCV, RSV, H5N1, HBV and DENV were used as screening viruses for the antiviral activities of the compounds. In addition, most antiviral compounds showed anti-H1N1 activity, followed by anti-HIV and anti-HSV activities. Only one compound exhibited anti-DENV activity. Truncateol M (50) showed potent anti-H1N1 activity, eutypellazines E (20), I–K (24–27) and 3β-hydroxyergosta-8,14,24(28)-trien-7-one (75) exhibited promising anti-HIV activity, trichobotrysins A (1) and D (3), aspergilols H (10) and I (11) had strong anti-HSV activity. Asteltoxins E (47) and F (48) showed anti-H3N2 activity, trypilepyrazinol (6), raistrickindole A (7) and raistrickin (8) exhibited potent anti-HCV activity. These provide guidance for the later screening of antiviral activity of new compounds.

Fig. 16
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The type of marine microbial-derived antiviral compounds

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Fig. 17
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Marine microbial-derived compounds with antiviral activity

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In summary, marine natural products are an important source of discovery of lead compounds and drug candidates for antiviral drugs. Nevertheless, it is undeniable that the current research and development of marine natural products still face bottlenecks. First, it is difficult to apply screening techniques to obtain lead compounds. Second, it is difficult to fully synthesize complex marine natural products. The most important thing is that most active marine natural products are limited to in vitro cell experiments, and few animals in vivo and clinical trials because of the limited availability of natural products. Today’s rapidly evolving technologies and an increasing understanding of the molecular processes and mechanisms of secondary metabolite production will continue to increase the possibility of extracting natural products from marine microorganisms. By using marine natural product compound libraries and computing virtual screening can quickly obtain good active lead compounds; explore the synthetic route of complex products by fusing artificial intelligence technology with the total synthesis of natural products; finally, promote the activity evaluation of high-activity and low-toxic natural products and conduct animal experiments.

The purpose of this review is to help interested readers understand the current status of marine-derived antiviral compounds, and in the process identify areas for further research that may accelerate the development of more effective and selective drugs to treat this global disease.