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. 2015 Jul 23;13(8):4594–4616. doi: 10.3390/md13084594

A Brief Review of Bioactive Metabolites Derived from Deep-Sea Fungi

Yan-Ting Wang 1, Ya-Rong Xue 1, Chang-Hong Liu 1,*
Editor: Johannes F Imhoff1
PMCID: PMC4556995  PMID: 26213949

Abstract

Deep-sea fungi, the fungi that inhabit the sea and the sediment at depths of over 1000 m below the surface, have become an important source of industrial, agricultural, and nutraceutical compounds based on their diversities in both structure and function. Since the first study of deep-sea fungi in the Atlantic Ocean at a depth of 4450 m was conducted approximately 50 years ago, hundreds of isolates of deep-sea fungi have been reported based on culture-dependent methods. To date more than 180 bioactive secondary metabolites derived from deep-sea fungi have been documented in the literature. These include compounds with anticancer, antimicrobial, antifungal, antiprotozoal, and antiviral activities. In this review, we summarize the structures and bioactivities of these metabolites to provide help for novel drug development.

Keywords: deep-sea fungi, bioactive compounds, anticancer, antimicrobial, antiviral, antifungal

1. Introduction

Fungi are well known for their vast diversity of secondary metabolites, which include many life-saving drugs and highly toxic mycotoxins [1]. Deep-sea fungi are the fungi that inhabit the sea and its sediment at a depth of over 1000 m below the surface [2]. Although the conditions in deep-sea environments are extreme and can be characterized by the absence of sunlight irradiation, predominantly low temperature, high hydrostatic pressure, and oligotrophy, it has been reported that fungi are abundant and diverse in these environments [3,4,5]. According to literature surveys, the first documented deep-sea fungi were isolated from the Atlantic Ocean at a depth of 4450 m approximately 50 years ago [6]; however, it was not until 2006 that the first bioactive metabolite of the deep-sea fungus Chromocleista sp. was described by Park et al. [7]. After that, many biologically active secondary metabolites have been isolated from deep-sea fungi and evaluated for their activities against cancer, pathogenic fungi, bacteria, virus, and larval settlement [1,7,8,9]. Many bioactive metabolites have shown potential as an excellent resource for the discovery of new drugs [10,11]. The intent of this review is to summarize the new and/or bioactive compounds produced by deep-sea fungi.

2. Diversity of Deep-Sea Fungi

Although the environmental conditions in the deep sea cannot support many organisms, it is now well recognized that the deep sea is home to rich and diverse microbial communities [12]. Apart from bacteria and archaea [13,14,15], fungi in deep-sea environments have been extensively studied [5,16,17] in the past 50 years since the isolation of the first reported deep-sea fungi from the Atlantic Ocean at a depth of 4450 m [6]. The investigated deep-sea environments include the Gulf of Mexico [12], the Mariana Trench (11,500 m) [18], the Chagos Trench (5500 m) [19], the Central Indian Basin (5000 m) [17], the South China Sea [20,21,22,23], the Antarctic Ocean [24,25], the Eastern Mediterranean [26], the Pacific Ocean [27], the Black Sea [28], the North Pacific Ocean [29], the East Indian Ocean [30], and the Central Arabian Sea [31]. For instance, Xu et al. [32] have described 175 deep-sea fungi that were isolated from 15 sediments in the Eastern Pacific Ocean, the South Atlantic Ocean, and the Southwest Indian Ocean. These fungi, including 93 yeast and 82 filamentous fungi, belonged to 17 genera: Rhodosporidium, Rhodotorula, Aspergillus, Cladosporium, Penicillium, Alternaria, Fusarium, Acremonium, Phoma, Tritirachium, Chaetomium, Exophiala, Engyodontium, Sistotrema, Schizophyllum, Tilletiopsis, and Hormonema. Most of the fungi were either isolated using culture-dependent method or proved based on sequence analysis of the ribosomal RNA gene, and are classified into Ascomycota and Basidiomycota. Particularly, Aspergillus and Penicillium belonging to Ascomycota are dominant in deep-sea environments [32,33].

Along with the development of modern instruments and techniques used for sampling and researching, more and more deep-sea fungi have been collected [20,22,34,35,36,37,38]. The rich and diverse communities of deep-sea fungi increase the pool of fungi available for natural bioactive product screening and new drug discoveries.

3. Bioactive Metabolites of Deep-Sea Fungi

3.1. Anticancer

With the changes in the living environment, cancer has become one of the major causes of death worldwide [39]. Many techniques have been applied to control cancer, such as surgery, radiotherapy, and chemotherapy. Out of all these techniques, chemotherapy is the most commonly used and the most effective method to treat cancer so far. However, the application of chemotherapeutic agents has been greatly restricted because most of them have high cell toxicity and provoke severe adverse reactions in human beings [40]. Therefore, seeking for high-efficiency, low-toxicity anticancer agents from deep-sea fungi has become one of the research subjects in the current pharmacy field.

3.1.1. Polyketides Compounds

Eight new chromones, engyodontiumones A–H (1–8), and eight known polyketides (9–16) (Figure 1) have been isolated from the deep-sea fungus Engyodontium album DFFSCS021. These polyketide compounds show a significant selective cytotoxicity against human histiocytic lymphoma U937 cell line with IC50 of 4.9–8.8 μM. In addition, compounds 8, 12, and 13 exhibit mild antibacterial activity against Escherichia coli and Bacillus subtilis, and compound 12 shows potent antilarval activity against barnacle Balanus amphitrite larval settlement [41].

Figure 1.

Figure 1

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Chemical structures of compounds 1–16.

Nine new C9 polyketides, named aspiketolactonol (17), aspilactonols A–F (18–23), aspyronol (25), and epiaspinonediol (27), together with five known polyketides, (S)-2-(2′-hydroxyethyl)-4-methyl-γ-butyrolactone (24), dihydroaspyrone (26), aspinotriol A (28), aspinotriol B (29), and chaetoquadrin F (30) (Figure 2), have been isolated from the secondary metabolites of Aspergillus sp. 16-02-1, which was isolated from a deep-sea sediment at a Lau Basin hydrothermal vent (depth 2255 m, temperature 114 °C) in the southwest of the Pacific Ocean. All of these compounds show strong cytotoxic activities against human cancer cell lines such as K562, HL-60, HeLa, and BGC-823 [42].

Figure 2.

Figure 2

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Chemical structures of compounds 17–30.

Five new nitrogen-containing sorbicillinoids, named sorbicillamines A–E (31–36) (Figure 3), have been isolated from an agitated culture of a deep-sea fungus Penicillium sp. F23-2. The structures of 31 to 36, including absolute configurations, were determined based on MS, NMR, and circular dichroism (CD) data. Unfortunately, all these compounds show weak cytotoxicity (IC50 > 10 μM) against the HeLa, BEL-7402, HEK-293, HCT-116, and P388 cell lines. Moreover, the strain F23-2 is able to produce indole alkaloids and terpenoids when it is cultured under static conditions [43].

Figure 3.

Figure 3

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Chemical structures of compounds 31–36.

Two highly oxygenated polyketides, penilactone A (37) and B (38) (Figure 4), containing a new carbon skeleton formed from two 3,5-dimethyl-2,4-diol-acetophenone units and a γ-butyrolactone moiety, have been isolated from a fungus named Penicillium crustosum PRB-2, which was derived from deep water environments of the Antarctic Ocean. Penilactones A and B possess antipodal absolute stereochemistry and show weak antitumor activity. However, penilactone A exhibits weak cytotoxic activity against NF-κB (40%) at the concentration of 10 mM [25].

Figure 4.

Figure 4

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Chemical structures of compounds 37–40.

Two new fungal hybrid polyketides, cladosin F (39) and G (40) (Figure 4), with a rare 6(3)-enamino-8,10-dihydroxy-tetraketide system have been discovered from the deep-sea-derived fungus Cladosporium sphaerospermum 2005-01-E3, guided by the OSMAC approach. Both exhibit weak in vitro antitumor activity [44].

3.1.2. Steroid Derivatives

Seven secondary metabolites including 9(11)-dehydroergosterol peroxide (41), ergosterol peroxide (42), (22E,24R)-5α,6α-epoxy-3β-hydroxyergosta-22-ene-7-one (43), and cerebroside A (44), B (45), C (46), and D (47) (Figure 5) have been described by Cui et al. in 2013 from the deep-sea fungus Paecilomyces lilacinus ZBY-1. These compounds exhibit cytotoxic activity against K562, MCF-7, HL-60, and BGC-823 cells with IC50 of 22.3 to 139.0 μM [45].

Figure 5.

Figure 5

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Chemical structures of compounds 41–47.

Li et al. (2012) reported two sterols, sterolic acid (48) and sterol (49) (Figure 6), which were isolated from the crude extract of the deep-sea fungus Penicillium sp. metabolites. Compounds 48 and 49 show slight cytotoxic effects against MCF-7 cells and A549 cells [46].

Figure 6.

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Chemical structures of compounds 48–51.

Compounds ergosterol (50) and ergosterol peroxide (51) (Figure 6) have been isolated from the cultures of the deep-sea fungus Penicillium sp. F00120, which was collected from the northern South China Sea at a depth of 1300 m [47]. Compound 51 also has been isolated from the deep-sea-derived fungus Aspergillus sp. CXCTD-06-6a [48]. Both compounds show good cytotoxicity (27.2%–31.5%) against the HeLa cell line at 10 μM [47].

(17R)-17-Methylincistererol (52) and cerevisterol (53) (Figure 7) were isolated from the deep-sea fungus Aspergillus sydowi by a bioassay-guided method. Compound 52 has been considered as a highly degraded product of sterol, while compound 53 is a common metabolite of fungi. Both exhibit cytotoxicity [49]. Shang et al. (2012) [50] also reported compound 53 together with compound 54 (Figure 7), which was isolated from the deep-sea fungus Penicillium commune SD-118. All of them show a slight cytotoxicity against MCF-7 [50].

Figure 7.

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Chemical structures of compounds 52–54.

3.1.3. Indole Derivatives

Three new prenylated indole alkaloids, including two β-carbolines, penipaline A (55) and B (56), and one indole carbaldehyde derivative, penipaline C (57), as well as two known indole-derived analogs (58,59) (Figure 8), have been isolated from the metabolites of the deep-sea fungus Penicillium paneum SD-44, which was cultivated in a 500-L bioreactor. All these metabolites show cytotoxicity against A549 (IC50: 20.4–21.5 μM) and HCT-116 (IC50: 14.9–18.5 μM) cell lines [51].

Figure 8.

Figure 8

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Chemical structures of compounds 55–61.

5-Chlorosclerotiamide (60) and 10-epi-sclerotiamide (61) (Figure 8) are the secondary metabolites of the deep-sea fungus Aspergillus westerdijkiae DFFSCS013, which show excellent cytotoxicity against K562 cell line with IC50 of 44 μM and 53 μM, respectively [52].

3.1.4. Sesquiterpenoids

Chemical investigation of the Penicillium sp. PR19 N-1 isolated from the Antarctic deep-sea has yielded five new eremophilane-type sesquiterpenes (62–66) (Figure 9). These compounds show strong cytotoxicity against HL-60 cells (IC50: 28.3–45.8 μM) and the A-549 cells (IC50: 5.2–82.8 μM) [53]. In 2013, Wu et al. [24] isolated a new chloro-trinoreremophilane sesquiterpene 67, three new chlorinated eremophilane sesquiterpenes (68–70), and a known compound, eremofortine C (71) (Figure 9), from the same strain, PR19N-1. They found that all the compounds (67–71) exhibit cytotoxic activity against HL-60 and A549 cell lines. Particularly, compound 67 shows great cytotoxicity against HL-60 and A549 cell lines with IC50 of 11.8 and 12.2 μM, respectively [24].

Figure 9.

Figure 9

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Chemical structures of compounds 62–72.

In 2010, Chen et al. reported a new sesquiterpene, hydroquinone (72) (Figure 9), which was isolated from the metabolites of the deep-sea fungus Phialocephala sp. This compound displays strong cytotoxic activity against P388 and K562 cells with IC50 of 0.16 μM and 0.05 μM, respectively [54].

3.1.5. Alkaloid Compounds

Shang et al. (2012) reported three alkaloids (73–75) (Figure 10) that were isolated from the deep-sea fungus Penicillium commune SD-118. These alkaloid compounds show potent cytotoxicity against the DU145 cell line with IC50 of 4.3–5.0 μM. Moreover, compound 75 shows moderate cytotoxicity toward the HepG2, NCIH460, HeLa, and MDA-MB-231 cell lines with IC50 of 0.03, 0.05, 0.05, and 0.03 mM, respectively [50].

Figure 10.

Figure 10

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Chemical structures of compounds 73–75.

3.1.6. Aromatic Compounds

Five new anthranilic acid derivatives, penipacids A–E (76–80), together with one known analogue (81) (Figure 11), which was previously synthesized, have been obtained from the ethyl acetate extract of the deep-sea fungus Penicillium paneum SD-44. These compounds exhibit cytotoxic activity against the RKO cell line (IC50: 8.4–9.7 μM). Especially, compound 81 displays remarkable cytotoxicity against the HeLa cell line with an IC50 of 6.6 μM [55].

Figure 11.

Figure 11

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Chemical structures of compounds 76–81.

A compound (2′S)-4-methoxy-3-(2′-methyl-3′-hydroxy) propionyl-methyl benzoate (82) (Figure 12) has been isolated from the metabolites of the deep-sea fungus Aspergillus sp. 16-02-1. This compound possesses 34.5%, 25.2%, 3.2%, and 15.5% cytotoxicity against human cancer cell lines K562, HL-60, HeLa, and BGC-823, respectively, at 100 μg/mL [56].

Figure 12.

Figure 12

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Chemical structures of compounds 82–84.

A secondary metabolite of 5-hydroxy-2-methoxy benzoic acid (83) (Figure 12) was isolated from the deep-sea fungus Aspergillus sp. CXCTD-06-6a, which shows 7.29% of cytotoxic activity against the HeLa cell line at 1.68 μg/mL [48].

An aromatic compound (84) (Figure 12) has been isolated from the metabolites of the deep-sea sediment-derived Penicillium commune SD-118. It exhibits moderate cytotoxicity against the SW1990 cell line with IC50 of 0.11 mM [50].

A new methyl 2-(4-((2-hydroxy-3-methylbut-3-en-1-yl)oxy)phenyl) acetate (85), together with five known compounds (86–90) (Figure 13), has been isolated from the culture of the deep-sea fungus Aspergillus westerdijkiae SCSIO 05233. All of these display weak cytotoxic activities. Compound 89 displays weak antiproliferation activities towards K562 and promyelocytic HL-6 (IC50: 25.8–44.9 mM), while compound 90 shows strong antifouling activity with EC50 of 27.5 mM [57].

Figure 13.

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Chemical structures of compounds 85–90.

3.1.7. Fatty Acids

Four fatty acid compounds, methyl myristate (91), methyl linoleate (92), linoleate (93), and oleinic acid (94) (Figure 14), have been isolated from the metabolites of the deep-sea fungus Paecilomyces lilacinus ZBY-1. All of them exhibit 30%–80% cytotoxicity against human cancer cell lines K562, MCF-7, HL-60, and BGC-823 at 100 mg/L [58].

Figure 14.

Figure 14

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Chemical structures of compounds 91–94.

3.1.8. Pyrone Analogues

Two new compounds, 2,3,5-trimethyl-6-(3-oxobutan-2-yl)-4H-pyran-4-one (95) and (2R)-2,3-dihydro-7-hydroxy-6,8-dimethyl-2-[(E)-prop-l-enyl]chromen-4-one (96), together with six known compounds (97–100) (Figure 15), were isolated from the deep-sea fungus Aspergillus sydowi by a bioassay-guided method. All these compounds exhibit various degrees of cytotoxicity. Compounds 96 and 100 show strong cytotoxicity against P388 cells with IC50 of 0.14 and 0.59 μM, respectively [49].

Figure 15.

Figure 15

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Chemical structures of compounds 95–100.

3.1.9. Sorbicillin Derivative

A novel sorbicillin trimer, trisorbicillinone A (101) (Figure 16), was isolated from the deep-sea fungus Phialocephala sp. FL30r. Trisorbicillinone A shows cytotoxicity against P388 and HL60 cells with IC50 of 9.1 and 3.1 μM, respectively [59].

Figure 16.

Figure 16

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Chemical structures of compounds 101–103.

Two new bisorbicillinoids, named oxosorbiquinol (102) and dihydrooxosorbiquinol (103) (Figure 16), have been isolated from the deep-sea fungus Phialocephala sp. Both of them show cytotoxicity (IC50: 8.9–103.5 μM) against P388, A549, HL60, BEL-7402, and K562 cell lines [60].

3.1.10. Breviane Derivative

Three new breviane spiroditerpenoids, breviones I–K (104–106), and the known breviones (107–110) (Figure 17) have been isolated from the crude extract of the deep-sea fungus Penicillium sp. and display strong cytotoxic effects against MCF-7 cells (IC50: 7.44–28.4 μM). Compound 106 exhibits cytotoxic activity against A549 cells with IC50 of 32.5 μM [46]. Similar compounds, Breviones F–H (111–113) (Figure 17), have been isolated from the same fungal species by Li et al. (2009) [61]. These compounds (111–113) show 25.2%–44.9% cytotoxicity against HeLa at 10 μg/mL. Particularly, compound 111 displays a very strong cytotoxicity to HIV-1 replication in C8166 cells with an EC50 of 14.7 μM [61].

Figure 17.

Figure 17

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Chemical structures of compounds 104–113.

3.1.11. Compounds Containing Amino Acid Structure

Six metabolites, cyclo(d-Pro-d-Phe) (114), cyclo(d-Tyr-d-Pro) (115), phenethyl 5-oxo-l-prolinate (116), cyclo(l-Ile-l-Pro) (117), cyclo(l-Leu-l-Pro) (118), and 3β,5α,9α-trihydroxy-(22E,24R)-ergosta-7,22-dien-6-one (119) (Figure 18), have been isolated from the secondary metabolites of a mutated deep-sea fungal strain of Aspergillus versicolor ZBY-3. These compounds show certain cytotoxicity against K562 cells at a concentration of 100 μg/mL [62].

Figure 18.

Figure 18

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Chemical structures of compounds 114–119.

3.1.12. Other Compounds

A novel cyclopentenone, trichoderone (120), and a known compound, cholesta-7,22-diene-3b,5a,6b-triol (121) (Figure 19), were identified from the deep-sea fungus Trichoderma sp., which was isolated from the deep-sea sediment of the South China Sea. Compound 120 shows more than 80% cytotoxicity against A549 and NCIH460 cancer cell lines. The selectivity index for 120 was greater than 100. The two compounds also act as enzyme inhibitors against HIV protease and Taq DNA polymerase [18].

Figure 19.

Figure 19

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Chemical structures of compounds 120 and 121.

New aspergillic acid (122), ferrineoaspergillin (123), aflatoxin (124), and (11S)-hydroxyl aspergillic acid (125) (Figure 20) have been isolated from the deep-sea fungus Aspergillus sp. 16-02-1. These compounds possess certain cytotoxicity against human cancer cell lines K562 (33.6%–43.6%), HL-60 (24.1%–53.3%), HeLa (18.8%–45.4%), and BGC-823 (36.2%–51.2%) at the concentration of 100 μg/mL [56].

Figure 20.

Figure 20

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Chemical structures of compounds 122–127.

A known antibacterial compound, xanthocillin X (126) (Figure 20), was isolated for the first time from the deep-sea fungus Penicillium commune SD-118. This compound displays not only remarkable antimicrobial activity against Staphylococcus aureus and Escherichia coli with MIC of 1–64 μg/mL, but also significant cytotoxicity against MCF-7, HepG2, H460, HeLa, DU145, and MDA-MB-231 cell lines (IC50: 7–22 μg/mL) [50,63].

One new sesquiterpene quinone, named penicilliumin A (127) (Figure 20), was isolated from the deep-sea fungus Penicillium sp. F00120. It inhibits in vitro proliferation of mouse melanoma (B16), human melanoma (A375), and human cervical carcinoma (HeLa) cell lines with IC50 of 0.08, 0.06, and 0.12 mM, respectively [47].

Three new sterigmatocystin derivatives, oxisterigmatocystin A (128), oxisterigmatocystin B (129), and oxisterigmatocystin C (130), together with one known compound, 5-methoxysterigmatocystin (131) (Figure 21), have been isolated from the deep-sea fungus Aspergillus versicolor. The structures of the new compounds were elucidated by spectroscopic methods. All the compounds show cytotoxic activity against A549 and HL-60 cell lines, and compound 131 is the best with IC50 of 3.86 mM and 5.32 mM, respectively [64].

Figure 21.

Figure 21

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Chemical structures of compounds 128–131.

Seven gliotoxin-related compounds including two new metabolites, bis(dethio)-10a-methylthio-3a-deoxy-3,3a-didehydrogliotoxin (132) and 6-deoxy-5a,6-didehydrogliotoxin (133), and five known metabolites (134–138) (Figure 22) have been isolated from the fungus Penicillium sp. strain JMF034, which was obtained from the deep-sea sediments of Suruga Bay, Japan. All these types of compounds exhibit significant cytotoxic activity against P388 (IC50: 0.02–3.40 μM), whereas compounds 136–138 containing a disulfide or tetrasulfide bond show potential inhibitory activity against histone methyltransferase (HMT) G9a (IC50: 2.1–6.4 μM) [65].

Figure 22.

Figure 22

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Chemical structures of compounds 132–138.

3.2. Antibacterial

Antimicrobials are the most important drugs to protect human beings from infective diseases. Deep-sea fungi are one of the potential pools for screening antimicrobial metabolites, which can be developed into new drugs.

3.2.1. Prenylxanthones

Four new prenylxanthones, emerixanthones A–D (139–143), together with six known analogues (144–148) (Figure 23), were isolated from the culture of the deep-sea fungus Emericella sp. SCSIO 05240. All of them show weak growth inhibition against bacteria. The inhibition zone of compounds 139 and 141 against Escherichia coli (ATCC 29922), Klebsiella pneumonia (ATCC 13883), Staphylococcus aureus (ATCC 29213), Enterococcus faecalis (ATCC 29212), Acinetobacter baumanii (ATCC 19606), and Aeromonas hydrophila (ATCC 7966) is 1–3 mm in diameter. Moreover, compound 143 displays broad antifungal activities (3–4 mm in diameter) against Fusarium sp., Penicillium sp., Aspergillus niger, Rhizoctonia solani, Fusarium oxysporium f. sp. niveum, and Fusarium oxysporium f. sp. cucumeris [8].

Figure 23.

Figure 23

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Chemical structures of compounds 139–148.

3.2.2. Depsidone-Based Analogues

Fifteen new depsidone-based analogues, named spiromastixones A–O (149–163) (Figure 24), have been isolated from the fermentation broth of the deep-sea fungus Spiromastix sp. These compounds exhibit significant growth inhibition (MIC: 0.1–8.0 μg/mL) against Gram-positive bacteria including Staphylococcus aureus, Bacillus thuringiensis, and Bacillus subtilis. In addition, compounds 154–158 display potential inhibitory effects on methicillin-resistant bacterial strains of Staphylococcus aureus (MRSA) and Staphylococcus epidermidis (MRSE). Moreover, compound 158 inhibits the growth of the vancomycin-resistant bacteria of Enterococcus faecalis and Enterococcus faecium (VRE) [66].

Figure 24.

Figure 24

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Chemical structures of compounds 149–163.

3.2.3. Triple Benzene Compound

Liu et al. (2013) [67] have reported a compound (164) (Figure 25) that was isolated from the deep-sea fungus Aspergillus candidus and possesses broad and high antibacterial activity (inhibition: 83.9%–100%) against Staphylococcus aureus, Bacillus subtilis, Vibrio sp. 385, Vibrio sp. 333, and Vibrio sp. 1758 [67].

Figure 25.

Figure 25

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Chemical structure of compound 164.

3.2.4. Citromycetin Analogue

A new citromycetin analogue, diorcinol (165) (Figure 26), has been isolated from the metabolites of Ascomycota sp. Ind19F07, which was collected from the deep-sea sediment in the Indian Ocean. Based on in vitro tests, compound 165 shows strong antibacterial activity against both Gram-positive and -negative bacteria such as Acinetobacter baumanii, Escherichia coli, Enterococcus faecalis, and Staphylococcus aureus [68].

Figure 26.

Figure 26

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Chemical structure of compound 165.

3.2.5. Other Compounds

Recently, Zhang et al. (2014) [23] have evaluated the antimicrobial activities of the secondary metabolites produced by eight novel deep-sea-derived fungal species, Acremonium implicatum DFFSCS001 (AI001), Aspergillus westerdijkiae DFFSCS013 (AW013), Alternaria tenuissima DFFSCS003 (AT003), Cladosporium cladosporioides DFFSCS016 (CC016), Cladosporium sphaerospermum DFFSCS019 (CS019), Engyodontium album DFFSCS021 (EA021), Geomyces vinaceus DFFSCS022 (GV022), and Tritirachium sp. DFFSCS034 (TS034). These fungal species were isolated from sediments of the South China Sea [23], and almost all the ethyl acetate extracts of the fungal species show strong antibacterial activity against two larval-settlement-inducing bacteria Loktanella hongkongensis and Micrococcus luteus, and one marine pathogenic bacterium. Based on bioassay-guided isolation technique, they have isolated five compounds (166–170) (Figure 27) from the extract of Aspergillus westerdijkiae DFFSCS013 that show antifouling activity against Bugula neritina larval settlement with an EC50 of 6.4–34.9 μg/mL [25].

Figure 27.

Figure 27

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Chemical structures of compounds 166–170.

3.3. Antiviral

Polyketides

Although many polyketide compounds have been identified, the compounds derived from deep-sea fungi with antiviral activity are rare. Only one fungal hybrid polyketide with a new structure, cladosin C (171) (Figure 28), has been reported from the deep-sea fungus Cladosporium sphaerospermum 2005-01-E3. However, this compound shows good antiviral activity against influenza A H1N1 virus with an IC50 of 276 μM [9].

Figure 28.

Figure 28

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Chemical structure of compound 171.

3.4. Antioxidant and Antifouling

3.4.1. Diketopiperazine Derivatives

Kong et al. (2014) [69] have reported a new diketopiperazine, brevianamide W (172), and five known diketopiperazine derivatives, diketopiperazine V (173), brevianamide Q (174), brevianamide R (175), brevianamide K (176), and brevianamide E (177) (Figure 29), which were isolated from the EtOAc extract of the deep-sea fungus Aspergillus versicolor CXCTD-06-6. These compounds exhibit moderate radical scavenging activity against DPPH with clearance ratios of 55.0% (172 and 173), 53.7% (174), 46.2% (175), 61.4% (176), and 19.3% (177) at 13.9 μM, respectively [69].

Figure 29.

Figure 29

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Chemical structures of compounds 172–177.

3.4.2. Hydroxyphenylacetic Acid

Compound 178 (Figure 30) has been reported from the deep-sea-derived fungus Aspergillus westerdijkiae SCSIO 05233 and shows strong antifouling activity with an EC50 of 8.8 mg/mL [57].

Figure 30.

Figure 30

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Chemical structure of compound 178.

3.5. Antifungal

One compound, p-hydroxyphenopyrrozin (179) (Figure 31), with a new structure has been isolated from the deep-sea fungus Chromocleista sp. and characterized on the basis of mass spectroscopy, NMR experiments, derivatization, and X-ray crystallography studies. The MIC of this compound is 25 μg/mL against Candida albicans [1]. In 2013, Liu et al. reported a compound (180) (Figure 31) that was isolated from the deep-sea fungus Aspergillus candidus and shows great growth inhibition against Candida albicans [67].

Figure 31.

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Chemical structures of compounds 179–180.

3.6. Compounds with Other Bioactivities

Two citrinin type compounds, phenol A acid (181) and penicitrinone A (182) (Figure 32), with anti-Aβ peptide aggregation inhibition activity have been isolated from the deep-sea fungus Aspergillus sp. SCSIOW 3, which show Aβ42 assembling inhibition activity (40.3%–72.3%) at 100 μM [70].

Figure 32.

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Chemical structures of compounds 181 and 182.

4. Conclusions

The fungi in deep-sea environments are very diverse and abundant, making them a versatile reservoir of metabolites with both new structures and bioactivities that can be of potential use, acting as leading compounds to synthesize new modern medicine. Although the research on deep-sea fungi is not as up-to-date as the research on fungi in other environments such as terrestrial soil, fresh water, and shallow marine areas due to difficulties in both sample collection and fungal cultivation methods, more and more fungi have been cultivated from the deep sea based on culture-dependent methods. These deep-sea fungi can provide a potential source for natural bioactive product screening and new drug discovery. Up to now, more than 180 new and/or bioactive secondary metabolites from deep-sea fungi with broad bioactivities, such as anticancer, antimicrobial, antifungal, anti-larval settlement, and antiviral, have been described in the literature. Most of the investigated bioactive compounds exhibit cytotoxic activity, then antimicrobial activity. These bioactive compounds not only help deep-sea fungi to defend themselves against predators in the natural ecosystem, but also have the potential of becoming treatments for human diseases and probes for new biological targets. Work to isolate fungi from deep-sea environments and characterize their bioactive metabolites is underway and is of increased importance due to the urgent need for new drugs to overcome emerging and drug-resistant diseases.

Acknowledgments

This work was supported by the National Natural Science Foundation of China (31272081, 31471810), the Jiangsu Science and Technology Support Program (BE2012372), and the Research Fund for the Doctoral Program of Higher Education (20130091110036).

Conflicts of Interest

The authors declare no conflict of interest.

References

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