Endophytic Fungi: An Effective Alternative Source of Plant-Derived Bioactive Compounds for Pharmacological Studies.

Plant-associated fungi (endophytic fungi) are a biodiversity-rich group of microorganisms that are normally found asymptomatically within plant tissues or in the intercellular spaces. Endophytic fungi promote the growth of host plants by directly producing secondary metabolites, which enhances the plant's resistance to biotic and abiotic stresses. Additionally, they are capable of biosynthesizing medically important "phytochemicals" that were initially thought to be produced only by the host plant. In this review, we summarized some compounds from endophyte fungi with novel structures and diverse biological activities published between 2011 and 2021, with a focus on the origin of endophytic fungi, the structural and biological activity of the compounds they produce, and special attention paid to the exploration of pharmacological activities and mechanisms of action of certain compounds. This review revealed that endophytic fungi had high potential to be harnessed as an alternative source of secondary metabolites for pharmacological studies.

1. Introduction

The term “endophytic fungi” refers to fungi that live in plant tissues throughout the entire or partial life cycle by establishing a mutually beneficial symbiotic relationship with its host plant without causing any adverse effect or disease [1,2]. They are natural components of the plant micro-ecosystem that positively affect the physiological activities of the host plant in several ways, including producing hormones such as indoleacetic acid, biosynthesizing and acquiring nutrients for plant growth and development, secreting stress-adaptor metabolites to protect the host plant from the invasion of herbivores, pathogens, and improving the host’s adaptability to abiotic stressors. In return, plants provide habitats and nutrients for endophytic fungi [3,4]. Endophytic fungi are capable of producing a rich variety of bioactive substances and can produce compounds that are identical or similar to pharmacological activities identified from plants [5]. They produce a range of metabolites of different chemical classes, including alkaloids, flavonoids, steroids, terpenoids, and phenolic compounds. Some compounds show pleiotropic and interesting pharmacological activities, including antimicrobial, antioxidant, anti-diabetic, anti-malarial, and antitumor properties. The discovery of these structurally novel and diverse active compounds provides a valuable resource for studying natural medical products from the microbiome [6,7,8]. In the search for bioactive molecules as pro-drug compounds or in the development of medicines, endophytic fungi can serve as an alternative source for valuable active plant compounds. Endophytic fungi can be harnessed to produce bioactive compounds for human pharmaceutical use when the bioactive secondary metabolites are not commercially available, derived from slow-growing or rare and endangered plants, and difficult to synthesize due to heavy molecular weight or structural complexity. Endophytic fungal secondary metabolites have drawn extensive attention among medicinal plants, mangroves, and marine microorganisms [9,10].

Endophytic fungi are a highly biodiverse and versatile microbial community that seems to be ubiquitous in nature. Studies have shown that almost all plants contain endophytic fungi, including colonized plants in the Arctic and Antarctic regions, deserts, oceans, and tropical rainforests [11,12]. They have been isolated and cultured from the roots and above-ground parts of various plants, including algae, mosses, ferns, gymnosperms, and angiosperms. Evidence from microorganism’s records in the fossil plant tissue indicated that the plant-endophytic fungal interactions have existed for approximately 400 million years, and during this time, endophytic fungi co-evolved unique biosynthetic pathways and metabolic mechanisms to synthesize complex secondary metabolites [13]. To date, only 5% of 1.5 million fungal species on Earth have been described in detail, and out of this percentage (69,000 fungal species), only 16% (11,500 species) have been cultured and studied. About 0.035–5.1 million fungal species have been found on Earth according to results from next-generation sequencing technologies [14]. Approximately 300,000 known species of higher plants exist on Earth, and each of which is a host for one or more obligate endophytic fungi. The high number of bioactive secondary metabolites found in endophytic fungi is due to their rich species diversity [15,16]. Endophytic fungi have been studied for more than 100 years, with the first endophytic strain isolated from the seeds of ryegrass (Lolium temulentum L.) by Vogl et al. in 1898 [17]. Stierle et al. [18] discovered the paclitaxel-producing endophytic fungus (Taxomyces andreanae) from the Pacific yew and then from other plant species successively. This discovery aroused the attention of mycologists and pharmaceutical chemists on endophytic fungi as a new source of bioactive substances and stimulated the interest in endophytic fungi as a sustainable source of plant metabolites. As shown in Table 1, many compounds that were isolated from endophytic fungi were also identified in some plant species as well as exhibited similar biological activity even though there were isolated from different sources, confirming endophytic fungi as an alternative source of bioactive compounds [19,20,21,22,23,24,25,26,27,28,29,30,31,32]. An overview of the recent literature surveys revealed that 51% of the bioactive substances isolated from endophytic fungi were previously unknown, with about 38% being isolated from soil microbiota [19]. Over the past decade, there has been a surge in the number of patents for endophytic fungi with new molecular secondary metabolites, which play a key role in the pharmaceutical industry, phytoremediation, and biomedicine [20,21]. Researchers are now searching for an economical, environmentally safe, and sustainable way to obtain new bioactive secondary metabolites from endophytic fungi.

Table 1

Several endophytic fungi of host plants have been reported to produce compounds with similar activity.

No.	Endophytic Fungus	Host Plant	Regions/Countries	Compound	Biological Activity	Ref.
1	Lophiostoma sp.	Eucalyptus exserta	Guangzhou, China.	Scorpinone	Antibacterial	[22]
2	Mycosphaerella sp.	Myrciaria floribunda	Amazon rainforest, Brazil.	Myriocin	Antifungal	[23]
3	Mucor sp.	Centaurea stoebe	Idaho, USA	Terezine E	Antifungal and cytotoxicity	[24]
4	Aspergillus calidoustus	Acanthospermum australe	Jalapao State Park, Tocantins, Brazil.	Ophiobolin K6-epi-ophiobolin K	Antifungal, trypanocidal and cytotoxicity	[25]
5	Phomopsis sp.	Garcinia kola (Heckel) nut	Yaounde, Cameroon	Cytochalasins H	Antibacterial and cytotoxicity	[26]
6	Aspergillus nidulans	Nyctanthes arbor-tristis Linn	Karachi, Pakistan	Sterigmatocystin	Antiproliferative activity	[27]
7	Trichoderma asperellum and Trichoderma brevicompactum	Vinca herbacea	Hamedan, Iran	4b-hydroxy-12,13-epoxytrichothec-9-ene	Antimicrobialand antiproliferative activity	[28]
8	Phyllosticta elongata	Cipadessa baccifera	Western Ghats, India	Camptothecin	Anticancer agent	[29]
9	Fusarium verticillioides	Huperzia serrata	Gucheng Mountain, Sichuan, China	Huperzine A	Treatment of Alzheimer’s disease	[30]
10	Fusarium solani	Cassia alata	Bangladesh	NapthaquinonesAzaanthraquinones	Cytotoxicity, antimicrobial andantioxidant activity	[31]
11	Fusarium sp. andLasiodiplodia theobromae	Avicennia lanata	Terengganu, Malaysia	Anhydrofusarubindihydrojavanicin	Antitrypanosomal	[32]
12	Corynespora cassiicola	Gongronema latifolium	Nigeria	Corynesidone D	Anti-inflammatory/anticancer agent	[33]
13	Pestalotiopsis theae	Camellia sinensis Theaceae	Hangzhou, China	punctaporonin H	Antibacterial and cytotoxicity	[34]
14	Phialocephala fortinii	Podophyllum peltatum	Tamilnadu, India	Podophyllotoxin	Antiviral, antioxidant, and antirheumatic activities	[35]

This article reports 220 new compounds with rare or novel structures or skeleton structures from endophytic fungi from 82 journal articles between 2011 and 2021 and briefly describes the sources of endophytic fungi, chemical structures, and biological activities of these compounds. Among all the new compounds reported in this review, terpenoids (35%) were largest in proportion, followed by alkaloids (26%). The proportion of different types of compounds among all the new compounds are presented in Figure 1. These new compounds were obtained from different species of endophytic fungi, which had diverse chemical skeletons and exhibited diverse and interesting biological activities. Additionally, the most common pharmacological activities these compounds showed were antimicrobial and antitumor activities. However, some of the compounds showed anti-angiogenic, anti-phytotoxic, and α-glucosidase inhibitory effects. Therefore, this review summarized different insights into the prospects and challenges of endophytic fungi as an alternative source of plant-derived bioactive compounds for drug development. In addition, this review will affirm that endophytic fungi produce similar bioactive compounds just as their host plants to give knowledge for the development of drug candidates from endophytic fungi using different strategies, thus making Endophytic fungi a treasure trove of new secondary metabolites.

Figure 1

The proportion of different types of compounds among all new compounds.

2. Bioactive New Metabolites Isolated from Endophytic Fungi and Their Biological Activities

2.1. Polyketides

2.1.1. Chromones

The induction of endophyte metabolism by adding Host components was used to add the same phytocomponents (2R, 3R)-3, 5, 7- trihydroxyflavanone 3-acetate in Botryosphaeria ramosa L29 potato dextrose broth culture to induce the production of 5-hydroxy2,3-dihydroxymethyl-7-methoxychromone 1 (Figure 2), 5-hydroxy-3-acetoxymethyl-2-methyl-7- methoxychromone 2 (Figure 2) and 5,7-dihydroxy-3-hydroxymethyl-2-methylchromone 3 (Figure 2), where Compounds 1–3 displayed acceptable antimicrobial activities against Fusarium oxysporum with MIC values of 50 μg/mL, 50 μg/mL, and 6.25 μg/mL, respectively. These values were superior compared to those of the positive drug—triadimefon—for the antimicrobial test (with an MIC value of 100 μg/mL) [36]. This indicated that the induction of endophytes metabolism to produce bioactive components of interest might be an ideal strategy for easy identification of drug candidates from these microbes; however, there is the need for long-term studies on how specific components influence endophytes metabolism and the bioactive compounds there are linked with. Phaeosphaonesa A 4 (Figure 2), isolated from Phaeosphaeria fuckelii, contains a β-(oxy)thiotryptophan motif structure that is rare in nature. Compound 4 showed stronger inhibition activity of mushroom tyrosinase than the positive control kojic acid (IC50 value of 40.4 μM) at 100 μM concentration, with an IC50 value of 33.2 μM [37]. Two aromatic chromones, Chaetosemins B–C 5–6 (Figure 2), were isolated from Chaetomium seminudum brown rice cultures, and compounds 5–6 contained L-cysteine and D-cysteine units, respectively. Compound 5 showed antifungal activity against Magnaporthe oryzae and Gibberella saubinetti, with MIC values of 6.25 μM and 12.5 μM, respectively. Compound 6 showed significant antioxidant activity at a concentration of 50 μM with a DPPH radical scavenging rate of 50.7% [38]. Pestaloficiols M–P 7–10 (Figure 2), which are new isoprenylated chromone derivatives, were isolated from brown rice culture extract of the plant endophytic fungus Pestalotiopsis fici. The structures of these compounds were elucidated primarily by MS and NMR techniques. Compounds 7–8 displayed inhibitory effects on HIV-1 replication in C8166 cells, with EC50 values of 56.5 μM and 10.5 μM, respectively (the EC 50 value of the positive control Indinavir Sulfate was 8.2 μM), whereas compounds 9–10 showed cytotoxic activity against the human tumor cell line HeLa, with IC50 values of 56.2 μM and 74.9 μM, respectively (the positive control 5-fluorouracil has an IC50 of 10.0 μM). Compound 10 exhibited a potent antifungal activity against Aspergillus fumigatus at IC50 = 7.35 μM) [39].

Figure 2

Chemical structures of chromones.

2.1.2. α-Pyrones

Two tetrasubstituted α-pyrone derivatives—Neurospora udagawae udagawanones A-B 11–12 (Figure 3)—were isolated from oak endophytic fungi, with both containing unique oxidation functional groups at the C-2 position. Compound 11 exhibited potent antifungal activity against Rhodoturula glutinis with MIC = 66 μg/mL). Additionally, compounds 11 and 13 showed moderate cytotoxic activity against KB3.1 cells with IC50 = 27 μg/mL [40]. The study revealed moderate activity of compounds 11 and 12 against fungi and mammalian cells, and this may be as a result of the method (serial dilution antimicrobial assay) used; therefore, it is suggested that other biological tests be employed to verify these findings. The nigerapyrones A–B 13–14 (Figure 3) were obtained from Aspergillus niger MA-132, which was isolated from the mangrove plant Avicennia marina. Compounds 13–14 both showed potent antifungal activities against two tumor cell lines (HL60 and A549), with IC50 values ranging from 0.3 to 5.41 μM [41]. The ficipyrones A–B 15–16 (Figure 3) were isolated from solid cultures of Pestalotiopsis fici. Compound 15 showed significant antifungal activity against Gibberella zeae CGMCC 3.2873, with an IC50 value of 15.9 μM, but had no activity against Fusarium culmorum CGMCC 3.4595 and Verticillium aiboatrum CGMCC 3.4306 [42]. The endophytic fungus Aspergillus oryzae was isolated from the rhizome of Paris polyphylla in Dali, Yunnan, China, and 4-hydroxy-6-[(2S, 3S)-3-hydroxybutan-2-yI]-3-methyl-2H-pyran-2-one 17 (Figure 3) and (R)-4-hydroxy-6-(l-hydroxy-2-methylpropyl)-3-methyl-2H-pyran-2-one 18 (Figure 3) were obtained from this fungi. However, the biological activities of these compounds were not tested in the study; hence, investigating the biological activities of these compounds is needed, as it may yield a very important source of drug activity [43].The pyran-2-one scaffold compounds 19–21 (Figure 3) were isolated by adding 10 mg/L DNA methyltransferase inhibitor 5-aza-2-deoxycytidine to Penicillium herquei liquid cultures, whereas the MTT method was used to measure the cytotoxicity of all compounds in MDA-ME-231 and MV-411 cell lines. Compounds 19–21 showed weak cytotoxicity only against the MV4-11 cell line with IC50 values of 90.09 µM, 74.16 µM, and 70.00 µM, respectively [44].

Figure 3

Chemical structures of α-pyrone compounds.

2.1.3. Other Polyketides

The phomaketides A–E 22–26 (Figure 4), pseurotins A3 27 (Figure 4), and pseurotins G 28 (Figure 4) were isolated from fermentation broth and mycelial extracts of the marine red algae endophytic fungus Phoma sp. NTOU4195. The mouse macrophages RAW264 were induced using the endothelial progenitor cells of human umbilical cord blood, lipopolysaccharide (LPS), to assess the anti-angiogenic and anti-inflammatory activities of all compounds. Compound 22 showed potent anti-angiogenic activity by inhibiting endothelial cell proliferation, with an IC50 value of 8.1 μM. Compound 24 at the concentration of 20 μM induced effective nitric oxide (NO) inhibition activity against LPS-induced RAW264.7 cells, with an IC50 value of 8.8 μM [45]. There were two tetracyclic polyketide compounds, simplicilone A–B 29–30 (Figure 4), containing helical centers obtained from the broth culture of the endophytic fungus Simplicillium sp., which was isolated from the bark of the medicinal plant Duguetia staudtii (Engl. and Diels) Chatrou in the Cameroon region. Compounds 29–30 showed weak cytotoxic activities against the KB3.1 cell line, with IC50 values of 1.25 μg/mL and 2.29 μg/mL, respectively, but had no antimicrobial activity against the tested bacteria (Staphylococcus aureus DSM 346 and Bacillus subtilis DSM 10) [46]. 5R-hydroxyrecifeiolide 31 (Figure 4), 5S-hydroxyrecifeiolide 32 (Figure 4), and ent-cladospolide F–H 33–35 (Figure 4) were also isolated from the endophytic fungal strain Cladosporium cladosporioides MA-299, which was obtained from the leaves of the mangrove plant Bruguiera gymnorrhiza from Hainan Island, China. Compounds 31–35 showed potent antimicrobial activities against Escherichia coli and Staphylococcus aureus, with MIC values ranging from 1.0 to 64 μg/mL. Compound 33 showed moderate inhibition activity against acetylcholinesterase, with an IC50 value of 40.26 μM [47]. The antimicrobial polyketide compound, palitantin 36 (Figure 4), was obtained from Aspergillus fumigatiaffnis and isolated from healthy leaves of Tribulus terrestris L. In addition, compound 36 showed effective antimicrobial activity against the multi-drug-resistant pathogens Enterococcus faecalis UW 2689 and Streptococcus pneumoniae 25697, both with an MIC value of 64 μg/mL [48]. The four polyketide derivatives—isotalaroflavone 37 (Figure 4), (+/−)-50-dehydroxytalaroflavone 38–39 (Figure 4), and bialternacin G 40 (Figure 4)—were obtained from the endophytic fungus Alternaria alternata ZHJG5 isolated from the leaves of Cercis chinensis, which was collected from the Nanjing Botanical Garden, Nanjing, China. They exhibited potent antimicrobial activity against Xanthomonas oryzae pv. oryzicola (Xoc) and Ralstonia solanacearum, with MIC values ranging from 0.5 to 64 μg/mL. Compound 37 at the concentration of 200 μg/mL showed a significant protective effect against the bacterial blight of rice caused by Xanthomonas oryzae pv. oryza, with a protection rate of 75.1% [49]. Four polyketide derivatives containing the benzoisoquinoline-9-one moiety structure peyronetides A–D 41–44 (Figure 4) were isolated from the mycelial crude acetone extract of Peyronellaea sp. FT431. Compounds 41–42 showed moderate to weak cytotoxic activity against human kidney cancer cell line TK10 and human ovarian cancer cell line A2780cisR, with IC50 values ranging from 6.7 to 29.2 μM [50]. The aromatic polyketide compound, (−)alternamgin 45 (Figure 4), was obtained from potato dextrose broth cultures of the endophytic fungus Alternaria sp. MG1 isolated from Vitis quinquangularis. This compound was of particular interest because it had the rare dibenzopyrone functionality of 6/6/6/6/5/6/6/6 heptacyclic backbone. Compound 45 displayed a weak cytotoxic activity against cells from two tested cell lines (Hela and HepG2), both with IC50 values exceeding 20 μM [51].

Figure 4

Chemical structures composition of other polyketides.

In summary, Polyketides, such as chromones and α-pyrone, and their derivatives identified from plant sources have also been found in endophytic fungi in recent studies. Chromones and their derivatives isolated from both plant and endophytic fungi sources all showed antimicrobial properties against specific pathogens; therefore, chromones from endophytic fungus can be used in the development of antimicrobials in the place of plant chromones to reduce the depletion of plants’ resources in the ecosystem.

2.2. Alkaloids

2.2.1. Cytochalasin

The methylation-deficient backbone, Phomopsisin A–C 46–48 (Figure 5), was obtained from brown rice cultures of Phomopsis sp. sh917, which was isolated from Isodon eriocalyx var. laxiflora stems. Compound 46 contained an unusual 5/6/11/5 tetracyclic ring system 2H-isoxazole moiety and showed significant inhibition activity against LPS-induced NO production in RAW264.7 cells, with an IC50 value of 32.38 μM, which was more potent than the positive control L-NMMA (IC50 value of 42.34 μM) [52]. The highly oxidized cytochalasin alkaloids—armochaetoglobins S–Z 49–57 (Figure 5) and 7-O-acetylarmochaetoglobin S 50 (Figure 5)—were identified and isolated from Chaetomium globosum TW1-1. The effects of all compounds on five tested human cancer cell lines (HL-60, A-549, SMMC-7721, MCF-7, and SW-480) were measured using the MTT method. Compounds 56–57 showed potent cytotoxic activities, with IC50 values ranging from 10.45 to 30.42 µM [53]. Furthermore, diaporthichalasins D–H 58–62 (Figure 5) were obtained from solid cultures of the endophytic fungus Diaporthe sp. SC-J0138 isolated from the leaves of the pteridophyte Cyclosorus parasiticus, and the MTS method was used to evaluate the cytotoxic activities of these compounds on four human cancer cell lines (A549, HeLa, HepG2, and MCF-7). Compound 58 exhibited significant cytotoxic activity against all tested human cancer cell lines; compounds 59–62 exhibited selective cytotoxic activities against some cell lines [54]. Cytochrysins A–C 63–65 (Figure 5) were obtained from rice cultures of Cytospora chrysosperma HYQZ-931, an endophytic fungus isolated from the desert plant Hippophae rhamnoides. Compound 63 showed significant antimicrobial activity to Enterococcus faecium, with an MIC value of 25 μg/mL. Compound 65 showed potent antimicrobial activity to Staphylococcus aureus, with an MIC value of 25 μg/mL [55].

Figure 5

Chemical structures composition of cytochalasins.

2.2.2. Indole Alkaloids

Six prenylated indole alkaloids, asperthrins A–F 66–71 (Figure 6), were derived from the marine endophytic fungus Aspergillus sp. YJ191021. Compound 66 showed moderate antimicrobial activity against Vibrio anguillarum, with an MIC value of 8 μg/mL. Additionally, the compounds 66 and 69 showed potent–weak anti-inflammatory activities against propionibacterium acnes-induced human mononuclear cell line (THP-1), with IC50 values of 1.46 μΜ and 30.5 μΜ, respectively, while compound 66 showed higher anti-inflammatory activity than the positive control Tretinoin at an IC50 value of 3.38 μM [56]. The α-pyrone meroterpenoid-type alkaloid, oxalicine C 72 (Figure 6), was obtained from Penicillium chrysogenum XNM-12, which was isolated from the marine brown algae Leathesia nana. Compound 72 showed potent antimicrobial activity against the phytopathogenic fungus Ralstonia solanacearum, with an MIC of 8 μg/mL [57]. Scalarane 73 (Figure 6) was isolated from Hypomontagnella monticulosa Zg15SU through the potato dextrose liquid culture. Compound 73 showed potent cytotoxic activity against cancer cell lines Panc-1, NBT-T2, and HCT116, with IC50 values of 0.05, 0.75, and 0.05 μg/mL, respectively [58]. Asperlenines A–C 74–76 (Figure 6) were isolated from Aspergillus lentulus DTO 327G5 cultures, and the antimicrobial activity of all compounds was evaluated using the broth-microdilution method against five tested agricultural pathogens (Xanthomonas oryzae pv. Oryzae, Xanthomonas oryzae pv. Oryzicola, Rhizoctonia solani, Fusarium oxysporum, and Colletotrichum gloeosporioides). Compounds 74–76 showed moderate to weak antimicrobial activities against Xanthomonas oryzae pv. Oryzae and Xanthomonas oryzae pv. Oryzicola, with MIC values ranging from 25 to 100 μg/mL [59].

Figure 6

Chemical structures of indole alkaloids.

2.2.3. Diketopiperazine Derivatives

The thiodiketopiperazine alkaloid, phaeosphaones D 77 (Figure 7), featuring an unusual β-(oxy) thiotryptophan motif, was obtained from endophytic fungus Phaeosphaeria fuckelii isolated from the medicinal plant Phlomis umbrosa. Compound 77 showed stronger mushroom tyrosinase inhibition activity than the positive control kojic acid (IC50 value of 40.4 μM), with an IC50 value of 33.2 μM. [60]. The oxepine-containing diketopiperazine-type alkaloids, varioloids A-B 78–79 (Figure 7), were obtained from Paecilomyces variotii EN-291, which was isolated from the marine red alga Grateloupia turuturu. Compounds 78–79 showed potent antifungal effects against Fusarium graminearum, with MIC values of 8 μg/mL and 4 μg/mL, respectively [61]. Aspergiamides A–F 80–85 (Figure 7) were isolated from the endophytic fungus Aspergillus sp. 16-5 of mangroves, and all compounds were evaluated for their inhibition activities against protein-tyrosine phosphatase 1B (PTP1B) and α-glucosidase. Compounds 80 and 81 showed potent to moderate α-glucosidase inhibition activities, with IC50 values of 18.2 µM and 40.7 µM, respectively. Compounds 80–85 did not show significant PTP1B inhibition activities (<10% inhibition) at 100 µg/mL [62]. Five sulfide diketopiperazines derivatives, penicibrocazines A–E 86–90 (Figure 7), were obtained from the endophytic fungus Penicillium brocae MA-231 isolated from the mangrove plant Avicennia marina. The antimicrobial effects of all compounds were evaluated by the agar diffusion method against five tested pathogens (Aeromonas hydrophilia, Escherichia coli, Staphylococcus aureus, Vibrio arveyi, and V. parahaemolyticus). Compounds 86–90 showed potent antimicrobial activities against S. aureus, with MIC values ranging from 0.25 to 32 μg/mL [63]. Spirobrocazines A–C 91–93 (Figure 7) were isolated from the mangrove-derived Penicillium brocae MA-231. Compounds 91–93 contained a 6/5/6/5/6 cyclic system with a rare spirocyclic center at C-2. All compounds showed moderate antimicrobial activities against S. aureus, Aeromonas hydrophilia, and Vibrio harveyi, with MIC values ranging from 16 to 64 μg/mL [64].

Figure 7

Chemical structures of diketopiperazine derivatives.

2.2.4. Other Types of Alkaloids

The quinazoline alkaloid (-)-(1R,4R)-1,4-(2,3)-indolmethane-1-methyl-2,4-dihydro-1H-pyrazino-[2,1-b]-quinazoline-3,6-dione 94 (Figure 8) was obtained from the endophytic fungus Penicillium vinaceum X1, which was isolated from corms of Crocus sativus (Iridaceae). The in vitro cytotoxicity of compound 94 was evaluated against three human tumor cell lines (A549, LOVO, and MCF-7), to which compound 94 showed weak cytotoxic activities against all human tumor cell lines, with IC50 values of 76.83, 68.08, and 40.55 μg/mL, respectively [65]. The enantiomeric bromotyrosine alkaloids S-Acanthodendrilline 95 (Figure 8) and R-Acanthodendrilline 96 (Figure 8) were isolated from the ethyl acetate extract of the sponge endophytic fungus Acanthodendrilla sp. The cytotoxic activities of compounds 95–96 against human non-small cell lung cancer H292 and normal human immortalized fibroblast HaCaT cell lines were evaluated using the MTT method. Compound 95 (IC50 value of 58.5 µM) was approximately three times more potent than compound 96 (IC50 value of 173.5 µM) against the H292 cell line. Compounds 95–96 exhibited efficient and selective cytotoxic activities against H292 and HaCaT cell lines, with IC50 values ranging from 58.5 to 173.5 µM and >400 µM, respectively [66]. Three phenylpyridone derivatives, citridones E–G 97–99 (Figure 8), were obtained from the endophytic fungal strain Penicillium sumatrense GZWMJZ-313 9, which was isolated from the leaves of Garcinia multiflora. These compounds showed moderate to weak antimicrobial activities against Staphylococcus aureus ATCC6538, Pseudomonas aeruginosa ATCC10145, and Escherichia coli ATCC11775, with MIC values ranging from 32 to 128 μg/mL [67]. Two isoprenylisoindole alkaloids, diaporisoindoles A-B 100–101 (Figure 8), were obtained from the endophytic fungus Diaporthe sp. SYSU-HQ3, which was isolated from a fresh branch of the mangrove plant Excoecaria agallocha. Compound 100 showed potent inhibition activity against Mycobacterium tuberculosis protein-tyrosine phosphatase B, with an IC50 value of 4.2 µM [68].

Figure 8

Chemical structure of other types of alkaloids.

In a nutshell, anti-angiogenic and anti-inflammatory activities were the main activities of alkaloids in both plants and endophytic fungi. In addition, phomaketides and their derivatives that were isolated from fungal endophytes possess antimicrobial activity just as those isolated in plants; therefore, alkaloids producing endophytic fungi can be used in the development of anti-angiogenic, anti-inflammatory, and antimicrobial drugs for both human and animal use.

2.3. Terpenoids

2.3.1. Sesquiterpenoids and Their Derivatives

The 1-methoxypestabacillin B 107 (Figure 9) was obtained from brown rice cultures of endophytic fungus Diaporthe sp. SCSIO 41011 isolated from the stem of the mangrove plant Rhizophora stylosa. Compound 107 was evaluated for the reversal of HIV incubation period and anti-influenza A virus activities, to which compound 107 did not show antiviral activity. However, its structure could serve as the backbone for the synthesis of more potent antiviral compounds [69]. The eremophilane-type sesquiterpenoids rhizoperemophilanes A-N 102–115 (Figure 9) were isolated from the ethyl acetate extract of Rhizopycnis vagum Nitaf22. Compound 111 contained a C-4/C-11 epoxide, and compound 115 had a 3-nor-eremophilane lactone-lactam skeleton. All compounds were evaluated for their cytotoxic activities against five tested human cancer cells (BGC823, Daoy, HCT116, HepG2, and NCI-H1650) and inhibition activities against radicle growth in rice seedlings. Compound 115 showed high selective cytotoxicity against NCI-H1650 and BGC823 cell lines, with IC50 values of 15.8 µM and 48.2 µM, respectively, while no significant cytotoxic activity was observed for other compounds at IC50 > 50 μm. Compounds 106–107 and 113–114 showed strong phytotoxic activities against radicle growth in rice seedlings at a concentration of 200 µg/mL, where the inhibition exceeded 50% [70]. The bisabolane-type sesquiterpene, trichoderic acid 116, (Figure 9) and acorane-type sesquiterpene, 2β-hydroxytrichoacorenol 117 (Figure 9), were obtained from Trichoderma sp. PR-35 culture, an endophytic fungus isolated from stems of Paeonia delavayi. Compounds 116–117 were tested for antimicrobial activity against two pathogens (Escherichia coli, and Shigella sonnei) using an agar diffusion method. Compounds 116–117 showed moderate to weak antimicrobial activities, with MIA values ranging from 50 to 175 µg/mL [69]. The ring flores aurantii alkane-type sesquiterpene, cyclonerotriol B 118 (Figure 9), and the α-pinene skeleton-containing sesquiterpene, 3β-hydroxy-β-acorenol 119 (Figure 9), were obtained from Fusarium proliferatum AF-04 isolated from Chlorophytum comosum roots via a combination of high-performance liquid chromatography (HPLC) and a bioassay-guided method. Compounds 118–119 showed weak antimicrobial activities (MIC values > 100 μg/mL) against Bacillus subtilis, Clostridium perfringens, E. coli, and methicillin-resistant Staphylococcus aureus (MRSA) [71]. The aromatic bisabolene-type sesquiterpene (7S, 8S)-8-hydroxysydowic acid 120 (Figure 9) was obtained from the brown rice culture of the endophytic fungus Aspergillus sydowii EN-434 isolated from the marine red alga Symphyocladia latiuscula from Qingdao, China. Compound 120 showed potent DPPH radical scavenging activity, with an IC50 value of 113.5 μmol/L [72]. The ophiobolane sesquiterpenes ophiobolins P–T 121–125 (Figure 9) were isolated from the acetone extract of the endophytic fungus Ulocladium sp. using the one-strain many-compound (OSMAC) strategy. Compounds 121–125 were evaluated for their cytotoxicity and antibacterial activities against two tested human cancer cell lines (KB and HepG2 cell lines) and three tested pathogens (Bacillus subtilis, MRSA, and Bacille Calmette-Guerin). Compounds 121–125 showed moderate antimicrobial activities against B. subtilis and multi-drug-resistant S. aureus, with MIC values ranging from 15.6 to 62.5 μM. Compound 125 showed moderate antimicrobial activity against Bacille Calmette-Guerin, with an MIC value of 31.3 μM. Additionally, compound 125 showed potent cytotoxic activity against the HepG2 cell line, with an IC50 value of 0.24 μM, which was stronger than the positive control etoposide (IC50 value of 2.02 μM) [73]. The daucane-type sesquiterpenes trichocarotins I-M 126–130 (Figure 9) were obtained from Trichoderma virens QA-8 isolated from the roots of Artemisia argyi H. Lév. and Vaniot, and these compounds showed significant antimicrobial activities against E. coli EMBLC-1, with MIC values ranging from 0.5 to 16 μg/mL [74].

Figure 9

Chemical structures of sesquiterpenoids and derivatives.

2.3.2. Diterpenoids

The ring diterpene diaporpenoid A 131 (Figure 10), containing a 5/10/5-fused tricyclic ring system, was isolated from the MeOH extract obtained from cultures of the mangrove endophytic fungus Diaporthe sp. QYM12. Compound 131 showed significant anti-inflammatory activity by inhibiting LPS-induced NO production in a mouse macrophage cell line RAW264.7, with an IC50 value of 21.5 μM [75]. The pimarane-type diterpene Libertellenone M 132 (Figure 10) was isolated from the marine source endophytic fungus Phomopsis sp. S12. Compound 132 inhibited pro-inflammatory cytokines IL1β and IL-18 mRNA expression in colon tissue, significantly reduced the cleavage of pro-caspase1, and dose-dependently inhibited the NF-κB nuclear translocation in macrophages. Clinical indications of acute colitis induced by 3% dextran sulphate sodium in mice were attenuated by intravenous administration of different doses of compound 132 (10 or 20 mg/kg), which is a potent inhibitor of NLRP3 inflammatory vesicles and may be a new medicine for treating acute colitis [76]. Three pimarane-type diterpenoids—pedinophyllol K 133 (Figure 10), pedinophyllol L 134 (Figure 10), and libertellenone T 135 (Figure 10)—were isolated from the endophytic fungal Phomopsis sp. S12 culture using the OSMAC strategy. The anti-inflammatory activities of all compounds were assessed using an LPS-induced inflammation model of mouse macrophage RAW264.7. Compound 135 dose-dependently inhibited the expression of inflammatory factors IL-1β and IL-6 at the mRNA level. Additionally, the anti-inflammatory activity of compounds 133–134 was similar to that of compound 135 in terms 0f IL-6 inhibition [77]. Two tetranorlabdane diterpenoids botryosphaerins G–H 136–137 (Figure 10) were obtained from the ethyl acetate extract of Botryosphaeria sp. P483 isolated from the branches of the herb Huperzia serrata (Thunb.) Trev. and tested for their antifungal activities against Gaeumannomyces graminis, Fusarium solani, and Pyricularia oryzae by the disk diffusion method. Compound 137 showed effective antifungal activity at a concentration of 100 μg/disk with an inhibitory zone diameter of 9 mm. (The inhibitory zone diameter of positive control carbendazim was 15–18 mm.) Compounds 136–137 were evaluated for their nematicidal activities against Panagrellus redivivus and Caenorhabditis elegans and showed weak nematicidal activities, with 30% and 28% fatality rates at a 24h action concentration of 400 mg/L, respectively [78]. The isopimarane diterpene sphaeropsidin A 138 (Figure 10) was isolated from the ethyl acetate extract of the endophytic fungus Smardaea sp. AZ0432 of Ceratodon purpureus. The in vitro cytotoxic activities of compound 138 against five human cancer cell lines (NCI- H460, MDA-MB-231, MCF-7, PC-3M, and SF-268) and human embryonic lung fibroblast cell line WI-38 were evaluated using the resazurin colorimetric assay. The results showed that compound 138 showed a high cell selectivity when it was applied at a concentration of 10 μM for 72 h and inhibited the migration of MDA-MB-231 cells by 50% at a subcytotoxic concentration of 1.5 μM [79]. (10S)-12,16-epoxy-17(15→16)-abeo-3,5,8,12,15-abietapentaene-2,7,11,14-tetraone 139 (Figure 10) was obtained from the cultures of the endophytic fungus Pestalotiopsis adusta isolated from stems of the medicinal plant Clerodendrum canescens. The cytotoxicity of compound 139 to the HL-60 tumor cell line was evaluated using the MTT assay, by which compound 139 showed moderate cytotoxic activity, with an IC50 value of 12.54 μM [80]. (The IC50 value of the positive control cisplatin was 9.20 μM.) The trichodermanin A 140 (Figure 10), a diterpene containing a 6-5-6-6 ring system, was obtained from the endophytic fungus Trichoderma atroviride S361 of Cephalotaxus fortunei and was not tested for any biological activities [81]. Therefore, further studies are needed to identify the potential biological activity of this compound in the future. The new tetranorlabdane diterpenoids, asperolides A–C 141–143 (Figure 10), were isolated from the ethyl acetate extract of the marine brown alga Aspergillus wentii EN-48 and the cytotoxic activities of compounds 141–143 to seven tested human cancer cell lines (NCI-H460, MDA-MB-231, HeLa, MCF-7, SMMC-7721, HepG2, and SW1990) were evaluated using the MTT method. Compounds 141–143 showed moderate cytotoxic activities, with IC50 values ≤ 10 Μm [82].

Figure 10

Chemical structures of diterpenoids and derivatives.

2.3.3. Triterpenoids

The 24-homo-30-nor-cycloartane triterpenoid 154 (Figure 11) was isolated from the endophytic fungus Mycoleptodiscus indicus FT1137. Compound 154 showed no activity against the human ovarian cancer cell line A2780 at a concentration of 20 μg/mL [83]. Three Lanostane-type triterpenes—sclerodols A–B 144–145 (Figure 11) and lanosta-8,23-dien-3β,25-diol 146 (Figure 11)—were obtained from Eucalyptus grandis cultures derived from the endophytic fungus Scleroderma UFSMSc1, and the antifungal activities of compounds 144–146 against Candida albicans and Candida parapsolosis were evaluated by the agar diffusion method. Compounds 144–146 showed moderate to weak antifungal activities, with MIC values ranging from 12.5 to 50 μg/mL. The antifungal effects of these compounds against C. albicans were associated with the inhibition of the selenocysteine methyltransferase (SMT) activity [84]. Fusidic acid 147 (Figure 11) was obtained from the cultures of the endophytic fungus Acremonium pilosum F47, isolated from the stem of Mahonia fortunei using the bioactivity-guided assay, and the antimicrobial activities of compound 147 against four human pathogens were tested (S. aureus ATCC 6538, B. subtilis ATCC 9372, P. aeruginosa ATCC 27853, and E. coli ATCC 25922) and evaluated. Compound 147 showed effective antimicrobial activities against S. aureus ATCC 6538 and B. subtilis ATCC 9372. The acetylation of the C-16 hydroxyl group of compound 147 was essential for antimicrobial action [85]. Two new ring A-cleaved lanostane-type triterpenoids, glometenoid A–B 148–149 (Figure 11), were obtained from the ethyl acetate extract of the mason pine endophytic fungus Glomerella sp. F00244. The cytotoxic activity of compounds 148–149 against the human ovarian cancer cell line HeLa was tested using the MTT assay. Compound 148 showed weak cytotoxic activity at a concentration of 10 μM with 21% inhibition [83]. Nine highly oxygenated schitriterpenoids—kadhenrischinins A–H 150–157 (Figure 11) and 7β-schinalactone C 158 (Figure 11)—were isolated from Penicillium sp. SWUKD4.1850, and compounds 154–157 contained a unique 3-one-2-oxabicyclo [1,2,3]-octane motif. All compounds were tested for their cytotoxic activities against the HepG2 tumor cell lines using the MTT assay, and these compounds showed weak cytotoxic activities, with IC50 values ranging from 14.3 to 40 μM [86]. Two tetracyclic triterpenoids—integracide E 159 (Figure 11) and isointegracide E 160 (Figure 11)—were isolated from the mycelia of Hypoxylon sp. 6269. Compound 159 showed weak inhibition activity against the HIV-1 integrase, with an IC50 value of 31.63 μM [87]. The tetracyclic triterpenoids, integracides H–J 161–163 (Figure 11), were obtained from the endophytic fungus Fusarium sp., which was isolated from the roots of Mentha longifolia L. (Labiatae) and were evaluated for antileishmanial activity against L. donovani promastigotes. Compound 161 showed significant antileishmanial activity, with an IC50 value of 4.75 μM, exceeding the positive control Pentamidine (IC50 value of 6.35 μM) [88]. The tetracyclic triterpenoids, integracides F–G 164–165 (Figure 11), were obtained from the endophytic fungus Fusarium sp. of Mentha longifolia L. (Labiatae). Compounds 164–165 were evaluated for their antileishmanial and cytotoxic activities to BT-549 and SKOV-3 cells and Leishmania donovani promastigotes. Compounds 164–165 showed significant cytotoxic activities against SKOV-3 and BT-549 cell lines, with IC50 values ranging from 0.16 to 1.97 μg/mL and 0.12 to 1.76 μg/mL, respectively. (The IC50 value of the positive control Pentamidine was 2.1 μg/mL.) Compounds 164–165 showed potent antileishmanial activities against L. donovani promastigotes, with IC50 values of 3.74 μg/mL and 2.53 μg/mL, respectively [89].

Figure 11

Chemical structures of terpenoids.

2.3.4. Meroterpenoids

Guignardones P–S 166–169 (Figure 12) were obtained from Guignardia mangiferae A348 cultures, and the cytotoxic activities of compounds 166–169 against three human cancer cell lines (SF-268, MCF-7, and NCI-H460) were tested using an MTT assay. Compounds 167 and 169 only showed weak cytotoxic activities against MCF-7 cell lines, with IC50 values ranging from 83.7 to 92.1 µM [90]. Six 3, 5-demethylorsellinic acid-based meroterpenoids emeridones A–F 170–175 (Figure 12) were isolated from Emericella sp. TJ29 cultures. Compound 171 possessed a 2,6 dioxabicyclo [2.2.1] heptane and a spiro [bicycle [3.2.2] nonane-2,1′-cyclohexane] moiety. The cytotoxic activities of all compounds against five human cancer cell lines (HL-60, SMMC7721, A549, MCF-7, and SW-480) were tested using the MTT assay, and compounds 172, 173, and 175 showed moderate cytotoxic activities against all tested cell lines, with IC50 values ranging from 8.19 to 18.8 µM [91]. Phyllomeroterpenoids A–C 176–178 (Figure 12) were isolated from the crude extract of Phyllosticta sp. J13-2-12Y fermentation broth. Compounds 176–178 showed moderate antimicrobial activities against Staphylococcus aureus 209P, Candida aureus 209P, and Candida albicans FIM709, with MIC values ranging from 32 to 128 μg/mL [92]. Austin 179 (Figure 12) was obtained from the ethyl acetate extract of Talaromyces purpurogenus H4 and Phanerochaete sp. H2 co-cultures, which showed moderate trypanocidal activity against T. cruzi at a concentration of 100 μg/mL, with an IC50 value of 36.6 µM. Notably, neither of the two endophytic fungi produced compound 179 when cultured separately under similar conditions [93].

Figure 12

Chemical structures of Meroterpenoids.

To sum up, Meroterpenoids and their derivatives, which are mainly known for their antifungal properties in most plants species, have been found in endophytic fungi. However, recent studies have also reported anti-oxidative, anti-inflammatory, and anti-cancer activities from these compounds. Therefore, these microorganisms can be used in the development of drugs candidates for human, animal, and other agricultural activities.

2.4. Lactones

Helicascolide F 180 (Figure 13) was obtained from Talaromyces assiutensis JTY2 isolated from Ceriops tagal leaves. The cytotoxic activities of compound 180 against three human cancer cell lines (HeLa, MCF-7, and A549) were tested using an MTT assay, in which compound 180 showed a moderate cytotoxic effect on all tested cell lines, with an IC50 value range of 14.1–38.6 μM [94]. Two β-lactones, polonicin A–B 181–182 (Figure 13), were obtained from the brown rice culture of the endophytic fungus Penicillium polonicum in the fruit of Camptotheca acuminata. Compound 181 showed effective glucose uptake activity at a concentration of 30 μg/mL on rat skeletal myoblast cell line L6, which enhanced 1.8-fold compared to that of the control. Compound 182 was used to assess its effect on GLUT4 translocation by using the fluorescent protein, IRAP-mOrange, which is stably expressed in L6 cells. It showed a 2.1-fold increase in fluorescence intensity on L6 cell membranes compared to the untreated controls [95]. The spirodilactone compound chaetocuprum 183 (Figure 13) was obtained from cultures of the endophytic fungus Chaetomium cupreum of wild Anemopsis californica from New Mexico, U.S.A. Compound 183 showed a weak antimicrobial activity against S. aureus, with an MIC value of 50 μg/mL [96]. A phytotoxic bicyclic lactone, (3aS,6aR)-4,5-dimethyl-3,3a,6,6a-tetrahydro-2H-cyclopenta [b] furan-2-one 184 (Figure 13), was obtained from the fermentation broth of Xylaria curta 92092022. Compound 184 contained a rare 5/5 rings-fusion system and was tested for antimicrobial activities against four pathogens (Pseudomonas aeruginosa ATCC 15442, Staphylococcus aureus NBRC 13276, Aspergillus clavatus F318a, and Candida albicans ATCC 2019) and the phytotoxicity against lettuce seedlings. Compound 184 showed moderate antimicrobial activities against Pseudomonas aeruginosa ATCC 15442 and Staphylococcus aureus NBRC 13276 at a concentration of 100 μg/disk, with inhibitory zone diameters of 13 mm and 12 mm, respectively. At the concentration of 25 μg mL −1, compound 184 showed 50% inhibition on lettuce roots with a root length of 1.6 ± 0.3 cm (3.2 ± 0.5 cm for the control). At a concentration of 200 μg mL −1, compound 184 strongly inhibited lettuce seed germination, with 90% inhibition [97]. Lasiodiplactone A 185 (Figure 13) was obtained from the mangrove endophytic fungus Lasiodiplodia theobromae ZJ-HQ1 and contained a unique tetracyclic system (12/6/6/5) of RAL 12 (12-membered β-resorcylic acid lactone) with a pyran ring and a furan ring. Compound 185 showed significant anti-inflammatory activity by inhibiting the LPS-induced NO production in RAW 264.7 cells, with an IC50 value of 23.5 μM, which was stronger than the positive control indomethacin (IC50 = 26.3 μM). Additionally, compound 185 showed potent α-glucosidase inhibition activity, with an IC50 value of 29.4 μM, which was superior to the commonly used clinical drug acarbose (IC50 = 36.7 μM) [98]. (+)-phomalactone 186 (Figure 13), hydroxypestalopyrone 187 (Figure 13), and pestalopyrone 188 (Figure 13) were isolated from the endophytic fungus Aspergillus pseudonomiae J1 cultures and evaluated for in vitro anti-trypanosomal activity against the Trypanosoma cruzi Y strain using an anti-epimastigote assay. Compounds 186–188 showed moderate to weak anti-trypanosomal activities, with IC50 values of 0.86 μM, 88.33 μM, and 580.19 μM, respectively [99].

Figure 13

Chemical structures of Lactones.

In summary, this review reported that fungal endophytes could produce Lactones and their derivatives through their metabolic activities. In addition, these compounds possessed biological activities, such as antimicrobial, anti-cancer, allelopathic, and anti-inflammatory; thus, fungal endophytes that produce these compounds may be utilized in the pharmacological setup as alternatives to plant-derived compounds.

2.5. Anthraquinones, Quinones, and Related Glycosides

6,8-di-O-methylbipolarin 189 (Figure 14), aversin 190 (Figure 14), and 6,8-di-O-methylaverufin 191 (Figure 14) were obtained from rice cultures of the marine red algae endophytic fungus Acremonium vitellinum from Qingdao, China. Compounds 189–191 showed moderate insecticidal activities against the third-instar larvae of Helicoverpa armigera, with LC50 values of 0.72 mg/mL, 0.78 mg/mL, and 0.87 mg/mL, respectively. (The LC50 value for the positive control, matrine, was 0.29 mg/mL.) Additionally, the molecular mechanism of the insecticidal activity of compound 191 was investigated based on transcriptome sequencing. The identification of 5,732 differentially expressed genes was performed, of which 2,904 genes were downregulated and 2,828 genes were upregulated. The upregulated genes were primarily involved in cell autophagy, apoptosis, DNA mismatch repair, and replication [100]. A new quinone, identified as 1,3-dihydroxy-4-(1,3,4-trihydroxybutan-2-yl)-8-methoxy-9H-xanthen-9-one 192 (Figure 14), was obtained from Phomopsis sp. isolated from the rhizome of Paris polyphyllavar. in Yunnan, China. Compound 192 showed significant cytotoxic activities against A549 and PC3 cell lines, with IC50 values of 5.8 μM and 3.6 μM, respectively [101]. The anthraquinone derivative eurorubrin 193 (Figure 14) was obtained from the ethyl acetate extract of the endophytic fungus Eurotium cristatum EN-220 of the seaweed Sargassum thunbergii and tested for its antimicrobial activities against three tested pathogens (E. coli, Physalospora obtuse, and Valsa mali), including its fatal activity against brine shrimp larvae. Compound 193 only showed a weak antimicrobial activity against E. coli, with an MIC value of 64 μg/mL. At the concentration of 10 μg/mL, compound 193 showed moderate fatal activity against brine shrimp larvae, with a fatality rate of 41.4% [102]. Isorhodoptilometrin-1-methyl ether 194 (Figure 14), emodin 195 (Figure 14), and 1-methyl emodin 196 (Figure 14) were obtained from cultures of the endophytic fungus Aspergillus versicolor of the red seaweed Halimeda opuntia. Compounds 194–196 were evaluated for their inhibiting activities against the hepatitis C virus NS3/4A protease, where Compounds 195–196 showed weak inhibition activities, with IC50 values ranging from 22.5 to 40.2 μg/mL [103]. The quinone altersolanol A 197 (Figure 14) was isolated from the endophytic fungus Stemphylium globuliferum of the medicinal plant Mentha pulegium (Lamiaceae). Compound 197 inhibited the proliferation of K562 and A549 cells in a time-dependent, dose-dependent manner and caused apoptosis by cleaving Caspase-3 and Caspase-9 and decreasing anti-apoptotic protein expression [104].

Figure 14

Chemical structure of anthraquinones, quinones, and related glycosides.

Anthraquinones, quinones, and related glycosides are known for their anti-viral and anti-apoptotic activity both in vitro and in vivo. Interestingly, these compounds have been identified and isolated from fungal endophytes by various studies and have similarly shown anti-viral and anti-apoptotic activities. Thus, endophytes that produce these compounds may serve as cheap and environmentally friendly alternative sources for the development of antimicrobial drugs instead to plant sources.

2.6. Steroids

Phomosterols A–B 198–199 (Figure 15) were isolated from the endophytic fungus Phoma sp. SYSU-SK-7 of mangrove plants. Compounds 198–199 had an unusual aromatic B ring skeleton and showed significant inhibition activities against LPS-induced NO production in RAW 264.7 cells, with IC50 values of 13.5 μM and 25.0 μM, respectively. Additionally, compounds 198–199 showed potent α-glucosidase inhibition activities with IC50 values of 51.2 μM and 46.8 μM, respectively, exceeding the positive control 1-deoxynojirimycin (IC50 value of 62.8 μM) [105]. The ergosterol derivative fusaristerol A 200 (Figure 15) was obtained from the endophytic fungus Fusarium sp., which was isolated from the root of Mentha longifolia L. This compound showed significant antimicrobial activity against Candida albicans, with an MIC value of 8.3 μg/disc. Additionally, compound 200 showed moderate cytotoxic activity against human colorectal cancer cell line HCT 116, with an IC50 value of 0.21 μΜ, compared to the positive control adriamycin (IC50 value of 0.06 μΜ) [106]. (5,6,15,22E)-6-ethoxy-5,15-dihydroxyergosta-7,22-dien-3-one 201 (Figure 15) and (14,22E)-9,14-dihydroxyergosta-4,7,22-triene-3,6-dione 202 (Figure 15) were isolated from the endophytic fungus Phomopsis sp. of Aconitum carmichaeli in Yunnan, China. Compounds 201–202 were analyzed against six tested pathogenic fungi (Candida albicans, Aspergillus niger, Fusarium avenaceum, Pyricularia oryzae, Hormodendrum compactum, and Trichophyton gypseum) using a broth microdilution assay. Compounds 201–202 showed weak antifungal activities against C. albicans and F. avenaceum, with MIC values ranging from 64 to 128 μg/mL [107].

Figure 15

Chemical structures of steroids.

To summarize, endophytic fungi are alternative sources of steroids and their derivatives; thus, they may be harnessed for the production of various drugs since they have shown antimicrobial and anticancer activity in previous studies.

2.7. Other Types of Compounds

Four lignans, terrusnolides A–D 203–206 (Figure 16), were obtained from the endophytic fungus Aspergillus sp. isolated from the root of Tripterygium wilfordii. Compounds 203–206 showed significant inhibition of LPS-induced IL-1β, TNF-α, and NO production in RAW264.7 cells, with IC50 values ranging from 16.21 to 35.23 μΜ, 19.83 to 42.57 μΜ, and 16.78 to 38.15 μΜ, respectively, which were comparable to the positive control indomethacin (IC50 value of 15.67–21.34 μΜ) [108]. The indene derivative methyl 2-(4-hydroxybenzyl)-1,7-dihydroxy-6-(3-methylbut-2-enyl)-1H-indene-carboxylate 207 (Figure 16) obtained from the endophytic fungus Aspergillus flavipes Y-62 isolated from Suaeda glauca Bunge in Zhoushan, Zhejiang, China, showed weak antimicrobial activities against Pseudomonas aeruginosa, Klebsiella pneumonia, and Staphylococcus aureus, with MIC values ranging from 32 to 128 μg/mL [109]. The polychlorinated triphenyl diether simatorone 208 (Figure 16) was isolated from Microsphaeropsis sp. cultures, and its antimicrobial activities against three pathogens (Escherichia coli, Bacillus megaterium, and Microbotryum violaceum) were evaluated using an agar diffusion assay. Compound 208 showed effective antimicrobial activities against B. megaterium and E. coli with inhibitory zone diameters of 14 mm and 18 mm, respectively [110]. Two alkylated furan derivatives—5-(undeca-3′,5′,7′-trien-1′-yl) furan-2-ol 209 (Figure 16) and 5-(undeca-3′,5′,7′-trien-1′-yl) furan-2-carbonate 210 (Figure 16)—were obtained from the methanol extract of the endophytic fungus Emericella sp. XL029 isolated from Panax notoginseng leaves in Hebei, China. Compounds 209–210 both showed potent antifungal activities against six tested plant pathogenic fungi (Rhizoctorzia solani, Verticillium dahliae Kleb, Helminthosporium maydis, Fusarium oxysporum, Fusarium tricinctum, and Botryosphaeria dothidea), with MIC values ranging from 25 to 3.1 μg/mL [111]. The new azaphilone, isochromophilone G 211 (Figure 16), was obtained from the endophytic fungus Diaporthe perseae sp. isolated from Pongamia pinnata (L.) Pierre. Compound 211 showed significant DPPH and ABTS radical scavenging activities, with IC50 values of 7.3 μmol/mL and 1.6 μmol/mL, respectively [112]. The furan derivative, 3-(5-oxo-2,5-dihydrofuran-3-yl) propanoic acid 212 (Figure 16), was obtained from the endophytic fungus Aspergillus tubingensis DS37 isolated from Decaisnea insignis (Griff.) Hook & Thomson, and showed significant inhibition activities against Fusarium graminearum and Streptococcus lactis, with MIC values of 16 μg/mL and 32 μg/mL, respectively [113]. The pyrrolidinone derivative, nigrosporamide A 213 (Figure 16), was isolated from the endophytic fungus Nigrospora sphaerica ZMT05 of Oxya chinensis Thunberg and showed a three-fold higher α-glucosidase inhibition activity than the positive control acarbose (IC50 value of 446.7 µM) with an IC50 value of 120.3 µM. Compound 213 has the potential to be a lead compound for the development of α-glucosidase inhibitors [114]. The production of the terrein derivative asperterrein 214 (Figure 16) was induced by co-culturing endophytic fungi Aspergillus terreus EN-539 and Paecilomyces lilacinus EN-531 of the marine red alga Laurencia okamurai. Compound 214 showed weak antimicrobial activities against Physalospora piricola and Staphylococcus aureus, with MIC values ranging from 32 to 64 μg/mL. Additionally, compound 214 was not detected in the sterile cultures of the two fungi alone [115]. The endophytic fungus Lachnum palmae of Przewalskia tangutica was isolated to halogenated dihydroisocoumarins palmaerones A–F 215–220 (Figure 16) under the guidance of UPLC-ESIMS. The antimicrobial activities of all compounds against five tested pathogens (Cryptococcus neoformans, Penicillium sp., Candida albicans, Bacillus subtilis, and Staphylococcus aureus) were evaluated using the broth microdilution method. Compounds 215–220 showed potent to weak antimicrobial activities against all tested pathogens, with MIC values ranging from 10 to 55 μg/mL. Additionally, compounds 215 and 219 showed moderate inhibition of LPS-induced NO production in RAW264.7 macrophages, with IC50 values of 26.3 μM and 38.7 μM, respectively [116].

Figure 16

Chemical structures of other new compounds.

Over the past few years, plants have been a major source of numerous compounds that possess biological activities; however, this review revealed that most of these compounds were also produced by various endophytes, especially fungi. Therefore, the isolation and development of these compounds as novel drug candidates would be of great importance to the pharmacological industry since endophytes are easy to manage, keep, and work with compared with plants. Thus, we conclude that endophytic fungi may serve as alternative sources of bioactive compounds of pharmacological interest.

All the information about the new compounds have been summarized below in Table 2.

Table 2

Brief summary of new compounds.

Compound	Molecular Formula	Color and Morphology	Endophytic Fungus	Host Plant	Site and Nation	Pharmacological Activity	Ref.
Polyketides Chromones
1	C12H13O6	colorless powder	Botryosphaeria ramosa L29	leaf of Myoporum bontioides	Leizhou Peninsula, China	Displayed acceptable antimicrobial activities against Fusarium oxysporum	[36]
2	C14H15O6	white powder
3	C11H11O5
4	C17H19N3O3S2	yellow crystals	Phaeosphaeria fuckelii	Phlomis umbrosa	Mount Hua, China	Mushroom tyrosinase inhibitory activity	[37]
5	C15H16O7S	yellow powder	Chaetomium seminudum			Showed antifungal activity (5–6); Exhibited radical scavenging activity against DPPH; Showed significant antioxidant activity ((5)	[38]
6	C16H18O7S
7	C16H24O5	colorless oil	Pestalotiopsis fici W106-1	Camellia sinensis	Hangzhou, China	Displayed inhibitory effects on HIV-1 replication in C8166 cells ((7–8); Showed low to moderate cytotoxic activity (9–10); Displayed significant antifungal activity (9)	[39]
8
9	C32H54O6
10	C32H54O6Na
Polyketides α-pyrones
11	C11H14O4	colorless crystals	Neurospora udagawae	shoot of Quercus macranthera		Exhibited moderate antifungal (vs. Rhodoturula glutinis) activity and cytotoxicity against KB3.1 cells (12)	[40]
12	C10H10O4	colorless oil
13	C28H42O4	colorless amorphous powder	Aspergillus niger MA-132	Avicennia marina	Hainan Province, China	Showed potent antifungal and cytotoxic activities	[41]
14
15	C14H22O5	yellow oil	Pestalotiopsis fici	branches of Camellia sinensis (Theaceae)	Hangzhou, China	Displayed significant antifungal against Gibberella zeae	[42]
17	C10H14O4	yellow oil	Aspergillus oryzae	Paris polyphylla var. yunnanensis	Dali, Yunnan Province, China	The biological activities of compounds 17–18 were not tested	[43]
18
19	C11H16O4	yellow gum	Penicillium herque	Cordyceps sinensis	Xiahe, China	Weak cytotoxic activity	[44]
20	C12H16O5
21
Polyketides: Other polyketides
22	C22H35ClO7	white powder	Phoma sp. NTOU4195	Pterocladiella capillacea	Taiwan, China	Showed potent anti-angiogenic activity (22); Exhibited inhibition of nitric oxide production in lipopolysaccharide (LPS)-stimulated RAW264.7 macrophage cells (24)	[45]
23
24
25
26
27	C22H34O6
28	C22H26NO8
29	C24H35NO5	colorless oil	Simplicillium subtropicum SPC3	fresh bark of Duguetia staudtii	Cameroon	Weak cytotoxic activity	[46]
30	C24H35NO6
31	C12H20O3	colorless oil	Cladosporium cladosporioides MA-299	leaves of the mangrove plant Bruguiera gymnorrhiza	Hainan Island, China	Showed potent antimicrobial((vs. Escherichia coli and Staphylococcus aureus) activity and moderate inhibition activity against acetylcholinesterase (33)	[47]
32
33	C12H22O4	pale yellow powder
34	C14H24O5	pale yellow oil
35	C12H20O4	colorless crystals
36	C14H20O5	colorless powder	Aspergillus fumigatiaffnis	Tribulus terestris		Weak antimicrobial activities	[48]
37	C14H12O6Na	white amorphous solid	Alternariaalternata ZHJG5	leaf of Cercis hinensis	Nanjing, China	Exhibited potent antimicrobial activity; Showed significant protective effect against the bacterial blight of rice (37)	[49]
38	C14H12O5Na	white powder
39	C14H12O5Na
40	C29H22O12Na
41	C24H27NO5	brown solid	Peyronellaea sp. FT431	healthy leaf of a Hawaiian indigenous plant, Verbena sp.	Lyon, France	Showed weak to moderate cytotoxic activity (41–42)	[50]
42	C24H26O7
43	C24H26O7
44	C18H20O5
45	C29H22O9	red wine colored lump crystal	Alternaria sp. MG1	Vitis quinquangularis		Showed weak cytotoxicity	[51]
Alkaloids Cytochalasin
46	C22H32N2O5	white amorphous solid	Phomopsis sp. sh917	Fresh stems of I. eriocalyx var. laxiflora	Kunming, China	Significant inhibitory activity against NO production in LPS-induced RAW264.7 cells (46)	[52]
47	C22H33NO4
48
49	C32H40N2O6	colorless amorphous powder	Chaetomium globosum TW1-1	Armadillidium vulgare	Hubei Province, China	Showed potential cytotoxic activities against cancer cell lines (HL-60, A-549, SMMC-7721, MCF-7, and SW-480)	[53]
50	C32H38N2O6
51
52	C32H40N2O6
53	C32H38N2O5	white amorphous powder
54	C32H83N2O6
55	C32H36N2O4
56		colorless amorphous powder
57	C34H42N2O7Na
58	C28H37NO3	white amorphous solid	Diaporthe sp. SC-J0138	Cyclosorus parasiticus (Thelypteridaceae)	Guangdong Province, China	Showed significant cytotoxic activities against four human cancer cell lines (A549, HeLa, HepG2, and MCF-7) (58); Exhibited selective cytotoxic activity (59–62)	[54]
59	C28H37NO
60
61	C28H37NO4
62
63	C25H37NO4	colorless crystal	Cytospora chrysosperma HYQZ-931	Hippophae rhamnoides		Exhibited significant antibacterial activity (63,65)	[55]
64		white amorphous powder
65	C26H41NO5
Alkaloids Indole alkaloids
66	C26H28N3O4	brilliant yellowish powder	Aspergillus sp. YJ191021		Zhejiang Province, China	Exhibited moderate antibacterial activity (66); Displayed notable anti-inflammatory; Exhibited notable cytotoxicity (66–69)	[56]
67	C26H29N3O5	white powder
68	C27H31N3O6Na
69	C27H31N3O6
70	C28H31N3O6
71	C26H31N3O6
72	C30H33NO7	white amorphous powder	Penicillium chrysogenum XNM-12	Leathesia nana	Shandong Province, China	Exhibited moderate antibacterial effects against Ralstonia solanacearum	[57]
73	C23H38N1NaO3	amorphous powder	Hypomontagnella monticulosa Zg15SU	fresh rhizome of Zingiber griffithii Baker	Indonesia	Showed potent cytotoxic activity	[58]
74	C20H22N2NaO4	yellowish powder	Aspergillus lentulus DTO 327G5	Caenagrion	Shanghai, China	Displayed weak to moderate antibacterial activity	[59]
75	C19H21O4N2	white powder
76	C24H25N3NaO3
Alkaloids Diketopiperazine derivatives
77	C20H27N3O3S2Na	white solid powder	Phaeosphaeria fuckelii	Phlomis umbrosa	Mount Hua, China	Showed strong inhibitory effects on mushroom tyrosinase	[60]
78	C26H29N3O5	colorless oil	Paecilomyces variotii EN-291	Grateloupia turuturu	Qingdao Province, China	Exhibited potent antifungal effects	[61]
79	C22H23N3O4
80	C21H25O3N3	yellow powder	Aspergillus sp. 16-5c	leaf of S. apetala	Hainan Island, China	Showed potent to moderate α-glucosidase inhibitory activity (80–81)	[62]
81	C21H23O4N3	white powder
82	C21H23O3N3	yellow powder
83	C21H25O3N3
84	C22H27O3N3
85	C18H15O4N3	white powder
86	C19H24N2O6S	colorless crystals	Penicillium brocae MA-231	Avicennia marina		Displayed moderate to high activities against Staphylococcus aureus	[63]
87	C19H22N2O5S	yellowish solid
88	C20H26N2O6S2	colorless crystals
89	C20H26N2O6S2	colorless solid
90	C20H24N2O6S2
91	C19H18N2O4S	colorless crystals	Penicillium brocae MA-231			Showed moderate antimicrobial activities against S. aureus and Aeromonas hydrophilia	[64]
92	C19H16N2O4S
93	C18H14N2O4
Alkaloids: Other types of alkaloids
94	C21H16N4O2	colorless needles	Penicillium vinaceum (X17)	corm of Crocus sativus	Shanghai, China	Showed weak cytotoxic activities against three human tumor cell lines (A549, LOVO, and MCF-7)	[65]
95	C14H16Br2N2O5	colorless amorphous powder	Acanthodendrilla sp.		Thailand	Exhibited efficient and selective cytotoxic activities against two human tumor cell lines (H292 and HaCaT)	[66]
96
97	C19H20NO3	colorless needles crystal	Penicillium sumatrense GZWMJZ-313	leaf of Garcinia multiflora	Guizhou, China	Showed moderate to weak antimicrobial activities against Staphylococcus aureus, Pseudomonas aeruginosa, and Escherichia coli	[67]
98	C20H24NO3	white powder
99	C20H21NO3
100	C25H29O5N	white powder	Diaporthe sp. SYSUHQ3	fresh branch of the mangrove plant Excoecaria agallocha		Showed potent inhibition activity against Mycobacterium tuberculosis protein-tyrosine phosphatase B	[68]
101	C25H29O5N
Terpenoids Sesquiterpenoids and their derivatives
102	C15H22O3Na	colorless oil	Rhizopycnis vagum Nitaf22	Nicotiana tabacum		Exhibited high selective cytotoxicity against NCI-H1650 and BGC823 cell lines (115); Showed strong phytotoxic activities against radicle growth in rice seedlings (106–107, 113–114)	[70]
103	C15H23O3
104	C15H22O4Na	colorless amorphous solid
105	C15H20O3Na	colorless oil
106	C15H24O3Na
107	C15H22NaO3
108	C15H21O4
109	C15H25O4
110	C15H22O3Na
111	C15H19O5	colorless amorphous solid
112	C15H13O5	brown amorphous solid	Rhizopycnis vagum Nitaf22 Rhizopycnis vagum Nitaf22	Nicotiana tabacum Nicotiana tabacum		Exhibited high selective cytotoxicity against NCI-H1650 and BGC823 cell lines (115); Showed strong phytotoxic activities against radicle growth in rice seedlings (106–107, 113–114)	[70]
113	C15H14O4Na	yellowish oil
114	C17H18NO4	greenish-yellow amorphous solid
115	C14H15NO4	light-yellowish amorphous solid
116	C15H22O3	colorless oil	Trichoderma sp. PR-35	healthy stem of Paeonia delavayi	Yunnan Province, China	Showed moderate to weak antimicrobial activities against Escherichia coli and Shigella sonnei	[69]
117	C15H26O2
118	C15H28O3Na	colorless oil	Fusarium proliferatum AF-04		Lanzhou, China	Displayed weak antimicrobial against Bacillus subtilis, Clostridium perfringens, E. coli, and MRSA	[71]
119	C15H26O2Na
120	C15 H 20 O5	colorless oil	Aspergillus sydowii EN-434	Symphyocladia latiuscula	Qingdao Province, China	Exhibited radical scavenging activity against DPPH	[72]
121	C25H37O4	amorphous powder	Ulocladium sp.		Yunnan Province, China	Showed moderate antimicrobial activities against B. subtilis and multi-drug-resistant S. aureus (121–125); Exhibited high selective cytotoxicity against the HepG2 cell line (125)	[73]
122
123	C26H38O4Na
124	C26H40O5Na
125	C25H34O3Na
126	C15H26O3	colorless crystals	Trichoderma virens QA-8	fresh inner root tissue of the grown medicinal herb Artemisia argyi H. Lév. and Vaniot	Hubei Province, China	Showed significant antimicrobial activities against E. coli	[74]
127		amorphous powder
128		colorless oil
129	C15H24O2
130	C15H26O3	colorless waxy solid
Terpenoids Diterpenoids
131	C20H32O6Na	colorless oil	Diaporthe sp. QYM12	healthy leaves of Kandelia candel	Hainan Province, China	Showed significant anti-inflammatory effects through the inhibition of NO production	[75]
132	C21H28O6	colorless crystals	Phomopsis sp. S12	seed of Illigera rhodantha		Showed excellent inhibitory effects on the production of IL-1β and IL-18; Effects on the NF-κB signaling pathway	[76]
133	C20H26O5	colorless needle crystal	Phomopsis sp. S12	seed of Illigera rhodantha		Exhibited anti-inflammatory activity against the production of IL-1b and IL-6 induced by lipopolysaccharide (LPS) in macrophages	[77]
134	C20H28O4	colorless oil
135	C20H26O6
136	C16H20O5	colorless needles	Botryosphaeria sp. P483	Chinese Herbal Medicine Huperzia serrata	Kunming, China	Showed effective antifungal antifungal activities against Gaeumannomyces graminis, Fusarium solani, and Pyricularia oryza (136); Showed weak nematicidal activities	[78]
137	C16H20O6	colorless solid
138	C20H28O6	white amorphous solid	Smardaea sp. AZ0432	photosynthetic tissue of the moss Ceratodon purpureus	Chiricahua Mountains of southeastern Arizona, USA	Exhibited selective cytotoxicity	[79]
139	C20H16O5	yellowish needles	Pestalotiopsis adusta	Fresh, healthy stems of Clerodendrum canescens	Yandang, Zhejiang Province, China	Demonstrated cytotoxic activities against the HL-60 tumor cell line	[80]
140	C20H34O2	colorless needles	Trichoderma atroviride S361	Cephalotaxus fortunei	Jiande, Zhejiang, China	Bioactivity tests were not performed	[81]
141	C16H16O5	colorless needles	Aspergillus wentii EN-48	unidentified marine brown algal species of the genus Sargassum	Qingdao Province, China	Showed moderate cytotoxic activities against seven human tumor cell lines (NCI-H460, MDA-MB-231, HeLa, MCF-7, SMMC-7721, HepG2, and SW1990)	[82]
142	C16H16O5
143	C16H24O5
Terpenoids Triterpenoids
144	C30H48O	colorless solid	Scleroderma UFSMSc1	Eucalyptus grandis		Showed moderate to weak antifungal activities against Candida albicans and Candida parapsolosis	[84]
145
146
147	C29H46O5	white powder	Acremonium pilosum F47	pedicel of the Chinese medicinal plant Mahonia fortunei	Qingdao Province, China	Displayed effective antimicrobial activities against S. aureus and B. subtili	[85]
148	C30H50O6	yellow amorphous powder	Glomerella sp. F00244	stem of mason pine	Fujian Province, China	Showed weak cytotoxic activity (148)	[83]
149	C31H52O6	white amorphous powder
150	C30H40O6	yellowish needle crystals	Penicillium sp. SWUKD4.1850	healthy branches of Kadsura angustifolia	Yunnan Province, China	Exhibited moderate in vitro cytotoxic activities	[86]
151	C30H40O6	white needle crystals
152	C30H40O6	white amorphous solid
153	C30H41O6
154	C32H44O7	white amorphous powder
155	C30H42O6	white powder
156	C34H46O8	yellow amorphous solid
157	C31H44O6
158	C30H46O6	white amorphous powder
159	C32H50O5	white amorphous powder	Hypoxylon sp. 6269	Artemisia annua		Weak inhibition activity against the HIV-1 integrase (159)	[87]
160	C29H44O4
161	C36H55O7	white amorphous powder	Fusarium sp.	roots of Mentha longifolia	Saudi Arabia	Showed significant antileishmanial activity (161)	[88]
162	C32H51O5
163	C39H55O7
164	C34H53O6	colorless powder	Fusarium sp.	roots of Mentha longifolia	Saudi Arabia	Displayed potent cytotoxic activity towards BT-549 and SKOV-3; Showed potent antileishmanial activities against L. donovani promastigotes	[89]
165	C42H68O7	white amorphous powder
Terpenoids Meroterpenoids
166	C18H26O5	colorless crystal	Guignardia mangiferae A348	Medicinal Plant Smilax glabra	Luofu Mountain Natural Reservation, Guangdong Province, China	Showed weak cytotoxic activities against MCF-7 cell lines(167,169)	[90]
167	C17H22O4
168	C18H28O5	white powder
169	C17H24O4
170	C25H30O5	colorless amorphous powder	Emericella sp. TJ29	root of the plant Hypericum perforatum	the Shennongjia areas of Hubei Province, China	Showed moderate cytotoxic activities against five human tumor cell lines (HL-60, SMMC7721, A549, MCF-7, and SW-480) (172, 173, 175)	[91]
171	C27H34O6	white powder
172	C26H32O6	colorless crystals
173	C25H30O6	colorless crystals
174	C25H32O6	white powder
175	C25H28O6	colorless crystals
176	C31H35O9	yellowish oil	Phyllosticta sp. J13-2-12Y	leaf of Acorus tatarinowii	Guangxi Province, China	Exhibited moderate antimicrobial activities against Staphylococcus aureus 209P, Candida aureus 209P, and Candida albicans FIM709	[92]
177	C31H37O9
178	C31H34O9
179	C27H32O9	white powder	Co-culture Talaromyces purpurogenus H4 and Phanerochaete sp. H2	Handroanthus impetiginosus	Alfenas, Minas Gerais, Brazil.	Showed moderate trypanocidal activity against T. cruzi	[93]
Lactones
180	C13H22O3	colorless gum	Talaromyces assiutensis JTY2	leaf of Ceriops tagal	South China Sea, China	Showed moderate cytotoxic activities against three human cancer cell lines (HeLa, MCF-7, and A549)	[94]
181	C21H34O5	yellow oil	Penicillum polonicum	fruits of Camptotheca acuminata Decne	Wuhan, China	Showed effective glucose uptake activity on rat skeletal muscle myoblast L6 (181); Significantly promoted GLUT4 translocation in L6 cells	[95]
182	C16H28O5	light red oil
183	C24H33NO8	colorless crystal	Chaetomium cupreum	Anemopsis californica	New Mexico, U.S.A.	Showed weak antimicrobial activity against S. aureus	[96]
184			Xylaria curta 92092022		Taiwan, China	Showed moderate antimicrobial activities against Pseudomonas aeruginosa and Staphylococcus aureus; Displayed strongly inhibited lettuce seed germination	[97]
185	C24H34O5	white powder	Lasiodiplodia theobromae ZJ-HQ1	healthy leaves of the marine mangrove Acanthus ilicifolius	South China Sea, China	Exhibited inhibitory effects on lipopolysaccharide-induced nitric oxide production in RAW 264.7 macrophage cells; Showed moderate inhibitory activity against α-glucosidase	[98]
186	C8H10O3		Aspergillus pseudonomiae J1	Euphorbia umbellata (Pax) Bruyns (Euphorbiaceae)	Bahia, Brazil	Showed moderate to weak anti-trypanosomal activity	[99]
187	C10H12O4
188	C10H12O3
Anthraquinones, quinones, and related glycosides
189	C20H19O7	Brilliant yellowish oil	Acremonium vitellinum	Acanthus ilicifolius Linn	Qingdao Province, China	Showed moderate insecticidal activities against the third-instar larvae of Helicoverpa ar-migera	[100]
190	C20H16O7	yellow solid
191	C22H21O7
192	C18H18O8Na	yellow amorphous powder	Phomopsis sp.	Paris polyphyllavar	Yunnan Province, China	Showed significant cytotoxic activities against A549 and PC3 cell lines	[101]
193	C21H20O10	red amorphous powder	Eurotium cristatum EN-220	Sargassum thunbergii	Qingdao Province, China	Showed weak antimicrobial activity against E. coli only; Showed moderate fatal activity against brine shrimp larvae	[102]
194	C18H15O6	orange yellow powder	Aspergillus versicolor	Halimeda opuntia	South Sinai, Egypt	Weak inhibitory activity against hepatitis C virus NS3/4A protease	[103]
195	C12H11O4	red powder
196	C16H11O5	orange powder
197	C16H21O7	red powder	Stemphylium globuliferum	healthy stems of Mentha pulegium	Beni Mellal, Morocco	Showed significant inhibition of proliferation of K562 and A549 cells	[104]
Steroids
198	C27H40O3	white crystals	Phoma sp. SYSU-SK-7		Guangdong Province, China	Exhibited inhibitory effects on lipopolysaccharide-induced nitric oxide production in RAW 264.7 macrophage cells; Showed moderate inhibitory activity against α-glucosidase	[105]
199	C28H41O3	white solid
200	C38H64O4	white amorphous powder	Fusarium sp.	Mentha longifolia	Egypt	Showed moderate cytotoxic activity against human colorectal cancer cell line HCT 116	[106]
201	C28H40O4		Phomopsis sp.	Aconitum carmichaeli	Huize County, Yunnan Province, China	Showed weak antifungal activities against C. albicans and F. avenaceum	[107]
202	C30H48O4
Other types of compounds
203	C20H22O3	yellow oil	Aspergillus sp.	root of Tripterygium wilfordii	Wuhan, China	Showed significant inhibition of LPS-induced IL-1β, TNF-α, and NO production in RAW264.7 cells	[108]
204	C24H26O6
205	C24H26O6	colorless oil
206	C23H24O6
207	C23H24O5	brown powder	Aspergillus flavipes Y-62	stems of plant Suaeda glauca Bunge	Zhoushan coast, Zhejiang province, China	Exhibited antimicrobial activities against the Gram-negative pathogens Pseudomonas aeruginosa and Klebsiella pneumoniae	[109]
208	C23H21O5	white powder	Microsphaeropsis sp.			Showed effective antimicrobial activities against B. megaterium and E. coli	[110]
209	C15H20O2	brown amorphous powder	Emericella sp. XL029	leaf of Panax notoginseng	Shijiazhuang, Hebei province, China	Showed potent antifungal activities against six tested plant pathogenic fungi (Rhi-zoctorzia solani, Verticillium dahliae Kleb, Helminthosporium maydis, Fusarium oxysporum, Fusarium tricinctum, and Botryosphaeria dothidea)	[111]
210	C16H20O4
211	C18H18O6Cl	yellow powder	Diaporthe perseae sp.	stem of Chinese mangrove Pongamia pinnata	Hainan city, China	Showed significant DPPH and ABTS radical scavenging activities	[112]
212	C7H7O4	colorless flake crystal	Aspergillus tubingensis DS37	Decaisnea insignis (Griff.) Hook. f. and Thomson		Showed significant inhibition activities against Fusarium graminearum and Streptococcus lactis	[113]
213	C13H15NO4Na	amorphous powder	Nigrospora sphaerica ZMT05	Oxya chinensis Thunber	Guangdong Province, China.	Showed significant α-glucosidase inhibitory activity	[114]
214	C9H14O2	colorless oil	Co-culture Aspergillus terreus EN-539 & Paecilomyces lilacinus EN-531	Laurencia okamurai	Qingdao, China	Showed weak antimicrobial activities against Physalospora piricola and Staphylococcus aureus	[115]
215	C11H11BrO4	white amorphous powder	Lachnum palmae	Przewalskia tangutica		Exhibited potent to weak antimicrobial activities against Cryptococcus neoformans, Penicillium sp., Candida albicans, Bacillus subtilis, and Staphy-lococcus aureus (215–220); Showed moderate inhibitory effects on NO production in LPS-induced RAW 264.7 cells (215,219)	[116]
216
217	C12H13BrO4
218	C10H9BrO4
219	C11H11BrO5
220	C11H11ClO4

3. Future Prospects and Challenges of Using Endophytic Fungi as an Alternative Source of Plant Bioactive Compounds

Endophytic fungi are hidden and subtle dwellers in several plant tissues and intercellular spaces and can produce diverse chemical structures and efficient, low-toxic new secondary metabolites that were initially thought to be produced by the host plants. The current reports on the biosynthesis of plant metabolites by endophytic fungi, in conjunction with recent research advances in fermentation culture, extraction, isolation, and structure identification techniques, permit us to rapidly uncover new valuable compounds. Generally, fungi are chemically diverse, easily cultured, and biologically active modalities that have great flexibility to be regulated by adding precursors, elicitors, and specific enzymes to effectively increase the quantity and yield of bioactive compounds. Table 3 represents the culture conditions and specific bioactive secondary metabolites and yields produced by various endophytic fungi. Endophytic fungi can convert active compounds of the host plant into more potent derivatives. This makes endophytic fungi an alternative and sustainable source of plant bioactive compounds [117,118]. The search for new compounds in endophytic fungi requires specific theories and ingenious bioprospecting strategies. Along with the continuously growing literature reports, the most promising host plants can be selected. It includes the selection of (A) plants from special habitats or growing in biodiversity-rich areas, including mangrove plants in tropical marine intertidal zones, and (B) medicinal and indigenous plants with ethnopharmacological uses, including Camptotheca acuminata and Ageratina adenophora. These selection criteria provide a reference for the current and future screening of host plants for endophytic fungi with new bioactive compounds [119,120]. This review has summarized 220 new compounds obtained between 2011 and 2021 from endophytic fungi using different culture methods, including the common culture, co-culture with bacteria or other fungi, and the addition of metal ions. These new compounds have unique molecular structures, and these rare structures allow these compounds to possess diverse biological activities, including significant antimicrobial and cytotoxic activities and α-glucosidase inhibition. These compounds have the potential to be modified as pro-drug molecules or directly developed as drugs for treating certain diseases. However, most of the current studies on the activity of new compounds with endophytic fungal sources are limited to in vitro studies; therefore, animal experiments and human intervention clinical trials are needed to further investigate the in vivo activities and mechanisms of action of the new compounds.

Table 3

Culture conditions and yields of bioactive secondary metabolites produced by endophytic fungi.

No.	Endophytic Fungus	Host Plant	Culture Conditions	Secondary Metabolites	Yield	Ref.
1	Hansfordia biophila	Hedychium acuminatum Roscoe	Inoculated in potato glucose broth (PDB) medium and shaken at 120 rpm at 25 °C for 7 days.	Tannin	41.6 μm·mL−1	[121]
2	Aspergillus terreus	Ficus elastica	Inoculated into PDB medium and incubated at 30 °C for 20 days on a rotatory shaker incubator at 140 rpm.	Camptothecin	320 μg/L	[122]
3	Guignardia mangiferae HAA11	Taxus x media	Inoculated into (PDB) medium and incubated at 200 rpm at 28 °C for 5 days.	Paclitaxel	720 ng/L	[123]
4	Papulasora sp.S6	Phellodendron amurense Rupr	Mutagenesis by UV, X-ray rays, and NaNO2, inoculated in PDB medium, and shaken at 100 rpm at 28 °C for 7 days.	Berberine	12.28 mg/L	[124]
5	Actinoplanes teichomyceticus		Improvement of the output of teicoplanin by genome shuffling; Inoculated teicoplanin medium and cultured at 28 °C for 15–20 days.	Teicoplanin	3016 μm·mL−1	[125]
6	Phialocephala fortinii	Podophyllum peltatum	Inoculated in Sabouraud’s dextrose agar (SDA) and cultured at 23 °C for 4–6 weeks.	Podophyllotoxin	189 µg/L	[126]
7	Entrophospora infrequens RJMEF001	Nothapodytes foetida	Inoculated into wheat bran containing Sabouraud’s broth, and incubation was carriedout at 28 ± 2 °C for 28 days.	Camptothecin	503 ± 25 μg/100 g dry cell mass (in Sabouraud broth)	[127]
8	Epicoccum nigrumSZMC 23769	Hypericum perforatum	Fungal isolates were grown in potato dextrose broth (PDB) for 7 days at 25 °C.	Hypericin, Emodin	117.1 μg/mL, 87.7 μg/mL	[128]

Unfortunately, endophytic fungi as new sources of bioactive secondary metabolites encounter various limitations, including the attenuated yield of secondary metabolites due to long-term storage and repeated passages under laboratory culture conditions, silencing of biosynthetic gene clusters or low level of expression (activation of gene clusters depends on environmental factors). Thus, the ability of endophytic fungi to produce new compounds of interest has been underestimated [129]. The expression could be upregulated by physicochemical and genetic manipulation techniques to increase the production of specific metabolites in endophytic fungi and to produce analogs of new active secondary metabolites. Methods including the OSMAC strategy (activation of silent biosynthetic gene clusters mediated by changes in medium composition, temperature, and aeration efficiency to produce desired metabolites), co-culture (mimicking natural ecosystems and triggering silent gene clusters to promote metabolite secretion and enhance bioactive metabolite production by microbial interaction-induced stress responses), and chemical epigenetic modification methods have been used to isolate new compounds. It was found that the addition of micromolar or even nanomolar small-molecule chemicals to cultures inhibits or activates relevant enzymes and remodels the fungal epigenome to increase the diversity of its secondary metabolites, including DNA methyltransferases (DNMTs) and histone deacetylase inhibitors (HDACs) [130,131]. The addition of epigenetic modifiers (5 μM SAHA and 10 μM AZA) to the endophytic fungus Xylaria psidii isolated from leaves of Vitis vinifera showed elevated resveratrol concentrations of 52.32 μg/mL and 48.94 μg/mL, respectively, by HPLC analysis (control concentration was 35.43 μg/mL). The treatments with 5 μM SAHA and 10 μM AZA showed stronger antioxidant activity with 30.92% and 33.82% DPPH radical scavenging, respectively, compared to the wild strain (19.26%) [132]. Unlike the chemical epigenetic modification methods reported, introducing exogenous substances as precursors into the cultures, including methyl jasmonate, causes the production of new compounds containing their structural units [133]. However, the addition of host plant components to the culture to induce the production of new compounds has rarely been reported. Additionally, it is necessary to elucidate the pathways by which endophytic fungi biosynthesize secondary metabolites, including the enzymes and genes involved via “omics” techniques—genomics, transcriptomics, and metabolomics—in regulating and manipulating the biosynthetic process to increase the number of new compounds [134].

4. Conclusions

Pharmaceutical chemists are turning their focus on the development of safe, efficient, and low-toxic new drugs from natural sources. Endophytic fungi may serve as renewable sources of novel bioactive compounds with pharmacological activities, as the number of new compounds to be isolated in the future tends to increase exponentially and rapidly. In addition, numerous studies have also reported that these bioactive compounds isolated from the endophytic fungi are also present in plants and have similar biological activities as the compounds from plant sources. Therefore, we conclude that endophytic fungi may be the best alternative for harnessing pharmacological bioactive compounds for the development of drugs for both human and animal use. Hence, there is a need for the identification of more compounds with pharmacological activity from endophytic fungi and elucidate their mechanisms of action through biological, pharmacodynamic, biochemical, bioinformatics, and pre-clinical approaches.