- Original Article
- Open Access
Antimicrobial and iNOS inhibitory activities of the endophytic fungi isolated from the mangrove plant Acanthus ilicifolius var. xiamenensis
Botanical Studiesvolume 60, Article number: 4 (2019)
Acanthus ilicifolius var. xiamenensis (Acanthaceae) is an old world mangrove species and has long been used as a folk remedy for treating various ailments in traditional medicine. The nature source of A. ilicifolius var. xiamenensis is now in short supply because of the urban development and habitat destruction. To better utilize this resource, biodiversity and bioactivity of endophytic fungi isolated from A. ilicifolius var. xiamenensis were investigated.
A total of 168 fungal isolates were cultured from leaves and stems of the mangrove plant collected in January (winter) and July (summer) 2014 at Kinmen County, Taiwan. Spent culture extract of 28 isolates were found to have bioactivities against one of the following pathogenic microorganisms: the bacteria Bacillus subtilis, Staphylococcus aureus (Gram-positive) and Escherichia coli (Gram-negative) and the fungi Candida albicans and Cryptococcus neoformans. These positive extracts were mostly active against the Gram-positive bacteria and C. albicans. Corynespora cassiicola NTOU4889 and Xylaria sp. NTOU4900 inhibited growth of all 3 test bacteria whereas Phellinus noxius NTOU4917 inhibited both test fungi. A further anti-inflammatory study of culture extracts of these 28 isolates revealed that extracts with a high iNOS inhibition caused a low viability of cells, and those with a low iNOS inhibition had a high cell viability. Three extracts showed low cytotoxicity (i.e. > 100% cell viability) and high iNOS inhibition (< 15% of NO production) of cells and they were Phoma sp. 2 NTOU4338, Nodulisporium sp. NTOU4868 and Guignardia sp. NTOU4871.
These results indicate that the endophytic fungi associated with A. ilicifolius var. xiamenensis can be a potential source of novel natural active substance.
With the emergence of antibiotic-resistant bacteria, finding new antibiotic drugs is in dire need (Strobel 2002; Guo et al. 2008). Over the years, medicinal plants have been explored for bioactive substances with anti-bacterial, anti-fungal, anti-cancer and/or anti-viral activities, for example, Paclitaxel (generic name Taxol) (Lin et al. 2007). Paclitaxel, the most famous natural-sourced cancer drug in the world, is derived from the bark of the Pacific yew tree (Taxus brevifolia) and is used to treat ovarian, breast, lung, pancreatic and other cancers. Stierle et al. (1993) isolated the fungus Taxomyces andreanae from T. brevifolia, which was found to produce taxol and this discovery provided a more feasible and practical way to mass-produce this compound. As an increasing number of endophytic fungi with novel metabolites of pharmaceutical importance has been isolated from medicinal plants, these plants may serve as a reservoir of untold numbers of endophytic microorganisms capable of synthesizing bioactive compounds that may act against plant pathogens (Cui et al. 2011). In the past, soil-borne microorganisms were the major sources of medicinal compounds. Currently, endophytic fungi from medicinal plants have been one of the main targets for drug leads, and many undescribed endophytic fungal species may be the sources of new medicines (Huang et al. 2001; Guo et al. 2008; Cui et al. 2011).
Around 50–70 species of mangrove plants are distributed in tropical and subtropical climates in the world (FAO 2007). Several mangrove plants have been studied for their endophytic fungal association, such as A. ilicifolius, Aegiceras corniculatum, Arthrocnemum indicum, Avicennia officinalis, Av. marina, Bruguiera gymnorrhiza, Ceriops decandra, Excoecaria agallocha, Kandelia candel, Lumnitzera racemosa, Rhizophora apiculata, Rh. mucronata, Sesuvium portulacastrum, Sonneratia caseolaris, Suaeda fruticosa and Su. maritima (Fisher and Petrini 1987; Purkayastha and Pal 1996; Suryanarayanan et al. 1998; Suryanarayanan and Kumaresan 2000; Kumaresan and Suryanarayanan 2001; Okane et al. 2001; Ananda and Sridhar 2002). The Ascomycota is dominant with many asexual species while the Basidiomycota is uncommon (Sebastianes et al. 2013).
Acanthus ilicifolius var. xiamenensis (Acanthaceae) is an old world mangrove species and characterized by spiny leaves, spicate terminal inflorescences, two bracteoles and uniform anthers (Duke 2006). This plant has long been used as a folk remedy for treating various ailments in traditional medicine (Ragavan et al. 2015; Saranya et al. 2015). Various parts of the plant have been used as crude drugs for treatment of asthma, diabetes, dyspepsia, leprosy, hepatitis, paralysis, snake bite, rheumatoid arthritis and diuretic (Bandaranayake 1998). In Taiwan, the only distribution of A. ilicifolius var. xiamenensis is at the Kinmen Island. Little is known on the endophytic fungi associated with this plant and therefore, we initiated a study on the diversity of endophytic fungi of A. ilicifolius var. xiamenensis and their anti-microbial and anti-inflammatory activities. In the present study, we report the antimicrobial and iNOS inhibitory activities of the endophytic fungi isolated from leaves and stems of A. ilicifolius var. xiamenensis.
Endophytic fungi of A. ilicifolius var. xiamenensis
One hundred and sixty-eight isolates of endophytic fungi were isolated from 95 leaves of A. ilicifolius var. xiamenensis (5 trees) collected in January and July 2014 and identified based on sequencing of a region of the rDNA spanning from 18S to 28S including ITS1 (internal transcribed spacer 1), ITS2 and 5.8S rDNA and comparing these sequences with those in the GenBank using nucleotide BLAST search. (Chi et al. unpublished results). These fungi were subcultured on malt extract agar (MEA) plates for 1 week (Table 1). Two agar plugs (8 mm in diameter) were made from the growing edge of the colonies and inoculated into 100 ml GYP broth (0.2 g peptone, 1 g dextrose, 0.1 g yeast extract) in 250 ml Erlenmeyer flasks. The flasks were incubated for 14 days at 25 °C on an orbital shaker at 220 rpm/min.
Secondary metabolite extraction
After incubation, the mycelia were separated from the spent culture broth by filtration. The filtered broth was partitioned two times with an equal volume of recycled ethyl acetate (AcOEt) and concentrated in vacuum to dryness. The solid AcOEt extracts were dissolved in sterilized water to a final concentration of 0.5 mg/ml for the antimicrobial assays described below.
Test indicator organism
The test indicator bacteria included Gram-negative Escherichia coli and two Gram-positive Bacillus subtilis and Staphylococcus aureus, all available at the Institute of Fisheries Science, National Taiwan University. All bacteria were cultured in Luria broth (LB) at 37 °C for 18 h and maintained on LB agar. Two test indicator fungi, namely Candida albicans and Cryptococcus neoformans, obtained from Faculty of Kinmen County Health Bureau, were used in the study. Both fungi were cultured in Yeast Mold (YM) broth at 30 °C for 48 h and maintained on YM agar.
The agar well diffusion method was used to evaluate antimicrobial activity of the spent culture broth of the endophytic fungi (Rios et al. 1988; Cui et al. 2011). The bacteria were diluted using beef extract peptone (BEP) medium (5 g beef extract, 5 g NaCl, 10 g peptone, 15 g agar, 1 L of sterilized water) to give a concentration of 1 × 106 bacteria/ml and poured into a Petri dish (9 cm diameter) containing BEP agar medium. Test fungi were spread evenly on the surface of YM agar plates, and incubated for 3–5 days at 25 °C. Cell concentrations of the test fungi were diluted using molten Sabouraud agar (SA) medium to 1 × 105 spores/ml, and 10 ml of this diluted medium were poured into a Petri dish containing 8 ml of solidified SA medium. A flame-sterilised cork borer was used to make circular wells (7.8 mm in diameter) in the BEP and SA agar. Fungal extracts (40 μl) with a final concentration of 0.5 mg/ml were added into the wells. After incubation at 37 °C for 24 h and at 25 °C for 48 h for bacteria and fungi, respectively, antibacterial and antifungal activities were measured in terms of diameter of the inhibition zone in triplicates.
Nitrite production and cell viability assay were used to assess the effects of the fungal extracts on LPS-induced NO production (Wang et al. 2007). The ethyl acetate soluble fraction, two positive controls [Nω-nitro-l-arginine (L-NNA, a non-selective iNOS inhibitor) and aminoguanidine (a specific inhibitor of iNOS)] and the vehicle (0.1%, DMSO) were added to the RAW 264.7 cells in the presence of LPS (200 ng/mL). Nitrite formation and cell viability were measured with the Griess reagent and the redox indicator Alamar Blue, respectively (Wang et al. 2007).
Spent culture extract of the 168 endophytic fungi isolated from A. ilicifolius var. xiamenensis was tested for their antimicrobial and anti-inflammatory activities. A total of 28 isolates (16.67%) of the tested endophytic fungi showed antimicrobial activities to at least one indicator organism (Table 1). Within each season, 9 (11.54%) active isolates out of 78 isolates were cultured from winter and 19 (21.11%) out of 90 isolates from summer (Fig. 1). Seven isolates were active against three indicator organisms, 7 against two indicator organisms and 14 against one indicator organisms. No extracts were able to act against all test bacteria and fungi.
Twenty (11.90%) and seventeen (10.12%) extracts were active against the Gram-positive B. subtilis and S. aureus, respectively (Fig. 2). However, only 4 (2.38%) extracts were active against the Gram-negative bacterium E. coli. Few extracts were active against the test fungal pathogens; 5 (2.98%) and 3 (1.79%) extracts showed anti-fungal activity against C. albicans and C. neoformans, respectively.
Concerning the isolates affiliated with the Ascomycota, the Xylariales (Nodulisporium sp. NTOU4868 and Xylaria sp. NTOU4900) were only active against the tested bacteria but not the fungal pathogens, and the same is true for the Amphisphaeriales, the Botryosphaeriales, the Capnodiales, the Dothideales, the Hypocreales, the Mycosphaerellales and the Pleosporales (Table 1). Most extracts were active against the Gram-positive bacteria, but only the extracts of Didymella sp. NTOU4354 and NTOU4878, Corynespora cassiicola NTOU4889 and Xylaria sp. NTOU4900 were active against E. coli. Only the ascomycetous orders Diaporthales, Glomerellales, the basidiomycetous orders Hymenochaetales and Polyporales were able to inhibit growth of the pathogenic fungi, especially C. albican. Growth of C. neoformans were only inhibited by extracts of Diaporthe endophytica NTOU4920 (Diaporthales), Phellinus noxius NTOU4917 (Hymenochaetales) and Tinctoporellus epimiltinus NTOU4916 (Polyporales). For C. albicans, the extracts of Colletotrichum spp., Phellinus noxius NTOU4917 and Phomopsis sp. 2 NTOU4918 were active against it.
The 28 isolates with anti-microbial activity were further tested for their anti-inflammatory activity through Griess (nitric oxide production) and Alamar Blue (cell viability) assays and the results are shown in Table 1 and Fig. 3. The highest value (% of vehicle) of Griess assay was 155.02 (Phellinus noxius NTOU4917), followed by 138.82 (Cladosporium sp. 2 NTOU4352), whereas the lowest was Alternaria alternata NTOU4330 and Nodulisporium sp. NTOU4868 (Fig. 3a). The values (% of vehicle) of Alamar Blue assay ranged from 0 (Alternaria alternata NTOU4330) to 114.35 (Phoma sp. 2 NTOU4338) (Fig. 3b). Generally, extracts with high iNOS inhibition (i.e. low NO production) also caused low viability of cells, except Nodulisporium sp. NTOU4868 and the reverse is true, i.e. low iNOS inhibition and high cell viability. Low (< 10%, % of vehicle) nitric oxide (NO) production was found for cells treated with extracts of six isolates: Alternaria alternata NTOU4330, Nodulisporium sp. NTOU4868, Corynespora cassiicola NTOU4889, Didymella sp. NTOU4878, Pseudocercospora nymphaeaceae NTOU4893 and Colletotrichum sp. 1 NTOU4370; no NO production was in fact produced by the first two isolates (Fig. 3a). On the other hand, high (> 100%, % of vehicle) NO production was recorded from cells of Hortaea werneckii NTOU4320, Cladosporium sp. 2 NTOU4352 and Phellinus noxius NTOU4917. For cell viability, 23 of the 28 test extracts showed high cell viability (> 89.56%, % of vehicle) (Table 1, Fig. 3b). No cells were viable when they were treated with extract of Alternaria alternata NTOU4330. Low cell viability (3.18%) was also observed in cells treated with extract of Pseudocercospora nymphaeacea NTOU4893. Three extracts showed low cytotoxicity (i.e. > 100% cell viability) and high iNOS inhibition (< 15% of NO production) of cells and they were Phoma sp. 2 NTOU4338, Nodulisporium sp. NTOU4868 and Guignardia sp. NTOU4871.
This is the first report that fungal endophytes associated with A. ilicifolius var. xiamenensis at Kinmen have been found to possess the potential of the iNOS inhibitory and antimicrobial activity. Acanthus ilicifolius var. xiamenensis and its congeners are widely used in traditional medicine (Saranya et al. 2015). Acanthus montanus is used in the treatment of diseases such as backache, cough, rheumatic pains and chest pain (Adeyemi et al. 2005), and pain, female infertility (Thierry et al. 2011). The methanolic fraction of A. ilicifolius leaf extract produced significant inhibition of rat paw oedema (Adeyemi et al. 2005). Endophytic fungi isolated from Acanthus have also been shown to have anti-microbial properties (Maria et al. 2005; Chen et al. 2007). In this study, anti-microbial and anti-inflammatory properties of spent culture extracts of 168 endophytic fungi isolated from surface-sterilised leaves and stems of A. ilicifolius var. xiamenensis were examined. These extracts were mostly active against the Gram-positive B. subtilis (20 active extracts) and S. aureus (17), in contrast to only 4 active extracts against the Gram-negative bacterium E. coli. These results are in agreement with reports of anti-bacterial activity of endophytic fungi from mangrove plants showing stronger activities against Gram-positive over Gram-negative bacteria (Chareprasert et al. 2010; Ebrahimia et al. 2010). This difference of anti-bacterial activity between Gram-positive and Gram-negative bacteria might be due to their differences in cell wall composition. The outer layer of cell wall of Gram-negative bacteria composes of lipopolysaccharide, in contrast to a thick layer of peptidoglycan in Gram-positive bacteria. Ethyl acetate extracts comparatively less polar natural products than other solvents such as methanol (Borquaye et al. 2016), suggesting that less polar natural products might be responsible for the anti-microbial activity of the majority of the extracts observed against Gram-positive bacteria in this study. Corynespora cassiicola NTOU4889 and Xylaria sp. NTOU4900 showed activity to all test pathogenic bacteria in this study. An endophytic Xylaria sp. from the mangrove A. ilicifolius in Thailand also had anti-bacterial properties against both Gram-positive and Gram-negative bacteria (Chareprasert et al. 2010). The Xylariales is known to produce anti-bacterial compounds (Xu et al. 2015).
Generally, the extracts of the spent culture of the isolated fungi showed weak anti-fungal activity towards the two test fungal pathogens. Two crude extracts out of six fungi isolated from A. ilicifolius var. xiamenensis using submerged fermentation showed anti-fungal activity against C. albicans, while anti-fungal activity against C. albidus was shown after these extracts were partially purified and they suggested a possible interference between different active principles in the crude extracts. Whether the same reason caused a weak anti-fungal activity by the fungal extracts in this study requires further studies (Maria et al. 2005).
Crude extracts of many fungi in this study showed comparable high iNOS inhibition activity but some also with high cell toxicity. Three crude extracts (Phoma sp. 2 NTOU4338, Nodulisporium sp. NTOU4868 and Guignardia sp. NTOU4871) showed high iNOS inhibition and low cytotoxicity and these extracts should be fractionated to determine the active chemical constituents. In a similar research, Chen et al. (2017) reported that culture extracts of the endophytic fungus Lasiodiplodia theobromae isolated from A. ilicifolius showed anti-inflammatory activities and they isolated some active components from the extracts including Lasiodiplactone A, an unprecedented lactone that possesses a unique tetracyclic system. Compounds such as meroterpenoid identified from Aspergillus terreus H010, an endophytic fungus from Kandelia obovata, also exhibited anti-inflammatory activities (Liu et al. 2017). Results from these reports and those from our study strongly support the view that endophytic fungi of mangrove plants are promising sources of natural bioactive compounds (Stierle et al. 1993; Strobel et al. 1997; Strobel and Daisy 2003; Chen et al. 2016).
Figure 4 shows the percentage of fungi (at the ordinal level) with antimicrobial activities, calculated from the original 168 cultures isolated from leaves of A. ilicifolius var. xiamenensis. The highest percentages were found in Mycosphaerellales (50.00%), following by Amphisphaeriales (33.33%), Xylariales (28.57%) (Ascomycota) and Hymenochaetales (33.33%) (Basidiomycota); the lowest in Diaporthales (11.76%), Dothideales (11.11%) (Ascomycota) and Polyporales (8.70%) (Basidiomycota). Future screening of bioactive substances from endophytic fungi of mangrove plants can focus on the four orders of fungi with a higher likelihood of finding fungi with anti-microbial and anti-inflammatory activities. However, Moron et al. (2018) found that culture extracts of taxa of the Hypocreales (Fusarium, Trichoderma) isolated from roots of mangrove plants produced good antimicrobial activities against Gram-positive bacteria. In another study, Handayani et al. (2017) found that culture extracts of the endophytic Eurotiales (Aspergillus spp.) isolated from Sonneratia grifithii produced good antimicrobial activities against S. aureus and E. coli.
In this study, 28 out of 168 endophytic isolates of fungi cultured from leaves and stems of A. ilicifolius var. xiamenensis were found to have various levels of anti-microbial and anti-inflammatory activities, which may be of pharmaceutical potentials. Endophytes are omnipresent in plants, with diversity dependent on host species and location (Tan and Zou 2001). Endophytic fungi of mangrove plants may include one to several taxa that are only adapted to each of these plant species (Schulz and Boyle 2005). The largest area and highest diversity of mangrove region are found in Asia (FAO 2007), suggesting that there is a high diversity of endophytic fungi in Asia, representing an untapped resource for bioactivity screening (Huang et al. 2014).
The present study demonstrates that the mangrove plant support wide spectrum of endophytes with significant bioactive potential. Thus, concerted efforts should be carried out for bioprospection in the A. ilicifolius var. xiamenensis to tap and conserve the microbial resources of this important biodiversity and utilize their potential for human welfare.
Adeyemi OO, Okpo SO, Onakade AA (2005) Anti-inflammatroy activity of the mehanolic extract of Acanthus montanus. West Afr J Pharmacol Drug Res 21:13–17
Ananda K, Sridhar KR (2002) Diversity of endophytic fungi in the roots of mangrove species on the west coast of India. Can J Microbiol 48:871–878
Bandaranayake WM (1998) Traditional and medicinal uses of mangroves. Mangr Salt Marshs 2:133–148
Borquaye LS , Darko G, Oklu N, Anson-Yevu C, Ababio A, Li G (2016) Antimicrobial and antioxidant activities of ethyl acetate and methanol extracts of Littorina littorea and Galatea paradoxa. Cogent Chem. https://doi.org/10.1080/23312009.2016.1161865
Chareprasert S, Piapukiew J, Whalley AJS, Sihanonth P (2010) Endophytic fungi from mangrove plant species of Thailand: their antimicrobial and anticancer potentials. Bot Mar 53:555–564
Chen G, Zhu Y, Wang HZ, Wang SJ, Zhang RQ (2007) The metabolites of a mangrove endophytic fungus, Penicillium thomii. J Asian Nat Prod Res 9:159–164
Chen YS, Chang HS, Cheng MJ, Chan HY, Wu MD, Hsieh SY, Wang HC, Chen IS (2016) New chemical constituents from the endophytic fungus Xylaria papulis cultivated on Taiwanese Lepidagathis stenophylla. Rec Nat Prod 10(6):735–743
Chen S, Liu Z, Liu H, Long Y, Chen D, Lu Y, She Z (2017) Lasiodiplactone A, a novel lactone from the mangrove endophytic fungus Lasiodiplodia theobromae ZJ-HQ1. Org Biomol Chem 15(30):6338–6341
Cui JL, Guo SX, Xiao PG (2011) Antitumor and antimicrobial activities of endophytic fungi from medicinal parts of Aquilaria sinensis. J Zhejiang Univ-Sci B 12(5):385–392
Duke NC (2006) Australia’s mangroves: the authoritative guide to Australia’s mangrove plants. University of Queensland, Brisbane, p 200
Ebrahimia A, Asghariana S, Habibianb S (2010) Antimicrobial activities of isolated endophytes from some Iranian native medicinal plants. Iranian J Pharm Sci 6:217–222
FAO (2007) The World’s Mangroves 1980–2005. FAO Forestry Paper No. 153. Rome, Italy. P. 77
Fisher PJ, Petrini O (1987) Location of fungal endophytes in tissues of Suaeda fruticosa: a preliminary study. Trans Br Mycol Soc 89(2):246–249
Guo B, Wang Y, Sun X, Tang K (2008) Bioactive natural products from endophytes: a review. Appl Biochem Micro 44(2):153–158
Handayani D, Rivai H, Hutabarat M, Rasyid R (2017) Antibacterial activity of endophytic fungi isolated from mangrove plant Sonneratia griffithii Kurz. J Appl Pharm Sci 7(4):209–212
Huang Y, Wang J, Li G, Zheng Z, Su W (2001) Antitumor and antifungal activities in endophytic fungi isolated from pharmaceutical plants Taxus mairei, Cephalataxus fortunei and Torreya grandis. FEMS Immunol Med Microbiol 31:163–167
Huang MY, Zhong LJ, Wang F, Liu QY, Zhang YH (2014) Chemical constituents from the roots of Acanthus ilicifolius var. xiamenensis. Biochem Syst Ecol 55:145–147
Kumaresan V, Suryanarayanan TS (2001) Occurrence and distribution of endophytic fungi in a mangrove community. Mycol Res 105:1388–1391
Lin X, Lu CH, Huang YJ, Zheng ZH, Su WJ, Shen YM (2007) Endophytic fungi from a pharmaceutical plant, Camptotheca acuminata: isolation, identification and bioactivity. World J Microbiol Biotechnol 23:1037–1040
Liu Z, Liu H, Chen Y, She Z (2017) A new anti-inflammatory meroterpenoid from the fungus Aspergillus terreus H010. Nat Prod Res 13:1–5
Maria GL, Sridhar KR, Raviraja NS (2005) Antimicrobial and enzyme activity of mangrove endophytic fungi of southwest coast of India. J Agric Technol 1:67–80
Moron LS, Lim YW, dela Cruz TEE (2018) Antimicrobial activities of crude culture extracts from mangrove fungal endophytes collected in Luzon Island, Philippines. Philipp Sci Lett 11:28–36
Okane I, Nakagiri A, Ito T (2001) Assemblages of endophytic fungi on Bruguiera gymnorrhiza in the Shiira River Basin, Iriomote Is. IFO Res Commun 20:41–49
Purkayastha RP, Pal AK (1996) New foliicolous fungi from Indian mangroves (Sunderbans). Indian Phytopath 49(1):9–21
Ragavan P, Saxena A, Mohan PM, Jayaraj RSC, Ravichandran K (2015) Taxonomy and distribution of species of the genus Acanthus (Acanthaceae) in mangroves of the Andaman and Nicobar Islands. India. Biodiversita 16(2):225–237
Rios JL, Recio MC, Villar A (1988) Screening methods for natural products with antimicrobial activity: a review of the literature. J Ethnopharmaco 23:127–149
Saranya A, Ramanathan T, Kesavanarayanan KS, Adam A (2015) Traditional medicinal uses, chemical constituents and biological activities of a mangrove plant, Acanthus ilicifolius Linn.: a brief review. American-Eurasian. J Agric Environ Sci 15(2):243–250
Schulz B, Boyle C (2005) The endophytic continuum. Mycol Res 109(6):661–686
Sebastianes FLS, Dumaresq ASR, Lacava PT, Harakava R, Azevedo JL, Melo IS, Pizzirani-Kleiner AA (2013) Species diversity of culturable endophytic fungi from Brazilian mangrove forests. Curr Genet 59:153–166
Stierle A, Strobel GA, Stierle D (1993) Taxol and taxane production by Taxomyces andreanae, an endophytic fungus of Pacific yew. Science 260:214–216
Strobel G (2002) Rainforest endophytes and bioactive products. Crit Rev Biotechnol 22(4):315–333
Strobel G, Daisy B (2003) Bioprospecting for microbial endophytes and their natural products. Microbiol Mol Biol Rev 67:491–502
Strobel GA, Torczynski R, Bollon A (1997) Acremonium sp.-a leucinostatin A producing endophyte of European yew (Taxus baccata). Plant Sci 128:97–108
Suryanarayanan TS, Kumaresan V (2000) Endophytic fungi of some halophytes from an estuarine mangrove forest. Mycol Res 104:1465–1467
Suryanarayanan TS, Kumaresan V, Johnson JA (1998) Foliar fungal endophytes from two species of the mangrove Rhizophora. Can J Microbiol 44:1003–1006
Tan RX, Zou WX (2001) Endophytes: a rich source of functional metabolites. Nat Prod Rep 18(4):448–459
Thierry DTA, Acha AE, Paulin N, Aphrodite C, Pierre K, Tzoacha A (2011) Subacute toxicity study of the aqueous extract from Acanthus montanus. Electron J Biol 7(1):11–15
Wang GJ, Chen SM, Chen WC, Chang YM, Lee TH (2007) Selective inducible nitricoxide synthase suppression by new bracteanolides from Murdannia bracteata. J Ethnopharmacol 112:221–227
Xu L, Meng W, Cao C, Wang J, Shan W, Wang Q (2015) Antibacterial and antifungal compounds from marine fungi. Mar Drugs 13:3479–3513
WCC and KLP took charge of experimental design. The leaves of Acanthus ilicifolius var. xiamenensis collected in Kinmen were carried out by WCC. WCC and WLC isolated and identified endophytic fungi. THL and GJW performed the determination of antioxidant activity and interpretation of results. WCC and KLP interpretation of results, phytochemical screening, wrote and finalized the manuscript. All authors read and approved the final manuscript.
The first author thanks the members in Ka-Lai Pang’s laboratory for their assistance with all taxonomy works.
The authors declare that they have no competing interests.
Availability of data and materials
The specimens of fungi after identified were deposited at the Institute of Marine Biology, National Taiwan Ocean University, Keelung, Taiwan. All data generated during the study are interpreted in the manuscript.
Consent for publication
Ethics approval and consent to participate
Not applicable. All applicable international, national, and/or institutional guidelines for the care and use of animals were followed.
Financial support from the Kinmen County Fisheries Research Institute through the Grant Number 106G019-1 to W.-C. Chi.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.