Bioactive Metabolites from the Deep Subseafloor Fungus Oidiodendron griseum UBOCC-A-114129

Four bioactive compounds have been isolated from the fungus Oidiodendron griseum UBOCC-A-114129 cultivated from deep subsurface sediment. They were structurally characterized using a combination of LC–MS/MS and NMR analyses as fuscin and its derivatives (dihydrofuscin, dihydrosecofuscin, and secofuscin) and identified as polyketides. Albeit those compounds were already obtained from terrestrial fungi, this is the first report of their production by an Oidiodendron species and by the deepest subseafloor isolate ever studied for biological activities. We report a weak antibacterial activity of dihydrosecofuscin and secofuscin mainly directed against Gram-positive bacteria (Minimum Inhibitory Concentration (MIC) equal to Minimum Bactericidal Concentration (MBC), in the range of 100 μg/mL). The activity on various protein kinases was also analyzed and revealed a significant inhibition of CDC2-like kinase-1 (CLK1) by dihysecofuscin.


Introduction
The ocean harbors a tremendous diversity of habitats, ranging from coastal waters to the deep biosphere, where microorganisms, through their biotic and abiotic interactions, are the major actors of the biogeochemical processes [1,2]. Bacteria, Archaea, and protists are the most commonly documented microorganisms in the marine environment. However, recent studies strongly support the idea that marine microbial communities also host fungi as an important component in different kinds of habitats, including the deep biosphere [3]. Deep subseafloor sediment microbial communities are in constant interactions though the production of a wide array of secondary metabolites, as recently revealed using metatranscriptomics [4,5]. Given that a large number of marine microorganisms can produce a wide array of bioactive metabolites and has consequently received a great amount of attention in the search for natural compounds [6][7][8], the deep biosphere appears to remain an untapped reservoir.
Recently, an exhaustive culture-based approach allowed us to isolate 183 deep subsurface marine fungi [3]. An antimicrobial screening on 110 of those fungal isolates highlighted that 33% of the the assayed strains had antimicrobial properties [9]. Among those 110 fungal isolates, 14 were considered as promising based on their antimicrobial activities, and finally the strain Oidiodendron griseum CB_36 UBOCC-A-114129 (isolated at 765 m below the sea floor) was selected for further investigation since it seemed to be the bioactive strain with the deepest origin known to date.
In this study, the bioactive metabolites of O. griseum CB_36 were investigated using a bioguided fractionation. Four antimicrobial compounds have been characterized using Nuclear Magnetic Resonance (NMR): fuscin (1), dihydrofuscin (2), dihydrosecofuscin (3), and secofuscin (4). Surprisingly, although those structures have been known for years from terrestrial fungi [10,11], no biological activity has been ever described to the best of our knowledge for secofuscin and dihydrosecofuscin.
Antimicrobial resistance represents an increasing threat jeopardizing global public health. The antibiotic resistance crisis has been partly attributed to the lack of new drug development by the pharmaceutical industry. The "old" chemical structures discovered in the golden age of antibiotics and abandoned because of their toxicity or lack of efficiency, such as polymyxins, fosfomycin, fusidic acid, or chloramphenicol, are currently being re-investigated for therapeutic use [12]. Therefore, we re-analyzed biological properties of fuscin and its derivatives using recent technologies. We describe herein their antibacterial activity but also their ability to inhibit protein kinase activity. Our results suggest that these "old" known structures may not be obsolete for biotechnological applications and notably for human therapeutics.

Purification and Characterization of the Bioactive Compounds Produced by Oidiodendron griseum UBOCC-A-114129
Antimicrobial activities were only recovered in the F10-90 extract supporting previous data [9]. The F10-90 extract was afterwards analyzed by Reversed Phase-High-Performance Liquid Chromatography (RP-HPLC) ( Figure 1). Fractions were collected along the elution, freeze-dried, resolubilized in 20% Acetonitrile (ACN), and assayed for antimicrobial activity. Only, three fractions eluted from 24 to 32 min exhibited antimicrobial activity against Enterococcus faecalis ( Figure 1).

Kinetics of Fuscin Derivative Production
The fungal biomass and the production of fuscin derivatives were quantified over time ( Figure 3). Fuscin and its derivatives were only detected when O. griseum UBOCC-A-114129 reached the stationary phase of fungal growth. Fuscin and its derivatives were detected after 7 days of culture at 25 °C and their production increased and achieved a maximal production after 18 days of culture. To date, the ecological role of these compounds is still unknown. Nevertheless, such a constitutive production during the stationary phase is commonly described for antimicrobial metabolites, such as citrinin produced by Penicillium chrysogenum [14]. Interestingly, fuscin and its derivatives were clearly the main amphiphilic metabolites produced by the strain of O. griseum since they represented almost 68% of the area of the chromatogram.

Kinetics of Fuscin Derivative Production
The fungal biomass and the production of fuscin derivatives were quantified over time ( Figure 3). Fuscin and its derivatives were only detected when O. griseum UBOCC-A-114129 reached the stationary phase of fungal growth. Fuscin and its derivatives were detected after 7 days of culture at 25 • C and their production increased and achieved a maximal production after 18 days of culture. To date, the ecological role of these compounds is still unknown. Nevertheless, such a constitutive production during the stationary phase is commonly described for antimicrobial metabolites, such as citrinin produced by Penicillium chrysogenum [14].

Antimicrobial Activity
We investigated the antimicrobial activity of secofuscin and dihydrosecofuscin since these metabolites (HPLC fractions) exhibited antimicrobial activity against E. faecalis. Their minimal inhibitory concentrations (MICs) were defined in accordance with the international standards by Clinical and Laboratory Standards Institute (CLSI guidelines M7-A09) against a panel of nine bacterial targets. A weak antibacterial activity was detected (MIC in the range of 100 μg/mL). To attain insight into the antibacterial mode of action (bactericidal versus bacteriostatic), 5 μL of suspension at MIC and MIC/2 was dropped onto tryptone soy agar (TSA) medium and incubated at the optimal temperature for bacterial target growth. These compounds were not only bacteriostatic but also bactericidal at MICs for Staphylococcus aureus, methicillin-resistant S. aureus (MRSA), Acinetobacter baumannii, and Klebsiella pneumoniae (Table 1). Table 1. Antimicrobial activity of isolated compounds. Minimal inhibitory concentrations (MICs) were determined according the clinical and laboratory standards Institute (CLSI) guidelines M7-A09. Controls for Gram-negative and Gram-positive bacteria were polymixin B and erythromycin, respectively. NA: Not Assayed. (*) indicates that a bactericidal mode of action was highlighted.

Antimicrobial Activity
We investigated the antimicrobial activity of secofuscin and dihydrosecofuscin since these metabolites (HPLC fractions) exhibited antimicrobial activity against E. faecalis. Their minimal inhibitory concentrations (MICs) were defined in accordance with the international standards by Clinical and Laboratory Standards Institute (CLSI guidelines M7-A09) against a panel of nine bacterial targets. A weak antibacterial activity was detected (MIC in the range of 100 μg/mL). To attain insight into the antibacterial mode of action (bactericidal versus bacteriostatic), 5 μL of suspension at MIC and MIC/2 was dropped onto tryptone soy agar (TSA) medium and incubated at the optimal temperature for bacterial target growth. These compounds were not only bacteriostatic but also bactericidal at MICs for Staphylococcus aureus, methicillin-resistant S. aureus (MRSA), Acinetobacter baumannii, and Klebsiella pneumoniae (Table 1). Table 1. Antimicrobial activity of isolated compounds. Minimal inhibitory concentrations (MICs) were determined according the clinical and laboratory standards Institute (CLSI) guidelines M7-A09. Controls for Gram-negative and Gram-positive bacteria were polymixin B and erythromycin, respectively. NA: Not Assayed. (*) indicates that a bactericidal mode of action was highlighted. ) and of fuscin and derivatives production resulting from three independent experiments. The latter were quantified by the area below the elution peak detected by RP-HPLC after solid-phase extraction (SPE) extraction of the cell-free supernatant.  . Biological Activities

MIC (μg/mL) Dihydrosecofuscin Secofuscin Control
We investigated the antimicrobial activity of secofuscin and dihydrosecofuscin since these tabolites (HPLC fractions) exhibited antimicrobial activity against E. faecalis. Their minimal ibitory concentrations (MICs) were defined in accordance with the international standards by inical and Laboratory Standards Institute (CLSI guidelines M7-A09) against a panel of nine cterial targets. A weak antibacterial activity was detected (MIC in the range of 100 μg/mL). To ain insight into the antibacterial mode of action (bactericidal versus bacteriostatic), 5 μL of spension at MIC and MIC/2 was dropped onto tryptone soy agar (TSA) medium and incubated at optimal temperature for bacterial target growth. These compounds were not only bacteriostatic t also bactericidal at MICs for Staphylococcus aureus, methicillin-resistant S. aureus (MRSA), inetobacter baumannii, and Klebsiella pneumoniae (Table 1).  . Biological Activities .

Antimicrobial Activity
We investigated the antimicrobial activity of secofuscin and dihydrosecofuscin since these tabolites (HPLC fractions) exhibited antimicrobial activity against E. faecalis. Their minimal ibitory concentrations (MICs) were defined in accordance with the international standards by nical and Laboratory Standards Institute (CLSI guidelines M7-A09) against a panel of nine cterial targets. A weak antibacterial activity was detected (MIC in the range of 100 μg/mL). To ain insight into the antibacterial mode of action (bactericidal versus bacteriostatic), 5 μL of pension at MIC and MIC/2 was dropped onto tryptone soy agar (TSA) medium and incubated at optimal temperature for bacterial target growth. These compounds were not only bacteriostatic t also bactericidal at MICs for Staphylococcus aureus, methicillin-resistant S. aureus (MRSA), inetobacter baumannii, and Klebsiella pneumoniae (Table 1).  . Biological Activities .

Antimicrobial Activity
We investigated the antimicrobial activity of secofuscin and dihydrosecofuscin since these tabolites (HPLC fractions) exhibited antimicrobial activity against E. faecalis. Their minimal ibitory concentrations (MICs) were defined in accordance with the international standards by nical and Laboratory Standards Institute (CLSI guidelines M7-A09) against a panel of nine cterial targets. A weak antibacterial activity was detected (MIC in the range of 100 μg/mL). To ain insight into the antibacterial mode of action (bactericidal versus bacteriostatic), 5 μL of pension at MIC and MIC/2 was dropped onto tryptone soy agar (TSA) medium and incubated at optimal temperature for bacterial target growth. These compounds were not only bacteriostatic t also bactericidal at MICs for Staphylococcus aureus, methicillin-resistant S. aureus (MRSA), inetobacter baumannii, and Klebsiella pneumoniae (Table 1).

Antimicrobial Activity
We investigated the antimicrobial activity of secofuscin and dihydrosecofuscin since these metabolites (HPLC fractions) exhibited antimicrobial activity against E. faecalis. Their minimal inhibitory concentrations (MICs) were defined in accordance with the international standards by Clinical and Laboratory Standards Institute (CLSI guidelines M7-A09) against a panel of nine bacterial targets. A weak antibacterial activity was detected (MIC in the range of 100 µg/mL). To attain insight into the antibacterial mode of action (bactericidal versus bacteriostatic), 5 µL of suspension at MIC and MIC/2 was dropped onto tryptone soy agar (TSA) medium and incubated at the optimal temperature for bacterial target growth. These compounds were not only bacteriostatic but also bactericidal at MICs for Staphylococcus aureus, methicillin-resistant S. aureus (MRSA), Acinetobacter baumannii, and Klebsiella pneumoniae (Table 1).

Disease-Related Kinase Inhibition
Dihydrosecofuscin obtained from O. griseum UBOCC-A-114129 was assayed on a panel of 11 disease-related kinases. It was first assayed at a final concentration of 50 µg/mL. When enzymatic inhibition was lower than 50% (half maximal inhibitory concentration (IC 50 ) > 50 µg/mL), dihydrosecofuscin was considered inactive (Table 2). At 50 µg/mL, dihydrosecofuscin was able to inhibit the activity of the CDC2-like kinase-1 (CLK1) by 83%. Bold values showed inhibition of kinase activity at 50 µg/mL.
When kinase inhibition was higher than 50%, the IC 50 was defined from the dose-response curves using a wide range of concentrations (usually from 0.015 µg/mL to 50 µg/mL) (Figure 4). The IC 50 value of diyhdrosecofuscin against CLK1 was estimated at 15.6 µg/mL.

Disease-Related Kinase Inhibition
Dihydrosecofuscin obtained from O. griseum UBOCC-A-114129 was assayed on a panel of 11 disease-related kinases. It was first assayed at a final concentration of 50 μg/mL. When enzymatic inhibition was lower than 50% (half maximal inhibitory concentration (IC50) > 50 μg/mL), dihydrosecofuscin was considered inactive (Table 2). At 50 μg/mL, dihydrosecofuscin was able to inhibit the activity of the CDC2-like kinase-1 (CLK1) by 83%. Bold values showed inhibition of kinase activity at 50 μg/mL. When kinase inhibition was higher than 50%, the IC50 was defined from the dose-response curves using a wide range of concentrations (usually from 0.015 μg/mL to 50 μg/mL) (Figure 4). The IC50 value of diyhdrosecofuscin against CLK1 was estimated at 15.6 μg/mL.

Discussion
Ocean covers almost 70% of the earth surface with a wide array of contrasting habitats harboring complex microbial communities. Marine microorganisms were proven to be a great reservoir of secondary bioactive metabolites [15]. Among them, marine fungi represent a potential new reservoir of bioactive natural and sustainable products [16,17]. Deep-sea and subseafloor fungi are the least studied marine fungi and therefore may appear as an untapped diversity with biotechnological potential [18,19]. Indeed, deep sea fungal communities can feed natural compound libraries with putatively novel structures and mode of actions [20].

Discussion
Ocean covers almost 70% of the earth surface with a wide array of contrasting habitats harboring complex microbial communities. Marine microorganisms were proven to be a great reservoir of secondary bioactive metabolites [15]. Among them, marine fungi represent a potential new reservoir of bioactive natural and sustainable products [16,17]. Deep-sea and subseafloor fungi are the least studied marine fungi and therefore may appear as an untapped diversity with biotechnological potential [18,19]. Indeed, deep sea fungal communities can feed natural compound libraries with putatively novel structures and mode of actions [20].
To reveal the chemical structure of the bioactive metabolites, we investigated the deepest fungal strain (765 m below the sea floor), O. griseum UBOCC-A-114129. Fuscin (1), dihydrofuscin (2), dihydrosecofuscin (3), and secofuscin (4) were structurally characterized from O. griseum UBOCC-A-114129. These compounds have already been described from terrestrial O. fuscum [10], O. griseum [13], and P. gallicola n. sp. [11]. However, to the best of our knowledge, this is the first report of (i) the production of fuscin and its derivatives by a marine fungus in the meantime and (ii) the antimicrobial activity of secofuscin and dihydrosecofuscin.
The production of fuscin (1), dihydrofuscin (2), dihydrosecofuscin (3), and secofuscin (4) occurred after the fungus has completed his growth and can thus be qualified as secondary metabolites [21]. Secondary metabolites are small molecular weight molecules produced by microorganisms to compete with environmental stressing conditions such as temperature, pressure, salinity, and those arising from other microorganisms [22]. Some of them could be beneficial as antimicrobial or antitumor activities, whereas other could be deleterious to humankind (e.g., mycotoxins) [23]. Dihydrosecofuscin has been previously described as a biosynthetic precursor of fuscin [24]. It was here the most produced metabolite and appeared to co-occur with the other derivatives. This is the first report on their co-production in an Oidiodendron species. Although fuscin and its derivatives appear as the major metabolites produced during the stationary phase, their ecological role remains to be clarified. The chemical structure of those compounds suggested a polyketide, a terpenoid structure, or a hybrid of both, as suggested by Birch and his colleagues [25]. Previous investigation of genes coding polyketides synthases and terpene synthases revealed the unique presence of polyketide synthases in the O. griseum UBOCC-A-114129 genome [3] and thus likely highlighted the polyketide nature of the bioactive metabolites produced by this isolate.
Although fuscin (1) and dihydrofuscin (2) were previously investigated for antimicrobial activities, no data were available regarding dihydrosecofuscin (3) and secofuscin (4). MIC values reflected a weak but significant antimicrobial activity. A bactericidal mode of action was also revealed against various Gram-positive bacterial targets.
Finally, dihydrosecofuscin showed in vitro inhibition of kinase activity against CLK1. Penicillium terrestre, a marine fungus isolated from marine sediment, has also been described for its anti-kinase activity. A 35% inhibition of tyrosine kinases was observed when incubated with 3 µg/mL of the bioactive metabolite terrestrol G synthetized by Penicillium terrestre [26]. Therefore, dihydrosecofuscin weakly inhibited CLK1 activity with an IC 50 of 15.6 µg/mL. Since this kinase has been reported to be a relevant target for Alzheimer's disease treatment, dihydrosecofuscin may provide a structural pattern for developing new therapeutic drugs.

Fungal Isolation and Identification
Isolation and identification of the fungal isolate selected in this study has been described in an earlier report [3]. Briefly, sediment samples were plated onto five low nutrient media with or without sea salts, at different temperatures and at different hydrostatic pressures. Subcultures of each colony were performed to obtain pure cultures. Purified isolates were then cryo-preserved on beads at −80 • C.
The sequence analysis of 18S rDNA and internal transcribed spacer (ITS) genetic markers revealed O. griseum as the nearest relative of our strain with 99% of similarity in GenBank database. The 18S and ITS rDNA sequence were respectively deposited in Genbank under the accession number KM222226 and KM232506, respectively. The O. griseum isolate studied here has been deposited in the Université de Bretagne Occidentale Culture Collection under the UBOCC-A-114129 number (www.univ-brest.fr/ubocc).

Cultivation Method and Fermentation
One cryobead containing a spore suspension of the preserved fungus was plated onto potato dextrose agar (PDA) and incubated at 25 • C for 10 days for revitalization. Then, the strain was subcultured onto PDA for 14 days at 25 • C. Six 250 mL Erlenmeyer flasks, containing 50 mL of Potato Dextrose Broth PDB complemented with 0.2% agar (PDA 0.2%), were inoculated with 2 plugs with a 4-mm diameter cut from the edge of the actively growing culture that was 14 days old. They were incubated under rotary shaking (100 rpm) at 25 • C for 21 days.

Kinetics of Biomass and Metabolite Production
The production of biomass and bioactive metabolites were assessed for 21 days. At 4,7,11,14,18, and 21 days of incubation, antimicrobial assays were performed using the well diffusion method [9] before extraction of the culture. The culture was filtered on Whatman filter paper (No. 1) (Fisher, Illkirch, France) under vacuum to separate biomass from the culture medium. The biomass was dried in a 58 • C incubator for at least one week and was weighed to draw the kinetic curve. The culture medium was centrifuged (8000× g, 20 min, 4 • C) to pellet residual biomass. The supernatant (25 mL) was loaded and fractionated onto a Solid Phase Extraction C-18 column. The first elution step was performed using 10% acetonitrile +0.07% TFA) (Fractions 0-10). The second elution step was conducted using 90% acetonitrile +0.07% TFA and led to Fractions 10-90. Fractions 0-10 and 10-90 were freeze-dried and suspended into 2.5 mL of 20% acetonitrile to obtain extracts 10 times, concentrated at, respectively, 1 mg/mL and 4 mg/mL (±10%)

Bio-Guided Isolation
Antimicrobial assays were performed on E. faecalis CIP-A-186 as the most sensitive target of this fungal strain [9]. An overnight culture of the target was performed in tryptone soy broth. This culture was then diluted and included in TSA to obtain 1.0 × 10 6 cfu/mL. Finally, 20 µL crude extracts or fractions were dropped into wells, previously performed in the TSA with E. faecalis. Inhibition diameter was measured after 24 h of incubation at 37 • C.

Characterization/Spectral Data
The pure compounds were further characterized using liquid chromatography-mass spectrometer (LC-MS) and NMR. The LC-MS analyses were conducted using an ultra Performance Liquid Chromatography (UPLC) system (Acquity H Class Bio, Waters, Milford, MA, USA) coupled with detection by spectrophotometry (PDA eλ detector, Waters) and mass spectrometry (QuattroMicro). Elutions were performed on a C-18 column (BEH, 2.1 × 50 mm, 1.7 µm) using a linear gradient of acetonitrile (0.1% Formic Acid). All the LC-MS instruments and column come from Waters Corporation. 1 H NMR measurements were carried out on a Bruker AVANCE 500 spectrometer (Bruker, Wissembourg, France) with a TCI cryoprobe. The spectra were recorded at 298 K. Homo-nuclear (Correlation Spectroscopy COSY), Total Correlation Spectroscopy (TOCSY), and hetero-nuclear (Heteronuclear Single Quantum Coherence (HSQC), Heteronuclear Multiple Bond Correlation (HMBC), and HSQC-TOCSY) standard pulse sequences of the Bruker database were used. Samples were solubilized in DMSO-d 6 and chemical shifts were expressed as ppm. Gram-negative bacteria. Experiments were performed as described in CLSI standard M07-A9: methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically [27]. Briefly, a 96-well microplate containing a 2-fold serial dilution of pure compounds (50 µL) ranging from 512 µg·mL −1 to 1 µg·mL −1 was prepared. Targets were cryo-preserved at −20 • C. Strains were streaked onto TSA and incubated for 24 h at 37 • C. One colony was suspended into 5 mL of Mueller-Hinton agar and incubated 4 h at 37 • C under rotary shaking. A bacterial suspension (1.0 × 10 6 cfu/mL) was performed in Mueller-Hinton 2× and dispensed (50 µL) in the previous microplates. Finally, the bacterial concentration reached 5.0 × 10 6 cfu/mL, and antibiotic final concentrations ranged from 256 µg/mL to 0.5 µg/mL. To validate our results, we verified that the MICs of the positive controls was in agreement with MICs listed by CLSI [27].

Conclusions
In this study, we characterized four bioactive compounds produced by O. griseum, isolated from a sample collected at 765 m below the sea floor. To our knowledge, this strain is the deepest subseafloor isolate ever studied for biological activities. Although all compounds had been previously described from terrestrial fungus, two of them, dihydrosecofuscin and secofuscin, had not been previously described as bioactive. Here we investigated their biological activities and showed their antibacterial activities against Gram-positive bacteria, with a bactericidal mode of action. Moreover, dihydrosecofuscin inhibited CLK1 kinase activity with an IC 50 of 15.6 µg/mL, highlighting a possible interest for putative applications in human disease treatment such as Alzheimer's. Such compounds, especially dihydrosecofuscin, could represent new structural patterns in the search for new bioactive compounds to fight antimicrobial resistance and neurodegenerative disease threats. Although no new structures were revealed here for O. griseum UBOCC-A-114129, the collection of deep subsurface isolates still represents an untapped reservoir of bioactive compounds since many other promising isolates remain to be screened for their secondary metabolites.