Introduction

The genus Keratinophyton was introduced in 1964 by Randhawa & Sandhu1 However, the nomenclatural history of this genus was confusing since untill recently all known Keratinophyton species were classified in Aphanoascus (Cooke) Apinis2,3,4. Members of Keratinophyton and Aphanoascus share cleistothecia with a pseudoparenchymatic peridium, and they can be found on keratinous substrata and dung3,5,6. Sutton et al. (2013) re-established the genus Keratinophyton with K. terreum as the type species, based on ascospore morphology5. These two genera are distinguished by their ascospore morphology, where ascospores with a conspicuous equatorial rim and pitted wall are characteristic for Keratinophyton, while Aphanoascus species produce reticulate ascospores without a rim5, and by result of phylogenetic analysis using ITS (the internal transcribed spacer) and LSU [the D1/D2 domains of the large-subunit (28S) rDNA gene] loci5,6,7. The monophyletic Keratinophyton clade currently encompasses six species, namely K. durum, K. hispanicum, K. multiporum, K. punsolae, K. saturnoideum, and K. terreum, known to form in vitro ascosporic state (sexual morph) as well as 19 taxa known only as asexual morphs, characterized mainly by a chrysosporium-like conidiogenesis6,7,8. Actually, the genus Keratinophyton includes several species described in Chrysosporium9,10,11,12,13,14. These species however, have been regarded as having a doubtful identity6.

The genus Keratinophyton is represented by a large group of keratinolytic soil-borne fungi rather common in areas with high animal activity resulting in transfer of keratinous material to the soil. Ecology and distribution of the genus has been reviewed in a previous study, stating that soil and soil-like substrata are primary habitats for this fascinating group of onygenalean fungi7. Currently, this genus comprises a total of 27 recognized and accepted taxa6,8.

We performed a mycological survey with emphasis on keratinophilic fungi in environmental samples taken from Republic of Kenya, Africa and Slovak Republic, Europe. Herein, we present description of two novel morphologically and phylogenetically distant species within the genus Keratinophyton being characterized by their unique chrysosporium-like morphs.

Material and methods

Sample collection and isolation of the fungi

The soil sample was collected in front of the Budúcnosť adit at the abandoned antimony (Sb) deposit Pezinok—Kolársky Vrch, 48°19′03.3" N 17°14′20.9" E, locality Rudné Mines, Pezinok (Slovak Republic) in December 2021. Sampling site was situated approximately one meter from neutral mine drainage contaminated by potentially toxic elements.

The second soil sample was collected from Egerton University campus, 0°22′09.3" S 35°55′24.2" E, Njoro (Republic of Kenya) in February 2022.

The samples from the surface layer (up to 20 cm deep) were dried and stored in at 5‒8 °C. Isolation of the keratinophilic fungi was performed as previously described15, with a modification according to7. A sample was divided into five subsamples. The subsamples (5 g each) were poured into Petri dishes (50 mm in diameter) and mixed with 0.5 g Vermiculite, then soaked with 3‒4 mL (depending on moiety of the sample) antibiotic solution containing 0.5 g/L cycloheximide and 0.1 g/L chloramphenicol. Sterile defatted horse hair fragments (10 pieces of ca 2.0 cm per plate) were used as baits. The Petri dishes were then incubated at laboratory temperature (23‒25 ± 1 °C), in dark, for a period of 2–3 months and remoistened with sterile deionized water when necessary7,15. The Petri dishes were checked weekly for the presence of fungi, and colonies were transferred on Sabouraud 4% dextrose agar (SDA; Merck, Darmstadt, Germany) supplemented with 0.5 g cycloheximide and 0.05 g chloramphenicol. Pure cultures were then transferred onto potato dextrose agar (PDA; Van Waters and Rogers (VWR) International, Leuven, Belgium)7.

Morphological analysis

The preliminary identification of the resulting keratinophilic fungi was carried out based on their phenotypic characteristics9,10,11.

For phenotypic determination, the strains were transferred by three-point inoculation onto PDA, Malt Extract Agar (MEA; Merck, Darmstadt, Germany), and SDA, and incubated for 14 d in the dark at 25 °C. Christensen´s urea agar (Sigma-Aldrich, St Louis, MO, USA) was used for additional physiological and biochemical characteristics (25 °C, 14 days, in the dark)7.

Colony growth rate (mm), colony structure and characteristics such as production of exudates and pigments were noted after 14 days (on PDA, MEA, and SDA). However, the cultivation was extended up to 3 months to observe and record changes in pigmentation of the colonies as well as to determine the onset of sexual reproduction7. In order to determine the optimal and minimum/maximum temperatures for growth, PDA, MEA and SDA plates were incubated at 5 °C, 8 °C, 10 °C, 12 °C, 15 °C, 18 °C, 20 °C, 25 °C, 28‒32 °C, 35 °C, and 37 °C, and the growth rate was measured on the 14th day of cultivation. For comparative descriptions of the macroscopic and microscopic characteristics, PDA was used according to7,11,16.

For observation of microscopic traits 14‒18 days growth on PDA was used. Conidiophore and conidia formation were observed in situ under low magnification (50–100×). Details of conidiophores, conidia (aleurioconidia) and other microscopic structures, such as width of hyphae, were observed in Melzer´s reagent and lactic acid with cotton blue7. Photomicrographs were taken using phase and Nomarski contrast optics on an Olympus BX51 microscope with Olympus DP72 camera and QuickPHOTO Micro 3.0 software. Photographs of the colonies were taken with a Sony DSC-RX100.

Dried fungal specimens were deposited as holotypes in the collections of the Mycological Department, National Museum in Prague, Czech Republic (PRM); ex-type cultures were deposited in the Bioactive Microbial Metabolites (BiMM) Fungal Collection, UFT- Tulln in Austria and in the Culture Collection of Fungi in Prague (CCF)7.

Keratinolytic activity

A hair perforation test was performed following de Hoog et al. (2020) using 25 mL water containing 2–3 drops 10% yeast extract (YEW)17. The hairs were examined microscopically 14 and 21 days after inoculation at 25 °C in the dark. At the end of the incubation period, a few pieces of hair were taken out from the testing medium. The overgrowing fungus was deactivated with 70% ethanol and then removed from the hair surface mechanically in a stream of a tap water7. The degree of hair digestion-degradation (keratinolytic activity) was assessed in the light microscope under 100× and 400× magnification. Water was used as mounting fluid for the observation and microphotography of the hair samples. Intensity of degradation18 of hair was estimated on a scale of 0 to 4: 0 = no degradation; 0–1 = light degradation on the cuticle; 1 = moderate degradation on the cuticle and/or rare formation of boring hyphae; 2 = degradation of cuticle and cortex, with about 20% degradation; 3 = degradation of cuticle and cortex, with about 50% degradation; 4 = degradation of cuticle and cortex, with about 80% degradation.

DNA extraction, PCR amplification and sequencing

DNA was extracted using a standard cetyltrimethyl ammonium bromide (CTAB) procedure, as described previously7,19. The internal transcribed spacer (ITS) region was amplified with primers ITS1-F20 and ITS421 using Taq-polymerase (GoTaq G2 Green Master Mix from Promega). The D1/D2 domains of the large-subunit (28S) rDNA gene (LSU) were amplified and sequenced using the primer pair ITS1/TW1421,22. All reactions were performed in an Eppendorf Gradient MasterCycler (Eppendorf, Hamburg, Germany). Conditions for amplification of ITS and LSU domains: 95 °C for 5 min; 35 cycles of 95 °C for 30 s, 54 °C for 30 s, 72 °C for 90 s, and finally 5 min at 72 °C7. The PCR products were sequenced with the same primers used for the PCR amplifications (LGC, Berlin, Germany). All sequences obtained in this study were deposited in GenBank nucleotide database (Table 1).

Table 1 List of the strains included in the study.
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Phylogenetic analysis

All sequences were aligned with MAFFT v7 with default settings. The percent similarity between strains was determined using BioEdit v7.223. ModelFinder24 on IQ-TREE web server25 was used to find the best-fitting model for ITS and LSU datasets according to the Bayesian Information Criterion (BIC). Phylogenetic trees were constructed using the maximum likelihood (ML) methods implemented in IQ-TREE web server. Branch support values were measured using ultrafast bootstraps. Additionally, MrBayes v3.2.726 with default settings on the CIPRES portal (http://www.phylo.org/) was used for both datasets. Ctenomyces serratus CBS 187.61 (Arthrodermataceae, Onygenales) was used as an outgroup. Phylogenetic trees were displayed and edited using Treeview v1.6.627 and iTOL v628.

Results

Morphological analyses and keratin degradation

The results of the morphological analyses are given for each novel species under the Taxonomy section below. Temperature dependent growth of the new Keratinophyton species on PDA, MEA and SDA after 14 days are provided in Table S1a‒c. Briefly, K. keniense grew better than K. kautmanovae on the same type of media and at the same incubation temperatures. All species showed good growth at 20‒25 °C on all three media. K. kautmanovae does not grow at 30 °C, while K. keniense reached up to 38 mm after 14 days at this temperature.

Ability to digest keratin was observed in the two new species after 21 days on testing medium (YEW). However, attack intensity on the hair according to the scale of18 Marchisio et al. was detected to be very weak in both species (= 0–1). Urease activity was negative in both new species on Christensen ´s urea agar.

Phylogenetical analysis

The ITS dataset consisted of 48 strains with 541 sites, LSU dataset consisted of 38 strains with 564 sites, and the ITS-LSU combined dataset included 38 strains with 564 sites. The best-fitting model was TNe + I + G4 for both datasets. Phylogenetic analyses of ITS (Fig. 1a) and combination of ITS-LSU data (Fig. 1b) of the species described in Keratinophyton and Aphanoascus revealed that strains BiMM-F297 and BiMM-296 (Keratinophyton kautmanovae sp. nov.) formed a basal clade in the genus Keratinophyton with 100% support. Strain BiMM-F335 (Keratinophyton keniense sp. nov.) was clustered together with K. hubeiense and K. sichuanense with 94% and 96% ITS similarity, respectively.

Figure 1
figure 1figure 1

(a) Phylogenetic tree of Keratinophyton and Aphanoascus strains based on ITS sequences. The new taxa of Keratinophyton are compared with available sequences of the other related species together with their conidium size, presence of intercalary conidia and ability to grow at 37 °C. Empty triangles and squares represent the absence of the characteristics. (b) Phylogenetic tree based on combination of ITS and LSU sequences for the new taxa of Keratinophyton together with available sequences of the other related species. Numbers at nodes indicate Bayesian probability/ maximum likelihood bootstrap values (≥ 60%). New species are shown in bold. Ctenomyces serratus was used as outgroup. A sequence for K. multiporum was not available for the study. T, ex-type culture.

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Taxonomy

Keratinophyton kautmanovae B.Voleková, Kubátová, Kandemir & Labuda, sp. nov.

(Figs. 2 and 3)

Figure 2
figure 2

Keratinophyton kautmanovae (BiMM-F297). (a) Colonies on PDA (after 14 days) at 25 °C (left—obverse, right—reverse). (b,c) Conidiophores with aleurioconidia (phase contrast microscopy). (d) Aleurioconidia under light microscopy (on PDA, after 14 days). Bars = 10 µm (b,c), 5 µm (d).

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Figure 3
figure 3

Line drawing of micromorphology of Keratinophyton kautmanovae (BiMM-F297). Conidiophores with young and mature aleurioconidia on PDA (at 25 °C, after 14 days). Branched conidiophore (at right) and unbranched conidiophore (at left) with sessile aleurioconidia. Fungus is not melanised. Bar = 10 µm.

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MycoBank: MB851666

Etymology: Named in honour of Ivona Kautmanová, Department of Botany, Slovak National Museum-Natural History Museum, Bratislava, Slovak Republic, an expert in the fungal ecology and taxonomy of higher fungi.

Type: Slovak Republic, Malé Karpaty, Pezinok, Rudné Mines, (coordinates: 48°19′03.3"N 17°14′20.9"E), from a soil sample close (1 m) to stream of contaminated water of abandoned antimony Sb deposit, coll. B. Voleková, December 2021, isol. R. Labuda, February 2022, holotype PRM 957896 (dried culture in metabolically inactive state), culture ex-type BiMM-F297 = CCF 6679 = CBS 150893, ITS sequence, GenBank PP062810; LSU sequence, GenBank PP062954.

Description: Sexual morph not observed on any of the media used. Asexual morph on PDA (25 °C, 14 days, in dark). Vegetative mycelium of hyaline, septate, smooth-walled, sparsely to pronouncedly branched hyphae, 1.0‒2.0 µm diam. Racquet hyphae not observed. Conidia (aleurioconidia), hyaline, white in mass, thin-walled, mostly smooth to finely roughened, some also coarsely roughened or irregularly warty. Terminal and lateral conidia born on main fertile hyphae or from side branches of variable length, sessile or on short protrusions, often slightly swollen (ampuliform) and of variable length, solitary, 1‒3 (–5) per conidiogenous cell, smooth to verrucose (warty), thick-walled, obovate to clavate, 1-celled, (3.5‒)4.0‒5.0(‒6.5) × (2.0‒)2.0‒2.5(‒3.0) µm (mean = 4.5 ± 0.5 × 2.4 ± 0.2 µm, n = 50). Intercalary conidia (arthroconidia) not observed. Chlamydospores not observed.

Culture characteristics: Colonies on PDA 13‒15 mm diam at 25 °C, after 14 d, floccose to downy (mealy), with abundant sporulation, white to creamy, flat, slightly umbonate at the centre, with slightly radial colony margin submersed into agar, reverse yellowish with dark yellow centre, no pigment or exudate produced. At 30 °C, no growth (germination only). Colonies on SDA 7‒10 mm diam at 25 °C, after 14 days, morphology similar to when on PDA with more floccose and plane colony surface and radial colony margin, poor sporulation, with orange reverse. At 30 °C, no growth (no germination). Colonies on MEA 15‒20 mm diam at 25 °C, after 14 days, morphology similar to PDA with more floccose colonies and plane structure, with moderate sporulation, limited hyaline exudate present, with yellow-orange reverse and vivid orange centre. At 30 °C, no growth (germination only). No ascomata observed after prolonged incubation (3 months).

Optimum temperature for growth on PDA, SDA and MEA at 20–25 °C. Minimum growth (2–5 mm in diam) at 12 °C. Germination of the conidia observed at 10 °C. Maximum temperature for growth (1–3 mm in diam) at 28 °C. Keratinolytic activity very weak, with hair attack intensity = 0–1. Urease activity negative (after 20 days of incubation).

Diagnosis: Keratinophyton kautmanovae molecularly can be distinguished from other Keratinophyton species by ITS locus analysis. Combination of the following phenotypic features can be used to differentiate this fungus from other species in the genus: (1) obovoid-clavate, smooth to coarsely verrucose or irregularly warty conidia, (2) absence of arthroconidia, (3) generally slow grow at 25 °C, poor growth at 28 °C and no growth at 30 °C, and (4) orange reverse at 25 °C on MEA and SDA.

Additional material examined: Slovak Republic, Malé Karpaty, Pezinok, Rudné Mines, (coordinates: 48°19′03.3" N 17°14′20.9" E), isolated from a different sub-sample, February 2022, R. Labuda, a strain BiMM-F296 (ITS sequence, GenBank PP062811; LSU sequence, GenBank PP062955). Phenotypically and molecularly (ITS and LSU) identical with ex-type culture BiMM-F297.

Notes: Based on a search of NCBI GenBank nucleotide database, the closest hit for Keratinophyton kautmanovae using the ITS sequence is Keratinophyton lemmensii (ex—type CCF 6359 = BiMM—F 76; GenBank acc. MN633082), with identity = 463/504 (92%) and gaps 16/504 (3%). Phenotypically, K. kautmanovae can be readily distinguished from the K. lemmensii by absence of intercalary conidia (arthroconidia) and filiform 2-celled conidia, presence of orange colony reverse at 25 °C on MEA and SDA, slower growth at 25 °C and inability to grow at 30 °C.

Keratinophyton keniense V. Scheffenacker, A. Schüller, Kubátová, Kandemir & Labuda, sp. nov.

(Figs. 4 and 5)

Figure 4
figure 4

Keratinophyton keniense (BiMM-F335). a Colonies on PDA (after 14 days) at 25 °C (left—obverse, right—reverse). (b) Conidiophores with aleurioconidia. (c–e) Aleurioconidia. (d) Arthroconidium—intercalary conidium (on PDA, after 14 days). Bars = 10 µm.

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Figure 5
figure 5

Line drawing of micromorphology of Keratinophyton keniense (BiMM-F335). Conidiophores with young and mature aleurioconidia on PDA (at 25 °C, after 14 days). Branched conidiophore (right) and unbranched conidiophore (left) with sessile aleurioconidia. Fungus is not melanised. Bar = 10 µm.

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MycoBank: MB851667

Etymology: Named according to the country of origin, Kenya, where the holotype was collected.

Type: Republic of Kenya, Njoro, Egerton University campus (approximate coordinates: 0°22′09.3" S 35°55′24.2" E), from a soil sample (top layer, 20 cm), February 2022, coll. Andreas Schüller, isol. V. Scheffenacker, July 2023, holotype PRM 960013 (dried culture in metabolically inactive state), culture ex-type BiMM-F335 = CCF 6712 = CBS, ITS sequence, GenBank PP062809; LSU sequence, GenBank PP062953.

Description: Sexual morph not observed on any of the media used. Asexual morph on PDA (25 °C, 14 days, in dark). Vegetative mycelium of hyaline, septate, smooth-walled, sparsely to pronouncedly branched hyphae, 2.0‒5.0 µm diam. Racquet hyphae present, rare. Conidia (aleurioconidia) hyaline, white in mass, thick-walled, smooth to very finely roughened. Terminal and lateral conidia born on main fertile hyphae or from side branches of variable length, sessile or on short protrusions of variable length, solitary, 1‒3(–7) per conidiogenous cell, obovate to clavate, mostly 1-celled, smooth, thick-walled, often apiculate and cymbiform (boat-like shaped), (4.0‒)5.0‒6.0(‒7.0) × (2.0‒)2.5‒3.0(‒3.5) µm, (mean = 5.7 ± 0.8 × 2.8 ± 0.3 µm, n = 60), some also 2-celled, oblong to cylindrical, up to 18 µm long, conidia at colony centre often (sub-)globose and rhomboid, (4.5‒)5.0‒6.0(‒7.0) × (4.0‒)4.5‒5.5(‒6.0) µm (mean = 5.7 ± 0.4 × 4.7 ± 0.3 µm, n = 60). Intercalary conidia (arthroconidia) very rare. Chlamydospores not observed.

Culture characteristics: Colonies on PDA 35‒38 mm diam at 25 °C, after 14 days, floccose to downy (mealy), with abundant sporulation, white to creamy, flat, slightly umbonate at the centre with a few concentric rings, even regular colony margin submersed into agar, reverse yellow with dull yellow centre, no pigment or exudate produced. At 30 °C, 33‒37 mm diam. Colonies on SDA 37‒40 mm diam at 25 °C, after 14 days, morphology similar to when on PDA, good sporulation, with darker yellow reverse at the centre. At 30 °C, 35‒38 mm diam. Colonies on MEA 43‒45 mm diam at 25 °C, after 14 days, powdery to downy (mealy), with abundant sporulation, white to creamy, flat, slightly umbonate at the centre, margin irregular, reverse yellow to dull yellow orange, no pigment or exudate produced. At 30 °C, 29‒31 mm diam. No ascomata observed after prolonged incubation (3 months).

Optimum temperature for growth on PDA, SDA and MEA at 20–30 °C. Minimum growth (2–6 mm in diam) at 10 °C. Germination of the conidia observed at 8 °C. Maximum temperature for growth (2–5 mm in diam) at 33 °C. Germination of the conidia and formation of microcolonies observed at 34 °C. Keratinolytic activity absent, with hair attack intensity = 0. Urease activity negative (after 20 days of incubation).

Diagnosis: Keratinophyton keniense molecularly can be distinguished from other Keratinophyton species by ITS locus analysis. Combination of the following phenotypic features can be used to differentiate this fungus from other species in the genus: (1) cymbiform and rhomboid conidia, (2) arthroconidia very rare, (3) good grow at 20–30 °C, (4) dull yellow reverse at 25 °C.

Notes: Based on a search of NCBI GenBank nucleotide database, the closest hit for Keratinophyton keniense using the ITS sequence is Keratinophyton sichuanense (ex—type CGMCC 3.20871; GenBank acc. NR182583), with identity = 529/550 (96%) and gaps 1/550 (0%). Phenotypically, K. keniense can be readily distinguished from the K. sichuanense by presence of rhomboid conidia, slower grow on PDA at 25 °C after 14 days (35‒38 vs 50‒54 mm), and inability to grow at 37 °C.

Discussion

Phylogeny

Phylogenetic reconstruction using ITS and LSU sequences (Fig. 1) resulted in clustering the both new taxa, Keratinophyton kautmanovae and K. keniense, with eight currently accepted species, namely K. alvearium14, K. durum2, K. chongqingense8, K. hubeiense12, K. lemmensii7, K. sichuanense8, K. siglerae29, and K. submersum11. Apart from the pronounced differences in the ITS regions, the species mentioned above can be distinguished by particular combinations of their phenotypic traits (e.g., colony characteristics, and morphology of conidia) as listed in Table 2. The monophyletic genus Keratinophyton is now extended and includes 29 species including six species known from sexual morphs5 and 23 species which are currently known only from asexual morphs8 and this study. The ability to produce ascosporic state (sexual morph) in vitro within this cluster is confined to K. durum2, characterized by discoid ascospores with flattened poles and with a broad equatorial rim, cruciform in side view, broad-ridged, with reticulate surface4. As noted by Li et al. (2022)8, the ability to form sexual morph in vitro is not phylogenetically conserved, as it can be seen from the phylogenetic analysis, showing that all known species forming ascosporic (sexual) structures within the genus are not clustered together and they are spread over the phylogenetic tree6,7,8.

Table 2 Comparison of the key phenotypic characteristics of the phylogenetically close related Keratinophyton spp.
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Ecology and distribution

Almost all known Keratinophyton species have been isolated from soil or soil-like substrates, such as river sediments, compost and sand, and as non-pathogenic fungi as a result of mycological screening for so-called keratinophilic/keratinolytic fungi using a horse-hair baiting method7,8. This highly selective method was introduced by Vanbreuseghem (1952) for soil fungi having affinity to keratinous material especially for onygenalean fungi such as dermatophytes19,30. According to Papini et al. (1998), Ajello reviewed the taxonomy of keratinophilic fungi for the first time in 196831. Later, Otčenášek et al. (1969) reported on the worldwide distribution of keratinophilic mycobiota in soil, claiming that the occurrence of keratinophilic fungi in soil depends on the presence of mammals, birds, and humans in a variety of ecological sites32. It is in fact the only method how this group of keratinophilic fungi can be isolated from the soil-like substrates and studied further. In this study, both fungi originated from the areas which are freely accessible by wild animals typically inhabiting these regions, and thus, these soils might be presumably reach on source of keratin as well as a source of biodiversity for this specific fungal group regardless of geochemical properties of soils15,33,34. As for the sample from the abandoned antimony (Sb) deposit (Slovakia, EU), the soil sample is rich in iron oxides and is also characterized by elevated concentrations of arsenic, antimony, aluminum and sulfates. More about mineralogy and geochemistry of the studied site was published previously35. On the other hand, the soils in Egerton Njoro area are Vintric Mollic andosols36,37. The sampled area is native, not influenced by agricultural or any industrial activities.

As mentioned above, the genus Keratinophyton harbours a total of 29 species, including the two new species described in this study. The majority of the new taxa have been so far described from Europe (15 spp.), followed by Asian continent (China, 8 spp. and India, 5 spp.)5,6,7,8. To the best to our knowledge, the description of K. keniense represents the first taxonomical novelty of the genus Keratinophyton from African continent. Thus, further research is needed because unknown strains may be isolated from similar environments on the African continent.

Hubálek provided a list of keratinolytic fungi associated with free-living mammals and birds of which ubiquitous K. durum, K. pannicola and K. terreum have been isolated from a variety of animals and from different geographical regions38. There are only a few reports of a human or animal clinical isolate belonging to Keratinophyton16,39, however, all these cases have doubtful etiological history and with no solid evidence of their pathogenicity16,40. On the other side, K. pannicola (as C. pannicola) is included in the Atlas of Clinical Fungi17 as a concern in skin infections. Even though the keratinophilic fungi were considered as potential pathogens by several researchers41,42; they rarely cause infections. Therefore, soil is proposed as an epidemiological and probably also an evolutionary link, that relates geophilic, zoophilic, and anthropophilic keratinophilic fungi42. Although being cycloheximide resistant, a potential pathogenicity to homeothermic vertebrates (mammals and birds) by these fungi seems highly unlikely because both new species are not able to grow at higher temperature (above 30‒34 °C), they are urease negative, and possess none or very mild keratinolytic activity in vitro. Rather contrary, these fungi might be interesting from a metabolic point of view, as they undoubtedly represent a yet unexplored source of new bioactive compounds as there is not much known of these properties in the genus34. Metabolic profile and investigation of the potential use of substances produced by these two novel fungi is an object of our further biochemical exploration.