Introduction
Subfertility is a leading global health issue affecting individuals of reproductive age worldwide. Available data over the past few years suggests that the percentage of infertile couples is steadily increasing in the world. Infertility may occur due to female or male factors or complications involving both (Malina and Pooley, Reference Malina and Pooley2017). It is a very sensitive issue of social concern, and many pharmacological, surgical, and assisted reproductive techniques (ART) have been developed to enable couples to have children. In vitro fertilization (IVF) is a type of ART commonly used in this field (Klemetti et al, Reference Klemetti, Gissler and Hemminki2004; Malina et al., Reference Malina, Błaszkiewicz and Owczarz2016). The use of porcine models in research is more popular due to their physiological similarity to humans. Many factors affect the success of the in vitro fertilization technique, including the condition of the sperm and the eggs. When conducting IVF with boar spermatozoa, the occurrence of polyspermy is of major concern (Alcântara-Neto et al., Reference Alcântara-Neto, Fernandez-Rufete, Corbin, Tsikis, Uzbekov, Garanina, Coy, Almiñana and Mermillod2020). The term polyspermy is simply defined as the interaction of more than one male sperm nucleus with the female nucleus (Markert, Reference Markert1979). The incidence of polyspermy can reach up to 30–40% with boar sperm compared to other mammalian species and under IVF conditions it can reach up to 65% (Xia et al., Reference Xia, Wang, Yang, Tan and Qin2001). The reasons for polyspermy are still unclear and several articles have suggested that it could occur due to factors such as the quality of mature oocytes, IVF conditions, and the semen quality at fertilization (Sirard et al., Reference Sirard, Dubuc, Bolamba, Zheng and Coenen1993; Wang et al., Reference Wang, Abeydeera, Okuda and Niwa1994; Marchal et al., Reference Marchal, Feugang, Perreau, Venturi, Terqui and Mermillod2001), as well as variations within the same species and the influence of the ejaculate on the sperm penetration and the polyspermy (Almiñana et al., Reference Almiñana, Gil, Cuell, Roca, Vazquez, Rodriguez-Martinez and Martinez2005; Gil et al., Reference Gil, Almiñana, Cuello, Parrilla, Roca, Vazquez and Martinez2007; Alcântara-Neto et al., Reference Alcântara-Neto, Fernandez-Rufete, Corbin, Tsikis, Uzbekov, Garanina, Coy, Almiñana and Mermillod2020). Polyspermy results in nuclear chromosomal abnormalities, a reduced number of cells in the blastocyst, and an overall reduction in the success rate of IVF (Nguyen et al., Reference Nguyen, Dang-Nguyen, Somfai, Men, Linh, Nguyen, Noguchi, Kaneko and Kikuchi2020). Therefore, researchers are paying attention to the use of artificially derived or naturally derived compounds to enhance the success rate of IVF.
Plant-derived compounds have been in use for many years and there is considerable ongoing research with regard to the medicinal uses of different plant extracts (Lee et al., Reference Lee, Lee and Wang2019). A wide variety of mushrooms are commonly considered nutritious foods with unique properties including their medicinal value (Wasser, Reference Wasser2011; Ma et al., Reference Ma, Zhang, Wang, Zhu, Wang, Feng and Ng2013). Secondary metabolites derived from the fungal strains of mushroom origin have antibacterial, antitumour, antiviral, anti-inflammatory, immunomodulatory, and antioxidant activities (Lindequist et al., Reference Lindequist, Niedermeyer and Jülich2005; Lee and Yun, Reference Lee and Yun2006; Wasser, Reference Wasser2011; Yi et al., Reference Yi, Lee, Lee and Yun2016). The fungal species Trichaptum fuscoviolaceum, commonly known as the violet tooth is of the order Hymenochaetales and is widely disseminated on coniferous trees in the temperate regions of the world (Seierstad et al., Reference Seierstad, Fossdal, Miettinen, Calsen, Skrede and Kauserud2021). However, little is known about its functional activity. In this study, while exploring the effects of fungal metabolites on pig oocytes, we found that stereumamide A (StA) derived from the culture broth of T. fuscoviolaceum exhibited activity in regulating sperm penetration during IVF.
Materials and methods
Isolation and purification of StA from the culture broth of T. fuscoviolaceum
The fungal strain T. fuscoviolaceum was cultured on potato dextrose agar at 27°C for two weeks. Small pieces of fresh mycelium were inoculated into 20 one-litre flasks containing 400 ml of potato dextrose broth and cultured on a rotary shaker at 120 rpm and 27°C for four weeks. The culture broth was filtered to separate mycelium and the broth filtrate. The broth filtrate was subjected to Diaion® HP-20 column chromatography eluted with 50% aqueous methanol (MeOH), followed by silica gel column chromatography with stepwise chloroform (CHCl3)-MeOH (30:1→0:100, v/v) to form fractions labelled A-C. Fraction B was chromatographed on a column of Sephadex® LH-20 eluted with MeOH. The fraction containing StA was separated using medium pressure liquid chromatography eluted with a gradient of an increasing amount of methanol in water. Finally, StA (142 mg) was obtained using a Sep-Pak C18 cartridge eluted with 10% aq. MeOH (Figure 1).
Figure 1. Structure of the isolated compound.
Structure determination of StA
The chemical structure of the isolated compound was determined by electrospray ionization (ESI)-mass spectrometry and nuclear magnetic resonance (NMR) measurements. The molecular weight was established as 345 by the ESI-mass spectrometry, which showed a quasi-molecular ion peak at m/z 245.9 [M+H]+ in the positive mode. The 1H NMR spectrum in dimethyl sulfoxide (DMSO)-d6 exhibited signals due to three aromatic methines at δ 9.31, 9.12 (d, J = 5.4 Hz), and 8.27 (d, J = 5.4 Hz), one olefinic methine at δ 6.90, three methines at δ 5.00 (d, J = 4.2 Hz), 4.51 (m), and 3.69 (m), one methylene at δ 1.97 (dd, J = 13.2, 8.4 Hz)/1.88 (dd, J = 13.2, 7.8 Hz), and four methyls at δ 1.21, 1.19, 1.10, and 0.98 (d, J = 6.6 Hz) (Figure 2). In the 13C NMR spectrum, 19 carbon peaks including two carbonyl carbons at δ 180.7 and 165.0, four sp2 methine carbons at δ 153.4, 148.5, 144.7, and 122.6, three sp2 quaternary carbons at δ 168.4, 136.3, and 128.8, two oxygen- or nitrogen-conjugated methines at δ 80.6 and 66.5, one oxygenated quaternary carbon at δ 72.3, one methine at δ 51.9, one quaternary carbon at δ 45.4, one methylene at δ 39.2, and four methyls at δ 28.0, 27.1, 24.8, and 20.7 were evident (Figure 2A). All the proton-bearing carbons were assigned by the heteronuclear multiple quantum correlation spectrum, and the 1H-1H homonuclear correlation spectroscopy spectrum revealed three partial structures. Further structural elucidation was performed with the aid of the Heteronuclear Multiple Bond Correlation spectrum, which showed long-range correlations from H-1 to C-8 and C-9, from H-3 to C-1, C-5 and C-9, from H-10 and H-11 to C-1, C-2, and C-3, from H-12 to C-4, C-5, and C-6, from H-13 to C-5 and C-7, from H-14 to C-6 and C-15, and from H-15 to C-6, C-8, and C-14, establishing the presence of sterostrein Q moiety. Finally, the long-range correlations from H-14 and H-15 to C-2´ and H-2´ to C-1´ indicated that the threonine moiety was connected to sterostrein Q via a carbon-nitrogen bond (Figure 2B). Therefore, the structure of the isolated compound was identified as a zwitterionic alkaloid StA (Duan et al., Reference Duan, Feng, Bai, Li, Zhang and Zhao2018).
Figure 2. 1H (italic) and 13C peaks assignments and two-dimensional nuclear magnetic resonance (NMR) data.
Assessment of boar sperm motility
Liquid boar semen was purchased from a local artificial insemination (AI) centre. Sperm motility was examined using a computer-assisted sperm analysis system (CASA; Sperm Class Analyzer®, Microptic, Barcelona, Spain). Spermatozoa were incubated for 2 h at 37.5°C with or without StA (controls; without addition of StA [w/o] or a solvent control with DMSO), and a 1 μl aliquot of sperm sample was then placed on a pre-warmed (38°C) Leja counting slide (Leja products B.V., Nieuw-Vennep, The Netherlands). Ten fields were analyzed at 37.5°C, assessing a minimum of 500 spermatozoa per sample. The proportion of total motile spermatozoa (%), progressive motile spermatozoa (%), and hyperactive spermatozoa (%) was determined. The kinetic parameters measured for each spermatozoon included: curvilinear velocity (VCL, µm/s), straight-line velocity (VSL, µm/s), average path velocity (VAP, µm/s), the percentage of linearity (LIN, %), the percentage of straightness (STR, %), and the wobble percentage (WOB, %).
Collection and in vitro maturation (IVM) of pig oocytes
Ovaries were collected from prepubertal gilts at a local slaughterhouse and transported to the laboratory. Cumulus-oocyte complexes (COCs) were aspirated from the antral follicles (3-6 mm in diameter), washed three times in N-2-hydroxyethylpiperazine-N’-2-ethanesulfonic acid (HEPES)-buffered Tyrode lactate (TL-HEPES) medium supplemented with 0.01% (w/v) polyvinyl alcohol (PVA), (TL-HEPES-PVA), followed by three washes with the oocyte maturation medium (Abeydeera et al., Reference Abeydeera, Wang, Prather and Day1998). A total of 50 COCs were transferred to 500 µl of the maturation medium and layered with mineral oil in a 4-well multi-dish equilibrated at 38.5°C in a 5% CO2 atmosphere. The oocyte maturation medium used was the tissue culture medium 199 supplemented with 0.1% PVA, 3.05 mM D-glucose, 0.91 mM sodium pyruvate, 0.57 mM cysteine, 0.5 µg/ml luteinizing hormone (Sigma-Aldrich, Seoul, Korea), 0.5 µg/ml follicle-stimulating hormone (Sigma), 10 ng/ml epidermal growth factor (Sigma), 75 µg/ml penicillin G, and 50 µg/ml streptomycin. The oocytes were cultured in TCM199 for 44 h at 38.5°C and 5% CO2 in air.
In vitro fertilization (IVF) and culture (IVC) of pig oocytes
After IVM, cumulus cells were removed by treating with 0.1% hyaluronidase in the TL-HEPES-PVA medium (Abeydeera et al., Reference Abeydeera, Wang, Prather and Day1998), and metaphase II oocytes were selected by observation under a stereomicroscope. Thereafter, in a 35-mm polystyrene culture dish, oocytes were placed into four 100 μl drops of modified Tris-buffered medium (mTBM) and covered with mineral oil. One millilitre of liquid semen preserved in Beltsville Thawing Solution was washed twice with phosphate-buffered saline (PBS) containing 0.1% PVA (PBS-PVA), at 800 x g for 5 min. The washed spermatozoa were resuspended in mTBM, appropriately diluted, and 1 µl of the sperm suspension was added to the medium containing the oocytes to give a final sperm concentration of 1 × 105 spermatozoa/ml. Oocytes were co-incubated with spermatozoa for 5 h at 38.5°C in an atmosphere containing 5% CO2. To observe the effects of StA on IVF, the following experiments were performed: i) Oocytes were inseminated in the absence or presence of StA (0–50 µg/ml), ii) Spermatozoa were incubated with 20 µg/ml StA for 30 min, and were then used for IVF, and iii) Oocytes were incubated with 20 µg/ml StA for 1 h, and then were used for IVF. After IVF, oocytes were transferred to 500 μl porcine zygote medium (PZM-3; Yoshioka et al., Reference Yoshioka, Suzuki, Tanaka, Anas and Iwamura2002) supplemented with 0.4% bovine serum albumin (BSA, A0281, Sigma), and cultured for an additional 20, 48, or 144 h. The IVM, IVF, and IVC studies were repeated five times for each treatment regimen.
Evaluation of fertilization and embryonic development
Oocytes/embryos were fixed with 2% formaldehyde for 40 min at room temperature, washed twice with PBS, permeabilized with PBS-Triton X-100 for 30 min, and stained with 2.5 mg/ml 4′,6-diamidino-2-phenylindole (DAPI; DNA staining; Molecular Probes, Eugene, OR, USA) for 40 min. The fertilization status of the zygotes (unfertilized, fertilized-monospermic, or fertilized-polyspermic), cleaved embryo number, blastocyst formation, and the cell number per blastocyst were assessed under a fluorescence microscope (Nikon Eclipse Ci microscope; Nikon Instruments Inc., Tokyo, Japan).
Statistical analysis
Values are exhibit as the mean ± standard error of the mean (SEM). Data analyses were conducted using one-way analysis of variance with SAS package 9.4 (SAS Institute Inc., Cary, NC, USA). The completely randomized design was used, and Duncan’s multiple range test was performed to compare values of individual treatments when the F-value was significant (p < 0.05).
Results
StA did not interfere with sperm movement during incubation
The boar spermatozoa were incubated in the presence of StA at concentrations of 10, 20 and 50 µg/ml for 2 h, or controls (W/O addition of StA or a solvent control with DMSO), and then sperm motility and progression were examined using a CASA system (Figure 3). As shown in Figure 3A, there was no significant difference in the percentage of motile spermatozoa between the treatment groups, and the controls. On the other hand, a significantly lower rate of progression was observed in spermatozoa incubated with 50 µg/ml StA, compared to those of spermatozoa incubated with 10 and 20 µg/ml StA or the controls (p < 0.05, Figure 3B).
Figure 3. Incubation of boar spermatozoa in the absence (W/O) or presence of StA or DMSO (a solvent control). Motile (A) And progressive (B) Spermatozoa were assessed after 2 h of incubation. Values are expressed as the mean ± SEM. The different superscripts (a&b) in each group of columns denote a significant difference at p < 0.05. StA: stereumamide A; DMSO: dimethyl sulfoxide.
StA inhibited sperm penetration during IVF, affected oocytes but not spermatozoa
To observe the effects of StA on IVF, oocytes were inseminated in the IVF medium in the absence or presence of StA for 5 h. Significantly lower rates of fertilization were observed in oocytes inseminated in the presence of 10–50 µg/ml StA compared with the fertilization rate of the controls (p < 0.05, Figure 4A). In addition, spermatozoa were pre-incubated with 20 µg/ml StA for 30 min and were then used for IVF (Figure 4B). When compared with the groups wherein StA was present in the IVF medium during insemination, the direct addition of StA inhibited sperm penetration significantly (p < 0.05, Figure 4B), while there were no differences in the fertilization rate of spermatozoa pre-incubated with or without StA (Figure 4B). Therefore, it is believed that StA affects oocytes rather than sperm during IVF.
Figure 4. Oocytes were inseminated in the IVF medium with different concentrations of StA or controls (without addition of StA [w/o] or a solvent control with DMSO) (A). StA (20 µg/ml) was directly added into the IVF medium or boar spermatozoa were incubated with 20 µg/ml StA, and then IVF was subsequently performed (B). Values are expressed as the mean ± SEM. The different superscripts (a&b) in each group of columns denote a significant difference at p < 0.05. StA: stereumamide A; DMSO: dimethyl sulfoxide; IVF: In vitro fertilization.
Incidence of polyspermy was reduced when IVF was performed with oocytes pre-incubated with StA
Based on the results, oocytes pre-incubated with 20 µg/ml StA for 1 h prior to the IVF process exhibited a significantly lower total fertilization rate, where controls showed above 60% of total fertilization (p < 0.05, Figure 5A). However, the incidence of polyspermy was significantly decreased in the oocytes pre-incubated with StA, and a higher percentage of monospermic oocytes was observed, compared with the controls (p < 0.05, Figure 5B). Further, in the fertilized oocytes cultured for 144 h, a higher rate of blastocyst formation was observed in oocytes pre-incubated with StA (p < 0.05, Figure 5C). Thus, StA at various concentrations and periods of incubation could reduce the frequency of polyspermy in IVF using pig oocytes.
Figure 5. Oocytes were incubated with 20 µg/ml StA or DMSO (a solvent control), and then IVF was performed subsequently. The rate of total fertilization (monospermic+polyspermic oocytes; (A), Polyspermy rate (B), And blastocyst formation (C) were examined after embryo culture for 16, and 144 h, respectively. Values are expressed as the mean ± SEM. The different superscripts (a&b) in each group of columns denote a significant difference at p < 0.05. StA: stereumamide A; DMSO: dimethyl sulfoxide; IVF: In vitro fertilization.
Discussion
IVF is a type of ART that involves retrieving oocytes after ovarian stimulation and combining them with sperm to accomplish fertilization in a well-established laboratory, and implanting one or more fertilized embryos in the uterine cavity. Among the factors that result in the success of IVF, the use of spermatozoa with good motility is one of the most important (Eskandar, Reference Eskandar2002; Xie et al, Reference Xie, Ma, Han, Su, Zhang, Qiu, Wang, Huang, Qiao, Wang and Cheng2010). Similarly, the survival of the oocyte also directly affects the success of the IVF process (Catalá et al., Reference Catalá, Izquierdo, Rodríguez-Prado, Hammami and Paramio2012; Ingilizova et al., Reference Ingilizova, Ivanov, Kovachev, Evrev, Kostov and Necheva2014; Lonergan and Fair, Reference Lonergan and Fair2016). Factors that reduce the success of IVF include impairments in the cumulus cell penetration, sperm/oocyte binding, sperm /oocyte fusion oocyte activation, sperm processing, and pronuclear formation (Swain and Pool, Reference Swain and Pool2008). Even though sperm penetration is a positive factor, polyspermy is a persistent obstacle to the success of IVF. Polyspermy could depend on the quality of oocyte and sperm, and their sperm number at the fertilization site (Hunter, Reference Hunter1991). In general, polyspermy is higher in IVF than in the IVM system and it is necessary to avoid polyspermy for successful fertilization and embryo development (Coy and Avilés, Reference Coy and Avilés2010). Polyspermy leads to abnormal embryo development, early embryonic death, or spontaneous abortions (Jacobs et al., Reference Jacobs, Angell, Buchanan, Hassold, Matsuyama and Manuel1978). Within the body, several mechanisms prevent polyspermy such as oviduct-based mechanisms which prevent the entrance of a large number of spermatozoa into the proximity of the oocytes, the egg-based mechanisms that alter the membrane, and the zona pellucida (ZP) reaction to the fertilizing sperm (Coy and Avilés, Reference Coy and Avilés2010). However, in in vitro systems, it is somewhat difficult to prevent polyspermy (Funahashi, Reference Funahashi2003; Li et al., Reference Li, Ma, Li, Hou, Jiao and Wang2003). Alcântara-Neto et al. (Reference Alcântara-Neto, Fernandez-Rufete, Corbin, Tsikis, Uzbekov, Garanina, Coy, Almiñana and Mermillod2020) stated that supplementation of extracellular vesicles (EVs) can decrease polyspermy and improve embryo production because EVs are the key components in the oviductal fluid. Chemical compounds that have the ability to inhibit sperm hyaluronidase activity and increase ZP hardening can reduce polyspermy (Tatemoto et al., Reference Tatemoto, Tokeshi, Nakamura, Muto and Nakada2006; Coy et al., Reference Coy, Grullon, Canovas, Romar, Matas and Aviles2008). Similar findings in the literature have shown that the resistance of ZP to proteolysis reduces the incidence of polyspermy (Coy et al., Reference Coy, Grullon, Canovas, Romar, Matas and Aviles2008; Mondéjar et al., Reference Mondéjar, Avilés and Coy2013a; Mondéjar et al., Reference Mondéjar, Martínez-Martínez, Avilés and Coy2013b). Also, the pre-incubation of the oocytes or sperm with oviductal epithelial cells prior to IVF can reduce penetration by multiple sperm (Wang et al., Reference Wang, Day and Wu2003). Several studies have shown that polyspermy is very commonly seen in pigs rather than in other mammals (Li et al., Reference Li, Ma, Li, Hou, Jiao and Wang2003; Hao et al., Reference Hao, Mathialagan, Walters, Mao, Lai, Becker, Li, Critser and Prather2006; Kitaji et al., Reference Kitaji, Ookutsu, Sato and Miyoshi2015). In the current study, we have observed that the polyspermy was significantly reduced in the StA incubated group (Figure 5B). This result indicates that StA has the ability to control polyspermy, which is commonly seen during IVF. Moreover, we observed that varying concentrations of StA did not affect sperm motility or the overall survival of the sperm and the oocytes and the percentage of the blastocysts was higher in the StA-treated group (Figure 3–5). Many studies have shown that a higher number of quality blastocysts help in carrying out the IVF process successfully (Gardner et al., Reference Gardner, Lane, Stevens, Schlenker and Schoolcraft2000; Xiong et al., Reference Xiong, Sun, Li, Yao, Chen, Wan, Zhong and Zeng2020). Currently, researchers are focusing on the use of different compounds extracted from plant materials to improve ART. Medicinal mushrooms have beneficial compounds like polysaccharides, triterpenoids, steroids, phenolic components, cordycepin, etc. that have anticancer, anti-inflammatory, antioxidant, anti-hypertensive, and immunomodulatory effects (Wasser, Reference Wasser2011; Johnson et al., Reference Johnson, Cheng, Tsou and Kong2019). Lin et al. (Reference Lin, Chen, Lee, Kuo, Lee and Lee2019) stated that the nutritive and essential trace elements, and/or concentrated compounds of medicinal plant extracts have the ability to improve fertility, but the underlying scientific mechanism is unclear. We can conclude from our results that the extracts of T. fuscoviolaceum have the ability to improve some aspects of the IVF process and we need more studies to identify the compounds responsible and their scientific mechanism during IVF. Also, these results indirectly indicate the possible benefits of the compounds derived from this medicinal mushroom in ART programmes.
Funding
Yi YJ was supported by the National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIT) (NRF-2020R1A2C1014007 and RS-2023-00245276).
Competing interests
Authors have no conflict of interest with this study.
Ethical standards
The ovaries were collected at a commercial slaughterhouse, and liquid boar semen was purchase from local AI centre, therefore it was not necessary to obtain approval of the Ethics Committee.
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