Yeast and Fertility: Effects of In Vitro Activity of Candida spp. on Sperm Quality.
Male fertility potential is related to the quality of the sperm present in the ejaculate. During ejaculation, semen is produced from a concentrated suspension of spermatozoa (~10%) stored in the paired epididymides, vas deferens and fluid secretions from the accessory sex organs (1). Seminal fluid can hold and transport bacteria, fungi, parasites and viruses that provide adequate conditions for microorganism survival in seminal plasma (2-5).
The male urogenital tract is colonized by these etiological agents that sometimes interference with sperm functions and cause infertility (6). The effect of viral and bacterial infections is commonly evaluated, while those caused by fungi are undervalued (7, 8). Candida spp., Aspergillus spp., Cryptococcus spp., and Coccidioides spp. account for more than 90% of the systemic mycoses reported and are caused by fungi. In the male reproductive tract, fungus causes urethritis, balanoposthitis, ulcers, pseudotumor, orchitis and prostatitis (7, 9, 10). Candidiasis is considered as the only sexually transmitted yeast infection; it is caused by Candida spp., Candida albicans and C. glabrata as the most prevalent species (11), and this infection is much more common in women than in men (2, 11). However, men can act as infection reservoir. Contact of C. albicans, or the soluble factor of fungal metabolism with seminal plasma alters sperm quality, either in the male reproductive tract (before ejaculation) or in the female reproductive tract (after ejaculation or sperm capacitation) (8, 12, 13).
Some in vitro studies report decreased motility and sperm viability, increased sperm DNA fragmentation, and alteration of the mitochondrial membrane affecting the potential of male fertility and nonspecific agglutinations (8, 12, 13). Conversely, the effects of C. glabrata on sperm cells are still unknown.
Burrello et al. (8, 14) reported that failure in the assisted reproductive program could occur in patients with C. albicans infections due to the increase of DNA fragmentation and apoptosis, but without affecting conventional sperm parameters. Even gradient methodologies commonly used in in semen processing reproductive programs cannot remove C. albicans contamination (8, 14). In addition, Tian et al. (13) demonstrated that C. albicans infection affects sperm motility and damages the ultrastructure of sperm cells.
Based on the previous demonstrations, within the diagnosis of yeast infection, it is mandatory to: i) determine the effect of C. albicans and C. glabrata on functional sperm parameters; ii) determine the possible receptor involved in the sperm and Candida spp. interaction, since this is important for medical and reproductive programs. These results will demonstrate further knowledge about Candida spp. infections and appropriate treatments to prevent possible negative results in the procedure of assisted reproduction.
The aim of this study was to evaluate the in vitro effects of C. albicans, C. glabrata and their soluble factors of fungal metabolism on sperm quality.
Yeast: C. albicans and C. glabrata strains (kindly donated by the Institucion Universitaria Colegio Mayor de Antioquia. Medellin, Colombia) were conserved on Sabouraud agar (Thermo Fisher Scientific, Waltham, MA, USA) at 4[degrees]C. Two days before use, each strain was reactivated in brain heart infusion (BHI, Thermo Fisher Scientific, Eugene, OR, USA) at 37[degrees]C.
Sperm samples: Thirty-five semen samples were donated by apparently healthy volunteers, aged between 18 and 32 years, collected by masturbation after a sexual abstinence period of 3 to 5 days and analyzed during the first hour after sample collection at the Reproduction Group, Medical School of the University of Antioquia. The conventional seminal parameters were determined in each semen sample following the guidelines established in the semen processing manual of the World Health Organization (WHO), and sperm concentrations were determined using a Makler chamber (Sefi-Medical Instruments). All the samples had seminal parameters equal to or above the lower reference limits established by WHO in 2010. Exclusion criteria for study participation were any history of urogenital surgery and leukocytospermia as well as self-reported illnesses or use of medication in the three months immediately preceding the study.
Sperm selection: Motile sperm were selected using the gradient technique (PureSperm[R] Nidacon, Gothenburg, Sweden). Briefly, in a 15 ml conical tube, 500 [micro]l of the denser phase (PureSperm[R] 80), 500 [micro]l of the less dense phase (PureSperm[R] 40) and 1000 [micro]l of semen over both phases were added, and the mixture was centrifuged 20 min at 300 g. Finally, the supernatant was removed and the motile sperm was re-suspended in 1 ml Ham's-F10 medium (Gibco Life Technologies, Breda, Netherlands).
Yeast inoculum and soluble factor of fungal metabolism: 2, 0.5 (1-5x[10.sup.6] yeast/ml) and 0.05 Mc Farland (McF) yeast inoculums in phosphate-buffered saline (PBS, Gibco Life Technologies, Grand Island, NY, USA) were incubated with three different relation between motile sperm and Candida spp. Candida and sperm ratios were 1 to 1 (0.5 McF), 1 to 10 (0.05 McF) and 4 to 1 (2 McF). The 0.05 McF inoculum was prepared from a 1:10 dilution of 0.5 McF.
Soluble factors of fungal metabolism (SFFM) of C. albicans and C. glabrata were obtained after a 0.5 McF PBS (Gibco Life Technologies) incubation for 1 hr at 37[degrees]C. Next, the medium was centrifuged for 5 min at 2300 g and subsequently filtered through a 0.2 [micro]m membrane (Advantec Industries, Yinzhou District, Ningbo, China). The filtrate was aliquoted and stored at -20[degrees]C until used.
Evaluation of the effect of C. albicans, C. glabrata and SFFM on conventional sperm parameters: Three concentrations (2, 0.5 and 0.05 McF) of each yeast strain and 0,5 McF SFFM were incubated with five million selected sperm and the effect of incubation over conventional sperm parameters was determined after 0, 1, 2 and 3 hr of incubation at 37[degrees]C following intervals previously described (8, 13). The results are expressed as the percentage of change in viability and progressive sperm motility relative to the control (Spermatozoa incubated in PBS).
Evaluation of the effect of C. albicans, C. glabrata and SFFM on capacitated spermatozoa: Five million selected sperm were incubated in four different conditions: i) Capacitation medium (MC, Ham's F10-Gibco Life Technologies- with 35 mg/ml bovine serum albumin (Sigma-Aldrich, St. Louis, MO, USA)), ii) Non-capacitation medium (Ham's F10-NC), iii) Capacitation medium with 0.5 McF SFFM (MC-FS), and iv) Capacitation medium with Candida spp., 0.05 McF (MC-0.05 McF). Finally, the progressive motility in the initial time (0 hr), and 6, 18 and 24 hr post capacitation was evaluated.
Evaluation of the effect of the SFFM of C. albicans and C. glabrata on the functional parameters: Fifteen million previously selected sperm were incubated with 0.5 McF SFFM of Candida spp. in a ratio of 1:1 v/v, for 3 hr at 37[degrees]C. The control was 15 million spermatozoa incubated with PBS. The following functional tests were evaluated, analyzing a total of 10000 events for each sample according to previously established protocols (15-22).
Mitochondrial membrane potential ([DELTA][[PSI].sub.m]): One million sperm were incubated with 3,3'-dihexyl-oxacarbocyanine iodide DIO[C.sub.6] (final concentration 10 nM, Molecular Probes Inc., Thermo Fisher Scientific) and propidium iodide (PI, final concentration 12 [micro]M, Molecular Probes Inc., Thermo Fisher Scientific) in the dark (30 min, 25[degrees]C). The samples were washed in PBS, centrifuged at 180 g for 5 min, and the pellets re-suspended in PBS and subjected to flow cytometry. Data were acquired as the percentage of living spermatozoa showing high ([DELTA][[PSI].sub.m.sup. high]) or low ([DELTA][[PSI].sub.m.sup. low]) green fluorescence, and dead spermatozoa-red fluorescence (19, 21).
Evaluation of plasma membrane integrity: One million sperm were incubated in Sybr-14 and PI (Final concentrations of 1 [micro]M and 12 [micro]M, respectively, The LIVE/DEAD[R] Sperm Viability Kit, Molecular Probes Inc., Thermo Fisher Scientific) in the dark (30 min, 25[degrees]C), washed once and re-suspended in PBS prior to flow cytometry analysis. The data are expressed as the percentage of viable spermatozoa (19, 21).
Lipid peroxidation assay: One million sperm were incubated in the dark (30 min, 25[degrees]C) with BODIPY C11 (Final concentration 6.6 [micro]M, Molecular Probes Inc., Thermo Fisher Scientific), washed and re-suspended in PBS before flow cytometry analysis. The results are expressed as the percentage of spermatozoa exhibiting a green fluorescence response (15).
Production of intracellular reactive oxygen species: One million sperm were incubated with PI (final concentration 12 [micro]M) and 2',7'-dichlorodihydro-fluorescein diacetate (DCFH-DA, Sigma-Aldrich, St Louis, MO, USA, final concentration 1 [micro]M) in the dark for 5 min, at 25[degrees]C, washed three times with PBS (180 g, 5 min) and the pellets re-suspended in PBS before being analyzed by flow cytometry. The results are expressed as the percentage of spermatozoa exhibiting the green fluorescence response (23-25).
Spermchromatin structureassay: Five million sperm were suspended in 200 [micro]l of TNE buffer (Tris-HCl, NaCl and EDTA, pH=7.4). Before reading on the cytometer, 200 ml of acid detergent solution (HCl, NaCl, Triton X-100, water, pH=1.2) was added and 30 s after, the sperm were stained with 600 [micro]l of acridine orange (Sigma-Aldrich) staining solution (6 [micro]g/ml). The ratio of single stranded DNA (red) to single plus double stranded DNA (green) media fluorescence intensity (MFI) is expressed as the DNA fragmentation index (DFI) (19, 21).
Detection of membrane phosphatidylserine exposure: An aliquot of 2x[10.sup.6] spermatozoa was re-suspended in binding buffer, labeled with Annexin-FITC plus PI, incubated for 15 min in the dark, followed by the addition of binding buffer (10x: 0.1 M Hepes pH=7.4, 1.4 M NaCl; 25 mm CaC[l.sub.2]) and then immediately transferred to a flow cytometer and analyzed according to the manufacturer's instructions (eBioscience Apoptosis Detection Kit FITC; BD, Thermo Fisher Scientific). The results are expressed as percentage of cells for each population of interest, phosphatidylserine exposure and PI positive (23).
Blockage of the mannose receptor: Sperm cells were incubated with mannose (Sigma-Aldrich, St. Louis, MO, USA, 100 [micro]M) for 1 hr and subsequently, the sperm cells were incubated with each yeast (0.5 McF). The results are expressed as the percentage change in progressive sperm motility relative to the control (spermatozoa incubated in PBS) at 0 and 3 hr.
Statistical analysis: The flow cytometry results of each functional parameter were processed using the FlowJo program 7.6 (TreeStar, San Carlos, CA, USA). Descriptive statistics were applied (Median and range). For the analysis of the conventional and functional parameters, a non-parametric Friedman was performed (Friedman test) considering a statistical significance of p<0.05. The assumption of normality was checked by Kolmogorov-Smirnov, Shapiro-Wilk test and D'Agostino-Pearson using Prism 5.0 (GraphPad Software, San Diego, CA) statistical software.
The effect of C. albicans, C. glabrata strains and their 0.5 McF SFFM on sperm viability is shown in figure 1. C. albicans progressively decreased sperm viability to 45% (2 McF, p<0.0001) and their SFFM to 18% (p< 0.0001) based on the control (Figure 1A), whereas C. glabrata strain achieved a maximum reduction of 42% (2 McF, p<0.0001) and their SFFM of 15% (p<0.01) with respect to the control (Figure 1B).
The effect of the strains of C. albicans, C. glabrata and their SFFM on progressive sperm motility is presented in figure 2. Immediately, when incubation began, both strains significantly decreased sperm motility, and increasing the time of incubation increased the negative effect, although this was higher when C. albicans strains (81%, p<0.0001) or their SFFM were incubated (58%, p<0.001) with respect to the control.
During the capacitation assays, the greatest effect was demonstrated with the strain of C. albicans that reduced motility to 94% (MCA-0.05 McF, p<0.0001) while C. glabrata reduced it to 89% (MCG-0.05 McF p<0.001) (Figure 3).
The effect of 0.5 McF SFFM of the two yeast strains on the sperm functional parameters did not show statistical differences. However, C. albicans decreased early apoptotic cells by 14%, but increased late apoptosis cells by 67%, necrotic cells by 4% and DNA fragmentation index by 4.3%. As for C. glabrata, it increased early apoptosis cells by 69% and late apoptosis to 37%, but it decreased necrotic cells to 17% and DNA fragmentation index to 19% (Table 1).
Finally, the effect of C. albicans and C. glabrata on progressive motility after 1 hr of sperm pre-incubation with mannose, at 0 and 3 hr with Candida spp. is shown in figure 4. Pre-incubation of sperm with mannose reduced the effect of yeast on mobility and no statistically significant differences were observed with control. Treatment with C. albicans or C. glabrata and without mannose decreased sperm motility in both cases (0 and 3 hr) (p<0.05) compared to the control.
In the present study, the effect of C. albicans and C. glabrata on sperm quality was evaluated. Candida spp. strains and their SFFM negatively affect the motility and sperm viability in vitro after 3 and 24 hr, and although both yeast strains significantly affect conventional parameters, C. albicans has a greater negative effect due to its virulence factors. However, with both strains, the effect is associated with yeast concentration and time of incubation. Three hours are sufficient to significantly modify the percentage of viable and progressive spermatozoa. These effects suggest that the sperm alterations caused by Candida spp. may be of greater importance during the fertility consultation.
Men infertility is associated with a decrease in the seminal quality that is frequently affected by uropathogenic or commensal microorganisms that colonize the male and female urogenital tract. Fungal infections are mostly asymptomatic and Candida spp. is the most common cause of fungal infections. However, this yeast has a high prevalence in infections of the female reproductive tract which can affect semen quality. Few studies have evaluated the effect of Candida spp. on seminal quality (8, 12-14).
The most frequently examined yeast until 2009 due to its prevalence was C. albicans (11); among the main virulence factors expressed by this microorganism are the cellular morphology, phenotypic change, extracellular enzymatic activity (proteases and phosphatases) and adhesion factors (11). In vitro studies have shown that yeasts and their filtrates or SFFM inhibit sperm motility, and this effect has been associated with the concentration and duration of contact (8, 13). Similarly, in the study published by Tuttle et al., C. albicans significantly reduced progressive sperm motility and form to nonspecific aggregates after 2 and 4 hr, suggesting that C. albicans affects male fertility potential (12).
Likewise, Tian et al. reported that C. albicans and its SFFM affect sperm morphology, causing the breakdown of the acrosome, inducing the formation of vacuoles in the head of the spermatozoa, damaging the middle piece and altering the normal function of mitochondria; in addition, these authors reported the formation of nonspecific aggregates (13). Rennemeire et al. reported that SFFM from C. albicans induces loss of acrosome and sperm viability (24), and Burrello et al. re ported that C. albicans sperm interaction increases the DNA fragmentation index and inhibits the fertilization process during assisted reproduction techniques (14). Burrello et al. later demonstrated alterations in sperm motility, mitochondrial membrane potential and cellular apoptosis after 3 and 24 hr of incubation with C. albicans (8). In contrast, Berktas et al. evaluated the effect of C. albicans on sperm motility at various concentrations, but found no influence of this microorganism on the seminal parameters (25).
With respect to sperm DNA damage, it is important to remark that several studies report that sperm incubation at 37 [degrees]C during 3 hr is associated with DNA damage (26, 27). In our case, the treatment during 3 hr with the SFFM was not different in relation to the control. However, the higher result of SCSA test could be originated by this incubation.
On the other hand, no reports examined the effect of C. glabrata on seminal quality, although C. glabrata causes balanitis and orchitis (25). During the last three decades, an increase in the number of cases of vaginal candidiasis, candidemia and systemic fungal infections caused by this species of yeast has occurred. It has even been considered an emerging pathogen, although it appears less virulent than other Candida species, due to the absence of pseudohifas, structures that increase the adherence and penetration of the fungus into tissues and cultures. However, it is known that C. glabrata produces proteases and presents hydro-phobicity on its cell surface, allowing adherence similar to that of C. albicans (28).
Regarding the functional parameters examined in the present study, no statistical differences were found. However, similar to what was reported in the literature (8), SFFM of C. albicans and C. glabrata affects some functional parameters. No reports regarding how the presence of Candida spp. affects reactive oxygen species have appeared and in this study, C. albicans decreases while C. glabrata increases them. In addition, C. glabrata decreases the lipoperoxidation of the sperm membrane.
On the other hand, during sperm travel to the female reproductive tract, sperm cells undergo the capacitation process. In the present study, Candida spp. strains, C. albicans and C. glabrata induce changes in the motility of the sperm during the capacitation process. If this same process occurs in vivo, the possibility to fertilize the oocyte decreases.
Candida spp. has mannan in the form of a glycoprotein that consists mainly of mannose residues and spermatozoa have receptors for this carbohydrate (29-32); these interactions explain these aggregations that are not present in mannose-pre-incubated samples. Therefore, in the future, a new methodology with blocked mannose receptor could be used to decrease the negative effects of Candida infection. In addition, there are several limitations in this study that should be noted. Sperm morphology and reversible effects of Candida spp. were not determined. Therefore, more studies are needed to determine the effects of in vitro or in vivo Candida spp. on motility, viability and sperm morphology.
The presence of C. albicans, C. glabrata and their SFFM affect seminal parameters, and this effect is related to incubation time and yeast concentration.
Conflict of Interest
The authors declare no conflict of interest.
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Elizabeth Ximena Castrillon-Duque, Jennifer Puerta Suarez, Walter Dario Cardona Maya (*)
- Grupo Reproduction, Departamento de Microbiologia y Parasitologia, Facultad de Medicina, Universidad de Antioquia, Medellin, Antioquia, Colombia
(*) Corresponding Author: Walter D. Cardona Maya, Grupo Reproduccion, Departamento de Microbiologia y Parasitologia, Facultad de Medicina, Universidad de Antioquia, Medellin, Antioquia, Colombia.
Received: Jun. 28, 2017
Accepted: Oct. 3, 2017
Table 1. Effect of the 0.5 McF soluble factors of Candida spp. on the functional parameters Parameter median (range) Control C. albicans Early apoptosis (%) 4 (2,2-9,9) 3,42 (1,7-11) (a) Late apoptosis (%) 7,38 (4,2-25,8) 12,34 (7,6-27,1) (a) Cells with high [DELTA][[PSI].sub.m] (%) 77,65 (53,1-81,4) 74,2 (48,5-76,1) (a) Lipoperoxidation of membrane (%) 60,4 (0,38-98,6) 59,9 (0,38-86,8) (a) Cells with intact membrane (%) 73,9 (36,9-84,5) 70,35 (54,8-76,7) (a) Necrotic cells (%) 21,7 (12,9-23,6) 24,7 (21,7-25,7) (a) Reactive oxygen species production (%) 70,7 (60,1-81,1) 67 (62-80,7) (a) DNA fragmentation index (%) 30,15 (9,3-52,5) 31,45 (9,3-56,6) (a) Parameter median (range) C. glabrata Early apoptosis (%) 6,76 (4,6-7,9) (a) Late apoptosis (%) 10,14 (2,2-41,5) (a) Cells with high [DELTA][[PSI].sub.m] (%) 77,35 (49,2-79,9) (a) Lipoperoxidation of membrane (%) 56,1 (0,51-73,6) (a) Cells with intact membrane (%) 74,4 (52,9-85,3) (a) Necrotic cells (%) 17,9 (12,7-26,4) (a) Reactive oxygen species production (%) 73,9 (47,4-78,6) (a) DNA fragmentation index (%) 24,5 (9,5-63,9) (a) (a): vs control p>0.05 (No statistical significant def.) Mitochondrial membrane potential ([DELTA][[PSI].sub.m])
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|Title Annotation:||Short Communication|
|Author:||Castrillon-Duque, Elizabeth Ximena; Suarez, Jennifer Puerta; Maya, Walter Dario Cardona|
|Publication:||Journal of Reproduction and Infertility|
|Date:||Jan 1, 2018|
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