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Korean J Parasitol > Volume 60(5):2022 > Article
Keum, Roh, Ryu, and Ryu: Excretory-Secretory Products of Trichomonas vaginalis Cause Apoptosis in Mouse Sperm in Vitro

Abstract

Excretory-secretory products (ESP) of T. vaginalis have been shown to inhibit sperm motility, viability, and functional integrity, leading to a decreased fertilization rate in vitro. This study investigated whether T. vaginalis induce apoptosis and ultrastructural changes of sperm using flow cytometry and electron microscopy. Incubation of sperm with T. vaginalis ESP increased phosphatidylserine externalization and DNA fragmentation, and decreased mitochondrial membrane potential. Transmission electron microscopy of sperm incubated with ESP revealed abnormal features such as distorted heads, broken necks, and acrosomes exocytosis. This is the first report that demonstrates a direct impact of T. vaginalis ESP on sperm apoptosis and architecture in vitro.

Trichomonas vaginalis infection is recognized as an important cause of infertility in men as well as women [1,2]. Many clinical studies have demonstrated decreased sperm motility and viability in men infected with T. vaginalis [37]. We previously demonstrated that T. vaginalis excretory-secretory products (ESP), which are composed of extracellular polymeric substances, reduced sperm motility, viability, and functional integrity, thus leading to a decreased fertilization rate in vitro [8]. The present study examined the impact of the ESP on the apoptosis of mouse spermatozoa.
Mouse sperm were obtained from 8- to 10-week-old 12 male ICR mice (Samtako Biokorea, Osan, Korea) and prepared as previously described [8]. Animal care followed institutional guidelines, and the Hanyang University IACUC approved all procedures, including animal experiments (HY-IACUC-090043). ESP were prepared as previously described [8]. Briefly, ESP were collected after incubating T. vaginalis (T016 isolate), which was kindly provided by Prof. John F. Alderete (Department of Microbiology, University of Texas Health Science Center at San Antonio, Texas, USA) for 1 h in 1 ml of Hank’s balanced salt solution (HBSS, pH 7.2) (Gibco, New York, New York, USA).
To investigate the effect of ESP on apoptosis of spermatozoa in vitro, sperm was prepared as follows. After exposure of the peritoneal cavity, the cauda epididymis was removed and washed immediately in prewarmed 1ml of collection medium (Whitten’s HEPES-buffered medium), and transferred to a 200 μl drop of human tubal fluid (HTF) medium (Quinn’s Advantage Fertilization, In-vitro Fertilization Inc, Trumbull, Connecticut, USA) containing 10% fetal bovine serum in a 35 mm culture dish equilibrated overnight under embryo-tested mineral oil in 5% CO2 humidified atmosphere at 37°C. Sperm were gently squeezed out of the epididymis using a 26-gauge needle, and the residual caudal tissue was discarded. The sperms were allowed to disperse for 15 min and large aggregations of immotile sperm in the culture drops were removed under a dissecting microscope. Aliquots of the sperm suspension (1.5×108 per ml) were incubated in the presence or absence of ESP for 3 h in a 37°C CO2 incubator and labelled with a fluorescence probe to detect apoptotic changes. The fluorescence signals of labelled sperm were evaluated by flow cytometry (FACSCalibur; BD Bioscience, San Jose, California, USA). A minimum of 20,000 events were measured for each sample at a flow rate of 200 to 300 events sec-1 using CellQuest pro software (BD Bioscience).
Since the release of phosphatidylserine (PS) from the plasma membrane is a hallmark of apoptosis [9], structural changes of the plasma membrane of spermatozoa were analyzed with an Annexin V-FITC apoptosis detection kit (BD Bioscience). The proportion of spermatozoa with PS externalization was markedly increased in the ESP-exposed group (ESP) compared to the control (CT) (MFI; CT, 79.6 vs. ESP, 220.6) (Fig. 1A). It has been reported that many factors including infection and toxins can alter the intermembrane permeability of mitochondria, triggering the intrinsic mitochondrial pathway of apoptosis [10]. To assess the integrity of the mitochondrial membrane potential (MMP), the green fluorescence (FL-1 channel) of sperm stained with fluorescein isothiocyanate (FITC)-conjugated 3,3′-dihexyloxacarbocyanine iodide (DiOC6; Molecular Probes, Eugene, Oregon, USA) was evaluated. ESS increased the proportion of spermatozoa with low MMP compared to the control (CT, 9.1% vs. ESP, 17.5%) (Fig. 1B). As loss of sperm motility is closely correlated with decreased MMP integrity [11], low MMP induced by ESP can explain how ESP decreases sperm motility. On the other hand, integrity of sperm DNA has been associated with male fertility in vivo and in vitro [12]. Damage to DNA, such as by fragmentation and denaturation, can cause infertility [13]. We therefore evaluated sperm DNA integrity using Terminal deoxynucleotidyl transferase-mediated dUTP Nick End Labelling (TUNEL) assays (Roche Diagnostics, Mannheim, Germany). Fig. 1C showed that ESP increased DNA fragmentation (MFI; CT, 28.4 vs. ESP, 65.12).
To further evaluate the effects of ESP on sperm, we examined their external and internal architecture after 3 h incubation with ESP using a scanning electron microscope (SEM; S-2380N, Hitachi, Tokyo, Japan) and a transmission electron microscope (TEM; Hitachi H-7600S, Hitachi). Ultrathin sections of the sperm were prepared as previously described [14]. As shown in Fig. 2, spermatozoa incubated with ESP had an abnormal appearance, with damaged or distorted heads and necks. The acrosome exocytosis was also evident. Considering that sperm membrane integrity and intact acrosomes are strongly associated with fertilization rate [15], our results show how T. vaginalis infection induces infertility and subfertility in women and men.
Many previous studies have concentrated on direct contact-dependent effects of T. vaginalis on sperm [1618], while little information has been available on the effects of ESP on sperm apoptosis. Apoptosis is an important and well-regulated form of cell death that occurs under a variety of physiological and pathological conditions [14]. T. vaginalis ESP has also been shown to induce apoptosis in human vaginal epithelial cells [19]. This study provides evidence that T. vaginalis ESP can induce sperm apoptosis in vitro. If this phenomenon also occurs in vivo, it should lead to a decrease in the number of spermatozoa and a decline in fertility. Indeed, testicular trichomoniasis has been known to lead to azoospermia [20]. A series of our studies employing T. vaginalis ESP broadens insight at the subcellular levels into how T. vaginalis infection causes infertility and subfertility in humans.

ACKNOWLEDGMENT

This work was supported by the research fund of Hanyang University (HY-2017).

CONFLICT OF INTEREST

The authors declare no conflict of interest related to this study.

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Fig. 1
Effect of T. vaginalis ESP on apoptosis of mouse sperm. Mouse sperms were treated with ESP for 3 h, and then used for the following assays. (A) Annexin V-PI staining, CT (upper panel); ESP (lower panel). (B) Determination of mitochondrial membrane potentials using FITC-conjugated DiOC6. CT (upper panel); ESP (lower panel). (C) DNA fragmentation by TUNEL assays. Solid and dotted lines indicate CT and ESP, respectively. Data are representative of 3 independent experiments. (CT, control; ESP, T. vaginalis excretory-secretory products-treated group)
kjp-60-5-357f1.jpg
Fig. 2
Effect of T. vaginalis ESP on ultrastructure of mouse sperm. Scanning electron micrographs of sperm (A) incubated in the absence of ESP (CT, left panel) or in the presence of ESP (ESP, right panel). Arrows indicate intact acrosome and arrowheads indicate injured head or neck. Transmission electron micrographs of sperm incubated (B) in culture medium (CT, left panel) or ESP (right panel). Arrows indicate acrosome and arrowheads depict acrosome exocytosis and head destruction. Data are representative of 3 biological replicates. (CT, control; ESP, T. vaginalis ESP-treated group)
kjp-60-5-357f2.jpg
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