Ultrastructure and Cytochemistry of the Mature Spermatozoon of Khawia Armeniaca (Cholodkovsky, 1915) (Caryophyllidea: Lytocestidae), a Parasite of Capoeta Capoeta Sevangi (De Filippi, 1865) (Teleostei, Cyprinidae).

The mature spermatozoon of Khawia armeniaca, a monozoic caryophyllidean parasite of templar fish Capoeta capoeta sevangi (De Filippi, 1865) from the Lake Sevan, Armenia, has been studied using transmission electron microscopy and cytochemical technique of Thiéry (1967) for the first time. The mature spermatozoon of K. armeniaca consists of a single axoneme with the 9+'1' trepaxonematan structure, cortical microtubules and nucleus which are situated parallel to the longitudinal axis of the spermatozoon, and a moderately electrondense cytoplasm with glycogen particles. The cortical microtubules are arranged in one continuous semicircle beneath the plasma membrane in Region II and anterior part of Region III of the mature spermatozoon. The two opposite rows of cortical microtubules are observed in the remaining nuclear and at the beginning of the postnuclear part (Regions III, IV) of the male gamete The number of cortical microtubules is remarkably variable in the spermatozoa of various Khawia species. K. armeniaca exhibits the highest number of cortical microtubules in comparison with K. sinensis and K. rossittensis. Glycogen was detected in the cytoplasm of prenuclear (II), nuclear (III) and postnuclear (IV) regions with different ultrastructural organization of the mature spermatozoon of K. armeniaca. Variations of sperm ultrastructural characters within caryophyllideans and other cestodes are discussed.

Introduction

Mature spermatozoa of the Eucestoda show a high variability and provide important characters useful for phylogenetic studies (Justine, 1998, 2001; Levron et al., 2010). In general, they contain one or two axonemes, cortical microtubules, a nucleus, and various granules in the cytoplasm (Justine, 2003). Male gametes of the order Caryophyllidea are of special interest, as phylogenetic relationships within this group and its interrelationships with other tapeworms remain unclear (Waeschenbach et al., 2012; Caira & Littlewood, 2013).

The Caryophyllidea is considered to comprise 42 genera and 122 valid species arranged in four families (Scholz & Oros, 2017). Uptodate, sperm characters of 12 caryophyllidean taxa of 3 families have been described (see Table 1). Of these taxa, 1 species (Breviscolex orientalis) belongs to the family Capingentidae, 5 species (Archigetes sieboldi, Caryophyllaeus laticeps, Glaridacris catostomi, Hunturella nodulosa, Wenyonia virilis) belong to the family Caryophyllaeidae, and 6 species (Atractolytocestus huronensis, Caryophyllaeides fennica, Khawia sinensis, Khawia rossittensis, Lytocestus indicus, Monobothrioides chalmersius) belong to the family Lytocestidae (see Yoneva et al., 2011; Bruňanská et al., 2019; Bruňanská & Kostič, 2012; Świderski & Mackiewicz, 2002; Yoneva et al., 2012a; Gamil, 2008; Bruňanská et al., 2011; Matoušková et al., 2018, Bruňanská, 2009; Matoušková et al., 2019; Yoneva et al., 2012b; Arafa & Hamada, 2004). It is of note that one of the most specious genera of caryophyllidean tapeworms is Khawia which includes 7 valid species (Scholz . Whereas complete spermatological data are available for two Khawia species (see Table 1), ultrastructural study of the third species, Khawia armeniaca, has been focused exclusively on spermiogenesis (Bruňanská & Poddubnaya, 2006).

Table 1

Variation of the maximum number of cortical microtubules (CM) in the spermatozoa of the Caryophyllidea.

Families	Genus Species	CM	References
Capingentidae	Breviscolex orientalis	15	Yoneva et al., 2011
Caryophyllaeidae	Archigetes sieboldi	11	Bruňanská et al., 2019
	Caryophyllaeus laticeps	15	Bruňanská & Kostič, 2012
	Glaridacris catostomi		Świderski & Mackiewicz, 2002
	Hunturella nodulosa	10	Yoneva et al., 2012a
	Wenyonia virilis	30	Gamil, 2008
Lytocestidae	Atractolytocestus huronensis		Bruňanská et al., 2011
	Caryophyllaeides fennica	19	Matoušková et al., 2018
	Khawia armeniaca	35	present study
	Khawia rossittensis	22	Matoušková et al., 2019
	Khawia sinensis	15	Bruňanská, 2009
	Lytocestus indicus	25	Yoneva et al., 2012b
	Monobothrioides chalmersius	40	Arafa & Hamada, 2004

Variation of the m<span class="Chemical">aximum number of cortical microtubules (CM) in the spermatozoa of the <span class="Chemical">Caryophyllidea.

Therefore, the present study aims to provide missing ultrastructural characters of the mature spermatozoa of K. armeniaca which are necessary for better understanding of the male gametes morphology within the genus Khawia, the order <span class="Chemical">Caryophyllidea, and the Eu<span class="Chemical">cestoda.

Materials and Methods

Adult specimens of <span class="Species">Khawia armeniaca (Cholodkovski, 1915) were collected from the intestine of <span class="Species">Capoeta capoeta sevangi (De Filippi, 1865) (Pisces: Cyprinidae), from Lake Sevan, Armenia.

Transmission electron microscopy

The tapeworms were cut into small pieces, fixed immediately in ice cold 3 % <span class="Chemical">glutaraldehyde in <span class="Chemical">sodium cacodylate buffer (pH 7.4) for 3 – 8 h, followed by three changes of cacodylate buffer and postfixed in 1 % OsO4 for 1 h. The material was dehydrated in a graded alcohol series, acetone, and embedded in Araldite. The ultrathin sections (90 nm) were cut on diamond knife using a Leica Ultracut UCT ultramicrotome, placed on copper grids, and double-stained with uranyl acetate (30 min.) and lead citrate (20 min.). The grids were examined in a JEOL 1010 transmission electron microscope operated at 80 kV.

Cytochemistry

Cytochemical technique of Thiéry (1967) with periodic acid-thiosemicarbazide-silver proteinate (PA-TSC-SP) was used for visualisation of glycogen in the mature spermatozooa. Ultrathin sections were placed on gold grids, treated in 1 % PA (20 – 25 min.), washed in destilled water, processed with 1 % TSC (40 min.), washed in 10 % acetic acid and destilled water, treated in 1 % SP (30 min.) and finally washed in destilled water. The grids were observed in JEOL 1010 transmission electron microscope.

Ethical Approval and/or Informed Consent

The research related to animals has been complied with all the relevant national regulations and institutional policies for the care and use of animals.

Results

A large number of cross- and longitudinal sections of the mature spermatozoa from <span class="Disease">vasa deferentia of Khawia armeniaca have been investigated in the present study.

Vas deferens

The vas deferens is situated between vasa eferentia and the ejaculatory duct of the cirrus pouch. The wall of convoluted vas deferens is formed by a thin syncytial epithelial layer, the <span class="Chemical">luminal surface of which is lined by numerous sinuous lamellae and/or rare cilia (measuring up to 3.5 μm) (Fig. 1a).

Fig. 1

Cross sections of the mature spermatozoon of K. armeniaca: (a) vas deferens with five different regions of the spermatozoon (I-V); (b) region I presents one axoneme and six cortical microtubules; (c) region II shows cortical microtubules which are arranged in a semi-circle under the plasma membrane; (d-g) region III or nucleated region: small diameter of anterior part of the nucleus (d), which gradually increases (e), reaches a maximum in the middle part (f), and diminishes again more posteriorly (g); (h-j) region IV shows cortical microtubules which are arranged in two opposite rows (note one single microtubule in the middle between the two opposite rows) (h), rapidly reduced volume of cytoplasm and number of cortical microtubules (i, j); (k-l) region V with one axoneme which lost its central structure (k) and undergoes disorganization into doublets (l). Ax, axoneme; Arrowheads, attachment zones; BB, basal body of the cilium; CM, cortical microtubules; D, doublets; L, lamellae; N, nucleus. Scale bars: a = 1000 nm, b-h, l = 200 nm, i = 250 nm, j, k =125 nm.

Mature spermatozoon

Male gametes are long, filiform cells, tapered at both extremities, with one incorporated axoneme of the 9+‘1’ trepaxonematan structure, cortical microtubules and a nucleus which are situated parallel to the longitudinal axis of the spermatozoon, and granules of glycogen. Five different regions (I – V) with specific ultrastructural organisation can be recognized (Figs. 1, 2, 3).

Fig. 2

Granules of glycogen in the cytoplasm of the mature spermatozoon of K. armeniaca after application of Thiéry method (1967): (a) cross section of region II; (b) cross section of region III; (c) cross section of region IV; (d) longitudinal section of region II. Ax, axoneme; CM, cortical microtubules; G, glycogen; N, nucleus. Scale bars: a-c = 200 nm, d = 250 nm.

Fig. 3

Schematic reconstruction of the mature spermatozoon of K. armeniaca. I–V, five different regions of the mature spermatozoon; ASE, anterior spermatozoon extremity; Ax, axoneme; AZ, attachment zones; CC, central core; CM, cortical microtubules; G, glycogen; N, nucleus; PM, plasma membrane; PSE, posterior spermatozoon extremity.

Region I (Figs. 1a, b; 3I) corresponds to the anterior extremity of the spermatozoon. It contains one <span class="Chemical">axoneme which is surrounded by a semiarc of up to 5 cortical microtubules (CM) located under the plasma membrane. The diameter of the spermatozoon is about 300 nm.

Region II (Figs. 1a, c; 2a, d; 3II) exhibits an increase of both the volume of cytoplasm and the number of CM. The CM are arranged in one continuous row composed of up to 23 elements (Fig. 1c). Granules of <span class="Chemical">glycogen (Figs. 2a, d), can be detected in the cytoplasm using Thiéry method (1967). One pair of attachment zones illustrates the points of fusion of the free flagellum with the median cytoplasmic process during spermiogenesis (Figs. 1c; 3II). The diameter of the spermatozoon reaches up to 460 nm.

Region III (Figs. 1a, d, e, f, g; 2b, 3III) corresponds to the middle part of the mature spermatozoon, containing the nucleus. The diameter of the nucleus is about 40 nm at the beginning (Fig. 1d), gradually enlarges (Fig. 1e) up to 500 nm in its middle region (Fig. 1f). Posteriorly, the nucles diameter diminishes again, having about 160 nm near its posterior extremity (Fig. 1g). The CM are arranged in a semicircle at first (Fig. 1d). Subsequently, an enlarged nucleus is approaching the plasma membrane of the spermatozoon, thus dividing originally continuous semicircle of CM in two opposite parts (Fig. 1e, f, g), each consisting of 12 – 15 elements. One pair of attachment zones can be recognized (Fig. 1f). Based on examination of cross sections, the m<span class="Chemical">aximum number of CM in the spermatozoon of K. armeniaca is 35 elements, which may occurr in the principal nucleated region of the male gamete. In addition, the cytoplasm of the spermatozoon contains scattered granules of <span class="Chemical">glycogen (Fig. 2b). The diameter of the mature spermatozoon in region III is ranging from 480 nm (anterior and posterior parts) to 720 nm (middle part).

Region IV (Figs. 1a, i, j, 2c, 3IV) is the postnuclear part of the spermatozoon. The CM are arranged at first in two opposite rows, each having 9 elements, and one single microtubule is situated in the middle between the two opposite rows (Fig. 1h). More posteriorly, a strong reduction of the cytoplasm volume, and only a few CM (up to 4) are observed (Fig. 1i). Here, the diameter of the spermatozoon is diminished to 380 nm. At the end of Region IV only one <span class="Chemical">axoneme is present (Fig. 1j).

Region V (Figs. 1a, k, l, 3V), or the posterior part of the spermatozoon, contains only one <span class="Chemical">axoneme which undergoes major disorganization: the central core unit disappears at first (Fig. 1k), and is followed by further disorganization of peripheral doublets (Figs. 1l, 3V). The very posterior extremity of the K. armeniaca spermatozoon is around 140 nm in diameter.

Discussion

This study provides an evidence that ultrastructural architecture of the mature spermatozoon of Khawia armeniaca principally resembles that of other lytocestiids and caryophyllideans. Their male gametes exhibit one axoneme; cortical microtubules and nucleus which are situated parallel to the long axis of the spermatozoon (Bruňanská, 2010; Levron et al., 2010). Caryophyllidean tapeworms have the spermatozoon with 9+‘1’ axonemal structure which is typical for the Trepaxonemata (Ehlers, 1984). Their axoneme is composed of the central core unit interconnected with nine peripheral doublet microtubules which are associated with inner and outer dynein arms. Traditionally, it was believed that the central core unit contains the central electron-dense core, electron-lucent intermediate area, and peripheral electron-dense cortical sheath. In contrast, recent electron tomography observations have revealed the presence of the two tubular structures in the central axonemal electron-dense core of two lytocestiid caryophyllideans, Caryophyllaeides fennica and Khawia rossittensis (Matoušková et al., 2018, 2019). Future electron tomography studies are necessary to elucidate the structure of the central electron-dense core of the axonemes in the spermatozoa of K. armeniaca.

The parallel alignment of CM in a longitudinal axis occurrs in most Eucestoda (except for the Cyclophyllidea and Tetrabothriidea, which have spiralled CM), Digenea and Monogenea (Justine, 2001; Bruňanská 2010; Bakhoum ). Based on the number of axonemes (one or two), the parallel/spiralled pattern of CM, the parallel/spiralled pattern of the nucleus, and some other ultrastructural characters, seven types of the male gametes have been proposed for the Eucestoda (Levron et al., 2010). In cross sections, CM are distributed either into two fields located between the two axonemes (Types I and II) or in one field (Types III –VII). Type III spermatozoon exhibits ultrastructural organisation, which is specific exclusively for the Caryophyllidea. According classification of Levron it includes one field of CM loosly scattered under the plasma membrane of the nucleated region of the spermatozoon in cross sections. In contrast, the present study reveals dual arrangement of CM, i.g. (i) in one field or a semicircle, and (ii) in two fields, or two opposite rows in regions III and IV of the spermatozoa in K. armeniaca. Whereas most caryophyllideans have the CM loosly scattered under the plasma membrane (Gamil, 2008; Bruňanská, 2009; Yoneva et al., 2011, 2012a, b; Bruňanská & Kostič, 2012; Matoušková et al., 2018; Bruňanská et al., 2019), the CM in K. armeniaca are tightly packed. A continuous field of tightly packed CM has been reported also in the spermatozoa of lytocestiid Monobothrioides chalmersius by Arafa and Hamada (2004). On the other hand, two opposite rows of CM have been reported in region II of the spermatozoa of lytocestiid Khawia rossittensis by Matoušková and caryophyllaeid Glaridacris catostomi by Świderski and Mackiewicz (2002). However, up to date, the simultaneous occurrence of both types of arrangement of CM has never been reported in the spermatozoa of caryophyllidean species. Here, it is worth to note that CM are distributed into two fields situated between the two axonemes in the gyrocotyllidean and amphilinidean cestodes (Xylander 1989, Bruňanská ) and in most digeneans (Bakhoum ). However, the latter taxa differs from that of any Eucestoda by the presence of a mitochondrion in the spermatozoon.

The location of the maximum number of CM would be an interesting ultrastructural criterion, especially in connection with their presumed role in spermatozoan movements. The maximum number of CM in the spermatozoa within the order Caryophyllidea is not constant (Tab. 1). It occurs in the anterior parts of the spermatozoa most frequently, and varies between 10 and 30 in the Caryophyllaeidae, or 15 – 40 in the Lytocestidae. At the intraspecific level of Khawia, the highest maxim number of the CM (35) has been reported in K. armeniaca (present study), whereas K. rossittensis exhibits maximum 22 CM (Matoušková et al., 2019) and K. sinensis only 15 elements (Bruňanská, 2009).

The occurrence of AZ in the mature spermatozoa of cestodes is not rare, as these structures represent the points of fusion of the free flagellum/flagella with the median cytoplasmic protrusion during spermiogenesis. The AZ were detected in the spermatozoa with one and/or two axonemes. The one-axoneme spermatozoa exhibit one pair of AZ. Within the Caryophyllidea, the AZ are situated in regions II, III or IV of the mature spermatozoa (Yoneva et al., 2012b; Matoušková et al., 2018, 2019; Bruňanská et al., 2019; present study). The two pairs of AZ have been reported in the two-axonemes spermatozoa of the Amphilinidea (Bruňanská et al., 2012a), Spathebothriidea (Bruňanská et al., 2006; Bruňanská & Poddubnaya, 2010), Bothriocephalidea (Levron et al., 2006a, b; Marigo et al., 2012), Diphyllobothriidea (Levron et al., 2006c, 2009, 2013; Bruňanská et al., 2012b), and Trypanorhyncha (Miquel & Świderski, 2006; Miquel et al., 2007; Marigo et al., 2011).

Glycogen is the major carbohydrate storage form in animals and represents the major energy store of the spermatozoa in the Eucestoda (Euzet et al., 1981). The presence of glycogen was detected using Thiéry method (1967) in the spermatozoa of the Caryophyllidea (Bruňanská, 2009; Yoneva et al., 2011; Bruňanská & Kostič, 2012; Matoušková et al., 2018; Bruňanská et al., 2019; present study), and in male gametes of other cestodes, e.g. Diphyllobothriidea, Bothriocephalidea, Haplobothriidea, Diphyllidea, Trypanorhyncha, Tetraphyllidea, Proteocephalidea, and Tetrabothriidea (Levron et al., 2010). In these cestodes, glycogen is localised in the sperm cytoplasm and it was never found in the sperm axonemes.

The spermatozoa travel on their route from the site of the origin towards the cirrus pouch through various canals of the male reproductive system, including vas deferens. The basic structure of the vasa deferentia of K. armeniaca resembles that in caryophyllidean Atractolytocestus huronensis (Bruňanská et al., 2011), gyrocotylideans or amphilinideans (Rohde & Watson, 1986; Xylander, 1989). Interestingly, vasa deferentia of other Caryophyllidea, Spathebothriidea, Diphyllobothriidea or Proteocephalidea have no cilia (Davydov et al., 1994; Korneva & Davydov, 2001; Poddubnaya, 2002; Poddubnaya et al., 2005).