Ultrastructure of the spermatozoa of the flatworms Phaenocelis peleca and Boninia divae (Platyhelminthes, Polycladida)

The ultrastructure of spermatozoa of the acotylean Phaenocelis peleca and the cotylean Boninia divae is described. All spermatozoa are filiform and biflagellate with a 9+"1" microtubular pattern in the axoneme. Sperm characters in P. peleca follow the morphologies described for other acotyleans, with axonemes exiting the sperm shaft at the distal end and remaining in close contact with the sperm membrane. The nucleus occupies the proximal region of the shaft, and two types of dense bodies and mitochondria are located at the distal end. Unlike other members of the Cotylea, the axonemes of B. divae spermatozoa are incorporated into the sperm shaft, leaving the shaft at some distance from the distal end and then remaining free. This type of morphology is characteristic for acotyleans. Additionally, the spermatozoa of B. divae contain only one type of dense bodies plus a unique structure, which we call a central core. The nucleus in this species is unique as well; it shows periodic constrictions and rings of electron-dense granules, characters that further contribute to the distinct status of Boniniidae.     

The plasama membrane of Xenopus laevis spermatozoon

Xenopus laevis sperm plasma membrane ultrastructure has been studied by means of freeze-fracture, deep-etching, and lectin-gold binding. Xenopus spermatozoa differ from those of other species in that their plasma membrane does not exhibit topographical domains. In fact, no geometric arrangement or characteristic array of particles is present on fractured plasma membrane. Fractures rarely occur in acrosomal or nuclear membranes. Wheat germ agglutinin receptors are distributed homogeneously, on the plasma membrane of the sperm head and tail.     

Is Sperm Ultrastructure Useful in Polychaete Systematics? An Example Using 20 Species of the Fabriciinae (Polychaeta: Sabellidae)

The utility of sperm morphology in the systematics of polychaetes has been questioned in the past. This doubt stems from a problem with methodology, not with sperm morphology. It is argued that sperm characters used in combination with other morphological features have utility at various hierarchical levels. As a test of this proposition males in species from each of the following 10 fabriciin genera: Augeneriella, Fabricia, Fabriciola, Fahricinuda, Manayunkia, Novafabricia, Parafabricia, Pseudofabricia, Pseudofabriciola and an undescribed new Genus A (Fitzhugh et al., in preparation), were examined in order to provide new characters for phylogenetic systematic studies. All species were found to have a dorsal sperm duct running beneath the faecal groove of the thoracic region. No sabellin sabellids or serpulids have this duct. The above Fabriciinae have spermatids developing in large clusters of several hundred cells. Serpulids and sabellins nearly always have sperm developing in tetrads or small groups. Fabriciins studied also have a sperm structure distinct from the Sabellinae and the Serpulidae. Proposed synapomorphies for the members of the Fabriciinae, based on sperm structure, include (1) a thick glycocalyx over the plasma membrane; (2) a distinctive nuclear projection, with an anterior thickening of the nuclear membrane; (3) a thickened. spiraling ridge of nuclear membrane; (4) an extra-axonemal sheath and (5) a unique sheath of mitochondrial material in the midpiece. Within the sub-family there were differences among species in sperm structure. This variability involves acrosome morphology; the structure of the sperm nucleus and nuclear projection; the spiral of thickened nuclear membrane; the structure of the extra-axonemal sheath; the mitochondrial sheath. The monophyly of the Fabriciinae (sensu Fitzhugh, 1991, 1993) is well supported by this analysis. The status of Caobangia is still unresolved and a close examination of this genus is warranted.     

Ultrastructural study of spermatogenesis in the free-living marine nematode <Emphasis Type="Italic">Paracyatholaimus pugettensis</Emphasis> Weiser et Hopper, 1967 (Chromadorida: Cyatholaimidae)

Spermatogenesis and the morphology of mature sperm in the free-living chromadorid Paracyatholaimus pugettensis from the Sea of Japan were studied using transmission electron microscopy. In spermatocytes fibrous bodies (FBs) appear; in spermatids, the synthetic apparatus is located in the residual body, whereas the main cell body (MCB) houses the nucleus, mitochondria, and FBs. The nucleus of the spermatid consists of a loose fibrous chromatin that is not surrounded by a nuclear envelope; centrioles lie in the perinuclear cytoplasm. The plasma membrane of the spermatid MCB forms numerous filopodia. Immature spermatozoa from the proximal part of the testis are polygonal cells with a central nucleus. The latter is surrounded by mitochondria and FBs with poorly defined boundaries. The immature spermatozoa bear lamellipodia all along their surface. Mature spermatozoa are polarized cells with an anterior pseudopodium, which is filled with filaments that make up the cytoskeleton; the MCB houses a nucleus that is surrounded by mitochondria and osmiphilic bodies. In many ultrastructural characteristics, the spermatozoa of P. Pugettensis are similar to those of most nematode species studied so far (i.e., they are ameboid, have no acrosome, axoneme, or nuclear envelope). On the other hand, as in other chromadorids, no aberrant membrane organelles were observed during spermatogenesis of P. Pugettensis.Original Russian Text Copyright © 2004 by Biologiya Morya, Zograf, Yushin.     

Spermatogenesis,sperm cell morphology and accompanying secretions from two interstitial marine mites

The sperm cell morphology and spermatogenesis of Halacaroides antoniazziae Pepato Tiago and da Rocha 2011 and Acaromantis vespucioi Pepato and Tiago 2004 was investigated. Halacaroides sperm cells have a complete acrosomal complex, dense tubules crossing the cytoplasm and modified mitochondria. Mature sperm cells are surrounded by two kinds of secretions. Inside the ejaculatory duct, they lie upon a centre composed of a secretion structured as heaps of elongated bodies. Acaromantis spermatozoa are spindle shaped and lack an acrosomal complex. The plasmalemma is deeply folded; the cytoplasm is very reduced and devoid of organelles. A single kind of globular secretion was found. The sperm mass is surrounded by two layers of amorphous secretions. These species share a peripheral pattern of nuclear condensation during spermatogenesis, a possible apomorphy for most halacarids, and no special adaptation to the interstitial environment could be related to their sperm cell morphology.     

Sperm morphology of five species of Colostethus (Anura, Dendrobatidae) from Brazil, with phylogenetic comments

We describe the sperm ultrastructure of five species of Colostethus from Brazil. The general structures of the spermatozoa (acrosomal complex and flagellar apparatus) were similar to species within the Bufonoidea. Colostethus brunneus, Colostethus sp. (aff. trilineatus), Colostethus nidicola and Colostethus sp. had biflagellated spermatozoa, whereas the spermatozoa of Colostethus stepheni had a single flagellum, a characteristic previously unknown for this genus. In addition, the spermatozoa of this species showed some mitochondria within the thick, undulating membrane. These characteristics are apparently common to dendrobatid species that have a single flagellum. Based on these findings, we tentatively consider biflagellarity to be an apomorphic condition in the Dendrobatidae. In addition, the results described here do not support the proposed regrouping of the ‘brunneus’ and ‘alagoanus’ groups in a monophyletic ‘trilineatus’ group.     

Spermatogenesis in a Free-Living Marine Nematode Neochromadora poecilosoma (Chromadorida,Chromadoridae) Studied Using TEM

Spermatogenesis and the structure of mature spermatozoa were studied using TEM in a free-living marine chromadorid nematode Neochromadora poecilosoma from the Sea of Japan. In spermatocytes, fibrous bodies (FB) develop; in spermatids, the synthetic apparatus lies in the residual body, while the nucleus, mitochondria, and FB are located in the main cell body (MCB). The nucleus consists of a diffuse chromatin of fibrous structure, which is not enclosed in a nuclear envelope. In the spermatid stage, the development of FB is completed, and immature spermatozoa from the proximal region of the testis do not show any structural differences from the MCB of spermatids. The mature spermatozoa are polarized cells. They attach to the uterus wall by a pseudopod filled with filaments of the cytoskeleton; in the MCB of spermatozoon, there is a nucleus surrounded by mitochondria and osmiophilic bodies. The spermatozoa of N. poecilosoma show typical ultrastructure features of sperm cells found in most studied nematodes (amoeboid nature and the absence of axoneme, acrosome, and nuclear envelope). However, no aberrant organelles characteristic of nematode spermatozoa were found throughout sperm development in N. poecilosoma and other chromadorids.     

A comparative study on the fine structure of developing spermatozoa in the isopod,Oniscus asellus,and the amphipod,Orchestoidea sp.

Summary Developing spermatids and mature spermatozoa from the isopod, Oniscus asellus and the amphipod, Orchestoidea sp. have been examined with the light microscope and the electron microscope and have been found to have similar morphologies. As spermiogenesis proceeds the nucleus migrates to one pole of the spermatid at which point an acrosome, contiguous rod, and cross-striated tail develop. The acrosomal vesicle elongates to a cone-shaped, mature acrosome lying at the apex of a cross-striated tail and nucleus which are situated at approximate forty-five degrees to each other. The cross-striated tail originates as an evagination of the spermatid plasma membrane near the acrosomal vesicle. The tail eventually grows to lengths of four to five hundred microns. The mature, tail-like appendage is cross-striated at major 750 to 800 Å, and minor 125 to 150 Å, periodicities. When observed in vitro, mature sperm of both species appear non-motile.Possible homologies of this unusual spermatozoon with other types of spermatozoa are made and it is concluded that: 1) isopod and amphipod spermatozoa should be classified as non-flagellate; 2) the cross-striated tail, previously thought to be a flagellum, is a non-motile structure associated in development and possible function with the acrosome; and 3) the rodlike structure contiguous with the acrosome is similar to perforatoria described in some vertebrate sperm.Supported by U.S.P.H.S. Grant No. NB-06285 and Training Grant No. 5-Tl-GM-202. — The author wishes to express his grateful appreciation for the technical assistance given by Miss Ann Barnett during the course of this investigation.     

Observations of spermiogenesis and epididymal sperm maturation in the rufous hare wallaby, Lagorchestes hirsutus (Metatheria, Mammalia)

Acrosomal development in the early spermatid of the rufous hare wallaby shows evidence of formation of an acrosomal granule, similar to that found in eutherian mammals, the Phascolarctidae and Vombatidae. Unlike the other members of the Macropodidae so far examined, the acrosome of this species appears to be fully compacted at spermiation and extends evenly over 90% of the dorsal aspect of the nucleus. During spermiogenesis, the nucleus of the rufous hare wallaby spermatid showed evidence of uneven condensation of chromatin; this may also be related to the appearance of unusual nucleoplasm evaginations from the surface of the fully condensed spermatid. This study was unable to find evidence of the presence of Sertoli cell spurs or nuclear rotation during spermiogenesis in the rufous hare wallaby. The majority of spermatozoa immediately before spermiation had a nucleus that was essentially perpendicular to the long axis of the sperm tail. Nuclei of spermatozoa found in the process of being released or isolated in the lumen of the seminiferous tubule were rotated almost parallel to the long axis of the flagellum; complete parallel alignment occurred during epididymal maturation. At spermiation spermatozoa have characteristically small cytoplasmic remnants compared to those of other macropods. Unlike the majority of macropodid spermatozoa so far described, the spermatozoa of the rufous hare wallaby showed little evidence of morphological change during epididymal transit. There was no formation of a fibre network around the midpiece or of plasma membrane specializations in this region; the only notable change was a distinctive flattening of midpiece mitochondria and scalloping of the anterior mitochondrial sheath to accommodate the sperm head. Preliminary evidence from spermiogenesis and epididymal sperm maturation supports the classification of the rufous hare wallaby as a separate genus but also indicates that its higher taxonomic position may need to be re‐evaluated.     

Ultrastructure of the spermatozoa of Aristaeopsis edwardsiana and Aristeus varidens (Crustacea, Dendrobranchiata, Aristeidae)

The acrosome-less spermatozoon of Aristaeopsis edwardsiana (Crustacea, Aristeidae), which consists of a central non-membrane bound nuclear region surrounded by a thin peripheral cytoplasm, much resembles that of the previously studied aristeid Aristaeomorpha foliacea. The marked spermatozoal similarities between these two species appear to indicate a close phylogenetic proximity. A considerably different spermatozoal pattern is observed in aristeids from the genus Aristeus (A. varidens and A. antennatus), whose spermatozoa possess an anterior spherical acrosome, lacking a spike, and partially embedded in (instead of capping) the main sperm body. The two distinct sperm types found in the Aristeidae differ significantly from the spiked sperm typically found in most penaeoids (Penaeidae, Solenoceridae and Sicyoniidae), thus suggesting a phylogenetic separation of the Aristeidae from the remaining Penaeoidea.     

Ultrastructure of the Geogarypus nigrimanus Spermatozoon (Arachnida,Pseudoscorpionida)

The ultrastructure of the spermatozoon of Geogarypus nigrimanus (Arachnida, Pseudoscorpionida) is described. The spermatozoon is composed of a small elliptic nucleus, a short flagellum and a very long and complex acrosome. In the male genital ducts, as in other studied species of pseudoscorpions, the sperm components are rolled up to form a globular structure enclosed in a cyst wall. The Geogarypus spermatozoon with a reduced flagellum and a giant acrosome seems to be evolutionary more advanced than spermatozoa from other pseudoscorpions.     

Characteristics of Spermatozoa from Five Gall-Midge Species (Diptera, Cecidomyiidae)

The gall-midge family Cecidomyiidae is one of the largest within the animal kingdom. Its characteristics include, among others, a chromosome elimination during spermiogenesis and a bewildering diversity in sperm ultrastructure. The sperm tail, in particular, is unusual in that it deviates from the conventional 9+2 pattern of microtubules. We describe here the spermatozoa of five gall-midge species, all belonging to the same supertribe Cecidomyiidi. In Bremia more than 100 microtubular doublets form a tight spiral around a central mitochondrion. In an undetermined binomen many doublets form a spiral around the mitochondria in the distal end of the sperm tail, but a single row along a peripheral cistern in the main part of the tail. In Coquillettomyia caricis a peripheral row of doublets resides in the proximal part and tightly packed doublets distally. In Arthrocnodax sp. the many doublets also form a peripheral single or double row around a central mitochondrion. In Massalongia bachmaieri there are more than 500 doublets which form several rows around the nucleus and tightly packed doublets distally. The nuclear membrane forms bundles of extensive outpocketings. There is no acrosome. The nucleus consists of both condensed and dispersed material. Only outer dynein arms are present in all this species and the spermatozoa are motile. Cecidomyiidi species that have been examined for sperm structure fall into two groups: those where the mitochondria are confined to the centre of the tail and those in which the mitochondria lie in the head region and have a peripheral location. Most species belong to the first group, while Massalongia belongs to the second one.     

A novel spermatozoan ultrastructure in the shrimp Hippolyte obliquimanus Dana, 1852 (Decapoda: Caridea: Hippolytidae)

The aim of this study was to describe and illustrate the morphology of the spermatozoon of the Western Atlantic shrimp, Hippolyte obliquimanus. Individuals were sampled from Itaguá Beach (Ubatuba, southern Brazil). The male reproductive system was dissected and morphological analysis was undertaken using a stereomicroscope, a light microscope, and transmission electron and scanning electron microscopes. When viewed from the nuclear or acrosomal poles, each spermatozoon has many translucent radiating arms (about 20) from a denser cell body, while laterally the cell body and arms resemble a “cnidarian medusa”, with all the arms projecting away from the bell-like cell body. This sperm morphology is distinct from the “thumbtack”-shaped spermatozoa observed in the majority of carideans but has similarities to the spermatozoa of Rhynchocinetes spp. The morphology of sperm of several species of the genus Hippolyte resembles the spermatozoon of H. obliquimanus with the presence of posterior nuclear arms, but it is necessary to study other Hippolyte species to place these arms in the context of the genus.     

A comparison of the structure of the spermatozoa and spermatogenesis of 16 species of patellid limpet (Mollusca: Gastropoda: Archaeogastropoda)

Light and transmission electron microscopy of the spermatozoa and spermatogenesis of 16 species (in three genera, Patella, Helcion, Cellana) of patellid limpet have shown that head lengths of the sperm range from 3 to 13 μm, and each species has a sperm with a unique morphology, indicating that the spermatozoa can be used as a taxonomic character. Although spermatozoon structure is species specific, five types can be recognized, based on the size, shape, and structure of the nucleus and acrosome. The occurrence of five morphological types of sperm, one of which (Cellana capensis) is particularly different from other patellids, suggests that the taxonomy of the family Patellidae be re-examined. The morphological changes that occur during spermatogenesis are very similar in all species, although two patterns of chromatin condensation are found. Those species with sperm that have short squat nuclei (length:breadth < 3.5:1) have a granular pattern of condensation. Species with sperm that have more elongate nuclei (length:breadth > 5:1) have an initial granular phase followed by the formation of chromatin fibrils. These fibrils become organized along the long axis of the elongating nucleus. The absence of a manchette suggests that nuclear elongation is brought about from within the nucleus.     

Spermatozoon Ultrastructure of Two Holothurian Species of the Genus Cucumaria (Dendrochirotida,Holothuroidea) from the Sea of Japan

The ultrastructure of spermatozoa of Cucumaria japonica and a congeneric morphologically similar deep-sea species was studied. The spermatozoa of both C. japonica and C. conicospermium are similar to those of other holothurians: the acrosome is composed of an acrosomal granule and periacrosomal material; the centrioles lie at an acute angle to one another; and the proximal centriole is connected to the nuclear envelope by a flagellar rootlet. The spermatozoa of C. japonica differ from those of C. conicospermium in the shape of the head and the dimensions and position of the acrosome. In C. japonica, the acrosome is completely embedded in the nuclear fossa and measures 0.7 m. In C. conicospermium, only one-third of the acrosome is embedded in the nuclear fossa; this acrosome measures 1.3 m. A correlation between the structure of the sperm acrosome and that of the egg envelope is discussed.     

Fine structure of spermatozoa inAnthopharynx sacculipenis (Plathelminthes,Solenopharyngidae)

Summary The organisation of the spermatozoa ofAnthopharynx sacculipenis is described, based on electron-microscopical observations. The male gametes are fili-form in shape. They are totally enclosed by cortical microtubules and possess two free cilia. Special features are dot-like dense granules arranged in regular rows and terraced elaborations of the nuclear membrane. Such terraced elaborations are not known in any other species of flatworms whereas dot-like dense granules are described for some other taxa of the Rhabdocoela. Male gametes do not show synapomorphic correspondences between the Solenopharyngidae and the Prolecithiphora.Abbreviations ci cilia - ct cortical microtubules - db dense bodies - gl glycogen - mi mitochondrion - n nucleus - nt nuclear terraces     

Freeze–thaw induced genotoxicity in buffalo (<Emphasis Type="Italic">Bubalus bubalis</Emphasis>) spermatozoa in relation to total antioxidant status

Use of cryopreserved semen has become an important tool in assisted reproduction but freezing and thawing cause sub-lethal damage to spermatozoa. This is detrimental to sperm because of the membrane damage including permeability and integrity. An excess generation of reactive oxygen species (ROS) creates oxidative stress due to reduced antioxidant status of the cryopreserved spermatozoa. In the present study fresh buffalo semen was collected and divided into two aliquots. One aliquot was used for fresh semen analysis and the other was cryopreserved in Tris-egg yolk-citrate extender. The semen samples were used to study different sperm quality parameters like motility, viability, membrane integrity and total antioxidant status. The DNA integrity in fresh and cryopreserved spermatozoa was also studied using comet assay. The sperm quality parameters like post-thaw sperm motility, viability, membrane integrity and total antioxidant status of cryopreserved spermatozoa were significantly lowered (P < 0.05) compared to fresh spermatozoa. The DNA fragmentation in cryopreserved spermatozoa was significantly higher (P < 0.01) as compared to fresh spermatozoa. The results show that the irreversible DNA damage occurs in spermatozoa during cryopreservation.     

The Cytoskeletal Proteins Actin and Tubulin in the Spermatozoa of Four Decapod Crabs (Crustacea,Decapoda)

The mature spermatozoa of four species of European decapod crabs (Clibanarius erythropus, Maja squinado, Cancer pagurusand Potamon fluviatile)have been investigated using indirect immuno-fluorescence techniques for the presence of the cytoskeletal proteins actin and tubulin. Indirect immunofluorescence labelling with monoclonal anti-actin antibody and three different monoclonal anti-tubulin antibodies indicate that actin is present in the spermatozoa of all four species, but tubulins are restricted to the two species with microtubular arms, Clibanariusand Maja.The pattern of actin fluorescence varies between the spermatozoa of the four species, with Majaand Cancershowing intense fluorescence in the acrosome vesicle and in elements of the sperm cell involved in the acrosome reaction. The spermatozoon of each species is described ultrastructurally using transmission electron microscopy and correlations made between observed patterns of fluorescence and the cellular components described. No obvious filamentous actin (F-actin) is visible in the electron micrographs of the spermatozoa of any of the species. In most cases the fluorescence is sufficiently specific to indicate in which region of the mature sperm cell the actin and tubulin occurs. Actin is acrosomal in Maja, Cancerand Potamonbut appears to be cytoplasmic in Clibanarius, while the tubulins appear only to be present in the cytoplasm of Clibanarius, Majaand Cancer.     

Interspecific Variation in Structural Organisation of the Spermatozoon in the Asian Bandicoot Rats,Bandicota Species (family Muridae)

The structural organisation of the spermatozoon from two species of bandicoot rats Bandicota bengalensis and Bandicota indica was investigated by light and electron microscopy together with the effect of incubation in Triton-X 100 and sodium dodecyl sulphate. The sperm head of B. bengalensis is invariably falciform, has a uniform electron-dense nucleus capped by an acrosome with a posteriolateral equatorial segment, a subacrosomal cytoskeleton with a large rostral perforatorium, and a sperm tail, attached to the lower concave surface of the sperm head, with typical coarse fibres and fibrous sheath. By contrast, the sperm head shapes of B. indica are generally conical or bulbous, the nucleus contains a few large vacuoles, the acrosome lacks an equatorial segment, no recognisable perforatorium occurs, and the sperm tail, which is attached basally, is very short with only modest development of coarse fibres and fibrous sheath. These results indicate that, within the genus Bandicota, huge interspecific differences in morphology of the spermatozoon have evolved. The spermatozoa of B. bengalensis are similar to those of Rattus and many other murids and thus presumably represent the ancestral condition, whereas those of B. indica (and B. savilei) are unlike spermatozoa from any other eutherian mammal so far described. © 1998 The Royal Swedish Academy of Sciences. Published by Elsevier Science Ltd. All rights reserved     

ELECTRON MICROSCOPE STUDIES OF EARLY STAGES OF SPERM PENETRATION IN HYDROIDES HEXAGONUS (ANNELIDA) AND SACCOGLOSSUS KOWALEVSKII (ENTEROPNEUSTA)

1. The early events of sperm entry in Saccoglossus and Hydroides are described and examined in relation to present knowledge of the acrosome reaction and of egg membrane lysins. In Saccoglossus and several other species these events occur in two phases. First. The acrosome filament of the spermatozoön spans the egg membrane barriers, reaches the reactive egg protoplasm, and causes the egg to begin its fertilization reaction. Second. The filament and its connected sperm head move through the egg membrane barriers and enter the egg proper. The first phase is completed in a matter of seconds but the second phase usually requires several minutes. 2. The peripheral areas of the eggs of the two species differ as seen in sections. In Hydroides, but not in Saccoglossus, the vitelline membrane is bounded by a distinct outer border layer of small concentrically differentiated bodies and penetrated by microvilli from the egg. 3. The acrosome filament, seen in the living condition as a delicate thread in Hydroides and as an exceedingly tenuous thread in Saccoglossus, appears to be tubular in both species when seen in electron micrographs of thin sections. 4. The acrosomal region of Hydroides appears to consist of two components—a peripheral one, which may collapse during the acrosome reaction, and a central one related to the acrosome filament. 5. Deliberately induced polyspermic material was used to increase the probability of finding examples of sperm penetration in thin sections. 6. As seen in sections, areas of low electron density, interpreted as spaces or pits from which the material of the membrane is absent, surround the attached or penetrating spermatozoa. (a) In Hydroides the spaces vary greatly in many characteristics including shape, position in the membrane, and size with relation to the enclosed sperm head. In one specimen a portion of the membrane is missing from border to border; no spermatozoön is seen but immediately beneath the space is the apex of a fertilization cone. (b) In every case in which a determination could be made, the spermatozoön in the membrane has undergone its acrosome reaction. (c) In Saccoglossus some pits are found with which several spermatozoa are associated. Generally, where the spermatozoa are more numerous the pit is larger. (d) Pits similar to those seen in Saccoglossus sections are observed in living eggs. They remain in Membrane I after sperm entry. (e) From the above and other considerations it is suggested that the pits and spaces are formed by local action of a lysin or lysins emanating from the individual spermatozoön at the site of sperm entry. 7. It is considered that the suggested lysin would participate in sperm entry by eroding the membrane barrier in the vicinity of the sperm head, thus permitting the sperm head to pass through the membrane. Since the acrosome filament much earlier stimulates the egg's initial fertilization response, this lysin would facilitate the second phase of the early events of sperm entry.