Exaptation of two ancient immune proteins into a new dimeric pore-forming toxin in snails.

The Membrane Attack Complex-Perforin (MACPF) family is ubiquitously found in all kingdoms. They have diverse cellular roles, however MACPFs with pore-forming toxic function in venoms and poisons are very rare in animals. Here we present the structure of PmPV2, a MACPF toxin from the poisonous apple snail eggs, that can affect the digestive and nervous systems of potential predators. We report the three-dimensional structure of PmPV2, at 17.2 Å resolution determined by negative-stain electron microscopy and its solution structure by small angle X-ray scattering (SAXS). We found that PV2s differ from nearly all MACPFs in two respects: it is a dimer in solution and protomers combine two immune proteins into an AB toxin. The MACPF chain is linked by a single disulfide bond to a tachylectin chain, and two heterodimers are arranged head-to-tail by non-covalent forces in the native protein. MACPF domain is fused with a putative new Ct-accessory domain exclusive to invertebrates. The tachylectin is a six-bladed ß-propeller, similar to animal tectonins. We experimentally validated the predicted functions of both subunits and demonstrated for the first time that PV2s are true pore-forming toxins. The tachylectin "B" delivery subunit would bind to target membranes, and then the MACPF "A" toxic subunit would disrupt lipid bilayers forming large pores altering the plasma membrane conductance. These results indicate that PV2s toxicity evolved by linking two immune proteins where their combined preexisting functions gave rise to a new toxic entity with a novel role in defense against predation. This structure is an unparalleled example of protein exaptation.

A novel approach for the characterisation of proteoglycans and biosynthetic enzymes in a snail model.

Proteoglycans encompass a heterogeneous group of glycoconjugates where proteins are substituted with linear, highly negatively charged glycosaminoglycan chains. Sulphated glycosaminoglycans are ubiquitous to the animal kingdom of the Eukarya domain. Information on the distribution and characterisation of proteoglycans in invertebrate tissues is limited and restricted to a few species. By the use of multidimensional protein identification technology and immunohistochemistry, this study shows for the first time the presence and tissue localisation of different proteoglycans, such as perlecan, aggrecan, and heparan sulphate proteoglycan, amongst others, in organs of the gastropoda Achatina fulica. Through a proteomic analysis of Golgi proteins and immunohistochemistry of tissue sections, we detected the machinery involved in glycosaminoglycan biosynthesis, related to polymer formation (polymerases), as well as secondary modifications (sulphation and uronic acid epimerization). Therefore, this work not only identifies both the proteoglycan core proteins and glycosaminoglycan biosynthetic enzymes in invertebrates but also provides a novel method for the study of glycosaminoglycan and proteoglycan evolution.

Ultrastructural analysis of the dorsal body gland of the terrestrial snail Megalobulimus abbreviatus (Becquaert, 1948) / Análise ultraestrutural da glândula corpo dorsal do caracol terrestre Megalobulimus abbreviatus (Becquaert, 1948)

The ultrastructure of the reproductive gland, dorsal body (DB), of Megalobulimus abbreviatus was analysed. Electron microscope immunohistochemistry was used to detect FMRFamide-like peptides in the nerve endings within this gland. Nerve backfilling was used in an attempt to identify the neurons involved in this innervation. In M. abbreviatus, the DB has a uniform appearance throughout their supraesophageal and subesophageal portions. Dorsal body cells have several features in common with steroid-secreting gland cells, such as the presence of many lipid droplets, numerous mitochondria with tubular cristae and a developed smooth endoplasmic reticulum cisternae. Throughout the DB in M. abbreviatus numerous axonal endings were seen to be in contact with the DB cells exhibiting a synaptic-like structure. The axon terminals contained numerous electron-dense and scanty electron-lucid vesicles. In addition, the DB nerve endings exhibited FMRFamide immunoreactive vesicles. Injection of neural tracer into the DB yielded retrograde labelling of neurons in the metacerebrum lobe of the cerebral ganglia and in the parietal ganglia of the subesophageal ganglia complex. The possibility that some of these retrograde-labelled neurons might be FMRFamide-like neurons that may represent a neural control to the DB in M. abbreviatus is discussed.

Foi analisada a ultraestrutura da glândula reprodutiva corpo dorsal (CD) de Megalobulimus abbreviatus. Imunoistoquímica para microscopia eletrônica foi utilizada para detectar peptídeos relacionados ao tetrapeptídeo FMRFamida nas terminações axonais existentes nessa glândula. Foi utilizada marcação neuronal retrógada com o intuito de localizar os neurônios envolvidos nesta inervação. O CD de M. abbreviatus possui um aspecto uniforme em toda sua extensão, tanto na porção supraesofágica como subesofágica. As células do CD possuem várias características de glândulas esteroidogênicas, tais como a presença de inúmeras gotículas lipídicas, numerosas mitocôndrias com cristas tubulares e cisternas bem desenvolvidas de retículo endoplasmático liso. Por toda a extensão do CD de M. abbreviatus foram encontradas numerosas terminações axonais fazendo contatos estruturalmente semelhantes a sinapses com as células do CD. As terminações axonais continham grande número de vesículas eletrodensas e esparsas vesículas eletrolúcidas. As terminações axonais no CD apresentavam vesículas com conteúdo imunorreativo à FMRFamida. A injeção de traçador neural no CD resultou em marcação retrógrada de neurônios no metacérebro dos gânglios cerebrais e nos gânglios parietais do complexo ganglionar subesofágico de M. abbreviatus. É discutida a possibilidade de que estes neurônios identificados por marcação retrógrada possam representar a via de controle neural do CD de M. abbreviatus, cujo mediador químico seria um neuropeptídeo relacionado à FMRFamida.

Ultrastructural analysis of the dorsal body gland of the terrestrial snail Megalobulimus abbreviatus (Becquaert, 1948).

The ultrastructure of the reproductive gland, dorsal body (DB), of Megalobulimus abbreviatus was analysed. Electron microscope immunohistochemistry was used to detect FMRFamide-like peptides in the nerve endings within this gland. Nerve backfilling was used in an attempt to identify the neurons involved in this innervation. In M. abbreviatus, the DB has a uniform appearance throughout their supraesophageal and subesophageal portions. Dorsal body cells have several features in common with steroid-secreting gland cells, such as the presence of many lipid droplets, numerous mitochondria with tubular cristae and a developed smooth endoplasmic reticulum cisternae. Throughout the DB in M. abbreviatus numerous axonal endings were seen to be in contact with the DB cells exhibiting a synaptic-like structure. The axon terminals contained numerous electron-dense and scanty electron-lucid vesicles. In addition, the DB nerve endings exhibited FMRFamide immunoreactive vesicles. Injection of neural tracer into the DB yielded retrograde labelling of neurons in the metacerebrum lobe of the cerebral ganglia and in the parietal ganglia of the subesophageal ganglia complex. The possibility that some of these retrograde-labelled neurons might be FMRFamide-like neurons that may represent a neural control to the DB in M. abbreviatus is discussed.

Ultrastructural features of the columellar muscle and contractile protein analyses in different muscle groups of Megalobulimus abbreviatus (Gastropoda, Pulmonata).

In Megalobulimus abbreviatus, the ultrastructural features and the contractile proteins of columellar, pharyngeal and foot retractor muscles were studied. These muscles are formed from muscular fascicles distributed in different planes that are separated by connective tissue rich in collagen fibrils. These cells contain thick and thin filaments, the latter being attached to dense bodies, lysosomes, sarcoplasmic reticulum, caveolae, mitochondria and glycogen granules. Three types of muscle cells were distinguished: T1 cells displayed the largest amount of glycogen and an intermediate number of mitochondria, suggesting the highest anaerobic metabolism; T2 cells had the largest number of mitochondria and less glycogen, which suggests an aerobic metabolism; T3 cells showed intermediate glycogen volumes, suggesting an intermediate anaerobic metabolism. The myofilaments in the pedal muscle contained paramyosin measuring between 40 and 80nm in diameter. Western Blot muscle analysis showed a 46-kDa band that corresponds to actin and a 220-kDa band that corresponds to myosin filaments. The thick filament used in the electrophoresis showed a protein band of 100kDa in the muscles, which may correspond to paramyosin.

Development beyond the gastrula stage and digestive organogenesis in the apple-snail Pomacea canaliculata (Architaenioglossa, Ampullariidae)

Development of Pomacea canaliculata from the gastrula stage until the first day after hatching is described. Trochophore embryos are developed after gastrulation, showing the prototroch as a crown of ciliated orange-brownish cells. However, no true veliger embryos are formed, since the prototroch does not fully develop into a velum. Afterward, the connection between the fore- and midgut is permeated and the midgut becomes full of the pink-reddish albumen, which is stored into a central archenterons lake, from where it is accumulated into the large cells forming the midgut wall ("giant cells"). Electron microscopy of giant cells in late embryos showed that albumen is engulfed by large endocytic vesicles formed between the irregular microvilli at the top of these cells. By the end of intracapsular development, giant cells become gradually replaced by two new epithelial cell types which are similar to those found in the adult midgut gland: the pre-columnar and the pre-pyramidal cells. Pre-columnar cells have inconspicuous basal nuclei and are crowned by stereocilia, between which small endocytic vesicles are formed. Pre-pyramidal cells have large nuclei with 2-3 nucleoli and show a striking development of the rough endoplasmic reticulum. The genesis of the three cell lineages (giant, pre-columnar and pre-pyramidal cells) is hypothetically attributed to epithelial streaks that occur at both sides of the midgut since early stages of development.(AU)

Development beyond the gastrula stage and digestive organogenesis in the apple-snail Pomacea canaliculata (Architaenioglossa, Ampullariidae)

Development of Pomacea canaliculata from the gastrula stage until the first day after hatching is described. Trochophore embryos are developed after gastrulation, showing the prototroch as a crown of ciliated orange-brownish cells. However, no true veliger embryos are formed, since the prototroch does not fully develop into a velum. Afterward, the connection between the fore- and midgut is permeated and the midgut becomes full of the pink-reddish albumen, which is stored into a central archenteron's lake, from where it is accumulated into the large cells forming the midgut wall ("giant cells"). Electron microscopy of giant cells in late embryos showed that albumen is engulfed by large endocytic vesicles formed between the irregular microvilli at the top of these cells. By the end of intracapsular development, giant cells become gradually replaced by two new epithelial cell types which are similar to those found in the adult midgut gland: the pre-columnar and the pre-pyramidal cells. Pre-columnar cells have inconspicuous basal nuclei and are crowned by stereocilia, between which small endocytic vesicles are formed. Pre-pyramidal cells have large nuclei with 2-3 nucleoli and show a striking development of the rough endoplasmic reticulum. The genesis of the three cell lineages (giant, pre-columnar and pre-pyramidal cells) is hypothetically attributed to epithelial streaks that occur at both sides of the midgut since early stages of development.

Microscopic anatomy of the male reproductive system in Echinolittorina peruviana (Mollusca: Caenogastropoda) / Anatomía microscópica del sistema reproductor masculino de Echinolittorina peruviana (Mollusca: Caenogastropoda)

Echinolittorina peruviana (Lamarck, 1822), a gonochoric representative of the Littorinidae on the SE Pacific coast, has a male reproductive system adapted for internal fertilization. We describe this system at both macro- and microscopic levels, particularly the compartmentalized organization of the gonad, and the morphology of the penis. The male reproductive system has a variegated conical gonad-digestive gland complex. The gonad presents three compartments, 1) gametogenic acinar among the glandular acini, 2) periacinar with a layer of fusiform somatic cells and, 3) interacinar with glycogen storage cells shared with glandular acini. Spermatogenesis occurs within the acinar gametogenic compartment, with the germinal line organized in centripetal form towards the lumen. The seminal vesicle stores the products of spermatogenesis; in its cephalic region the euspermatozoa are united to the epithelium and the paraspermatozoa are distributed in the lumen. A short duct connects the seminal vesicle to the prostate gland that is open to the pallial cavity over its entire length. The anterior zone of the prostate gland is joined to the cervical spermatic groove that runs along the neck of the snail through the right pallial region; this continues as the penile spermatic groove, ascending from the base to the point of the penis. The penis is acutely conical and unpigmented; towards the anterior and adjacent to its base there is a glandular complex with a mamilliform process and a discoidal glandular region. The secretion from the discoidal region is transformed in a spicule of unknown function, whose histology is described here for the first time. The mamilliform process is formed by the spicular projection and a connective-muscle tissue band which surrounds it and separates it from the discoidal follicular glandular region; the follicular secretion crosses this band and is incorporated into the epithelium which lines the interior of the process.

Echinolittorina peruviana (Lamarck, 1822), representante gonocórico de Littorinidae en el Pacífico Sur, tiene un sistema reproductor masculino adaptado para la fecundación interna, que en este estudio se describe a niveles macrocoscópico y microscópico; enfatizando la organización compartimentalizada de la gónada y la morfología del pene. El sistema reproductor masculino se presenta como un complejo cónico gónada-glándula digestiva abigarrado. La gónada presenta tres compartimientos: 1) gametogénico acinar entre los acinos glandulares, 2) periacinar con una capa de células somáticas fusiformes y 3) interacinar con células almacenadoras de glicógeno, compartido con los acinos glandulares. En el compartimiento gametogénico acinar ocurre la espermatogénesis con la línea germinal organizada en forma centrípeta hacia el lumen. Hacia anterior, la vesícula seminal almacena los productos de la espermatogénesis; en su región cefálica los euespermatozoides se unen al epitelio y los paraespermatozoides se distribuyen en el lumen. Este órgano se conecta con un conducto corto a la glándula prostática, abierta hacia la cavidad paleal en toda su longitud. La zona anterior de la glándula prostática se une al surco espermático cervical, que recorre el cuello del animal por la región paleal derecha; éste continúa como surco espermático peniano ascendiendo desde su base hasta la punta. El pene es cónico aguzado no pigmentado; hacia anterior adyacente a su base, hay un complejo glandular con un proceso mamiliforme y una región glandular discoidal. Su producto de secreción sería una espícula de función desconocida, cuya histología es descrita por primera vez. En este complejo glandular, el proceso mamiliforme está constituido por la proyección espicular y una banda conjuntivo-muscular que lo rodea y separa de la región glandular folicular discoidal; su secreción atraviesa dicha banda, incorporándose al epitelio de revestimiento interno del proceso.

Permeability of the haemolymph-neural interface in the terrestrial snail Megalobulimus abbreviatus (Gastropoda, Pulmonata): an ultrastructural approach.

The aim of this study was to investigate the ultrastructure of the interface zone between the nervous tissue and the connective vascular sheath that surround the central ganglia of the terrestrial snail of Megalobulimus abbreviatus and test its permeability using lanthanum as an electron dense tracer. To this purpose, ganglia from a group of snails were fixed by immersion in a 2% colloidal lanthanum solution, and a second group of animals was injected in the foot with either a 2%, 10% or 20% lanthanum nitrate solution and then sacrificed 2 or 24 h after injection. Ganglia from both groups were processed for transmission electron microscopy. The vascular endothelium, connective tissue and basal lamina of variable thickness that ensheathe the nervous tissue and glial cells of the nervous tissue constitute the interface zone between the haemolymph and the neurones. The injected lanthanum reached the connective tissue of the perineural capsule; however, it did not permeate into the nervous tissue because the basal lamina interposed between both tissues interrupted this passage. Moreover, the ganglia fixed with colloidal lanthanum showed electron dense precipitates between the glial processes in the area adjacent to the basal lamina. It can be concluded from these findings that, of the different components of the haemolymph-neuronal interface, only the basal lamina, between the perineural capsule and the nervous tissue, limits the traffic of substances to and from the central nervous system of this snail.

Testicular organization and spermatogenesis in Tegula (Chlorostoma) tridentata (Potiez and Michaud, 1838) (Mollusca: Archaeogastropoda: Trochidae).

The basic environment for the generation of spermatozoa in the gastropods is a gametogenic compartment resulting from somatic and germ cells interaction. In arachaeogastropods however, such association has not been characterized. In this study at the light and transmission electron microscopy level, evidences are given that in T. (C.) tridentata, spermatogenesis is centrifugal and occurs around seminiferous tubules surrounding the lumen that is a blood vessel. This basic organization presents somatic cells interacting with germ cells. There are three types of spermatogonia: primary spermatocytes with proacrosomic granules, and spermatids that undergo the following spermiohistogenic events: 1. Nuclear chromatin condensation to form a short cylindrical nucleus with an anterior invagination containing the base of the axial rod and a posterior invagination containing the proximal centriole. 2. Polarization of mitochondria attached to the posterior nuclear membrane to integrate the midpiece. 3. Coalescence of proacrosomic granules in one acrosomic vesicle, polarization of the acrosomic vesicle in the anterior nuclear region and transformation of the acrosomic vesicle in the conical acrosomic complex with a subacrosomic cavity containing the axial rod. 4. Tail formation from the distal centriole. Apparently the supporting cells do not associate closely with the spermatids. Therefore, they would not perform a mechanical role in the generation of spermatozoa shape that is characteristic of the Trochidae and other archaeogastropod families. This spermatozoon is peculiar due to its prominent acrosome larger than the nucleus.