The life cycle of Anguina agrostis: Embryogenesis

Bpird A. F. and Sptynes B. A. 1981. The life cycle of Anguina agrostis: embryogenesis. International Journal for Parasitology11: 23–33. Egg development, from laying to hatching, of two widely separated populations of Anguina agrostis, has been followed over a range of temperatures. Development rates for these two populations have been shown to be identical with a thermal optimum between 18 and 20°C. The minimum time recorded for embryogenesis through to hatching was 9–10 days.Embryogenesis was inhibited by temperatures of 27°C and above and hatching by temperatures greater than 23°C.No significant differences were detected in the dimensions of eggs from either population. These eggs have an average length of 95 μm and an average width of 38 μm.Electron microscope studies of sections through eggs undergoing synchronous development show that the first and apparently only moult of the larva in the egg commences about 7 days after the start of embryogenesis under optimal conditions. The sequence of morphological events that occur throughout embryogenesis are described and recorded for whole specimens observed at low resolution and the moulting sequence is described from high resolution electron micrographs of the cuticles of synchronously developing embryos and larvae.     

Mastophorus muris (Nematoda: Spirurina): Ultrastructure of somatic muscle development

Hamada G. S. and Wertheim G. 1978. Mastophorus muris (Nematoda: Spirurina): ultrastructure of somatic muscle development. International Journal for Parasitology8; 405–414. The ultrastructure of the somatic muscle cells of the adult and six developmental stages of Mastophorus were studied. In all stages the cells consisted of a contractile region containing myofibrils separated by dense bands and a noncontractile region with nuclei, mitochondria, glycogen, lipid droplets and vesicles. Two sizes of myofilaments were present. The dense band contained T tubules and sarcoplasmic reticulum, and, in more advanced stages, support filaments, glycogen and dense bodies. The contractile region of the adult muscle cell consisted of several hundred irregularly shaped myofibrils arranged in a random pattern. This pattern of myofibrils was defined as irregular-coelomyarian. The third stage larva had a shallow-coelomyarian myofibril configuration, which changed to coelomyarian in the late third stage through the addition of new myofibrils at the apical contractile border. In the fourth stage larvae, the subdivision of existing myofibrils changed the pattern to irregular-coelomyarian.     

The life history of Sulcascaris sulcata (Nematoda: Ascaridoidea), a parasite of marine molluscs and turtles

Berry G. N. and Cannon L. R. G. 1981. The life history of Sulcascaris sulcata (Nematoda: Ascaridoidea), a parasite of marine molluscs and turtles. International Journal for Parasitoiogy11: 43–54. The morphology, development and hatching of Sulcascaris sulcata eggs are described. Two moults occurred in the egg. Third stage larvae spontaneously hatched and were found to develop in marine bivalves and gastropods. Larvae grew steadily and after three to four months, when about 5 mm long, they moulted to fourth stage larvae characteristic of natural infections in bivalves from commercial catches. Experimentally, when fed to laboratory-reared Caretta caretta, the fourth stage larvae first attached at the oesophago-gastric junction where they moulted to adults in 7–21 days. Subsequent growth to mature adults was obtained by at least 5 months after infection. It is suggested that under natural conditions the life history may take up to 2 years to complete. These findings are discussed in relation to the predatory mode of feeding and the breeding habits of C. caretta and the significance of a possible health hazard to man.     

Spatio-temporal regulation of Rx and mitotic patterns shape the eye-cup of the photoreceptor cells in Ciona

The ascidian larva has a pigmented ocellus comprised of a cup-shaped array of approximately 30 photoreceptor cells, a pigment cell, and three lens cells. Morphological, physiological and molecular evidence has suggested evolutionary kinship between the ascidian larval photoreceptors and vertebrate retinal and/or pineal photoreceptors. Rx, an essential factor for vertebrate photoreceptor development, has also been suggested to be involved in the development of the ascidian photoreceptor cells, but a recent revision of the photoreceptor cell lineage raised a crucial discrepancy between the reported expression patterns of Rx and the cell lineage. Here, we report spatio-temporal expression patterns of Rx at single-cell resolution along with mitotic patterns up to the final division of the photoreceptor-lineage cells in Ciona. The expression of Rx commences in non-photoreceptor a-lineage cells on the right side of the anterior sensory vesicle at the early tailbud stage. At the mid tailbud stage, Rx begins to be expressed in the A-lineage photoreceptor cell progenitors located on the right side of the posterior sensory vesicle. Thus, Rx is specifically but not exclusively expressed in the photoreceptor-lineage cells in the ascidian embryo. Two cis-regulatory modules are shown to be important for the photoreceptor-lineage expression of Rx. The cell division patterns of the photoreceptor-lineage cells rationally explain the generation of the cup-shaped structure of the pigmented ocellus. The present findings demonstrate the complete cell lineage of the ocellus photoreceptor cells and provide a framework elucidating the molecular and cellular mechanisms of photoreceptor development in Ciona.     

Structure and development of Austramphilina elongata Johnston, 1931 (Cestodaria: Amphilinidea)

The life cycle and structure of the larva of Austramphilina elongata using light-microscopy, scanning and transmission electron microscopy are described. Eggs are round and non-operculate. Larvae hatch in freshwater and penetrate through the cuticle of juvenile crayfish, Cherax destructor, and of freshwater shrimps, Paratya australiensis and Atya (= Atyoida) sp., shedding their ciliated epidermis. In the last two hosts, development to the infective stage does not occur. In crayfish, larvae grow and reach the infective stage. Turtles, Chelodina longicollis, become infected by eating infected crayfish. Larvae penetrate through the oesophageal wall of the turtle and migrate toward the coelom, where maturation occurs. The free-swimming larva has a syncytial epidermis which covers most of the body except for the posterior region bearing the hooks. It is loosely attached to a thin underlying tegument, which is connected to ‘insunk’ nucleated cell bodies. It forms a thick surface layer in the posterior region. There are three flame cells on each side of the body and two postero-lateral excretory pores. There are no lateral flames. The weir apparatus of the flame cell has the structure typical of parasitic platyhelminths. The smaller capillaries have a smooth surface, that of the terminal ducts is covered by numerous microvilli. Three types of penetration glands open anteriorly. There are five pairs of hooks; one median ‘normal’, two submedian halberd-shaped, and two lateral serrate. Hook are not lost, they are arranged around the gonopore of the adult. Frontal glands opening into the proboscis were found in the anterior part of the body in all stages examined. Infective stages in crayfish have developing reproductive organs and ducts. The tegument of the adult has many microvilli.     

Brugia pahangi: Feeding and nutrient uptake in vitro and in vivo

Incubation in vitro of adult Brugia pahangi in an apparatus which permitted the separate exposure of the anterior, middle, or posterior region of the worms to medium-containing radioactively labeled d-glucose, l-leucine, and adenosine has provided evidence that these materials are taken up in physiologically significant amounts by a transcuticular route. No evidence for an oral ingestion of materials has been obtained from worms in vitro, but in vivo an oral uptake of Trypan blue has been demonstrated. The ultrastructure and cytochemical staining reactions for nonspecific esterase, acid phosphatase (EC-3.1.3.2), and leucine naphthylamidase of the gut and body wall are described.     

A multiciliate ‘starcell’ in the parenchyma of the larva of Austramphilina elongata (Amphilinidea)

Rohde K. and Garlick P. R. 1985. A multicilite ‘starcell’ in the parenchyma of the larva of Austramphilina elongata (Amphilinidea). International Journal for Parasitology15: 403–407. The ultrastructure of a new cell type is described. It is located at the posterior end of the penetration glands of larval Austramphilina. Large numbers of cilia of the cell protrude in all directions into adjacent fluidfilled spaces. The cell is rich in mitochondria and has a cavity which is separated from the surrounding tissue spaces by a sheath of cytoplasm and by ribs of cytoplasm with a membrane between them. Leptotriches project from the cell body into the cavity. Possible functions of the cell are discussed.     

Cholecystokinin and anorexia in sheep infected by the intestinal nematode Trichostrongylus colubriformis

Symons L. E. A. and Hennessy D. R. 1981. Cholecystokinin and anorexia in sheep infected by the intestinal nematode Trichostrongylus colubriformis. Internationaljournal for Parasitology11: 55–58. It was postulated that there is a correlation between anorexia in intestinal nematode infection and the plasma concentration of cholecystokinin (CCK). In the first experiment plasma concentration of CCK rose as food consumption fell until, when sheep infected with Trichostrongylus colubriformis were almost completely anorexic, it had increased by 65%. Plasma CCK and food consumption returned to pre-infection levels in from four to six days after administration of an anthelmintic. In the second experiment food consumption by uninfected sheep was reduced in the first ten minutes after intravenous infusion of 150–300 μg of the octapeptide of CCK. It was concluded that anorexia in these infections may be due to or be mediated by higher concentrations of CCK.     

uninflatable encodes a novel ectodermal apical surface protein required for tracheal inflation in Drosophila

The tracheal system of Drosophila melanogaster has proven to be an excellent model system for studying the development of branched tubular organs. Mechanisms regulating the patterning and initial maturation of the tracheal system have been largely worked out, yet important questions remain regarding how the mature tubes inflate with air at the end of embryogenesis, and how the tracheal system grows in response to the oxygen needs of a developing larva that increases nearly 1000-fold in volume over a four day period. Here we describe the cloning and characterization of uninflatable (uif), a gene that encodes a large transmembrane protein containing carbohydrate binding and cell signaling motifs in its extracellular domain. Uif is highly conserved in insect species, but does not appear to have a true ortholog in vertebrate species. uif is expressed zygotically beginning in stage 5 embryos, and Uif protein localizes to the apical plasma membrane in all ectodermally derived epithelia, most notably in the tracheal system. uif mutant animals show defects in tracheal inflation at the end of embryogenesis, and die primarily as larvae. Tracheal tubes in mutant larvae are often crushed or twisted, although tracheal patterning and maturation appear normal during embryogenesis. uif mutant larvae also show defects in tracheal growth and molting of their tracheal cuticle.     

Observations on crystals found in the intestinal cells of Haemonchus contortus and in the intestinal lumen of Ostertagia ostertagi.

Bird A. F., Waller P. J., Dash K. M. and Major G. 1978. Observations on crystals found in the intestinal cells of Haemonchus contortus and in the intestinal lumen of Ostertagia ostertagi. International Journal for Parasitology8: 69–74. Crystals are described which are located in the distal intestinal cells of the fourth stage larva of Haemonchus contortus and in the distal intestinal lumen of both larvae and adults of Ostertagia ostertagi.The crystals are thought to be by-products of degenerative processes in these nematodes. They are irregular hexagonal rod-shaped structures which measure approx. 2.5 × 15 um in H. contortus. In O. ostertagi they are also irregular hexagonal structures commonly reaching dimensions of 25 × 50 μm, but they vary considerably in size and are not rod-shaped.Histochemical tests. X-ray analysis and electron microscope studies reveal that both types of crystal contain protein and the element sulphur and are of uniform composition, being neither hollow nor having a core of different refractive index.They differ in that the crystals of O. ostertagi contain more sulphur, exhibit birefringence under polarized light, stain with methylene blue, toluidine blue and osmium tetroxide. The crystals from H. contortus on the other hand are not birefringent and do not stain with the dyes mentioned above.     

Identification and characterization of defensin genes from the endoparasitoid wasp Cotesia vestalis (Hymenoptera: Braconidae)

Defensins are members of a large and diverse family of antimicrobial peptides (AMPs) containing three or four intramolecular disulfide bonds. They are widely distributed from vertebrates to invertebrates, and serve as critical defense molecules protecting the host from the invasion of pathogens or protozoan parasites. Cotesia vestalis is a small endoparasitoid wasp that lays eggs in larvae of Plutella xylostella, a cosmopolitan pest of cruciferous crops. We identified and characterized three full-length cDNAs encoding putative defensin-like peptides from C. vestalis, named CvDef1, CvDef2 and CvDef3. Phylogenetic analyses of these sequences showed that they are present in two clades, CITDs and PITDs, indicating a diversity of defensins in C. vestalis. We analyzed their expression patterns in larvae, pupae and adults by semi-quantitative RT-PCR. The results showed that CvDef1 mRNA was expressed from the end stage of the second instar larva, CvDef3 mRNA from the early stage of the second instar larva, and CvDef2 mRNA was expressed in all developmental stages of C. vestalis. Furthermore, CvDef1 showed antimicrobial activity against gram-positive and gram-negative bacteria. Growth kinetics of Staphylococcus aureus indicated that CvDef1 had much better antimicrobial ability than ampicillin, making it a potential candidate for practical use. Transmission electron microscopic (TEM) examination of CvDef1-treated S. aureus cells showed extensive damage to the cell membranes. Our results revealed the basic properties of three defensins in C. vestalis for the first time, which may pave the way for further study of the functions of defensins in parasitism and innate immunity of C. vestalis.     

Sesquiterpene lactones from Vernonia scorpioides and their in vitro cytotoxicity

Fresh leaves of Vernonia scorpioides are widely used in Brazil to treat a variety of skin disorders. Previous in vivo studies with extracts of this species had also demonstrated a high antitumor potential. This paper reports isolation of four sesquiterpene lactones (hirsutinolides and glaucolides), together with diacetylpiptocarphol, 8-acetyl-13-etoxypiptocarphol, luteolin, apigenin, and ethyl caffeate from fresh leaves and flowers of Vernonia scorpioides. The hypothesis that hirsutinolide 3 is formed during extraction was verified theoretically using Density Functional Theory. The effects of isolated compounds on in vitro tumor cells were investigated, as well as their genotoxicity by means of an in vitro comet assay. The results indicate that glaucolide 2 and hirsutinolide 4 are toxic to HeLa cells. These compounds were genotoxic in vitro, a property that appears to be related to the presence of their epoxy groups, which has been a more reliable indication of toxicity than substitution on C-13 or the presence of α,β-unsaturated keto-groups. These results need to be replicated in vivo in order to ascertain their toxicity.     

In vitro development of the strobilar stage of Mesocestoides corti

Thompson R. C. A., Jue Sue L. P. and Buckley S. J. 1982. In vitro development of the strobilar stage of Mesocestoides corti. International Journal for Parasitology12: 303–314. Sexually mature strobilated adults of Mesocestoides corti were grown consistently from undifferentiated tetrathyridia in vitro using a conventional diphasic culture system. Development (growth, strobilisation and maturation) was compared in vitro and in vivo. Although growth and strobilisation were comparable in vitro and in vivo, during the first 18 days, total length and numbers of proglottids decreased in vivo but continued to increase in vitro after day 18. Both male and female reproductive systems appeared to develop normally in vitro and self copulation was frequently observed in cultured worms. However, fully developed oncospheres were not produced in vitro.     

The giant cells produced by Telenomus remus (Hymenoptera: Scelionidae)

The parasitic larva of Telenomus remus is surrounded by giant cells throughout its first instar. These cells arise in the embryonic serosa of the parasite and grow in size, starting with a radius of 5nm and ending with 27nm. Young cells are round and mononuclear, whereas older ones are often polynuclear and have varied, irregular contours. Most cells are profusely vacuolated, the vacuoles being especially large in some of the older cells. Only a few of the giant cells are devoured by the first instar parasite larva, but all disappear at the end of this stage. No giant cells seem to be produced by supernumerary larvae. Once the parasite egg hatches, the host tissue disintegrates almost instantaneously.     

Rugopharynx rosemariae new species (nematoda: Pharyngostrongylidae) from grey kangaroos (Macropus gig anteus and M. fuliginosus) with life cycle stages and associated pathology

Beverdge I. and Ppresidente P. J. A. 1978. Rugopharynx rosemarie sp. nov. (Nematoda: Pharyngostrongylidae) from grey kangaroos (Macropus giganteus and M. fuliginosus) with life cycle stages and associated pathology. International Journal for Parasitology8: 379–387. Rugopharynx rosemariae new species is described from the stomachs of grey kangaroos, Macropus giganteus Shaw, 1790 and Macropus fuliginosus (Desmarest, 1817) from south-eastern Australia. The new species differs from other species of the genus in spicule length and in the length and shape of the oesophagus. Parasitic life-cycle stages are described from natural infections; free-living life-cycle stages were obtained by culturing eggs from gravid females. Third stage larvae burrow into the gastric mucosa producing small elevated nodules resulting from a localized fibroplastic and inflammatory reaction in the lamina propria and submucosa. Fourth stage and adult worms occur in the stomach lumen. Rugopharynx brevis (Canavan, 1931) is made a synonym of Rugopharynx australis (Mönnig, 1926).     

Freshwater fishes of thailand as experimental intermediate hosts for Capillaria philippinensis

Bhaibulaya M., Indra-Ngarm S. and Ananthapruti M. 1979. Freshwater fishes of Thailand as experimental intermediate hosts for Capillaria philippinensis. The International Journal for Parasitology9: 105–108. Nine species of freshwater fishes from Thailand have been exposed to infection with embryonated eggs of Capillaria philippinensis. The eggs were fed to fishes with food or through a polyethylene tube. After 10–30 days larvae capable of establishing intestinal capillariasis in Mongolian gerbils were recovered from six fish species: Cyprinus carpio, Puntius gonionotus, Aplocheilus panchax, Gambusia holbrookii, Rasbora borapelensis, and Trichopsis vittatus. Larvae were not recovered from Tilapia nilotica, Osteochilus hasseltii and Trichogaster trichopterus. Five human cases of intestinal capillariasis have been reported from widely scattered areas of Thailand and the natural intermediate and definitive hosts remain to be determined.     

Ultrastructural studies on the microfilaria of Cardianema sp. Alicata, 1933 (Nematoda; Onchocercidae)

The ultrastructure of the sheath, cuticle and hypodermis of the microfilaria of Cardianema sp, is described from electron micrographs of in utero- and blood-stages. The trilaminiar sheath invests the microfilaria throughout development in utero and it acquires a superficial coat after the microfilaria enters the blood stream of its reptile host. The cuticle consists of external and internal cortex, fibrillar and subfibrillar layers. The cuticle is attached to the hypodermis without the intervention of a basal lamina. The structure of the external cortex is modified in the annular furrows in the cuticle. The cellular hypodermis forms a complete subcuticular layer, although over much of the circumference the cells exist as thin cytoplasmic processes and where these overlap there are extensive tight junctions. The case for classifying the microfilaria of Cardianema a first stage larva is advanced and a functional but speculative, role for the sheath is proposed.     

Prenylated acetophenones from Melicope obscura and Melicope obtusifolia ssp. obtusifolia var. arborea and their distribution in Rutaceae

Four prenylated acetophenones 2,6-dihydroxy-4-geranyloxyacetophenone (1), 4-geranyloxy-2,6,β-trihydroxyacetophenone (2), 2,6-dihydroxy-4-geranyloxy-3-prenylacetophenone (3), and 4-geranyloxy-3-prenyl-2,6,β-trihydroxyacetophenone (4) have for the first time been isolated from Melicope obscura (1 and 2) and Melicope obtusifolia ssp. obtusifolia var. arborea (3 and 4). The distribution of prenylated acetophenones in Rutaceae is reviewed and the results, including the new records, indicate that prenylated acetophenones are valuable as chemotaxonomic markers for the subfamily Rutoideae, tribe Xanthoxyleae sensu Engler.