The Development and Life History of Echinorhynchus truttae Schrank, 1788 (Acanthocephala)

1966 ◽  
Vol 40 (1-2) ◽  
pp. 11-32 ◽  
Author(s):  
J. B. E. Awachie

The details of the post-embryonic development of Echinorhynchus truttae in the intermediate host, Gammarus pulex, and the final host, Salmo truttae, are described.The cystacanths of this species are sexually mature and are formed about 82 days after infection at room temperature, ca. 17°C.Copulation takes place in the definitive host soon after the worms enter the pyloric region of the intestine. About 10 weeks after infection, mature eggs are passed out with the faeces of fish.

1972 ◽  
Vol 46 (1) ◽  
pp. 35-46 ◽  
Author(s):  
S. C. Dutt ◽  
H. D. Srivastava

The life cycle of Gastrodiscoidcs hominis has been described using Helicorbis coenosus as the experimental intermediate host and the pig as the definitive host.The morphology of the miracidium, redia and metacercaria has been described. Data have been furnished on the infection and longevity, of and production of cercariae by the snail host, and the growth and development of the adult-fluke in the definitive host.


Author(s):  
M. B. Jones ◽  
G. Smaldon

INTRODUCTIONAdults of the isopod genus Holophryxus (Dajidae) occur as ectoparasites on natant decapod crustaceans, but little is known of the ecology and life-history of most species. Species of Holophryxus are thought to have a typical dajid life cycle involving an intermediate host (copepod), a definitive host (prawn) and three larval stages (epicaridium, microniscus, cryptoniscus), and the one species for which details are available fits this pattern (Coyle & Mueller, 1981). The final host is infected by the cryptoniscus, a stage superficially resembling a cirolanid isopod, and the first cryptoniscus to settle loses its isopod-like appearance and develops through a juvenile stage into a rather inflated, highly modified female (Coyle & Mueller, 1981). Any subsequent settler becomes a male, retains the small cryptoniscus body form and lives within the marsupium of the female.


Parasitology ◽  
1932 ◽  
Vol 24 (2) ◽  
pp. 210-224 ◽  
Author(s):  
Cecil A. Hoare

This paper contains a report on a collection of parasitic protozoa from the blood of some vertebrate animals of Uganda.Seven new species and a number of parasites recorded for new hosts are described. New observations on some known parasites are also recorded.An account is given of the life history of the crocodile haemogregarine. It is shown that the schizogony of Hepatozoon pettiti (nomen novum for Haemogregarina pettiti) occurs in the liver of the crocodile, while the sporogony takes place in Glossina palpalis, its intermediate host.A list of all the blood parasites found, together with their hosts, is given.


1974 ◽  
Vol 106 (4) ◽  
pp. 367-376 ◽  
Author(s):  
W. W. Sawchyn ◽  
C. Gillott

AbstractLestes congener Hagen overwinters in the egg stage. There is a diapause just before blastokinesis, during which the egg is extremely resistant to low temperatures and desiccation. Post-diapause embryonic development can occur near 0 °C but will not take place until the eggs are wetted as the pond habitat fills in the spring. Hatching does not occur until the temperature exceeds about 5 °C and is highly synchronous. Larval development is rapid and is completed in the field in about 50 days. Emergence of the adults also is synchronous. Sexual maturation requires 3 weeks. Oviposition occurs immediately after copulation while the pair are still in tandem. It takes place only in dry stems of Scirpus. Adaptations of L. congener for life under rigorous prairie conditions are discussed.


1953 ◽  
Vol 31 (4) ◽  
pp. 351-373 ◽  
Author(s):  
Liang-Yu Wu

A cause of swimmer's itch in the lower Ottawa River is Trichobilharzia cameroni sp. nov. Its life cycle has been completed experimentally in laboratory-bred snails and in canaries and ducks, and the various stages are described. The eggs are spindle-shaped. The sporocysts are colorless and tubular. Mother sporocysts become mature in about a week. The younger daughter sporocyst is provided with spines on the anterior end and becomes mature in about three weeks. The development in the snail requires from 28 to 35 days. A few cercariae were found to live for up to 14 days at 50 °C., although their life at 16° to 18 °C. was about four days. Cercariae kept at room temperature for 60 to 72 hr. were found infective. The adults become mature in canaries and pass eggs in about 12 to 14 days. Physa gyrina is the species of snail naturally infected. It was found in one case giving off cercariae for five months after being kept in the laboratory. Domestic ducks were found to become infected until they were at least four months old, with the parasites developing to maturity in due course; no experiments were made with older ducks. Furthermore, miracidia were still recovered from the faeces four months after the duck had been experimentally infected, and it is suggested that migratory birds are the source of the local infection.


Parasitology ◽  
1953 ◽  
Vol 42 (3-4) ◽  
pp. 244-258 ◽  
Author(s):  
J. F. A. Sprent

The development of Ascaris devosi, a parasite of the fisher and marten, was followed from the egg to the adult stage using the white mouse and the ferret as the intermediate and final hosts respectively. The eggs contained motile 1st stage larvae 6 days after cleavage and were infective at 12 days, the 1st moult having already occurred. The eggs remained infective for at least 1 year. The 2nd stage larva after hatching from the egg in the intestine of the mouse passes through the intestinal wall to the liver and mesenteric tissues. At 3 days after infection they were recovered from the heart, lungs, brain, kidneys and from the carcass. The larvae grow and store food material during the 2nd stage and between 8 and 12 days after infection they undergo the 2nd moult. The mouse shows the most severe pulmonary symptoms on the 3rd and 4th days after infection, the lungs showing complete red hepatization at this time. The 3rd stage larva is relatively inactive and becomes encapsulated in various tissues, particularly in the muscular and subcutaneous tissues of the neck, shoulders and thorax. The chief developmental changes, apart from growth, which occur in the 2nd and 3rd stage larvae are: (i) the intestine develops from a single row of cells to a multi-cellular tube; (ii) the body cavity appears; (iii) the excretory lobes appear, the nucleus on the left side becoming prominent at the end of the 2nd stage; (iv) the cuticle shows transverse striations at the end of the 2nd stage; (v) the lateral lines become prominent.The encapsulated 3rd stage larvae remained alive for at least six months in the tissues of mice and at 25 days after infection of the mouse they were able to develop in the young ferret following killing and ingestion of the mouse. No infection of ferrets was obtained through oral administration of embryonated eggs or 3rd stage larvae digested from mouse tissues.The 3rd moult occurred in the intestine of the young ferret 3–4 days after infection; in adult ferrets the 3rd stage larvae were evidently unable to gain a hold and were passed out in the faeces. In the next 2–3 weeks the larva grew from about 2 to 16 mm. the 4th moult occurring between 2 and 3 weeks after infection. During the 4th stage the lips develop into the adult form and sexual differentiation occurs. In the female the genital rudiment moves forward and becomes differentiated into the vagina, uteri and ovaries. The vulva remains closed throughout the 4th stage.The adult parasites had developed to sexual maturity by 56 days after infection, but they continued to grow and were considerably longer at 6 months after infection. The position of the vulva relative to the body length was found to move from about midway along the body in the 4th stage larva to a position at the junction of the anterior and middle third of the body in the mature adult.The life history of this parasite is discussed in relation to that of A. lumbricoides and other species. It is considered that the life history of A. devosi, requiring as it does a true intermediate host for its completion, provides further information on the evolutionary development of the ascaris group. This work accordingly supports the hypothesis that the earliest members of this group utilized an intermediate host and does not support that which supposes that ascaris parasites are descended from skin-penetrating forms.During this investigation the writer has benefited considerably from correspondence with Dr J. D. Tiner, Department of Zoology, University of Illinois, Urbana, Illinois, U.S.A. His thanks are also due to Dr H. B. Speakman and Dr A. M. Fallis for their encouragement, guidance and help.This work was supported by the Province of Ontario on the recommendation of the Research Council of Ontario.Grateful acknowledgement is made to Mr Cliff Smith of the Connaught Medical Research Laboratories of the University of Toronto for photographic work.


Author(s):  
Marie V. Lebour ◽  
Richard Elmhirst

Parorchis acanthus is a Trematode described by Nicoll (1907) from the bursa Fabricii and rectum of the Herring Gull, Larus argentatus; in 1906 he first described it as Zeugorchis acanthus. Originally found at St. Andrews, it is now known to be common at Millport and also occurs in gulls from the Northumberland coast, and probably is abundant elsewhere. Nicoll found it once in the Common Gull, Larus canus. In 1907 (Lebour, 1907) one of the present writers described a cercaria occurring in rediæ from Purpura lapillus. This was named Cercaria purpurœ sp. inq., and afterwards identified with young stages of Parorchis acanthus in the Herring Gull (Lebour, 1914). It was thus shown that the first host of this Trematode is Purpura lapillus and the final host the Herring Gull, but the intermediate host was unknown. Localities for the cercaria were Loch Ryan, Wigtownshire; Budle Bay, Fenham Flats and Cullercoats in Northumberland; Robin Hood's Bay in Yorkshire; and Millport. Adults occur at St. Andrews, Northumberland coast and Millport, as already stated.The Cercaria appeared to be closely related to Echinostomum cercariæ, and it was suggested (Lebour, 1914) that the intermediate host would probably be some marine bivalve, as it is often so with Echinostomum (e.g. E. secundum in Mytilus edulis and Cardium edule, E. leptosomum in Scrobicularia tenuis). This suggestion now proves to be correct, and we are able to show that the intermediate host of Parorchis acanthus is Mytilus edulis or Cardium edule.On August 13th, 1921, at the Millport Station some larval cercariæ were noticed by Elmhirst swimming in a small glass aquarium, which contained a collection of Purpura lapillus, Cardium edule and Mytilus edulis.


1922 ◽  
Vol 36 (1) ◽  
pp. 135-140 ◽  
Author(s):  
J. Homer Wright ◽  
Eugene M. Craighead

1. The attempt to infect young rabbits and guinea pigs with material containing in all probability the virus of human infantile paralysis failed. 2. Failure to infect the primary animals almost of necessity brought failure with the secondary flea-bitten animals. It is, however barely conceivable that a non-infectious form of an organism might circulate in the blood of the primary animal and that this form, through development in an intermediate host, the flea, might become virulent for the secondary flea-bitten animal. 3. Incidentally, and presumably accidentally, a paralytic disease was observed in young rabbits associated with the presence of an organism showing certain definite characters. So far as we know this paralysis and the associated organism have not been previously described. 4. This organism is found widely distributed in the organs of the affected animals and can be demonstrated in the urine. The active destruction by the organism of the nerve cells of the spinal cord is particularly striking, and gives complete explanation for the paralysis observed clinically. 5. With the organism present in the urine the spread of the disease by contact can be easily understood. 6. The transfer of the infection from animal to animal by fleabites is possible but not probable. 7. The nature of the observed organisms is in doubt. They represent probably an intermediate stage in the life history of some protozoan parasite.


1960 ◽  
Vol 17 (6) ◽  
pp. 763-774 ◽  
Author(s):  
D. M. Scott ◽  
W. F. Black

Larvae of the parasitic ascarid (Porrocaecum decipiens) occurred commonly in the musculature and viscera of Atlantic cod (Gadus morhua) in the Bras d'Or Lakes. They were also present in the musculature of nine other species of teleosts and probably also in the viscera of skates (Raja sp.). Most larvae were longer than 20 mm. None was shorter than 10 mm, a fact which suggested the existence of some earlier intermediate host, probably an invertebrate. More than 8,000 mysids, an important food of fishes when they first become infected, were examined for nematodes. Although 110 nematodes were found, only one certainly and four dubiously appeared to be Porrocaecum. The definitive hosts were the harbour seal (Phoca vitulina) and the grey seal (Halichoerus grypus). The distribution of seals coincided with local variations in the incidence of the parasite in cod.


Sign in / Sign up

Export Citation Format

Share Document