STUDIES ON CESTODES OF THE GENUS TRIAENOPHORUS FROM FISH OF LESSER SLAVE LAKE, ALBERTA: III. NOTES ON TRIAENOPHORUS NODULOSUS (PALLAS) IN THE SECOND INTERMEDIATE HOST

1945 ◽  
Vol 23d (1) ◽  
pp. 1-5 ◽  
Author(s):  
Richard B. Miller

The plerocercoids of T. nodulosus were found in their earliest stages in the livers of burbot fry (Lota lota maculosa) in early July. At this time the worms occur scattered throughout the liver tissue, not enclosed in cysts. The anlagen of the scolex hooks are present.Later in July the cyst wall has developed and the plerocercoids are provided with a scolex identical with the adult structure. The cysts are small and compact and the contained worms strongly coiled in contrast to their earlier, diffuse state.During the second summer the plerocercoids begin to degenerate, the process proceeding from the posterior end forward. No burbot older than yearlings were found to contain cysts.A brief summary of the life history of T. nodulosus is given.

Parasitology ◽  
1935 ◽  
Vol 27 (1) ◽  
pp. 93-100 ◽  
Author(s):  
Wendell H. Krull

The life history of Panopistus pricei, as determined experimentally, has been described, together with the life history stages, including the sporocyst, cercaria and metacercaria. The snail Zonitoides arboreus has been determined experimentally to be a first and second intermediate host of the parasite.


Parasitology ◽  
1960 ◽  
Vol 50 (3-4) ◽  
pp. 551-575 ◽  
Author(s):  
P. Nasir

1. The life cycle of Cotylurus brevis Dubois and Rausch, from the cercaria to the adult, has been investigated for the first time by using laboratory-bred primary, secondary and definitive hosts. The holometabolic metamorphosis with the formation of a tetracotyle stage in a second intermediate host has been described in detail.2. The cercaria of C. brevis obtained from Lymnaea stagnalis in Edgbaston Pool has been found to be identical with Cercaria helvetica XXXIV Dubois from Lake Neuchâtel. The total number of flame cells in the cercaria is twenty, as opposed to the fourteen in the cercaria of Cotylurus cornutus Rudolphi (= ‘Strigea tarda’ described by Mathias (1925), Harper (1929, 1931) and Wesenberg-Lund (1934)).3. In nature the second intermediate host of Cotylurus brevis is Lymnaea stagnalis. Under experimental conditions L. pereger and L. auricularia were also found to act as second intermediate hosts, but neither Planorbis corneus, P. carinatus nor various leeches could act as second intermediate hosts.4. The tetracotyle stage of Cotylurus brevis is morphologically indistinguishable from the corresponding stage of other species of Cotylurus.


Parasitology ◽  
1933 ◽  
Vol 25 (3) ◽  
pp. 317-328 ◽  
Author(s):  
F. J. Brown

1. The life history of Lecithodendrium chilostomum has been established; C. Lecithodendrii chilostomi penetrates a second intermediate host, the larva of Phryganea grandis, and unlike other stylet cercariae does not encyst, but feeds and grows in the host tissue as a mobile metacercaria. During pupation of the host in the following year these mobile forms migrate from the abdominal segments of the larva to the thorax, where they then encyst in the thoracic muscles in which they are also found in the imago. The largest metacercariae and the excysted worms are typical early adult Lecithodendrium chilostomum. No case of progenesis in the metacercaria was found.2. It is estimated that the maximum swarming of the cercariae probably occurs during July, when first penetration of the intermediate host takes place. Subsequent diminished swarming and penetration proceed until November. The life of the larval trematode as a mobile metacercaria is approximately 8 months; the imagines of Phryganea grandis emerge during May and June, the infective period for the final host.3. The metacercariae are not distributed throughout the body cavity of their larval host, but the majority are confined to the three posterior segments.4. Limnophilus rhombicus may also serve as a second intermediate host, but the infection is very light and the metacercariae do not encyst during pupation of this host.5. The excretory system has been determined in all stages of Lecithodendrium chilostomum; it is of the 2 (6 × 2) type. The occurrence of this type of system in other groups of cercariae is reviewed and since it is found in several widely separated families, it is suggested that its presence does not necessarily imply relationship, but is due to convergence.6. The life histories of the following bat trematodes are indicated: Lecitho-dendrium lagena, Plagiorchis vespertilionis and Crepidostomum moeticus.7. The life history of Dicrocoelium dendriticum is discussed.


1944 ◽  
Vol 22d (1) ◽  
pp. 6-16 ◽  
Author(s):  
Thomas W. M. Cameron

A trematode, widely distributed in Canada, and occurring in man and other fish-eating mammals, is described and its taxonomy discussed. Its life cycle has been worked out and it is shown to involve a snail, Amnicola limosa porata as first intermediate host and a fish, the common sucker (Catostomus commersonii) as the second intermediate host. The larval stages are described.


Parasitology ◽  
1927 ◽  
Vol 19 (1) ◽  
pp. 86-99 ◽  
Author(s):  
F. J. Brown

1. Crepidostomum farionis inhabits the gall bladder, as well as the intestine and pyloric caeca, of the trout and grayling.2. The life history of Crepidostomum farionis has been worked out and is based on the similarity of organisation of the cercaria, encysted larval trematode and the adult.3. The first intermediate hosts in the life history of this trematode are Pisidium amnicum (Müll.) and Sphaerium corneum (L.) though the latter is unusual.4. The second intermediate host is the larva of the mayfly, Ephemera danica (Müll.).5. There are two generations of rediae, the first gives rise to daughter rediae, which in turn produce cercariae.6. The rediae are characterised by the absence of ambulatory processes and a functional intestine.7. The cercaria (n.sp.) possesses “eye spots,” stylet and gland cells (salivary?), and the excretory vesicle is tube-shaped.8. The excretory system of the redia and the cercaria has been worked out in detail.9. The relation of the parasites to their respective hosts is discussed. On account of the need for further observations definite conclusions are held over for a later paper.


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.


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.


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.


1961 ◽  
Vol 35 (S1) ◽  
pp. 179-186
Author(s):  
Gobind Singh Thapar

The life history of Olveria indica was worked out experimentally at Lucknow. Gyraulus convexiusculus was shown to be the intermediate host. The various stages in the larval development are described in detail.


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