scholarly journals INFECTIOUS MOTOR PARALYSIS IN YOUNG RABBITS

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.

Parasitology ◽  
1922 ◽  
Vol 14 (3-4) ◽  
pp. 268-281 ◽  
Author(s):  
F. W. Flattely

Lambs contract Moniezia infection either at or very soon after birth, since they have been observed to harbour adult worms at 2–3 months old and in one case, to pass proglottids at 4–6 weeks.The intermediate host, if such exists, must be frequent on the pasture in early spring, otherwise lambs would not be found to harbour adult tapeworms so regularly or in such numbers when slaughtered in early summer. In the small intestine of a lamb from 3–4 months old slaughtered at Aberystwyth, there occurred 75 individuals.The fact that lambs regularly harbour adult tapeworms before they are weaned suggests the possibility of their contracting the infection from the mother-ewes. No direct evidence in this direction has been obtained, however, and an attempt to produce a larval stage in the udder region of a ewe by feeding to it the eggs of a tapeworm proved abortive.Hitherto, all attempts to produce the adult tapeworms directly by feeding the eggs to sheep have failed; there is, however, the remote possibility that the eggs require to undergo some kind of maturation process outside the body of the sheep before they will develop. The fact that several species of Moniezia occur in the domestic sheep would seem to require an intermediate stage, which would occur in a corresponding number of intermediate-host species.The disease seems prevalent in flocks which are singularly free from ectoparasites.The invertebrates which seem most likely to harbour an intermediate stage are coprophagous insects, etc. (beetles, flies, mites). Attempts to infect species of Aphodius have nevertheless proved fruitless.Moisture favours the survival of the eggs of Moniezia: eggs kept in water for a period of several months seemed to remain perfectly viable. Nevertheless tapeworm is common among flocks on pastures about Rome which are characteristically dry.A comprehensive series of experiments under conditions of the most complete control would almost certainly clear up the life-history; on economic grounds alone the problem is urgent.The overwhelming majority of a quantity of worms collected from slaughter-houses in Aberystwyth, Aberdeen, Beauly (Inverness-shire) and Newcastle-on-Tyne proved to be of the species M. expansa. The only other species found were M. trigonophora and M. alba. The identification was based on anatomical characters and not on externals, which are useless.The writer intends directing his attention to coprophagous mites as carriers, viz. Gamasus coleoptratorum, G. fimetorum, Macrocheles glaber.


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.


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.


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.


The researches recorded in this paper were undertaken at the suggestion of Major Ross, who wished me to investigate the parasitological aspect of the numerical cyclical development discovered by him and Dr. D. Thomson (1910) in the trypanosome occurring in a patient suffering from Sleeping Sickness contracted in Rhodesia, particularly as regards the possible connection of the latent bodies of Salvin-Moore and Breinl (1907) with that cycle. The investigations have been conducted in the Liverpool School of Tropical Medicine, under a grant from the Tropical Diseases Research Fund. A complete and generally accepted life cycle of Trypanosoma gambiense has yet to be written. The following paper is offered as a contribution to the solution of this difficult problem, and deals with that portion of the life history of the parasite which takes place in a Vertebrate host.


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.


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