Studies on resistance in calves to experimental infection with the nodular worm, Oesophagostomum radiatum (Rudolphi, 1803). III. The stimulation of resistance by multiple infections with larval stages

1967 ◽  
Vol 18 (4) ◽  
pp. 707 ◽  
Author(s):  
RK Keith

Observations are reported on the influence of multiple infections with larval stages of Oesophagostomum radiatum on the stimulation of resistance in calves to reinfection with this parasite. Calves were given spaced doses of infective larvae, and the resulting infections were terminated in the early fourth stage by treatment with an anthelmintic. The egg counts, numbers of adult worms recovered at necropsy, and the pathological changes observed in the intestine subsequent to a test dose indicated that the reinfected calves had developed a high degree of resistance. The reinfected calves made significantly lower weight gains than uninfected control calves during the period of exposure to the larval infections. The results suggest that the immunogenic products of adult worms, and of third stage or early fourth stage larvae, are qualitatively similar.

1968 ◽  
Vol 42 (3-4) ◽  
pp. 269-278 ◽  
Author(s):  
D. N. Dhar ◽  
Kunwar Suresh Singh

1. A precipitate was formed at the oral opening, excretory pore and anal opening of the fourth stage juveniles of O. columbianum in the presence of immune serum in vitro, causing their immobilisation and subsequent death in large numbers. The precipitates failed to appear on these juveniles in normal serum or in saline; nor did they appear on the third stage juveniles on incubation in immune sera. Apparently the excretory-secretory products of the fourth stage juveniles of O. columbianum serve as antigen and play an important role in the stimulation of antibodies in the host.2. Inactivation of the immune serum did not destroy the precipitin type of antibody, nor was it affected when the immune animals had been treated with cortisone.3. Immune serum from animals receiving multiple infections showed a higher antibody titre.4. The possible way in which the antibody acts on the fourth stage juveniles, causing their immobilisation and subsequent death, is discussed.


1962 ◽  
Vol 40 (7) ◽  
pp. 1175-1186 ◽  
Author(s):  
Roy C. Anderson

Eggs of Diplotriaena bargusinica from worms found in a Hylocichla fuscescens from Algonquin Park, Ontario, hatched and developed in the fat body of grasshoppers (Melanoplus bilituratus, M. fasciatus, Camnula pellucida). At approximately 30–33 °C the first molt took place on the 9–11th day, the second on the 14–16th day. Most second- and third-stage larvae were enveloped in capsules, more than one larva often being present in a single capsule. The larval stages from grasshoppers are described. Grasshoppers with infective larvae were fed to two H. fuscescens, one H. ustulata. one Turdus migratorius, and one Quiscalus quiscula. Subadult worms were found in the two H. fuscescens and the H. ustulata 55–301 days later but none was found in the other birds examined 78–97 days later. Late fourth-stage larvae from the heart and aorta of a nestling H. ustulata captured in the field are described. It is believed tridents first make their appearance during development in the definitive host from the infective stage to the fourth stage. Observations on the morphology of adult D. bargusinica are also reported.


Parasitology ◽  
1946 ◽  
Vol 37 (3-4) ◽  
pp. 192-201 ◽  
Author(s):  
J. F. A. Sprent

A description is given of the processes of copulation, formation of the egg and spermatozoon, cleavage, embryogeny and hatching in B. phlebotomum. These processes were found to be essentially similar to those in other strongyle nematodes.The anatomy of the first three larval stages is described and the observations of Conradi & Barnette (1908) and Schwartz (1924) were largely confirmed.Penetration of the skin of calves by the infective larva was observed histologically. The larvae were found to have reached the dermis within 30 min. and to have penetrated the cutaneous blood vessels within 60 min. of application to the skin. The larvae were found in the lung where the third ecdysis was in progress 10 days after penetration of the skin. A description is given of the growth of the third-stage larva in the lung, the changes which take place during the third ecdysis, and the anatomy of the fourth-stage larva.The fourth-stage larvae exsheath in the lungs and travel to the intestine. After a period of growth in which sexual differentiation takes place, the fourth ecdysis occurs and the adult parasite emerges. The time required for the attainment of maturity was found to be somewhere between 30 and 56 days after penetration of the skin.This paper was written at the Ministry of Agriculture and Fisheries Veterinary Laboratories, Wey-bridge, and the writer would like to express his gratitude to the Director, Prof. T. Dalling, also to Dr W. R. Wooldridge, chairman of the Council of the Veterinary Educational Trust for their help and encouragement. The writer's thanks are also due to Dr H. A. Baylis, Prof. R. T. Leiper and Dr E. L. Taylor for their advice and help on technical points, and to Mr R. A. O. Shonekan, African laboratory assistant, for his able co-operation.


1982 ◽  
Vol 56 (2) ◽  
pp. 135-144 ◽  
Author(s):  
A. R. Hunter ◽  
Grace Mackenzie

ABSTRACTThe pathogenesis of H. contortus infection in lambs under 6 months of age challenged orally with 10,000 third stage infective larvae is described. The development of the parasite and its relationship to haematological and pathological changes are discussed, with particular reference to specific cellular mobilizations, and detailed descriptions are given of the haematology and parasitology, gross pathology and histopathology at 4, 7, 12, 18, 22 and 35 days after infection. Dramatic changes had developed by day 12.


1975 ◽  
Vol 53 (11) ◽  
pp. 1552-1568 ◽  
Author(s):  
T. F. Mace ◽  
R. C. Anderson

Dioctophyma renale was found in the right kidney of 48% of mink (Mustela vison) trapped in late fall and winter in the Black River area of Ontario. Eggs embryonated at temperatures from 14 C to 30 C. Eggs hatched in the intestine of the aquatic oligochaete Lumbriculus variegatus, and first-stage larvae migrated to the ventral blood vessel where development took place. The first molt occurred about 50 days after infection in oligochaetes kept at 20 C; the second molt occurred about 100 days after infection. Third-stage larvae removed from oligochaetes produced infection in a mink. Larvae given to frogs (i.e. Rana clamitans, melanota and R. pipiens) became encapsulated in the stomach wall or abdominal muscles. A mink was infected with larvae removed from frogs experimentally infected 25 days earlier. A mink was also infected with larvae found in a naturally infected bullhead (Ictalurus nebulosus). Infective larvae of D. renale were found in wild Rana catesbeiana (6.2%), R. septentrionalis (9.6%), and R. clamitans melanota (0.7%) in an area enzootic for dioctophymiasis. It is suggested frogs as well as bullheads are important natural paratenic hosts for D. renale. The various larval stages of D. renale are described and its third-stage larva is distinguished from that of Eustrongylides spp. which may also be found in frogs.


2000 ◽  
Vol 74 (4) ◽  
pp. 323-328 ◽  
Author(s):  
M. Køie

AbstractMature specimens of Cucullanus heterochrous Rudolphi, 1802 (Nematoda: Cucullanidae) were obtained from the intestine of the flounder, Platichthys flesus, from Danish waters. Eggs embryonate in seawater but do not hatch. Fully developed larvae pressed out of eggs are 430 μm long with amphids and dereids and enclosed within the cuticle of a previous larval stage. Infective larvae are believed to be in their third stage. Experimental studies showed that the polychaetes, Nereis spp., Scoloplos armiger, Brada villosa and Capitella sp., may act as intermediate hosts. In N. diversicolor the larvae increase their length to 1 mm within four weeks (15°C) without moulting. Experimental infections showed that larvated eggs are not infective to fish, whereas >550 μm long larvae from polychaetes survived in 4–24 cm long flounders and plaice, Pleuronectes platessa. Third-stage larvae 550 μm to 1.1 mm long were found in the submucosa of the intestine one week post infection. At a length of about 800 μm to 1.4 mm they moult to fourth-stage larvae. Fourth-stage larvae, immature and mature worms occur in the intestine and rectum. Fourth-stage larvae and adults survived experimental transfer from one flounder to another. Similar developmental stages survived for two weeks in the intestine of experimentally infected cod, Gadus morhua.


1992 ◽  
Vol 70 (8) ◽  
pp. 1576-1584
Author(s):  
Leslie A. Rye ◽  
Michael R. Baker

Larval stages of Hysterothylacium analarum are described from Lepomis gibbosus in Dawson Pond, Ontario (45°10′N, 78°50′W). Second-stage larvae were easily distinguished from all other stages by the presence of a conical boring tooth. Third-stage larvae lacked both a boring tooth and lips. Fourth-stage larvae had well-developed lips. The ratio of ventricular appendage length to intestinal caecum length varied greatly between larval stages and adults. Prevalence and intensity of larval stages and adult H. analarum showed a distinct seasonal pattern, with one generation of adult worms per year. In spring, third-stage larvae left nodules on the intestinal serosa of L. gibbosus and migrated to the intestinal lumen, where they rapidly moulted to the fourth-stage and then to adult worms. Eggs collected from gravid females developed to second stage larvae in approximately 5 days under laboratory conditions. In natural infections in the late summer second-stage larvae were found in nodules on the serosa and in the mesentery. Larvae apparently moulted to the third stage and overwintered in the nodules as third-stage larvae.


Parasitology ◽  
1963 ◽  
Vol 53 (1-2) ◽  
pp. 7-38 ◽  
Author(s):  
J. F. A. Sprent

The development ofAmplicaecum robertsihas been followed from the egg to the adult stage using laboratory mice and rats as intermediate hosts. The eggs were found to be resistant to desiccation and would develop under water; they were infective to mice after culturing for 18 days after removal from the uterus.Completion of the first moult occurred after hatching of the eggs in the intestine. Within 6 hr. of infection second-stage larvae had reached the liver. They also appeared in the lungs and carcass, but after 2 days were mostly confined to the liver.At 5–7 days after infection larvae underwent a period of lethargy followed by the second moult and the third-stage larvae commenced a period of growth reaching a length of 79 mm. at 28 weeks after infection in the liver of mice. In rats the growth of the larvae was slower for the first 2 months, but eventually they reached more or less the same proportions as in mice. The intestinal caecum appeared at a length of 3–4 mm., but there was no development of the reproductive organs throughout the third stage and no evidence of the third moult in rodents.Fifty carpet snakes were autopsied and searched for larvae and adults ofA. robertsi; in two snakes third-stage larvae were found in the aorta; in one snake the third moult was observed in the wall of the stomach and oesophagus; in three snakes the fourth moult was observed in the wall of the stomach; in twenty-six snakes adults were found.Experimental infection of laboratory-reared carpet snakes showed that infection with embryonated eggs resulted in second-stage larvae in the tissues which did not develop further. Infection with third-stage larvae, resulted in two distinct migratory patterns depending upon the maturity of the larvae administered. Larvae from the liver of laboratory rats which had been infected less than 12 weeks previously, migrated to various tissues, especially the aorta, of the snake, where they remained coiled in cysts filled with clotted blood for periods up to 112 days. Growth occurred within these cysts, but no evidence of moulting was observed. In contrast, larvae from the liver of laboratory rats infected 12 weeks or more previously, and from mice infected for 8 weeks or more, underwent the third moult in the wall of the oesophagus and stomach of the snake.With the onset of the fourth stage, the development of the reproductive organs became evident and continued during the fourth stage. It appeared that the fourth stage may occur in two phases, possibly depending on the size of the third-stage larva at the time of ingestion. Some experimental infections indicated that third-stage larvae may give rise to attached fourth stage larvae, probably capable of active growth. Other observations indicated that fourth-stage larvae may remain encapsulated in the wall of the stomach or oesophagus until sex differentiation is completed, after which the fourth moult occurs and the adult parasite emerges, leaving two sheaths of the same length within the capsule.The functional significance of each of the larval stages is discussed and it was concluded:—that the first-stage larva is one of tissue differentiation, whereby development proceeds to the infective stage; that the second stage represents a migratory phase without structural changes; that the third stage represents a growth phase, characterized by considerable increase in size, but without further radical changes in differentiation.In contrast, the fourth stage is characterized by absence of growth, inability to migrate, and by marked structural changes in the reproductive organs, whereby the sexes are differentiated. Evidently this development may take place while the fourth stage is attached to the wall of the stomach or oesophagus, or while the larva remains in the capsule in a state of quiescence.The fourth moult may occur in the attached state, but usually occurs within the capsule. After it is completed, the adult may remain for an indefinite period within the capsule with the two sheaths of the third and fourth stage. The emergence of the adult worms may be influenced by the arrival of food in the stomach. Once this phase is initiated, both growth and reproductive activity ensue during the adult stage.This work was financed by a research grant from the University of Queensland. The writer wishes to acknowledge the valuable assistance of Miss Ann Pritchard.


1983 ◽  
Vol 61 (4) ◽  
pp. 848-859 ◽  
Author(s):  
R. G. Appy ◽  
M. J. Dadswell

The cystidicolid nematode, Capillospirura pseudoargumentosa (Appy and Dadswell, 1978) (Habronematoidea) moulted twice and developed to the infective third stage in Gammarus tigrinus and G. fasciatus (Amphipoda) but not in isopods, decapods, mysids or other amphipods. At 10–14 °C development to the third stage in G. tigrinus took between 28 and 40 days and at 21–25 °C, it took between 10 and 15 days. Infective larvae fed to shortnose sturgeon, Acipenser brevirostrum, moulted from the third to the fourth stage within 15 days. Moulting third- and fourth-stage larvae were found in naturally infected sturgeon collected in the Saint John River estuary, New Brunswick. The developmental morphology of C. pseudoargumentosa is compared with that of other cystidicolid nematodes.


1925 ◽  
Vol 3 (1) ◽  
pp. 1-14 ◽  
Author(s):  
R. J. Ortlepp

1. During the free-living development the larvæ of Triodontophorus tenuicollis undergo two moults separating three larval stages, the last stage remaining ensheathed in the cuticule of the previous stage.2. The development takes about four days when the eggs are cultured in horse fæces and charcoal at 26° C.3. The infective or third stage larvæ are climbers, and also show a marked resistance to desiccation ; they can also withstand variations in temperature from – 8° C. to 60° C.4. They do not penetrate skin.5. Infection of the host is probably via the mouth during grazing.6. The fourth-stage larva is described. It is free in the lumen of the colon, possesses a well-marked larval buccal capsule and three stout and pointed œsophageal teeth. Sex differences are now present.7. The adult buccal capsule develops in the form of a vesicle round the base of the larval buccal capsule.8. The probable mode of its parasitic development is given.9. A fourth-stage larva, probably that of either T. brevicauda or T. serratus, is described.


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