Hostname: page-component-77c89778f8-vsgnj Total loading time: 0 Render date: 2024-07-23T19:51:01.157Z Has data issue: false hasContentIssue false

The life history and development of Amplicaecum robertsi, an ascaridoid nematode of the carpet python (Morelia spilotes variegatus). I. Morphology and functional significance of larval stages

Published online by Cambridge University Press:  06 April 2009

J. F. A. Sprent
Affiliation:
Department of Parasitology, University of Queensland, Brisbane

Extract

The development of Amplicaecum robertsi has 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 of A. 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.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1963

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Chabaud, A. G. (1955). Essai d'interpretation phylétique des cycles évolutif chez les nématodes parasites de vertébrés. Conclusions taxonomiques. Ann. Parasit. hum. comp. 30, 83126.CrossRefGoogle Scholar
Harrison, J. L. (1961). The food of some Innisfail mammals. Proc. Roy. Soc. Qd. (in the Press).Google Scholar
Johnston, T. H. & Mawson, P. M. (1948). Some new records of nematodes from Australian snakes. Rec. S. Aust. Mus. 9, 101–6.Google Scholar
Ortlepp, R. J. (1922). On the hatching and migration in a mammalian host of larvae of ascarids normally parasitic in cold-blooded vertebrates. J. Trop. Med. (Hyg.), 25, 97100.Google Scholar
Osche, G. (1955). Über Entwicklung, Zwischenwirt und Bau von Porrocaecum talpae, Porrocaecum ensicaudatum und Habronema mansioni (Nematoda). Z. Parasitenk. 17, 144–64.CrossRefGoogle Scholar
Osche, G. (1957). Die ‘Wirtskreiserweiterung’ bei parasitischen Nematoden und die sie bedingenden biologisch-ökologischen Faktoren. Z. Parasitenk. 17, 437–89.CrossRefGoogle Scholar
Osche, G. (1958). Beiträge zur Morphologie, Ökologie und Phylogenie der Ascaridoidea (Nematoda) Parallelen in der Evolution von Parasit und Wirt. Z. Parasitenk. 18, 479572.CrossRefGoogle Scholar
Petter, C. (1960). Étude zoologique de la larva migrans. Ann. Parasit. hum. comp. 35, 118–37.CrossRefGoogle Scholar
Sprent, J. F. A. (1952). On the migratory behaviour of the larvae of various ascaris species in white mice. I. Distribution of larvae in tissues. J. Infect. Dis. 90, 165–76.CrossRefGoogle ScholarPubMed
Sprent, J. F. A. (1953). Intermediate hosts in Ascaris infections. J. Parasit. 39 (Suppl.), p. 38.Google Scholar
Sprent, J. F. A. (1954). The life cycles of nematodes in the Family Ascarididae Blanchard 1896. J. Parasit. 40, 608–17.CrossRefGoogle ScholarPubMed
Sprent, J. F. A. (1956). The life history and development of Toxocara cati (Schrank, 1788) in the domestic cat. Parasitology, 46, 5478.CrossRefGoogle ScholarPubMed
Sprent, J. F. A. (1958). Observations on the development of Toxocara canis (Werner, 1782) in the dog. Parasitology, 48, 184209.CrossRefGoogle ScholarPubMed
Sprent, J. F. A. (1959). The life history and development of Toxascaris leonina (von Linstow, 1902) in the dog and cat. Parasitology, 49, 330–71.CrossRefGoogle Scholar
Sprent, J. F. A. & Mines, J. J. (1960). A new species of Amplicaecum (Nematoda) from the carpet snake (Morelia argus variegatus): with a redefinition and a key for the genus. Parasitology, 50, 183–90.CrossRefGoogle Scholar
Walton, A. C. (1937). The nematoda as parasites of Amphibia. III. Studies on life histories. J. Parasit. 23, 299300.CrossRefGoogle Scholar