Hostname: page-component-76fb5796d-22dnz Total loading time: 0 Render date: 2024-04-29T05:12:55.223Z Has data issue: false hasContentIssue false

The effect of temperature on the development and survival of the infective larvae of Strongyloides ratti Sandground, 1925

Published online by Cambridge University Press:  06 April 2009

J. Barrett
Affiliation:
The Molteno Institute, University of Cambridge

Extract

The development of the free-living infective larvae of a homogonic strain Strongyloides ratti is described.

The larvae develop only between 15 and 34 °C. Transfer experiments show the temperature block to be in the preparation for the second moult.

Within the temperature range 15–34 °C, increasing the temperature speeds up the rate of development of all the larval stages equally, the Q10 for development being 2·5.

The maximum percentage development occurs at 20 °C. The percentage development is highest in faeces–peat culture (95% development at 20 °C), whilst the percentage development in charcoal and vermiculite cultures is about the same (75% development at 20 °C.).

Larvae grown on charcoal cultures are larger than those grown on vermiculite, which are larger than those grown on peat. No significant difference was found in the length:oesophagus and length:width ratios or in the variability of larvae grown at different temperatures or on different culture media.

Different worm densities in the cultures of from 2000 to 10000 larvae per g of culture did not affect either the size of the infective larve or the percentage development.

The optimum temperature for survival is 15 °C. Worms grown at 20 °C lived longer than worms grown at any other temperature. There was no evidence of temperature adaptation by the larvae.

The infective larvae are positively thermotactic, and show maximum activity at 37 °C.

I should like to thank my supervisor, Dr Tate, for his advice and encouragement. The work was carried out during the tenure of a Medical Research Council Scholarship.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1968

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

Agrawal, V. (1966). The effects of temperature on the survival and development of the free living stages of Oesophagostomum columbianum Curtice, (1890) (Nematoda). Trans. Am. microsc. Soc. 85, 99106.CrossRefGoogle ScholarPubMed
Balasingham, E. (1964). Comparative studies on the effects of temperature on free living stages of Placoconus lotoris, Dochmoides stenocephala and Ancylostoma caninum. Can. J. Zool. 42, 907–18.CrossRefGoogle Scholar
Banda, Narain. (1965). Survival of the first stage larvae and infective larvae of Bunostomum trigonocephalum Rudolphi, 1808. Parasitology 55, 551–8.Google Scholar
Chhabra, R. C. & Singh, K. S. (1965). Effect of temperature on free living stages of two species of Oesophagostomum (Nematoda). Indian J. Helminth. 17, 125–37.Google Scholar
Costello, L. C. & Grollman, S. (1958). Oxygen requirements of Strongyloides papillosus infective larvae. Expl Parasit. 7, 319–27.CrossRefGoogle ScholarPubMed
Fenwick, D. W. & Franklin, M. T. (1942). Identification of Heterodera species by larval length. Technique for estimating the constants determining the length variations with a given species. J. Helminth. 20, 67114.CrossRefGoogle Scholar
Keeling, J. E. D. (1960). The effects of ultra-violet radiation on Nippostrongylus muris. I. Irradiation of infecting larvae: lethal and sublethal effects. Ann. trop. Med. Parasit. 54, 182–91.CrossRefGoogle ScholarPubMed
Poole, J. B. (1956). Reaction to temperature by infective larvae of Nematodirus filicolis Trichostrongylidae (Nematoda). Can. J. comp. Med. 20, 169–72.Google ScholarPubMed
Premvati, , (1958). Studies on Strongyloides of Primates. IV. Effect of temperature on the morphology of the free living stages of Strongyloides fulleborni. Can. J. Zool. 36, 623–8.CrossRefGoogle Scholar
Premvati, , & Lal, S. S. (1961). Effect of high temperature on the infective larvae of Oesophagostomum columbianum Curtice, 1890. J. Parasit. 47, 943–6.Google ScholarPubMed
Reesal, M. R. (1951). Observations on the development of Strongyloides agoutii of the Agouti in the guinea pig. Can. J. Zool. 29, 116–20.CrossRefGoogle Scholar
Rogers, W. P. (1939). The physiological ageing of Ancylostome larvae. J. Helminth. 17, 195202.CrossRefGoogle Scholar
Ronald, K. (1960). The effects of physical stimuli on the larval stages of Terranova decipiens (Krabbe, 1878) (Nematoda: Aniskidae). I. Temperature. Can. J. Zool. 38, 623–42.CrossRefGoogle Scholar
Rose, J. H. (1966). Investigations into the free living phase of the life cycle of Nematodirus helvetianus. Parasitology 56, 679–91.CrossRefGoogle ScholarPubMed
Shepherd, A. M. (1962). New blue R, a stain that differentiates between living and dead nematodes. Nematologica 8, 201–8.CrossRefGoogle Scholar
Spindler, L. A. (1936). Effects of various physical factors on the survival of eggs and infective larvae of the swine nodular worm Oesophagostomum dentatum. J. Parasit. 22, 529. (Abstr.)Google Scholar
Wallace, H. R. (1963). The Biology of Plant Parasitic Nematodes, 1st ed. p. 110. London: Arnold.Google Scholar
Wertheim, G. & Lengy, J. (1964). The seasonal occurrence of Strongyloides ratti Sandground, 1925, and of S. venezuelensis Brumpt, 1934, in a population of Rattus norvegicus. J. Helminth. 38, 393–8.CrossRefGoogle Scholar
Wilson, P. G. A. (1965). The effect of temperature change on the oxygen uptake of the infective larvae of Nippostrongylus brasiliensis. Expl Parasit. 17, 318–25.CrossRefGoogle ScholarPubMed