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Variable infectivity of third-stage larvae of Brugia malayi

Published online by Cambridge University Press:  18 November 2009

Mark L. Eberhard
Affiliation:
Department of Parasitology, Delta Regional Primate Research Center, Covington, Louisiana 70433, USA
Robert C. Lowrie Jr
Affiliation:
Department of Parasitology, Delta Regional Primate Research Center, Covington, Louisiana 70433, USA

Abstract

Infectivity of third-stage larvae of Brugia malayi was assessed following intraperitoneal inoculation into jirds, Meriones unguiculatus. Larvae were of two ages and were derived from two sites in Aedes aegypti mosquitoes, i.e., specimens collected from the thorax 11 days after infection and from the head on day 14. Larvae from the thorax had just completed the second moult and measured 990 to 1100μm in length. Only 6% of these specimens developed to adult worms in jirds. Larvae that migrated to the head were 1400 to 1700 μm long on day 14 and, in contrast, 23% of the inocula developed to adult worms. This study establishes that all third-stage larvae, regardless of their age or location in the arthropod host, are potentially infective. However, pronounced physical maturation does seem to be accompanied by a marked increase in infectivity.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1985

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References

REFERENCES

Addison, E. M. (1973) Life cycle of Dipetalonema sprenti Anderson (Nematoda: Filarioidea) of beaver(Castor canadensis). Canadian Journal of Zoology, 51, 403416.CrossRefGoogle ScholarPubMed
Bianco, A. E. & Muller, R. L. (1977) A hard tick as vector of a new rodent filaria. Transactions of the Royal Society of Tropical Medicine and Hygiene, 71, 383.Google Scholar
Feng, L. C. (1936) The development of Microfilaria malayi in A. hyrcanus var. sinensis Wied. China Medical Journal, 50, 345367.Google Scholar
Gwadz, R. W. & Chernin, E. (1972) Oral transmission of Brugia pahangi to jirds (Meriones unguiculatus). Nature, 239, 524525.CrossRefGoogle ScholarPubMed
Hollanda, J. C.Denham, D. A. & Suswillo, R. R. (1982) The infectivity of microfilariae of Brugia pahangi of different ages to Aedes aegypti. Journal of Helminthology, 56, 155157.CrossRefGoogle ScholarPubMed
Kartman, L. (1953) On the growth of Dirofilaria immitis in the mosquito. American Journal of Tropical Medicine and Hygiene, 2, 10621069.CrossRefGoogle ScholarPubMed
Lowrie, R. C. Jr & Eberhard, M. L. (1980) A new technique for immobilizing fllarial larvae using dimethyl sulfoxide (DMSO). Journal of Parasitology, 66, 169170.CrossRefGoogle Scholar
Nelson, G. S. (1959) The identification of infective filarial larvae in mosquitoes: with a note on the species found in “wild” mosquitoes on the Kenya coast. Journal of Helminthology, 33, 233256.CrossRefGoogle ScholarPubMed
Rosen, L. (1955) Observations on the epidemiology of human filariasis in French Oceania. American Journal of Hygiene, 61, 219248.Google Scholar
Wharton, R. H. (1957) Studies on filariasis in Malaya. Observations on the development of Wuchereria malayi in Mansonia (Mansonoides) longipalpis. Annals of Tropical Medicine and Parasitology, 51, 278296.CrossRefGoogle Scholar