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Human host selection by anophelines: no evidence for preferential selection of malaria or microfilariae-infected individuals in a hyperendemic area

Published online by Cambridge University Press:  06 April 2009

T. R. Burkot
Affiliation:
Papua New Guinea Institute of Medical Research, P.O. Box 378, Madang, Papua New Guinea
A. Narara
Affiliation:
Papua New Guinea Institute of Medical Research, P.O. Box 378, Madang, Papua New Guinea
R. Paru
Affiliation:
Papua New Guinea Institute of Medical Research, P.O. Box 378, Madang, Papua New Guinea
Patricia M. Graves
Affiliation:
Papua New Guinea Institute of Medical Research, P.O. Box 378, Madang, Papua New Guinea
P. Garner
Affiliation:
Papua New Guinea Institute of Medical Research, P.O. Box 378, Madang, Papua New Guinea

Summary

Host selection among humans by Anopheles punctulatus was studied in an area of Papua New Guinea endemic for malaria and filariasis. Blood films were made from the stomach contents of freshly engorged mosquitoes found resting on the walls of houses in which the parasite status of the occupants was known. Engorgement rates on humans were non-random but could not be consistently related to the parasite status of individuals in the houses for either malaria or filaria. In some households, anophelines preferentially fed on parasitaemic individuals while in other households aparasitaemic individuals were significantly more often selected. This finding is believed to reflect the fact that malaria and filarial infections in this endemic area are predominantly asymptomatic. There were no significant differences in axillary temperatures between malaria or microfilariae positive or negative individuals.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1989

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References

REFERENCES

Burkot, T. R. (1988). Non-random host selection by anopheline mosquitoes. Parasitology Today 4, 156–62.CrossRefGoogle ScholarPubMed
Burkot, T. R., Graves, P. M., Cattani, J. A., Wirtz, R. A. & Gibson, F. D. (1987). The efficiency of sporozoite transmission in the human malarias, Plasmodium falciparum and P. vivax. Bulletin of the World Health Organization 65, 375–80.Google ScholarPubMed
Burkot, T. R., Graves, P. M., Paru, R. & Lagog, M. (1988 a). Mixed blood feeding by the malaria vectors in the Anopheles punctulatus complex (Diptera: Culicidae). Journal of Medical Entomology 25, 205–13.CrossRefGoogle ScholarPubMed
Burkot, T. R., Graves, P. M., Paru, R., Wirtz, R. A. & Heywood, P. (1988 b). Human malaria transmission studies in the Anopheles punctulatus complex in Papua New Guinea: sporozoite rates, inoculation rates and sporozoite densities. American Journal of Tropical Medicine and Hygiene 39, 135–44.CrossRefGoogle ScholarPubMed
Cattani, J. A., Tulloch, J. L., Vrbova, H., Jolley, D., Gibson, F. D., Moir, J. S., Heywood, P. F., Alpers, M. P., Stevenson, A. & Clancy, R. (1986). The epidemiology of malaria in a population surrounding Madang, Papua New Guinea. American Journal of Tropical Medicine and Hygiene 35, 315.CrossRefGoogle Scholar
Covell, G. (1960). Relationship between malarial parasitaemia and symptoms of the disease. Bulletin of the World Health Organization 22, 605–19.Google ScholarPubMed
Day, J. F., Ebert, K. M. & Edman, J. D. (1983). Feeding patterns of mosquitoes (Diptera: Culicidae) simultaneously exposed to malarious and healthy mice, including a method for separating blood meals from conspecific hosts. Journal of Medical Entomology 20, 120–7.CrossRefGoogle ScholarPubMed
Day, J. F. & Edman, J. D. (1983). Malaria renders mice susceptible to mosquito feeding when gametocytes are most infective. Journal of Parasitology 69, 163–70.CrossRefGoogle ScholarPubMed
Day, J. F. & Edman, J. D. (1984). The importance of disease induced changes in mammalian body temperature to mosquito blood feeding. Comparative Biochemistry and Physiology 77A, 447–52.CrossRefGoogle ScholarPubMed
Dye, C. & Hasibeder, G. (1986). Population dynamics of mosquito-borne disease: effects of flies which bite some people more frequently than others. Transactions of the Royal Society of Tropical Medicine and Hygiene 80, 6977.CrossRefGoogle ScholarPubMed
Edman, J., Day, J. & Walker, E. (1985). Vector-host interplay – factors affecting disease transmission. In Ecology of Mosquitoes, (ed. Lounibos, L. P., Rey, J. R. and Frank, J. H.), pp. 273–85. New York: Chapman and Hall.Google Scholar
Graves, P. M., Burkot, T. R., Carter, R., Cattani, J. A., Lagog, M., Parker, J., Brabin, B. J., Gibson, F. D., Bradley, D. J. & Alpers, M. P. (1988). Measurement of malarial infectivity of human populations to mosquitoes in the Madang area, Papua New Guinea. Parasitology 96, 251–63.CrossRefGoogle ScholarPubMed
Kingsolver, J. G. (1987). Mosquito host choice and the epidemiology of malaria. The American Naturalist 130, 811–27.CrossRefGoogle Scholar
Mahon, R. & Gibbs, A. (1982). Arbovirus-infected hens attract more mosquitoes. In Viral Diseases in Southeast Asia and the western Pacific, (ed. Mackenzie, J. D.), pp. 502–4. Sydney: Academic Press.Google Scholar
Molineaux, L. & Gramiccia, G. (1980). The Garki Project: Research on the Epidemiology and Control of Malaria in the Sudan Savanna of West Africa, pp. 255–9. Geneva: World Health Organization.Google Scholar
Rossignol, P. A., Ribeiro, J. M. C., Jungery, M., Spielman, A. & Bailey, C. L. (1985). Enhanced mosquito blood-finding success on parasitemic hosts: evidence for vector-parasite mutualism. Proceedings of the National Academy of Sciences, USA 82, 7725–7.CrossRefGoogle ScholarPubMed
Turrell, M. J., Bailey, C. L. & Rossi, C. (1984). Increased mosquito feeding on Rift Valley fever virus-infected lambs. American Journal of Tropical Medicine and Hygiene 33, 1232–8.CrossRefGoogle Scholar