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The influence of host haematocrit on the blood feeding success of Anopheles stephensi: implications for enhanced malaria transmission

Published online by Cambridge University Press:  07 August 2001

P. J. TAYLOR
Affiliation:
Centre for Applied Entomology and Parasitology, School of Life Sciences, Keele University, Staffs. ST5 5BG, UK
H. HURD
Affiliation:
Centre for Applied Entomology and Parasitology, School of Life Sciences, Keele University, Staffs. ST5 5BG, UK

Abstract

Two studies were carried out to determine the effect of the rodent malaria Plasmodium yoelii nigeriensis on the blood feeding success of Anopheles stephensi. Initially, pairs of mice with similar packed cell volume (PCV) (measured by haematocrit) were selected. Following infection of one of the pair its PCV gradually fell. At various times post-infection, a comparison was made of the bloodmeal size (haemoglobin content) of mosquitoes feeding on these mice. The bloodmeal sizes increased with parasite-induced fall in PCV down to a haematocrit of 43–44%, which occurred approximately 48 h post-infection. Bloodmeals were significantly reduced, however, when mosquitoes fed on mice with higher parasitaemias and a haematocrit of 15–35%. Thus, at early stages of infection, mosquitoes ingested a bloodmeal significantly greater than did the mosquitoes feeding on the control mice. However, mosquitoes were not able to compensate for severe infection-associated anaemia. To compensate for variation due to innate differences in the mice, a second experiment was performed. Mosquitoes were fed on the same mice before (control) and after infection. Again, the bloodmeal size increased with decreasing PCV down to haematocrits of 42–45%, but declined thereafter. In this host–parasite–vector system, haematocrits that maximized erythrocyte intake were produced when gametocytes, capable of exflagellation, were present.

Type
Research Article
Copyright
2001 Cambridge University Press

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References

AHMED, A. M., MAINGON, R. G., TAYLOR, P. J. & HURD, H. (1999). The effects of infection with Plasmodium yoelii nigeriensis on the reproductive fitness of the mosquito Anopheles gambiae. Invertebrate Reproduction and Development 36, 217222.CrossRefGoogle Scholar
BRIEGEL, H. (1990). Fecundity, metabolism and body size in Anopheles (Diptera: Culicidae), vectors of malaria. Journal of Medical Entomology 27, 839856.CrossRefGoogle Scholar
BRIEGEL, H., LEA, A. O. & KLOWDEN, M. J. (1979). Hemoglobinometry as a method for measuring bloodmeal size of mosquitoes (Diptera: Culicidae). Journal of Medical Entomology 15, 235238.CrossRefGoogle Scholar
BRIEGEL, H. & REZZONICO, L. (1985). Concentration of host blood protein during feeding by anopheline mosquitoes (Diptera: Culicidae). Journal of Medical Entomology 22, 612618.CrossRefGoogle Scholar
CHUTMONGKONKUL, M., MAIER, W. A. & SEITZ, H. M. (1992). Trials to infect Anopheles stephensi with Plasmodium yoelii nigeriensis by membrane feeding technique. Angewandte Parasitologie 33, 217225.Google Scholar
DANIEL, T. L. & KINGSOLVER, J. G. (1983). Feeding strategy and the mechanics of blood sucking in insects. Journal of Theoretical Biology 105, 661672.CrossRefGoogle Scholar
DAVIES, C. R. (1990). Interrupted feeding of blood-sucking insects: causes and effects. Parasitology Today 6, 1922.CrossRefGoogle Scholar
DEARSLEY, A. L., SINDEN, R. & SELF, I. A. (1990). Sexual development in malarial parasites: gametocyte production, fertility and infectivity to the mosquito vector. Parasitology 100, 359368.CrossRefGoogle Scholar
HOGG, J. & HURD, H. (1995). Plasmodium yoelii nigeriensis: the effect of high and low intensity of infection upon egg production and bloodmeal size of Anopheles stephensi during three gonotrophic cycles. Parasitology 111, 555562.CrossRefGoogle Scholar
JAHAN, N. & HURD, H. (1997). The effects of infection with Plasmodium yoelii nigeriensis on the reproductive fitness of Anopheles stephensi. Annals of Tropical Medicine and Parasitology 91, 365369.CrossRefGoogle Scholar
KURTZHALS, J., ADDAE, M. M., AKANMORI, B. D., DUNYO, S., KORAM, K. A., APPAWU, M. A., NKRUMAH, F. K. & HVIID, L. (1999). Anaemia caused by asymptomatic Plasmodium falciparum infection in semi-immune African schoolchildren. Transactions of the Royal Society of Tropical Medicine and Hygiene 93, 623627.CrossRefGoogle Scholar
MENENDEZ, C., FLEMING, A. F. & ALONSO, P. L. (2000). Malaria-related anaemia. Parasitology Today 16, 469476.CrossRefGoogle Scholar
SHIEH, J.-N. & ROSSIGNOL, P. A. (1992). Opposite influences of host anaemia on blood feeding rate and fecundity of mosquitoes. Parasitology 105, 159163.CrossRefGoogle Scholar
SHIFF, C., CHECKLEY, W., WINCH, P., PREMJI, Z., MINJAS, J. & LUBEGA, P. (1996). Changes in weight gain and anaemia attributable to malaria in Tanzanian children living under holoendemic conditions. Transactions of the Royal Society of Tropical Medicine and Hygiene 90, 262265.CrossRefGoogle Scholar
SHULMAN, C. E., GRAHAM, W. J., JILO, H., LOWE, B. S., NEW, L., OBIERO, J., SNOW, R. W. & MARSH, K. (1996). Malaria is an important cause of anaemia in primigravidae: evidence from a district hospital in coastal Kenya. Transactions of the Royal Society of Tropical Medicine and Hygiene 90, 535539.CrossRefGoogle Scholar
SINDEN, R., BUTCHER, G. A., BILLIKER, O. & FLECK, S. L. (1996). Regulation of infectivity of Plasmodium to the mosquito vector. Advances in Parasitology 38, 54117.CrossRefGoogle Scholar
TAYLOR, L. H. & READ, A. F. (1997). Why so few transmission stages? Reproductive restraint by malaria parasites. Parasitology Today 13, 135140.CrossRefGoogle Scholar
VAUGHAN, J. A., NODEN, B. H. & BEIER, J. C. (1991). Concentration of human erythrocytes by anopheline mosquitoes (Diptera: Culicidae) during feeding. Journal of Medical Entomology 28, 780786.CrossRefGoogle Scholar