Hostname: page-component-848d4c4894-ttngx Total loading time: 0 Render date: 2024-05-26T22:31:21.130Z Has data issue: false hasContentIssue false

Optimization of breeding output for larval stage of Anopheles gambiae (Diptera: Culicidae): prospects for the creation and maintenance of laboratory colony from wild isolates

Published online by Cambridge University Press:  06 January 2011

T. Tchuinkam*
Affiliation:
Malaria Research Unit of the Laboratory of Applied Biology and Ecology (MRU-LABEA), Department of Animal Biology, Faculty of Sciences of the University of Dschang, PO Box 067 Dschang, Cameroon Laboratoire de Recherche sur le Paludisme, Organisation de Coordination pour la lutte contre les Endémies en Afrique Centrale (OCEAC), PO Box 288 Yaounde, Cameroon
M. Mpoame
Affiliation:
Malaria Research Unit of the Laboratory of Applied Biology and Ecology (MRU-LABEA), Department of Animal Biology, Faculty of Sciences of the University of Dschang, PO Box 067 Dschang, Cameroon
B. Make-Mveinhya
Affiliation:
Malaria Research Unit of the Laboratory of Applied Biology and Ecology (MRU-LABEA), Department of Animal Biology, Faculty of Sciences of the University of Dschang, PO Box 067 Dschang, Cameroon
F. Simard
Affiliation:
Laboratoire de Recherche sur le Paludisme, Organisation de Coordination pour la lutte contre les Endémies en Afrique Centrale (OCEAC), PO Box 288 Yaounde, Cameroon Laboratoire de Lutte contre les Insectes Nuisibles (LIN-UR 016), Institut de Recherche pour le Développement (IRD), 911 Avenue Agropolis, BP 64501, 34394 Montpellier, France
E. Lélé-Defo
Affiliation:
Malaria Research Unit of the Laboratory of Applied Biology and Ecology (MRU-LABEA), Department of Animal Biology, Faculty of Sciences of the University of Dschang, PO Box 067 Dschang, Cameroon
S. Zébazé-Togouet
Affiliation:
Hydrobiology laboratory, Faculty of Sciences of the University of Yaounde I, PO Box 812 Yaounde, Cameroon
A. Tateng-Ngouateu
Affiliation:
Malaria Research Unit of the Laboratory of Applied Biology and Ecology (MRU-LABEA), Department of Animal Biology, Faculty of Sciences of the University of Dschang, PO Box 067 Dschang, Cameroon
H.-P. Awono-Ambéné
Affiliation:
Laboratoire de Recherche sur le Paludisme, Organisation de Coordination pour la lutte contre les Endémies en Afrique Centrale (OCEAC), PO Box 288 Yaounde, Cameroon
C. Antonio-Nkondjio
Affiliation:
Laboratoire de Recherche sur le Paludisme, Organisation de Coordination pour la lutte contre les Endémies en Afrique Centrale (OCEAC), PO Box 288 Yaounde, Cameroon
T. Njiné
Affiliation:
Hydrobiology laboratory, Faculty of Sciences of the University of Yaounde I, PO Box 812 Yaounde, Cameroon
D. Fontenille
Affiliation:
Laboratoire de Lutte contre les Insectes Nuisibles (LIN-UR 016), Institut de Recherche pour le Développement (IRD), 911 Avenue Agropolis, BP 64501, 34394 Montpellier, France
*
*Author for correspondence Fax: +237 22 23 00 61 E-mail: timtchuinkam@yahoo.fr

Abstract

Domesticating anopheline species from wild isolates provides an important laboratory tool but requires detailed knowledge of their natural biology and ecology, especially the natural breeding habitats of immature stages. The aim of this study was to determine the optimal values of some parameters of Anopheles gambiae larval development, so as to design a standard rearing protocol of highland isolates, which would ensure: the biggest fourth instars, the highest pupae productivity, the shortest duration of the larval stage and the best synchronization of pupation. The density of larvae, the size of breeding water and the quantity of food supplied were tested for their effect on larval growth. Moreover, three cheap foodstuffs were selected and tested for their capability to improve the breeding yield versus TetraMin® as the standard control. The larval density was a very sensitive parameter. Its optimal value, which was found to be ≈1 cm−2 surface area, yielded a daily pupation peak of 38.7% on day 8 post-oviposition, and a global pupae productivity of 78.7% over a duration range of three days. Anopheles gambiae's larval growth, survival and developmental synchronization were density-dependent, and this species responded to overcrowding by producing smaller fourth instars and fewer pupae, over elongated immature lifetime and duration range of pupae occurrence, as a consequence of intraspecific competition. While shallow breeding waters (<3 cm) produced a higher number of pupae than deeper ones, no effect of the breeding habitat's absolute surface area on larval development was observed. Increasing the daily food supply improved the pupae productivity but also boosted the water pollution level (which was assessed by the biological oxygen demand (BOD) and the chemical oxygen demand (COD)) up to a limit depending on the food quality, above which a rapid increase in larval mortality was recorded. The food quality that could substitute the manufactured baby fish food was obtained with weighed mixture of 1 wheat+1 shrimp+2 fish. On establishing an anopheline mosquito colony in the laboratory, special care should be taken to design and maintain the appropriate optimal values of larval density, water depth, daily diet quantity and nutritional quality.

Type
Research Paper
Copyright
Copyright © Cambridge University Press 2011

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

Bayoh, M.N. & Lindsay, S.W. (2003) Effect of temperature on the development of the aquatic stages of Anopheles gambiae sensu stricto (Diptera: Culicidae). Bulletin of Entomological Research 93, 375381.CrossRefGoogle ScholarPubMed
Bayoh, M.N. & Lindsay, S.W. (2004) Temperature-related duration of aquatic stages of the Afrotropical malaria vector mosquito Anopheles gambiae in the laboratory. Medical and Veterinary Entomology 18, 174179.CrossRefGoogle ScholarPubMed
Bedhomme, S., Agnew, P., Sidobre, C. & Michalakis, Y. (2003) Sex-specific reaction norms to intraspecific larval competition in the mosquito Aedes aegypti. Journal of Evolutionary Biology 16, 721730.CrossRefGoogle ScholarPubMed
Blackmore, M.S. & Lord, C.C. (2000) The relationship between size and fecundity in Aedes albopictus. Journal of Vector Ecology 25, 212217.Google ScholarPubMed
Bradshaw, W.E. & Holzapfel, C.M. (1992) Reproductive consequences of density-dependent size variation in the pitcher plant mosquito, Wyeomyia smithii (Diptera: Culicidae). Annals of the Entomological Society of America 85, 274281.CrossRefGoogle Scholar
Briegel, H. (1990) Fecundity, metabolism, and body size in Anopheles (Diptera: Culicidae), vector of malaria. Journal of Medical Entomology 27, 839850.CrossRefGoogle ScholarPubMed
Clements, A.N. (2000) The Biology of Mosquitoes: Development, Nutrition and Reproduction, vol. 1. 511 pp. Wallingford, UK, CABI Publishing.Google Scholar
Edillo, F.E., Tripét, F., Touré, Y.T., Lanzaro, G.C., Dolo, G. & Taylor, C.E. (2006) Water quality and immatures of the M and S forms of Anopheles gambiae s.s. and An. arabiensis in a Malian village. Malaria Journal 5, 3544.CrossRefGoogle Scholar
Fillinger, U., Sonye, G., Killeen, G.F., Knols, B.G.J. & Becker, N. (2004) The practical importance of permanent and semipermanent habitats for controlling aquatic stages of Anopheles gambiae sensu lato mosquitoes: operational observations from a rural town in western Kenya. Tropical Medicine and International Health 9, 12741289.CrossRefGoogle ScholarPubMed
Gillies, M.T. & De Meillon, B. (1968) The Anophelinae of Africa South of the Sahara (Ethiopian Zoogeographiecal Region), vol. 54. 2nd edn. 343 pp. Johannesburg, South Africa, South African Institute for Medical Research.Google Scholar
Gimnig, J.E., Ombok, M., Otieno, S., Kaufman, M.G., Vulule, J.M. & Walker, E.D. (2002) Density-dependant development of Anopheles gambiae (Diptera: Culicidae) larvae in artificial habitats. Journal of Medical Entomology 39, 162172.CrossRefGoogle Scholar
Hawley, W.A. (1985) The effect of larval density on adult longevity of a mosquito, Aedes sierrensis: epidemiological consequences. Journal of Animal Ecology 54, 955964.CrossRefGoogle Scholar
Himeidan, Y.E., Zhou, G., Yakob, L., Afrane, Y., Munga, S., Atieli, H., El-Rayah, E.-A., Githeko, A.K. & Yan, G. (2009) Habitat stability and occurrences of malaria vector larvae in Western Kenya highlands. Malaria Journal 8, 234239.CrossRefGoogle ScholarPubMed
Howell, P. & Wilkins, L. (2007) Anopheles laboratory biology and culture: modifying fecundity, longevity and size. pp. 16 in MR4: Advance techniques in Anopheles culture workshop. 6–10 August 2007, Atlanta GA, USA. MR4-ATCC-NIAID-NIH, 1.Google Scholar
Klowden, M.J., Blackmer, J.L. & Chambers, G.M. (1988) Effects of larval nutrition on the host-seeking behaviour of adult Aedes aegypti mosquitoes. Journal of American Mosquito Control Association 4, 7375.Google ScholarPubMed
Koenraadt, C.J.M. & Takken, W. (2003) Cannibalism and predation among larvae of the Anopheles gambiae complex. Medical and Veterinary Entomology 17, 6166.CrossRefGoogle ScholarPubMed
Landry, S.V., De Foliart, G.R. & Hogg, D.B. (1988) Adult body size and survivorship in a field population of Aedes triseriatus. Journal of American Mosquito Control Association 4, 121128.Google Scholar
Lounibos, L.P., Larson, V.L. & Morris, C.D. (1990) Parity fecundity and body size of Mansonia dyari in Florida. Journal of American Mosquito Control Association 6, 121126.Google ScholarPubMed
Lucas, E.A. & Romoser, W.S. (2001) The energetic costs of diving in Aedes aegypti and Aedes albopictus pupae. Journal of the American Mosquito Control Association 17, 5660.Google ScholarPubMed
Lyimo, E.O. & Koella, J.C. (1992) Relationship between body size of adult Anopheles gambiae s.l. and infection with the malaria parasite Plasmodium falciparum. Parasitology 104, 233237.CrossRefGoogle ScholarPubMed
McCay, C.M., Crowell, M.F. & Maynard, L.A. (1989) The effect of retarded growth upon the length of life span and upon the ultimate body size. Nutrition 5, 155171.Google ScholarPubMed
Mercer, D.R. (1999) Effects of larval density on the size of Aedes polynesiensis adults (Diptera: Culicidae). Journal of Medical Entomology 36, 702708.CrossRefGoogle ScholarPubMed
Mercer, D.R. & Anderson, J.R. (1994) Tannins in tree hole habitats and their effects on Aedes sierrensis (Diptera: Culicidae) production and parasitism by Lambornella clarki (Ciliophora: Tetrahymenidae). Journal of Medical Entomology 31, 159167.CrossRefGoogle Scholar
Minakawa, N., Sonye, G. & Yan, G. (2005) Relationships between occurrence of Anopheles gambiae s.l. (Diptera Culicidae) and size and stability of larval habitats. Journal of Medical Entomology 42, 295300.CrossRefGoogle ScholarPubMed
Munga, S., Minakawa, N., Zhou, G., Barrack, O.O., Githeko, A.K. & Yan, G. (2005) Oviposition site preference and egg hatchability of Anopheles gambiae: effects of land cover types. Journal of Medical Entomology 42, 993997.Google ScholarPubMed
Mutuku, F.M., Bayoh, M.N., Gimnig, J.E., Vulule, J.M., Kamau, L., Walker, E.D., Kabiru, E.W. & Hawley, W.A. (2006) Pupal habitat productivity of Anopheles gambiae complex mosquitoes in a rural village in Western Kenya. American Journal of Tropical Medicine and Hygiene 74, 5461.CrossRefGoogle Scholar
Packer, M.J. & Corbet, P.S. (1989) Size variation and reproductive success of female Aedes punctor (Diptera: Culicidae). Ecological Entomology 14, 297309.CrossRefGoogle Scholar
Reisen, W.K. (1975) Intraspecific competition in Anopheles stephensi Liston. Mosquito News 35, 473482.Google Scholar
Reisen, W.K., Milby, M.M. & Bock, M.E. (1984) The effects of immature stress on selected events in the life history of Culex tarsalis. Mosquito News 44, 385395.Google Scholar
Remoser, W. S. (1975) Buoyancy and ventilation in Aedes aegypti pupae (Diptera: Culicidae). Journal of Medical Entomology 12, 547550.CrossRefGoogle Scholar
Sattler, M.A., Mtasiwa, D., Kiama, M., Premji, Z., Tanner, M., Killeen, G.F. & Lengeler, C. (2005) Habitat characterization and spatial distribution of Anopheles sp mosquito larvae in Dar es Salaam (Tanzania) during an extended dry period. Malaria Journal 4, 418.CrossRefGoogle Scholar
Schneider, P., Takken, W. & McCall, P.J. (2000) Interspecific competition between sibling species larvae of Anopheles arabiensis and An. gambiae. Medical and Veterinary Entomology 14, 165170.CrossRefGoogle ScholarPubMed
Suleman, M. (1982) The Effects of intraspecific competition for food and space on the larval development of Culex quinquefasciatus. Mosquito News 42, 347355.Google Scholar
Takken, W., Klowden, M.J. & Chambers, G.M. (1998) Effect of body size on host seeking and blood meal utilization in Anopheles gambiae sensu stricto (Diptera: Culicidae): the disadvantage of being small. Journal of Medical Entomology 35, 639645.CrossRefGoogle ScholarPubMed
Tchuinkam, T. (1994) Etude du pouvoir infectant des porteurs de gamétocytes de Plasmodium falciparum pour Anopheles gambiae en zone d'endémie palustre, Yaoundé; Cameroun. Thèse de doctorat du 3e cycle, Université de Yaoundé, Cameroun.Google Scholar
Timmerman, S.E. & Briegel, H. (1993) Water depth and larval density affect development and accumulation of reserves in laboratory populations of mosquitoes. Bulletin of the Society of Vector Ecology 18, 174187.Google Scholar
Tuno, N., Miki, K., Minakawa, N., Githeko, A., Yan, G. & Takagi, M. (2004) Diving ability of Anopheles gambiae (Diptera: Culicidae) larvae. Journal of Medical Entomology 41, 810812.CrossRefGoogle ScholarPubMed
Tuno, N., Githeko, A.K., Nakayama, T., Minakawa, N., Takagi, M. & Yan, G. (2006) The association between the phytoplankton, Rhopalosolen species (Chlorophyta: Chlorophycea) and Anopheles gambiae sensus lato (Diptera: Culicidae) larval abundance in western Kenya. Ecologycal Research 21, 476482.CrossRefGoogle Scholar
Washburn, J.O., Mercer, D.R. & Anderson, J.R. (1991) Regulatory role of parasites: impact on host population shifts with resource availability. Science 253, 185188.CrossRefGoogle ScholarPubMed