Source reduction of mosquito larval habitats has unexpected consequences on malaria transmission

Reduction of aquatic habitats through environmental management mitigates malaria transmission not only by reducing emergence of host-seeking mosquitoes, but also by increasing the amount of time required for vectors to locate oviposition sites. However, the consequence of source reduction on mosquito oviposition has largely been neglected in evaluations of environment-management programs. Here, by theoretically examining the relationship between the time spent for oviposition and the availability of aquatic habitats, we show that prolonged oviposition cycles induced by source reduction account for a great deal of reductions in the basic reproductive rate of malaria, especially when aquatic habitats are scarce and the mosquito's flight ability is limited. Neglecting this mechanism may lead to substantial underestimation of the impact of source reduction of aquatic habitats on malaria transmission. Our findings suggest that the prolonged duration of the gonotrophic cycle might be one of the important mechanisms underlying the effectiveness of environment-management interventions for malaria control.

[1]  E. Walker,et al.  Pupal habitat productivity of Anopheles gambiae complex mosquitoes in a rural village in western Kenya. , 2006, The American journal of tropical medicine and hygiene.

[2]  S. Lindsay,et al.  Can source reduction of mosquito larval habitat reduce malaria transmission in Tigray, Ethiopia? , 2005, Tropical medicine & international health : TM & IH.

[3]  Robert J Novak,et al.  Habitat-based modeling of impacts of mosquito larval interventions on entomological inoculation rates, incidence, and prevalence of malaria. , 2005, The American journal of tropical medicine and hygiene.

[4]  Antoine Flahault,et al.  The unexpected importance of mosquito oviposition behaviour for malaria: non-productive larval habitats can be sources for malaria transmission , 2005, Malaria Journal.

[5]  G. Killeen,et al.  Habitat characterization and spatial distribution of Anopheles sp. mosquito larvae in Dar es Salaam (Tanzania) during an extended dry period , 2005, Malaria Journal.

[6]  G. Killeen,et al.  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 , 2004, Tropical medicine & international health : TM & IH.

[7]  G. Yan,et al.  Habitat characteristics of Anopheles gambiae s.s. larvae in a Kenyan highland , 2004, Medical and veterinary entomology.

[8]  John C. Carlson,et al.  Field assessments in western Kenya link malaria vectors to environmentally disturbed habitats during the dry season , 2004, BMC public health.

[9]  G. Killeen,et al.  Rationalizing historical successes of malaria control in Africa in terms of mosquito resource availability management. , 2004, The American journal of tropical medicine and hygiene.

[10]  John-hwa Lee,et al.  Cloning and characterization of a new cysteine proteinase secreted by Paragonimus westermani adult worms. , 2004, American Journal of Tropical Medicine and Hygiene.

[11]  J. Sachs,et al.  A global index representing the stability of malaria transmission. , 2004, The American journal of tropical medicine and hygiene.

[12]  M. Reiskind,et al.  Culex restuans (Diptera: Culicidae) Oviposition Behavior Determined by Larval Habitat Quality and Quantity in Southeastern Michigan , 2004, Journal of medical entomology.

[13]  R. Bos Global Strategic Framework for Integrated Vector Management , 2004 .

[14]  A. Saul,et al.  Zooprophylaxis or zoopotentiation: the outcome of introducing animals on vector transmission is highly dependent on the mosquito mortality while searching , 2003, Malaria Journal.

[15]  Jacob C Koella,et al.  A Model for the Coevolution of Immunity and Immune Evasion in Vector‐Borne Diseases with Implications for the Epidemiology of Malaria , 2003, The American Naturalist.

[16]  James L Regens,et al.  An individual-based model of Plasmodium falciparum malaria transmission on the coast of Kenya. , 2003, Transactions of the Royal Society of Tropical Medicine and Hygiene.

[17]  M. Mangel,et al.  Oviposition habitat selection in response to risk of predation in temporary pools: mode of detection and consistency across experimental venue , 2003, Oecologia.

[18]  G. Killeen,et al.  Integrated programme is key to malaria control , 2002, Nature.

[19]  C. Shiff,et al.  Integrated Approach to Malaria Control , 2002, Clinical Microbiology Reviews.

[20]  P. McCall,et al.  Evidence for memorized site-fidelity in Anopheles arabiensis. , 2001, Transactions of the Royal Society of Tropical Medicine and Hygiene.

[21]  J. Nájera Malaria control: achievements, problems and strategies. , 2001, Parassitologia.

[22]  H. Stanley,et al.  Optimizing the success of random searches , 1999, Nature.

[23]  S. Lal,et al.  Epidemiology and control of malaria , 1999, Indian journal of pediatrics.

[24]  T. Scott,et al.  Aedes aegypti (Diptera: Culicidae) movement influenced by availability of oviposition sites. , 1998, Journal of medical entomology.

[25]  J. Lines,et al.  Anopheles gambiae gonotrophic cycle duration, biting and exiting behaviour unaffected by permethrin‐impregnated bednets in The Gambia , 1997, Medical and veterinary entomology.

[26]  M. Birley,et al.  Comparative effects of permethrin-impregnated bednets and DDT house spraying on survival rates and oviposition interval of Anopheles farauti No. 1 (Diptera:Culicidae) in Solomon Islands. , 1995, Annals of tropical medicine and parasitology.

[27]  P Reiter,et al.  Short report: dispersal of Aedes aegypti in an urban area after blood feeding as demonstrated by rubidium-marked eggs. , 1995, The American journal of tropical medicine and hygiene.

[28]  Bidlingmayer Wl How mosquitoes see traps: role of visual responses. , 1994 .

[29]  J. Charlwood,et al.  The effect of permethrin‐impregnated bednets on a population of Anopheles farauti in coastal Papua New Guinea , 1987, Medical and veterinary entomology.

[30]  C. Dye,et al.  Population dynamics of mosquito-borne disease: effects of flies which bite some people more frequently than others. , 1986, Transactions of the Royal Society of Tropical Medicine and Hygiene.

[31]  J. Frottier,et al.  [Septicemia due to staphylococcus albus. Report of 14 personal cases]. , 1974, La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris.

[32]  M. Gillies.,et al.  A comparison of the range of attraction of animal baits and of carbon dioxide for some West African mosquitoes. , 1969, Bulletin of entomological research.

[33]  M. Gillies. Studies on the dispersion and survival of Anopheles gambiae Giles in East Africa, by means of marking and release experiments , 1961 .

[34]  H. Kalmus,et al.  BEHAVIOUR OF AEDES MOSQUITOS IN RELATION TO BLOOD‐FEEDING AND REPELLENTS , 1960 .

[35]  M. Bates The natural history of mosquitoes , 1965 .

[36]  P. Russell,et al.  Some experiments on flight range of Anopheles culicifacies , 1944 .