BackgroundThe communities of Namawala and Idete villages in southern Tanzania experienced extremely high malaria transmission in the 1990s. By 2001-03, following high usage rates (75% of all age groups) of untreated bed nets, a 4.2-fold reduction in malaria transmission intensity was achieved. Since 2006, a national-scale programme has promoted the use of longer-lasting insecticide treatment kits (consisting of an insecticide plus binder) co-packaged with all bed nets manufactured in the country.MethodsThe entomological inoculation rate (EIR) was estimated through monthly surveys in 72 houses randomly selected in each of the two villages. Mosquitoes were caught using CDC light traps placed beside occupied bed nets between January and December 2008 (n = 1,648 trap nights). Sub-samples of mosquitoes were taken from each trap to determine parity status, sporozoite infection and Anopheles gambiae complex sibling species identity.ResultsCompared with a historical mean EIR of ~1400 infectious bites/person/year (ib/p/y) in 1990-94; the 2008 estimate of 81 ib/p/y represents an 18-fold reduction for an unprotected person without a net. The combined impact of longer-lasting insecticide treatments as well as high bed net coverage was associated with a 4.6-fold reduction in EIR, on top of the impact from the use of untreated nets alone. The scale-up of bed nets and subsequent insecticidal treatment has reduced the density of the anthropophagic, endophagic primary vector species, Anopheles gambiae sensu stricto, by 79%. In contrast, the reduction in density of the zoophagic, exophagic sibling species Anopheles arabiensis was only 38%.ConclusionInsecticide treatment of nets reduced the intensity of malaria transmission in addition to that achieved by the untreated nets alone. Impacts were most pronounced against the highly anthropophagic, endophagic primary vector, leading to a shift in the sibling species composition of the A. gambiae complex.
Swarming behaviour in the Anopheles gambiae complex was observed in the field, in the Gambia, West Africa, and in the laboratory. Naturally occurring swarms of A.melus were seen in a clearing at the edge of mangrove swamps close to their breeding sites. Males could be induced to swarm over artificial 'markers' within this 'arena' but not outside it. Females were observed entering the swarm and mating. In the laboratory, in an artificial 'dusk', male A-gambiae s.str. swarmed over a black marker on the floor of their 1.2-m cube cage. In contrast to the males, females made only short flights over the marker, performing brief turning movements at its edge. It is proposed that swarming brings about the aggregation necessary before short-range attraction can take place, and that, in nature, anopheline mosquitoes orientate visually first to an arena and then to a marker within the arena. Female behaviour can be interpreted as a process of scanning possible swarm sites until mating is achieved.
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