- Open Access
Diversity in anopheline larval habitats and adult composition during the dry and wet seasons in Ouagadougou (Burkina Faso)
Malaria Journalvolume 9, Article number: 78 (2010)
Several cases of malaria are frequently recorded during the dry period in Ouagadougou town (Burkina Faso). This has led to the design of a series of studies focusing on both parasitological and entomological investigations intended to provide relevant health data on the risk of local malaria transmission according to the way of urbanisation.
A cross-sectional entomological survey was carried out in various districts of Ouagadougou in April and October 2006. Adult malaria vectors were collected using CDC traps and indoor insecticide spraying performed in four houses during four consecutive days/nights. Intensive larval sampling was also done in available water ponds throughout the study sites.
In April, the anopheline breeding sites consisted only of semi-permanent or permanent swamps located mainly in the two peripheral districts. Despite the presence of anopheline larvae in these breeding sites, less than five Anopheles gambiae s.l. adults were caught by CDC traps and indoor insecticide spraying. In October, additionally to the permanent breeding sites reported in April, some rainfall swamps were also found positive to anophelines. The number of adults' mosquitoes was higher than that collected in April (2 vs 159 in October). Out of 115 larvae of An. gambiae s.l. analysed by PCR in April, 59.1% (68/115) were identified as Anopheles arabiensis, 39.1% (45/115) as An. gambiae M while the S form represented less than 2%. Overall 120 larvae and 86 females were identified by PCR in October as An. gambiae M form (51%) and An. arabiensis (42.2%). The S form represented only 6.8%. The global sporozoite rate recorded was high (6.8%) and did not differ between the districts except in the central district where no positive mosquito was detected.
Although only few adults' mosquitoes were actively caught during the driest month, malaria vectors persisted all year long that increases the risk of urban malaria transmission. The distribution of breeding sites and especially the occurrence of malaria vectors were more abundant in the periphery, which is more like that of a rural settlement. The evolution of malaria prevalence and the factors sustaining the risk of transmission in Ouagadougou as well in many African cities during the dry season are discussed.
Nowadays, human settlements in many African countries are gradually, but inadequately, experiencing an urbanization process that constitutes a great challenge. More often than not, rapid and unplanned urban growth is the source of many environmental hazards including overcrowding, water shortage and pollution, sub-standard housing, poor solid waste management. Generally, the urban landscape management is expected to reduce the risk of malaria transmission due to the lack of suitable breeding sites for vector development. Indeed, before any insecticide was invented, vector control meant mainly environmental management by drying up the swamps. This is not the case in urban agglomerations in Africa, where the convergent pattern of house dispersion and landscape use is more rural than urban, with precarious peripheral quarters surrounded by gardening and specialized small farming.
One consequence is the multiplication of aquatic habitats induced by the presence of non-formal and disordered hydro-agricultural installations co-occurring permanently with the urbanization and often suitable for vector development. This may increase the risk of vector proliferation in urban areas, where malaria transmission is deemed neglected because theoretically malaria is considered by health planners to be a seasonal and rural problem affecting particularly children. However, the threat of malaria vectors is a major concern for poorly immune populations living in African cities . Indeed, it has been estimated that the 200 million people living in town in Africa, which corresponds to 25% of the African global population, are exposed permanently to malaria infection . Projecting the extension of urbanization process towards 2025, more than 50% of African population will live in towns .
In Burkina Faso, available reports indicate that about 40.2% of global morbidity recorded in 2006 in health centres were ascribed to malaria, mainly affecting children aged 0-5 years. In fact, this vulnerable group represents 64.5% of hospitalized patients. On the whole, 45.8% of deaths are caused by malaria . Except for the study by Wang et al, no study has been explicitly undertaken on malaria epidemiology in Ouagadougou since the end of 1980s. The earlier studies of Rossi et al showed that malaria transmission was heterogeneous in the city: it was highest close to the urban dams and also in the peripheral areas and quite nil in the central districts. In order to provide a health database that will be correlated to the urbanization pattern in Ouagadougou town, a global health investigation including parasitological studies were conducted in 2004 . This survey clearly indicated that malaria prevalence averaged 21% for the 0-12 year age group, and varied greatly from one district to another but globally ranged from 31.7% in peripheral quarters to 13% in the central districts. However, complementary entomological data supporting this information is lacking. An increase awareness of the presence of malaria vectors and malaria transmission in Ouagadougou stimulated interest to provide entomological data allowing a better documentation of the database with the intended goal to record the presence of mosquito larval habitats according to urbanization pattern.
The present paper reports the preliminary investigation on the diversity of anopheline breeding sites and species composition in those habitats disseminated throughout the city during the dry season and the end of the rainy season.
For the entomological investigations four districts were chosen based on the level of urbanization and the density of housing (Figure 1). The selected sites included i) an old urbanized and densely populated district (Dapoya), ii) a recently urbanized district with more dispersed houses (Tanghin), iii) a peripheral and densely populated quarter (Yamtenga), and iv) a peripheral district with more dispersed houses (Zongo). These parameters were correlated to the dissemination of breeding sites favourable to mosquito development.
Dapoya is an old colonial district located in the centre of the town. It is characterized by close-together houses with numerous households. It is surrounded by a large dam collecting polluted domestic water and also rain water. While these water collections dry up progressively during the dry season, they offer fertile areas with some dispersed depressions constituting numerous small water pools. This landscape is much used for vegetable cropping that is intensively developed during the dry period. In addition, numerous wells are also made in the dam bed contributing to collect water for vegetable irrigation. Other domestic water collection channels are disseminated across the quarter. All these natural and anthropogenic factors contribute to the proliferation of temporal breeding sites.
Tanghin was formerly a rural village which has been gradually, but inadequately, urbanized since 1980. It is limited in the north by some rural villages and separated from the centre district (Dapoya) by the dam. In addition numerous spring-borne pools can be found throughout the district offering suitable habitats for mosquito development. As a relatively recent urban district, it shares some characteristics with the rural villages, such as dispersed housing pattern and the existence of spring as a water resource.
Yamtenga is a recent eastern peripheral non-urbanized district without formal limit with the urban districts and still slowly undergoing its urbanization process. It is characterized by condensed precarious houses built with local materials, such as mud. One permanent and large polluted-swamp occurs in the centre of the quarter constituting the principal breeding site all year long. In addition, some domestic pool or spring-borne pools are disseminated through the agglomeration constituting important breeding sites for mosquitoes.
Zongo is a recent peripheral non-urbanized area connecting to the town on its western side. It is characterized by dispersed houses. One major feature of this area is the presence of a natural and accidental ravine that has been exploited to collect rain water for brick making. Some small pools were disseminated in the bed of the ravine during the dry season and kept non-polluted water exposed to the sun. These water sources constituted the main breeding sites permitting the development of anophelines.
The meteorological data were provided by the National Meteorology Office located in Ouagadougou i.e. mean values of temperatures, rainfall and relative humidity for each month during the year 2006.
Mosquito adult collections
In each study site, both traditional and modern houses were sampled for mosquito collection. During four consecutive nights, CDC traps were used to catch adult's mosquitoes in each study site between 8:00 pm and 6:00 am according to four traps inside and four others just outside of four houses randomly selected. Indoor resting females were caught by spraying four houses in proximity of the CDC-sampling houses with insecticide aerosols between 6:00 am and 9:00 am, during four consecutive days in each study site. Female mosquitoes were knocked-down onto, and immediately retrieved from, white sheets laid down on the floor of sprayed huts.
Larva sampling and breeding sites productivity
In each study area, all water collections were numbered and prospected for the presence of anophelines larvae. A productivity index was assigned to each breeding site according to the presence or absence of anopheline larvae using the classical deeping technique . As the objective was not to count the total number of anopheline larva per breeding site, we just sampled some from each positive breeding site and stored into 1.5 ml tube containing alcohol 70° dedicated to PCR analysis for species identification. When anophelines species other than An. gambiae s.l. were suspected, as assumed in Yamtenga large swamp and Zongo ravine, larvae were sampled and bred in an insectary until adult stage. The adults were lately emerged and identified using standard keys as described below.
Laboratory processing of mosquitoes
Adults including both CDC and indoor spray catches and also insectary-emerged adults were identified using standard morphological identification keys . When numerous specimens were collected per site, a subsample of ~30 specimens of An. gambiae s.l. was processed by PCR to identify species belonging the An. gambiae complex and molecular forms of An. gambiae s.s. [9, 10]. Sporozoite rates were estimated from females of An. gambiae s.l. and Anopheles funestus collected indoors and by CDC traps, essentially in October 2006 using the ELISA CSP techniques .
The absolute values of the temperature exceeded 30°C in April and October. April was one of the driest months with 2.3 mm of rain and 37.7% of relative humidity while in October 41.7 mm rain with 94.3% of relative humidity were recorded (Figure 2).
Prevalence of malaria
Except in Zongo district, malaria prevalence differed significantly between dry and rainy seasons irrespective the district (P < 0.05). Indeed, it was similar in Zongo for the two seasons but varied significantly between districts in dry as well as in rainy season (P < 0.01) and ranged from 34% to 9% (Table 1).
Productivity of breeding sites
In April 2006, no anopheline larvae were found in any of breeding sites prospected in the central district of Dapoya, both in vegetable growing wells and domestic channels, where only Culex sp. larvae were collected. In Tanghin district, anopheline larvae were collected only in the brick holes closer to the dam surrounding the district. Anopheline larvae were mainly collected from the breeding sites located at Yamtenga and Zongo, the two peripheral non-urbanized areas. In these two areas, 87.5% (7/8) of prospected breeding sites were found positive to anophelines. All larvae identified at adult stage as An. gambiae s.l. were exclusively collected from the brick-made ravine of Zongo (Figure 3) and the large polluted swamp of Yamtenga (Figure 4). Additionally to An. gambiae s.l., Anopheles pharoensis and Anopheles rufipes were identified among those emerged from Yamtenga swamp. In October 2006, out of 50 breeding sites observed throughout the four sites, 42 were positive for anophelines. They mostly consisted of the sites mentioned above and also additional swamps and domestic channels produced by the rainfall (Table 2).
In April 2006, except Yamtenga where two anophelines (one male and one female) were collected indoor, all mosquitoes collected both by CDC-traps and indoor sprays were exclusively composed by mosquitoes belonging to the genus Culex sp in all districts. In October 2006, the CDC-light traps yielded 49 anopheline mosquitoes with respectively 15, 10, 22 and 2 in Zongo, Dapoya, Tanghin and Yamtenga. Overall 110 anophelines were collected by indoor sprays vs 3,402 Culex composed by 95.9% Cx. quinquefasciatus and less than 4% Cx. decens (Table 3). Considering the two sampling techniques overall 159 anophelines were collected and mainly dominated by An. gambiae s.l. with few specimens of other species such as An. funestus, An. pharoensis and An. rufipes. Some sandflies identified as Phlebotomus dubosqi and Sergentomya sp. belonging to the family of Psychodidae were collected both by CDC and indoor sprays in all districts.
Overall 115 mosquitoes were analysed in PCR to identify the species composition and to characterize the molecular forms of An. gambiae s.s (Table 4). Out of 44 mosquitoes analysed in Yamtenga, 59.1% were identified as An. gambiae M form vs 40.9% as An. arabiensis without any S molecular form. In Zongo district An. gambiae s.l. populations were dominated by An. arabiensis, representing 76.6% vs 22.3% for An. gambiae M form with only 3% of S molecular form. In Tanghin, four mosquitoes were identified as An. gambiae M form. Overall in April 2006, An. arabiensis was the predominant species (χ2 = 8.72, df = 1 P < 0.001) reaching 59.1% vs 40.8% of An. gambiae s.s., which was mainly composed by the M form (39.1%). The S form represented only 1.7% of total anophelines.
Overall 206 specimens including 120 larvae and 86 females were analysed in PCR in October 2006 to identify the species composition and to characterize the molecular forms of An. gambiae s.s. (Table 4). They were composed by 57.8% of An. gambiae s.s. (51% of M form and 6.8% of S form) vs 42.2% of An. arabiensis. An. funestus was found in low proportion (1.4%) only in Tanghin and Dapoya districts separated by the dam. The frequency of An. gambiae s.s. and An. arabiensis did not vary significantly between districts. However the M form predominated slightly (χ2 = 6.97, df = 3 P > 0.05). The proportion of each species between April and October 2006 as significantly different (χ2 = 10.23, df = 2 P < 0.01).
Out of 89 females, including An. gambiae M (39) and S forms (four), An. arabiensis (36) and An. funestus (three) analysed by ELISA for the presence of the circumsporozoite protein of P. falciparum, six were detected positive for the CSP antigen (Table 5). They were composed by three positive from Tanghin (including 2 An. gambiae M form and 1 An. arabiensis), two from Zongo (1 An. gambiae M form and 1 An. arabiensis) and one An. gambiae M form from Yamtenga. The global sporozoite rate was estimated higher (6.38%). Except Dapoya where no infected Anopheles was detected, the sporozoite rate did not differ significantly between districts (χ2 = 0.48, df = 3, P > 0.05).
According to the parasitological values, malaria prevalence is maintained all year long in Ouagadougou town. The parasitological values differed between the two seasons revealing that malaria transmission dynamic increased intensively during the rainy season where the density of vectors also increased accordingly. This result also showed that malaria transmission varied following the districts decreasing from the peripheral to the central ones that is in accordance with our entomological data.
Indeed, some vectors from three of the four districts surveyed were detected positive to Plasmodium falciparum by ELISA with a relative high value of sporozoite rate especially in the periphery. The occurrence of malaria affection during the dry period could be partially due to the persistence of malaria vectors sustaining the transmission even thought they had been found in low density. The vector species composition did not differ between the two months but their relative proportion varied: An. arabiensis and An. gambiae M were the main vectors, with a low proportion of S molecular form. Few specimens of An. funestus were reported in October in Tanghin and Dapoya the most urbanised districts probably due to the presence of dams which surface was covered by vegetation suitable to An. funestus development. The persistence of the S molecular form in April seemed atypical and the question is how does this form to adapt to the dry season conditions under urban pattern. Many studies had shown that An. gambiae S molecular form is well adapted to rainy season developing in the rainfall breeding sites and survived the dried conditions by living in aestivation but such mechanisms are not well known . If any, what mechanism does sustain this adaptation as only chromosomal arrangements had been pointed out as direct adaptation to the environment . In fact, larvae of S form had been collected in brick-made ravine in peripheral area which ecology is considered to be similar to humid savannah. Furthermore, An. gambiae M form was logically the most frequent vector found during this dry season where breeding sites were mainly dominated by permanent and semi-permanent water stamps and swamps in floodable areas favourable to its development . It was followed by An. arabiensis, which proportion had increased significantly compared to the latest study of Rossi et al. Here, the two vectors were found in polluted breeding sites, such as permanent swamp from Yamtenga receiving domestic wastes, from where they probably exploited the clear film of water at the edge of the swamp. Thus the survival of malaria vectors during the dry season re-launches the problematic of urban malaria pointed out over the last decade [15, 16]. Even though the sample size analysed was low, the sporozoite rate remained higher and mainly supported by An. gambiae M form and An. arabiensis. These results confirmed the malaria prevalence showing that the higher values were reported in the periphery. Although these results reflected those already observed in many African cities, they were important as they updated those published by Rossi et al.  since twenty years. Globally the tendency of transmission and vector distribution patterns was very similar to that reported by Rossi et al. It can be observed that after two decades no major modifications occurred in terms of vector composition in Ouagadougou town which kept mainly the same structure especially in the periphery (Zongo and Yamtenga). That meant that the town is extending in size but basically conserves a rural landscape structure in the periphery. Accordingly the vector composition looks like that observed in the neighbouring villages in rural setting (Dabiré unpublished. data). Indeed the recent study of Wang et al in Ouagadougou also reported a gradient of endemicity between the urban centre and the periphery and clearly linked the malaria prevalence to the seasonal availability of water supplies. The current results confirmed the distribution of the disease prevalence and provided additional information on the vector species and the sporozoite rate that is crucial to assess the risk of malaria transmission in Ouagadougou town. Herein the infection rates are higher reminding those observed in rural settings. This situation will probably progress drastically in the future with the increasing number of precarious and peripheral quarters. The occurrence of malaria vectors in urban areas in Africa is fairly well documented and local circumscribed malaria transmission had been reported in many cities [17, 18]. This situation could probably be ascribed to the failure of landscape management disseminating breeding sites, thus favouring vector-human contact. Moreover, during the last decade, gardening had expanded in the peripheral belts and also in the centre of many towns disseminating numerous breeding sites favourable to mosquito development [15, 19]. All these factors are contributing to maintain anophelines beyond to rainy period. In several African towns anophelines have been observed developing in wide range of habitats largely supplied to natural water resource such as lagoon or permanent swamps in Accra, Cotonou and Lagos or including polluted water dedicated to vegetable growing in Dakar [15, 20–23]. But in many cases the entomological inoculation rates were reported being low decreasing from the periphery to the centre. Nowadays many people originated of rural foci not necessary free of malaria are setting in periphery of the towns which could increase the picture of "urban" malaria transmission as being observed in Ouagadougou town. This landscape modification will probably modify the pattern of malaria transmission, while control measures are, so far, focused preferentially towards rural populations. This landscape modification must be monitored and controlled by a system of planning to prevent vector proliferation.
Keiser J, Utzinger J, Caldas de Castro M, Smith TA, Tanner M, Singer BH: Urbanization in sub-Saharan Africa and implication for malaria control. Am J Trop Med Hyg. 2004, 71 (Suppl 2): 118-127.
UNDP: World Urbanization Prospects: the 2001 Revisions. 2002, New York: Population Division Department of Economics and Social Affair of the United Nations
Ministère de la Santé: Annuaire statistique santé 2006. Direction des Etudes et de la Planification. 2005
Wang SJ, Lengeler C, Smith TA, Vounatsou P, Diadie DA, Pritroipa X, Convelbo N, Kientga M, Tanner M: Rapid urban malaria appraisal (RUMA) I: Epidemiology of urban malaria in Ouagadougou. Malar J. 2005, 4: 43-10.1186/1475-2875-4-43.
Rossi P, Belli A, Mancini L, Sabatinelli G: Enquête entomologique longitudinale sur la transmission du paludisme à Ouagadougou, Burkina Faso. Parassitologia. 1986, 28: 1-15.
Baragatti M, Fournet F, Henry MC, Assi S, Rogier C, Ouedraogo HZ, Salem G: Social and environmental malaria risk factors in urban areas of Ouagadougou, Burkina Faso. Malar J. 2009, 8: 13-10.1186/1475-2875-8-13.
Service MW: Mosquito ecology field sampling methods. 1993, Barking, Essex, UK: Elsevier Science Publishers, 2
Gillies MT, Coetze M: A Supplement to Anophelinae of Africa South of the Sahara. 1987, South African Institute for Medical Research, Johannesburg
Scott JA, Brogdon WG, Collins FH: Identification of single specimens of Anopheles gambiae complex by the polymerase chain reaction. Am J Trop Med Hyg. 1993, 49: 520-529.
Favia G, Lanfrancotti A, Spanos L, Sideén-Kiamos I, Louis C: Molecular characterization of ribosomal DNA polymorphisms discriminating among chromosomal forms of Anopheles gambiae s.s. Insect Mol Biol. 2001, 10: 19-23. 10.1046/j.1365-2583.2001.00236.x.
Burkot TR, Williams JL, Scheinder I: Identification of Plasmodium falciparum infected- mosquitoes by a double antibody enzyme-linked immunosorbent assay. Am J Trop Med Hyg. 1987, 33: 783-788.
Minakawa N, Githure JI, Beir JC, Yan G: Anopheline mosquito survival strategies during the dry period in western Kenya. J Med Entomol. 2003, 38: 388-392.
Touré YT, Petrarca V, Traoré SF, Coulibaly A, Maiga HM, Sangaré O, Sow M, Di Decco MA, Coluzzi M: The distribution and inversion polymorphism of chromosomally recognised taxa of the Anopheles gambiae complex in Mali, West Africa. Parassitologia. 1998, 40: 477-511.
Touré YT, Petrarca V, Traoré SF, Coulibaly A, Maiga HM, Sangaré O, Sow M, Di Decco MA, Coluzzi M: Ecological genetics studies in the chromosomal form Mopti of Anopheles gambiae s.s. in Mali, West Africa. Genetica. 1994, 94: 213-223. 10.1007/BF01443435.
Robert V, Awono-Ambene HP, Thioulouse J: Ecology of larval mosquito, with special reference to Anopheles arabiensis (Diptera: Culicidae) in market-garden wells in the urban area of Dakar, Senegal. J Med Entomol. 1998, 35: 948-955.
Keating J, Macintyre K, Mbogo C, Githeko A, Regens JL, Swalm C, Ndenga B, Steinberg LJ, Kibe L, Githure JI, Beier JC: A geographic sampling strategy for studying relationships between human activity and malaria vectors in urban Africa. Am J Trop Med Hyg. 2003, 68: 357-365.
Chinery WA: Effects of ecological changes on the malaria vector Anopheles funestus and the Anopheles gambiae complex of mosquitoes in Accra, Ghana. J Trop Med Hyg. 1984, 87: 75-81.
Robert V, Macintyre K, Keating J, Trape JF, Duchemin JB, Warren M, Beier JC: Malaria transmission in urban sub-Saharan Africa. Am J Trop Med Hyg. 2003, 68: 169-176.
Khaemba BM, Mutani A, Bett MK: Studies on the anopheline mosquitoes transmitting malaria in a newly developed highland urban area: a case study of Moi University and its environs. East Afr Med J. 1994, 71: 159-164.
Chinery WA: Variation in frequency in breeding of An. gambiae s.l. and its relationship with in-door adult mosquito density ion various localities in Accra, Ghana. J Trop Med Hyg. 1990, 87: 75-81.
Sattler MA, Mtasiwa D, Kiama M, Premji Z, Tanner M, Killeen GF, Lengeler C: Habitat characterization and spatial distribution of Anopheles sp. mosquito larvae in Dar es Salaam (Tanzania) during an extended dry period. Malar J. 2005, 4: 4-10.1186/1475-2875-4-4.
Awolola TS, Oduola AO, Obansa JB, Chukwurar NJ, Unyimadu JP: Anopheles gambiae s.s. breeding in polluted water bodies in urban Lagos, south-western Nigeria. J Vector Borne Dis. 2007, 44: 241-244.
Machault V, Gadiaga L, Vignolles C, Jarjaval F, Bouzid S, Sokhna C, Lacaux JP, Trape JF, Rogier C, Pages F: Highly focused anopheline breeding sites and malaria transmission in Dakar. Malar J. 2009, 8: 138-10.1186/1475-2875-8-138.
We are grateful to the people of the four districts of Ouagadougou for their helpful assistance during this study. We also thank MM Zoungrana Sougrinoma, Guel Hyacinthe field technicians from IRSS for their collaboration during the sampling period at Ouagadougou. This study was financially supported by the Ministry of Research of France and the UR178 (now UMR190) of IRD and also by MIM grant ID 60098A allocated to DKR.
The authors declare that they have no competing interests.
FF and DKR participated to the study design, undertook the field study, analysed data and wrote the paper. OA, CM, MPE and TKH participated to the field study and the laboratory analysis. GLC participated to the manuscript drafting. All authors have read and approved the final manuscript.