Low and seasonal malaria transmission in the middle Senegal River basin: identification and characteristics of Anopheles vectors

Mamadou O Ndiath, Jean-Biram Sarr, Lobna Gaayeb, Catherine Mazenot, Seynabou Sougoufara, Lassana Konate, Franck Remoue, Emmanuel Hermann, Jean-Francois Trape, Gilles Riveau, Cheikh Sokhna, Mamadou O Ndiath, Jean-Biram Sarr, Lobna Gaayeb, Catherine Mazenot, Seynabou Sougoufara, Lassana Konate, Franck Remoue, Emmanuel Hermann, Jean-Francois Trape, Gilles Riveau, Cheikh Sokhna

Abstract

Background: During the last decades two dams were constructed along the Senegal River. These intensified the practice of agriculture along the river valley basin. We conducted a study to assess malaria vector diversity, dynamics and malaria transmission in the area.

Methods: A cross-sectional entomological study was performed in September 2008 in 20 villages of the middle Senegal River valley to evaluate the variations of Anopheles density according to local environment. A longitudinal study was performed, from October 2008 to January 2010, in 5 selected villages, to study seasonal variations of malaria transmission.

Results: Among malaria vectors, 72.34% of specimens collected were An. arabiensis, 5.28% An. gambiae of the S molecular form, 3.26% M form, 12.90% An. pharoensis, 4.70% An. ziemanni, 1.48% An. funestus and 0.04% An. wellcomei. Anopheles density varied according to village location. It ranged from 0 to 21.4 Anopheles/room/day and was significantly correlated with the distance to the nearest ditch water but not to the river.Seasonal variations of Anopheles density and variety were observed with higher human biting rates during the rainy season (8.28 and 7.55 Anopheles bite/man/night in October 2008 and 2009 respectively). Transmission was low and limited to the rainy season (0.05 and 0.06 infected bite/man/night in October 2008 and 2009 respectively). During the rainy season, the endophagous rate was lower, the anthropophagic rate higher and L1014F kdr frequency higher.

Conclusions: Malaria vectors are present at low-moderate density in the middle Senegal River basin with An. arabiensis as the predominant species. Other potential vectors are An. gambiae M and S form and An. funestus. Nonetheless, malaria transmission was extremely low and seasonal.

© 2012 Ndiath et al; licensee BioMed Central Ltd.

Figures

Figure 1
Figure 1
Map of the studied area in the middle Senegal River basin.
Figure 2
Figure 2
Anopheles density in the 20 villages of the study area during the cross-sectional study. Anopheles density measured in September 2008 by Night Landing Catches NLC (number of Anopheles/person/night, n = 5 person/night) and by Pyrethrum Spray Catches PSC (number of Anopheles /room/day, n = 4 room/day) in all villages according to the different species studied Anopheles funestus, Anopheles gambiae s.s. molecular form M, An. arabiensis, Anopheles pharoensis and Anopheles ziemanni).
Figure 3
Figure 3
Anopheles density and malaria transmission from October 2008 to January 2010. Human biting rate (HBR, number of Anopheles bite/person/night) according to the different Anopheles species and entomologic inoculation rate (EIR, number of infected bite/person/night) during the longitudinal study, n = 40 person/night each month.

References

    1. Handschumacher P, Hervé J-P, Hébrard G. Des aménagements hydro-agricoles dans la valée du fleuve Sénégal ou le risque de maladies hydriques en milieu sahélien. Sécheresse. 1992;3:219–226.
    1. Ndiaye M. Le fleuve Sénégal et les barrages de l'OMVS:quels enseignements pour la mise en œuvre du NEPAD? VertigO - la revue électronique en sciences de l'environnement. 2003.
    1. Sow S, de Vlas SJ, Engels D, Gryseels B. Water-related disease patterns before and after the construction of the Diama dam in northern Senegal. Ann Trop Med Parasitol. 2002;96:575–586. doi: 10.1179/000349802125001636.
    1. Faye O, Konate L, Mouchet J, Fontenille D, Sy N, Hebrard G, Herve JP. Indoor resting by outdoor biting females of Anopheles gambiae complex (Diptera: Culicidae) in the sahel of northern Senegal. J Med Entomol. 1997;34:285–289.
    1. Carrara GC, Petrarca V, Niang M, Coluzzi M. Anopheles-Pharoensis and Transmission of Plasmodium-Falciparum in the Senegal River Delta, West-Africa. Med Vet Entomol. 1990;4:421–424. doi: 10.1111/j.1365-2915.1990.tb00460.x.
    1. Dia I, Konate L, Samb B, Sarr JB, Diop A, Rogerie F, Faye M, Riveau G, Remoue F, Diallo M, Fontenille D. Bionomics of malaria vectors and relationship with malaria transmission and epidemiology in three physiographic zones in the Senegal River Basin. Acta Tropica. 2008;105:145–153. doi: 10.1016/j.actatropica.2007.10.010.
    1. Faye O, Gaye O, Fontenille D, Hébrard G, Konate L, Sy N, Herve JP, Toure YT, Diallo S, Molez JF. Malaria decrease and drought in the Niayes area of northwestern Senegal. Cahiers santé. 1995;5:299–305.
    1. Konate L, Diop A, Sy N, Faye MN, Deng Y, Izri A, Faye O, Mouchet J. Comeback of Anopheles funestus in Sahelian Senegal. Lancet. 2001;358:336.
    1. Diabate A, Baldet T, Chandre F, Akoobeto M, Guiguemde TR, Darriet F, Brengues C, Guillet P, Hemingway J, Small GJ, Hougard JM. The role of agricultural use of insecticides in resistance to pyrethroids in Anopheles gambiae s.l. in Burkina Faso. Am J Trop Med Hyg. 2002;67:617–622.
    1. Donnelly MJ, Corbel V, Weetman D, Wilding CS, Williamson MS, Black WC. Does kdr genotype predict insecticide-resistance phenotype in mosquitoes? Trends Parasitol. 2009;25:213–219. doi: 10.1016/j.pt.2009.02.007.
    1. Diop A. Rapports annuels du Projet OMS/GATES sur le contrôle et la biologie des vecteurs du paludisme. Programme National de Lutte contre le Paludisme, Ministère de la Santé et de la Prévention, Sénégal. 2010.
    1. Gillies MT, De Meillon D. The Anophelinae of Africa South of the Sahara (Ethiopian zoogeographical region) 2. p. 343 pp.
    1. Beier JC, Perkins PV, Wirtz RA, Koros J, Diggs D, Gargan TP, Koech DK. Bloodmeal Identification by Direct Enzyme-Linked Immunosorbent-Assay (Elisa), Tested on Anopheles (Diptera, Culicidae) in Kenya. J Med Entomol. 1988;25:9–16.
    1. Fanello C, Santolamazza F, della TA. Simultaneous identification of species and molecular forms of the Anopheles gambiae complex by PCR-RFLP. Med Vet Entomol. 2002;16:461–464. doi: 10.1046/j.1365-2915.2002.00393.x.
    1. Wirtz RA, Zavala F, Charoenvit Y, Campbell GH, Burkot TR, Schneider I, Esser KM, Beaudoin RL, Andre RG. Comparative Testing of Monoclonal-Antibodies Against Plasmodium-Falciparum Sporozoites for Elisa Development. Bull World Health Organ. 1987;65:39–45.
    1. Martinez-Torres D, Chandre F, Williamson MS, Darriet F, Berge JB, Devonshire AL, Guillet P, Pasteur N, Pauron D. Molecular characterization of pyrethroid knockdown resistance (kdr) in the major malaria vector Anopheles gambiae s.s. Insect Mol Biol. 1998;7:179–184. doi: 10.1046/j.1365-2583.1998.72062.x.
    1. Coetzee M, Craig M, le Sueur D. Distribution of African malaria mosquitoes belonging to the Anopheles gambiae complex. Parasitology Today. 2000;16:74–77. doi: 10.1016/S0169-4758(99)01563-X.
    1. Lindsay SW, Parson L, Thomas CJ. Mapping the ranges and relative abundance of the two principal African malaria vectors, Anopheles gambiae sensu stricto and An-arabiensis, using climate data. Proc Biol Sci. 1998;265:847–854. doi: 10.1098/rspb.1998.0369.
    1. Toure YT, Petrarca V, Traore SF, Coulibaly A, Maiga HM, Sankare O, Sow M, Dideco MA, Coluzzi M. Ecological Genetic-Studies in the Chromosomal Form Mopti of Anopheles-Gambiae S-Str in Mali, West-Africa. Genetica. 1994;94:213–223. doi: 10.1007/BF01443435.
    1. Diuk-Wasser MA, Toure MB, Dolo G, Bagayoko M, Sogoba N, Traore SF, Manoukis N, Taylor CE. Vector abundance and malaria transmission in rice-growing villages in Mali. Am J Trop Med Hyg. 2005;72:725–731.
    1. Ndiath MO, Brengues C, Konate L, Sokhna C, Boudin C, Trape JF, Fontenille D. Dynamics of transmission of Plasmodium falciparum by Anopheles arabiensis and the molecular forms M and S of Anopheles gambiae in Dielmo, Senegal. Malar J. 2008;7
    1. Ndiath MO, Cohuet A, Gaye A, Konate L, Mazenot C, Faye O, Boudin C, Sokhna C, Trape JF. Comparative susceptibility to Plasmodium falciparum of the molecular forms M and S of Anopheles gambiae and Anopheles arabiensis. Malar J. 2011;10:269. doi: 10.1186/1475-2875-10-269.
    1. de SD, Kelly-Hope L, Lawson B, Wilson M, Boakye D. Environmental factors associated with the distribution of Anopheles gambiae s.s in Ghana; an important vector of lymphatic filariasis and malaria. PLoS One. 2010;5:e9927. doi: 10.1371/journal.pone.0009927.
    1. Toure YT, Petrarca V, Traore SF, Coulibaly A, Maiga HM, Sankare O, Sow M, Di Deco MA, Coluzzi M. The distribution and inversion polymorphism of chromosomally recognized taxa of the Anopheles gambiae complex in Mali, West Africa. Parassitologia. 1998;40:477–511.
    1. Yawson AE, McCall PJ, Wilson MD, Donnelly MJ. Species abundance and insecticide resistance of Anopheles gambiae in selected areas of Ghana and Burkina Faso. Med Vet Entomol. 2004;18:372–377. doi: 10.1111/j.0269-283X.2004.00519.x.
    1. Diabate A, Baldet T, Chandre C, Dabire KR, Kengne P, Guiguemde TR, Simard F, Guillet P, Hemingway J, Hougard JM. KDR mutation, a genetic marker to assess events of introgression between the molecular M and S forms of Anopheles gambiae (Diptera: Culicidae) in the tropical savannah area of West Africa. J Med Entomol. 2003;40:195–198. doi: 10.1603/0022-2585-40.2.195.
    1. Mouchet J, Faye O, Julvez J, Manguin S. Drought and malaria retreat in the Sahel, West Africa. Lancet. 1996;348:1735–1736.
    1. Sogoba N, Vounatsou P, Doumbia S, Bagayoko M, Toure MB, Sissoko IM, Traore SF, Toure YT, Smith T. Spatial analysis of malaria transmission parameters in the rice cultivation area of Office du Niger, Mali. Am J Trop Med Hyg. 2007;76:1009–1015.
    1. Rosenberg R, Wirtz RA, Lanar DE, Sattabongkot J, Hall T, Waters AP, Prasittisuk C. Circumsporozoite Protein Heterogeneity in the Human Malaria Parasite Plasmodium-Vivax. Science. 1989;245:973–976. doi: 10.1126/science.2672336.
    1. Lemasson JJ, Fontenille D, Lochouarn L, Dia I, Simard F, Ba K, Diop A, Diatta M, Molez JF. Comparison of behavior and vector efficiency of Anopheles gambiae and An-arabiensis (Diptera: Culicidae) in Barkedji, a Sahelian area of Senegal. J Med Entomol. 1997;34:396–403.
    1. Himeidan YE, Dukeen MY, El-Rayah E-A. Anopheles arabiensis: abundance and insecticide resistance in an irrigated area of eastern Sudan. East Mediterr Health J. 2004;10:167–174.
    1. Mwangangi JM, Mbogo CM, Nzovu JG, Githure JI, Yan GY, Beier JC. Blood-meal analysis for anopheline mosquitoes sampled along the Kenyan coast. J Am Mosq Control Assoc. 2003;19:371–375.
    1. Ameneshewa B, Service MW. Blood-feeding behavior of Anopheles arabiensis Patton (Diptera: Culicidae) in central Ethiopia. Ethiopia J Afr Zoo. 2011;11:235–245.
    1. Boreham PFL. Some Applications of Bloodmeal Identifications in Relation to Epidemiology of Vector-Borne Tropical Diseases. J Trop Med Hyg. 1975;78:83–91.
    1. 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
    1. Dia I, Ba H, Mohamed SAO, Diallo D, Lo B, Diallo M. Distribution, host preference and infection rates of malaria vectors in Mauritania. Parasit Vectors. 2009;2
    1. Fettene M, Hunt RH, Coetzee M, Tessema F. Behaviour of Anopheles arabiensis and An. quadriannulatus sp B mosquitoes and malaria transmission in southwestern Ethiopia. African Entomol. 2004;12:83–87.
    1. Waka M, Hopkins RJ, Akinpelu O, Curtis C. Transmission of malaria in the Tesseney area of Eritrea: parasite prevalence in children, and vector density, host preferences, and sporozoite rate. J Vec Ecol. 2005;30:27–32.
    1. Fontenille D, Lochouarn L, Diatta M, Sokhna C, Dia I, Diagne N, Lemasson JJ, Ba K, Tall A, Rogier C, Trape JF. Four years' entomological study of the transmission of seasonal malaria in Senegal and the bionomics of Anopheles gambiae and A-araibiensis. Trans R Soc Trop Med Hyg. 1997;91:647–652. doi: 10.1016/S0035-9203(97)90506-X.
    1. Joshi GP, Service MW, Pradhan GD. Survey of Species-A and Species-B of Anopheles-Gambiae Giles Complex in Kisumu Area of Kenya Prior to Insecticidal Spraying with Oms-43 (Fenitrothion) Ann Trop Med Parasitol. 1975;69:91–104.
    1. Ministère de la Santé et de la Prévention. Annual report. National Malaria Managment Programm. 2009.
    1. Ranson H, N'Guessan R, Lines J, Moiroux N, Nkuni Z, Corbel V. Pyrethroid resistance in African anopheline mosquitoes: what are the implications for malaria control? Trends Parasitol. 2011;27:91–98. doi: 10.1016/j.pt.2010.08.004.
    1. Diabate A, Brengues C, Baldet T, Dabire KR, Hougard JM, Akogbeto M, Kengne P, Simard F, Guillet P, Hemingway J, Chandre F. The spread of the Leu-Phe kdr mutation through Anopheles gambiae complex in Burkina Faso: genetic introgression and de novo phenomena. Trop Med Int Health. 2004;9:1267–1273. doi: 10.1111/j.1365-3156.2004.01336.x.
    1. Thwing JI, Perry RT, Townes DA, Diouf MB, Ndiaye S, Thior M. Success of Senegal's first nationwide distribution of long-lasting insecticide-treated nets to children under five - contribution toward universal coverage. Malar J. 2011;10:86. doi: 10.1186/1475-2875-10-86.
    1. Czeher C, Labbo R, Arzika I, Duchemin JB. Evidence of increasing Leu-Phe knockdown resistance mutation in Anopheles gambiae from Niger following a nationwide long-lasting insecticide-treated nets implementation. Malar J. 2008;7

Source: PubMed

3
Subscribe