C. Guerra, P. Gikandi, A. Tatem, A. Noor, D. Smith et al., The Limits and Intensity of Plasmodium falciparum Transmission: Implications for Malaria Control and Elimination Worldwide, PLoS Medicine, vol.3, issue.2, p.38, 2008.
DOI : 10.1371/journal.pmed.0050038.st001

P. Martens and L. Hall, Malaria on the Move: Human Population Movement and Malaria Transmission, Emerging Infectious Diseases, vol.6, issue.2, pp.103-109, 2000.
DOI : 10.3201/eid0602.000202

A. Tatem, C. Guerra, C. Kabaria, A. Noor, and S. Hay, Human population, urban settlement patterns and their impact on Plasmodium falciparum malaria endemicity, Malaria Journal, vol.7, issue.1, p.218, 2008.
DOI : 10.1186/1475-2875-7-218

S. Wang, C. Lengeler, T. Smith, P. Vounatsou, G. Cisse et al., Rapid urban malaria appraisal (RUMA) in sub-Saharan Africa, Malaria Journal, vol.4, issue.1, p.40, 2005.
DOI : 10.1186/1475-2875-4-40

J. Keiser, J. Utzinger, C. De-castro, M. Smith, T. Tanner et al., Urbanization in sub-saharan Africa and implication for malaria control

W. Chinery, Effects of ecological changes on the malaria vectors Anopheles funestus and the Anopheles gambia complex of mosquitoes in Accra, Ghana, J Trop Med Hyg, vol.87, pp.75-81, 1984.

V. Robert, K. Macintyre, J. Keating, J. Trape, J. Duchemin et al., Malaria transmission in urban sub-Saharan Africa, Am J Trop Med Hyg, vol.68, pp.169-176, 2003.

M. Donnelly, P. Mccall, C. Lengeler, I. Bates, D. 'alessandro et al., Mutero C: Malaria and urbanization in sub-Saharan Africa, Malaria Journal, vol.4, issue.1, p.12, 2005.
DOI : 10.1186/1475-2875-4-12

S. Diallo, L. Konate, O. Ndir, T. Dieng, Y. Dieng et al., Malaria in the central health district of Dakar (Senegal). Entomological, parasitological and clinical data, Sante, vol.10, pp.221-229, 2000.

L. Gadiaga, V. Machault, F. Pages, A. Gaye, F. Jarjaval et al., Conditions of malaria transmission in Dakar from 2007 to 2010, Malaria Journal, vol.10, issue.1, p.312, 2007.
DOI : 10.1603/0022-2585(2005)042[0104:COHCAO]2.0.CO;2

F. Pages, G. Texier, B. Pradines, L. Gadiaga, V. Machault et al., Malaria transmission in Dakar: A two-year survey, Malaria Journal, vol.7, issue.1, p.178, 2008.
DOI : 10.1186/1475-2875-7-178

URL : https://hal.archives-ouvertes.fr/pasteur-00634615

J. Trape, E. Lefebvre-zante, F. Legros, G. Ndiaye, H. Bouganali et al., Vector density gradients and the epidemiology of urban malaria in Dakar, Senegal, Am J Trop Med Hyg, vol.47, pp.181-189, 1992.

V. Machault, L. Gadiaga, C. Vignolles, F. Jarjaval, S. Bouzid et al., Highly focused anopheline breeding sites and malaria transmission in Dakar, Malaria Journal, vol.8, issue.1, p.138, 2009.
DOI : 10.1186/1475-2875-8-138

V. Machault, C. Vignolles, F. Pages, L. Gadiaga, A. Gaye et al., Spatial heterogeneity and temporal evolution of malaria transmission risk in Dakar, Senegal, according to remotely sensed environmental data, Malaria Journal, vol.9, issue.1, p.252, 2010.
DOI : 10.1186/1475-2875-9-252

N. Govella, P. Chaki, Y. Geissbuhler, K. Kannady, F. Okumu et al., A new tent trap for sampling exophagic and endophagic members of the Anopheles gambiae complex, Malaria Journal, vol.8, issue.1, p.157, 2009.
DOI : 10.1186/1475-2875-8-157

E. Mathenge, G. Omweri, L. Irungu, P. Ndegwa, E. Walczak et al., Comparative field evaluation of the Mbita trap, the Centers for Disease Control light trap, and the human landing catch for sampling of malaria vectors in western Kenya, Am J Trop Med Hyg, vol.70, pp.33-37, 2004.

L. Mboera, Sampling techniques for adult Afrotropical malaria vectors and their reliability in the estimation of entomological inoculation rate, Tanzania Journal of Health Research, vol.7, issue.3, pp.117-124, 2005.
DOI : 10.4314/thrb.v7i3.14248

A. Poinsignon, S. Cornelie, F. Ba, D. Boulanger, C. Sow et al., Human IgG response to a salivary peptide, gSG6-P1, as a new immuno-epidemiological tool for evaluating low-level exposure to Anopheles bites, Malaria Journal, vol.8, issue.1, p.198, 2009.
DOI : 10.1186/1475-2875-8-198

F. Remoue, S. Cornelie, A. Ngom, D. Boulanger, and F. Simondon, Immune responses to arthropod bites during vector-borne diseases, Update in tropical immunology Edited by, pp.377-400, 2005.

B. Schwartz, J. Ribeiro, and M. Goldstein, ANTI-TICK ANTIBODIES: AN EPIDEMIOLOGIC TOOL IN LYME DISEASE RESEARCH, American Journal of Epidemiology, vol.132, issue.1, pp.58-66, 1990.
DOI : 10.1093/oxfordjournals.aje.a115643

D. Champagne, Antihemostatic Strategies of Blood-Feeding Arthropods, Current Drug Target -Cardiovascular & Hematological Disorders, vol.4, issue.4, pp.375-396, 2004.
DOI : 10.2174/1568006043335862

J. Ribeiro, Blood-feeding arthropods: live syringes or invertebrate pharmacologists?, Infect Agents Dis, vol.4, pp.143-152, 1995.

H. Brummer-korvenkontio, K. Palosuo, T. Palosuo, M. Brummer-korvenkontio, P. Leinikki et al., Detection of mosquito saliva-specific IgE antibodies by capture ELISA, Allergy, vol.130, issue.3, pp.342-345, 1997.
DOI : 10.1016/0091-6749(85)90803-6

R. Lane, R. Moss, Y. Hsu, T. Wei, M. Mesirow et al., Anti-arthropod saliva antibodies among residents of a community at high risk for Lyme disease in California, Am J Trop Med Hyg, vol.61, pp.850-859, 1999.

A. Barral, E. Honda, A. Caldas, J. Costa, V. Vinhas et al., Human immune response to sand fly salivary gland antigens: a useful epidemiological marker?, Am J Trop Med Hyg, vol.62, pp.740-745, 2000.

R. Nascimento, J. Santana, S. Lozzi, C. Araujo, and A. Teixeira, Human IgG1 and IgG4: the main antibodies against Triatoma infestan (Hemiptera: Reduviidae) salivary gland proteins, Am J Trop Med Hyg, vol.65, pp.219-226, 2001.

A. Poinsignon, F. Remoue, M. Rossignol, S. Cornelie, D. Courtin et al., Human IgG antibody response to Glossina saliva: an epidemiologic marker of exposure to Glossina bites, Am J Trop Med Hyg, vol.78, pp.750-753, 2008.

K. Palosuo, H. Brummer-korvenkontio, J. Mikkola, T. Sahi, and T. Reunala, Seasonal Increase in Human IgE and lgG4 Antisaliva Antibodies to Aedes Mosquito Bites, International Archives of Allergy and Immunology, vol.114, issue.4, pp.367-372, 1997.
DOI : 10.1159/000237696

F. Remoue, A. E. Cornelie, S. Sokhna, C. Cisse, B. Doucoure et al., IgE and IgG4 antibody responses to Aedes saliva in African children, Acta Tropica, vol.104, issue.2-3, pp.108-115, 2007.
DOI : 10.1016/j.actatropica.2007.07.011

Z. Peng, N. Rasic, Y. Liu, and F. Simons, Mosquito saliva???specific IgE and IgG antibodies in 1059 blood donors, Journal of Allergy and Clinical Immunology, vol.110, issue.5, pp.816-817, 2002.
DOI : 10.1067/mai.2002.128736

P. Drame, A. Poinsignon, P. Besnard, L. Mire, J. Dos-santos et al., Human Antibody Response to Anopheles gambiae Saliva: An Immuno-Epidemiological Biomarker to Evaluate the Efficacy of Insecticide-Treated Nets in Malaria Vector Control, American Journal of Tropical Medicine and Hygiene, vol.83, issue.1, pp.115-121, 2010.
DOI : 10.4269/ajtmh.2010.09-0684

F. Remoue, B. Cisse, F. Ba, C. Sokhna, J. Herve et al., Evaluation of the antibody response to Anopheles salivary antigens as a potential marker of risk of malaria, Transactions of the Royal Society of Tropical Medicine and Hygiene, vol.100, issue.4, pp.363-370, 2006.
DOI : 10.1016/j.trstmh.2005.06.032

A. Waitayakul, S. Somsri, J. Sattabongkot, S. Looareesuwan, L. Cui et al., Natural human humoral response to salivary gland proteins of Anopheles mosquitoes in Thailand, Acta Tropica, vol.98, issue.1, pp.66-73, 2006.
DOI : 10.1016/j.actatropica.2006.02.004

B. Andrade, B. Rocha, A. Reis-filho, L. Camargo, W. Tadei et al., Anti-Anopheles darlingi saliva antibodies as marker of Plasmodium vivax infection and clinical immunity in the Brazilian Amazon, Malaria Journal, vol.8, issue.1, p.121, 2009.
DOI : 10.1186/1475-2875-8-121

P. Drame, A. Poinsignon, P. Besnard, S. Cornelie, L. Mire et al., Human Antibody Responses to the Anopheles Salivary gSG6-P1 Peptide: A Novel Tool for Evaluating the Efficacy of ITNs in Malaria Vector Control, PLoS ONE, vol.6, issue.12, p.15596, 2010.
DOI : 10.1371/journal.pone.0015596.g003

A. Poinsignon, S. Cornelie, M. Mestres-simon, A. Lanfrancotti, M. Rossignol et al., Novel Peptide Marker Corresponding to Salivary Protein gSG6 Potentially Identifies Exposure to Anopheles Bites, PLoS ONE, vol.3, issue.1102, p.2472, 2008.
DOI : 10.1371/journal.pone.0002472.g004

A. Poinsignon, B. Samb, S. Doucoure, P. Drame, J. Sarr et al., First attempt to validate the gSG6-P1 salivary peptide as an immuno-epidemiological tool for evaluating human exposure to Anopheles funestus bites, Tropical Medicine & International Health, vol.98, issue.10, pp.1198-1203, 2010.
DOI : 10.1111/j.1365-3156.2010.02611.x

M. Gillies and M. Coetzee, A supplement to the anophelinae of Africa south of the Sahara (Afrotropical region) The South African Institut for Medical Research No, 1987.

V. Robert and C. Boudin, Biology of man-mosquito Plasmodium transmission, Bull Soc Pathol Exot, vol.96, pp.6-20, 2003.

Y. Geissbuhler, P. Chaki, B. Emidi, N. Govella, R. Shirima et al., Interdependence of domestic malaria prevention measures and mosquito-human interactions in urban Dar es Salaam, Tanzania, Malaria Journal, vol.6, issue.1, p.126, 2007.
DOI : 10.1186/1475-2875-6-126

P. Dambach, A. Sie, J. Lacaux, C. Vignolles, V. Machault et al., Using high spatial resolution remote sensing for risk mapping of malaria occurrence in the Nouna district, Burkina Faso. Glob Health Action, 2009.

B. Matthys, N. Goran, E. Kone, M. Koudou, B. Vounatsou et al., Urban agricultural land use and characterization of mosquito larval habitats in a medium-sized town of C??te d'Ivoire, Journal of Vector Ecology, vol.40, issue.2, pp.319-333, 2006.
DOI : 0022-2585(2003)040[0860:ACOMPT]2.0.CO;2

Y. Afrane, E. Klinkenberg, P. Drechsel, K. Owusu-daaku, R. Garms et al., Does irrigated urban agriculture influence the transmission of malaria in the city of Kumasi, Ghana? Acta Trop, pp.125-134, 2004.

R. Holt, G. Subramanian, A. Halpern, G. Sutton, R. Charlab et al., The Genome Sequence of the Malaria Mosquito Anopheles gambiae, Science, vol.298, issue.5591, pp.129-149, 2002.
DOI : 10.1126/science.1076181

E. Calvo, A. Dao, V. Pham, and J. Ribeiro, An insight into the sialome of Anopheles funestus reveals an emerging pattern in anopheline salivary protein families, Insect Biochemistry and Molecular Biology, vol.37, issue.2, pp.164-175, 2007.
DOI : 10.1016/j.ibmb.2006.11.005