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BioMed Research International
Volume 2014, Article ID 746509, 8 pages
http://dx.doi.org/10.1155/2014/746509
Research Article

Human Antibody Response to Aedes albopictus Salivary Proteins: A Potential Biomarker to Evaluate the Efficacy of Vector Control in an Area of Chikungunya and Dengue Virus Transmission

1Institut de Recherche pour le Développement (IRD), Maladie Infectieuse et Vecteurs, Ecologie, Génétique, Evolution et Contrôle (MIVEGEC), UM1-CNRS 5290-IRD, Centre IRD de Montpellier, 34394 Montpellier, France
2URMITE 198 Campus IRD-UCAD, Route des Pères Maristes, BP 1386, 18524 Dakar, Senegal
3Agence Régionale de Santé, Océan Indien, CS 61002, 97743 Saint Denis Cedex 9, La Réunion, France
4Agence Régionale de Santé, Océan Indien, CS 60050, 97408 Saint Denis Cedex 9, La Réunion, France

Received 15 August 2013; Revised 6 March 2014; Accepted 19 March 2014; Published 13 April 2014

Academic Editor: Benoît Stijlemans

Copyright © 2014 Souleymane Doucoure et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. M. Q. Benedict, R. S. Levine, W. A. Hawley, and L. P. Lounibos, “Spread of the tiger: global risk of invasion by the mosquito Aedes albopictus,” Vector-Borne and Zoonotic Diseases, vol. 7, no. 1, pp. 76–85, 2007. View at Publisher · View at Google Scholar · View at Scopus
  2. N. G. Gratz, “Critical review of the vector status of Aedes albopictus,” Medical and Veterinary Entomology, vol. 18, no. 3, pp. 215–227, 2004. View at Publisher · View at Google Scholar · View at Scopus
  3. D. J. Gubler, “The global emergence/resurgence of arboviral diseases as public health problems,” Archives of Medical Research, vol. 33, no. 4, pp. 330–342, 2002. View at Publisher · View at Google Scholar · View at Scopus
  4. E. A. Gould, P. Gallian, X. De Lamballerie, and R. N. Charrel, “First cases of autochthonous dengue fever and chikungunya fever in France: from bad dream to reality!,” Clinical Microbiology and Infection, vol. 16, no. 12, pp. 1702–1704, 2010. View at Publisher · View at Google Scholar · View at Scopus
  5. C. H. Tan, P. S. J. Wong, M. Z. I. Li et al., “Entomological investigation and control of a chikungunya cluster in Singapore,” Vector-Borne and Zoonotic Diseases, vol. 11, no. 4, pp. 383–390, 2011. View at Publisher · View at Google Scholar · View at Scopus
  6. P. Barbazan, W. Tuntaprasart, M. Souris et al., “Assessment of a new strategy, based on Aedes aegypti (L.) pupal productivity, for the surveillance and control of dengue transmission in Thailand,” Annals of Tropical Medicine and Parasitology, vol. 102, no. 2, pp. 161–171, 2008. View at Publisher · View at Google Scholar · View at Scopus
  7. D. A. Focks and D. D. Chadee, “Pupal survey: an epidemiologically significant surveillance method for Aedes aegypti: an example using data from Trinidad,” American Journal of Tropical Medicine and Hygiene, vol. 56, no. 2, pp. 159–167, 1997. View at Google Scholar · View at Scopus
  8. D. Focks, A Review of Entomological Sampling Methods and Indicators for Dengue Vectors, World Health Organization TDR/ IDE/Den/03. 1, 2003.
  9. T. Lefèvre, L.-C. Gouagna, K. R. Dabiré et al., “Beer consumption increases human attractiveness to malaria mosquitoes,” PLoS ONE, vol. 5, no. 3, article e9546, 2010. View at Publisher · View at Google Scholar · View at Scopus
  10. R. C. Smallegange, N. O. Verhulst, and W. Takken, “Sweaty skin: an invitation to bite?” Trends in Parasitology, vol. 27, no. 4, pp. 143–148, 2011. View at Publisher · View at Google Scholar · View at Scopus
  11. B. S. Schwartz and M. D. Goldstein, “Lyme disease in outdoor workers: risk factors, preventive measures, and tick removal methods,” American Journal of Epidemiology, vol. 131, no. 5, pp. 877–885, 1990. View at Google Scholar · View at Scopus
  12. B. S. Schwartz, J. M. C. Ribeiro, and M. D. Goldstein, “Anti-tick antibodies: an epidemiologic tool in Lyme disease research,” American Journal of Epidemiology, vol. 132, no. 1, pp. 58–66, 1990. View at Google Scholar · View at Scopus
  13. A. Schwarz, S. Helling, N. Collin et al., “Immunogenic salivary proteins of Triatoma infestans: development of a recombinant antigen for the detection of low-level infestation of triatomines,” PLoS Neglected Tropical Diseases, vol. 3, no. 10, article e532, 2009. View at Publisher · View at Google Scholar · View at Scopus
  14. A. Schwarz, J. M. Sternberg, V. Johnston et al., “Antibody responses of domestic animals to salivary antigens of Triatoma infestans as biomarkers for low-level infestation of triatomines,” International Journal for Parasitology, vol. 39, no. 9, pp. 1021–1029, 2009. View at Publisher · View at Google Scholar · View at Scopus
  15. H. Brummer-Korvenkontio, K. Palosuo, T. Palosuo, M. Brummer-Korvenkontio, P. Leinikki, and T. Reunala, “Detection of mosquito saliva-specific IgE antibodies by capture ELISA,” Allergy: European Journal of Allergy and Clinical Immunology, vol. 52, no. 3, pp. 342–345, 1997. View at Google Scholar · View at Scopus
  16. H. Brummer-Korvenkontio, P. Lappalainen, T. Reunala, and T. Palosuo, “Detection of mosquito saliva-specific IgE and IgG4 antibodies by immunoblotting,” Journal of Allergy and Clinical Immunology, vol. 93, no. 3, pp. 551–555, 1994. View at Google Scholar · View at Scopus
  17. A. Poinsignon, S. Cornelie, F. Ba 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, no. 1, article 198, 2009. View at Publisher · View at Google Scholar · View at Scopus
  18. A. Poinsignon, S. Cornelie, M. Mestres-Simon et al., “Novel peptide marker corresponding to salivary protein gSG6 potentially identifies exposure to Anopheles bites,” PLoS ONE, vol. 3, no. 6, article e2472, 2008. View at Publisher · View at Google Scholar · View at Scopus
  19. A. Poinsignon, B. Samb, S. Doucoure 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 and International Health, vol. 15, no. 10, pp. 1198–1203, 2010. View at Publisher · View at Google Scholar · View at Scopus
  20. M. F. Clements, K. Gidwani, R. Kumar et al., “Measurement of recent exposure to Phlebotomus argentipes, the vector of indian visceral leishmaniasis, by using human antibody responses to sand fly saliva,” American Journal of Tropical Medicine and Hygiene, vol. 82, no. 5, pp. 801–807, 2010. View at Publisher · View at Google Scholar · View at Scopus
  21. S. Marzouki, M. Ben Ahmed, T. Boussoffara et al., “Characterization of the antibody response to the saliva of Phlebotomus papatasi in people living in endemic areas of cutaneous leishmaniasis,” American Journal of Tropical Medicine and Hygiene, vol. 84, no. 5, pp. 653–661, 2011. View at Publisher · View at Google Scholar · View at Scopus
  22. A. P. Souza, B. B. Andrade, D. Aquino et al., “Using recombinant proteins from Lutzomyia longipalpis saliva to estimate human vector exposure in visceral leishmaniasis endemic areas,” PLoS Neglected Tropical Diseases, vol. 4, no. 3, article e649, 2010. View at Publisher · View at Google Scholar · View at Scopus
  23. C. Teixeira, R. Gomes, N. Collin et al., “Discovery of markers of exposure specific to bites of Lutzomyia longipalpis, the vector of Leishmania infantum chagasiin Latin America,” PLoS Neglected Tropical Diseases, vol. 4, no. 3, article e638, 2010. View at Publisher · View at Google Scholar · View at Scopus
  24. P. M. Drame, A. Poinsignon, P. Besnard 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. 5, no. 12, article e15596, 2010. View at Publisher · View at Google Scholar · View at Scopus
  25. P. M. Drame, A. Poinsignon, P. Besnard 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, no. 1, pp. 115–121, 2010. View at Publisher · View at Google Scholar · View at Scopus
  26. A. Schwarz, J. A. Juarez, J. Richards et al., “Anti-triatomine saliva immunoassays for the evaluation of impregnated netting trials against Chagas disease transmission,” International Journal for Parasitology, vol. 41, no. 6, pp. 591–594, 2011. View at Publisher · View at Google Scholar · View at Scopus
  27. T. Reunala, H. Brummer-Korvenkontio, K. Palosuo et al., “Frequent occurrence of IgE and IgG4 antibodies against saliva of Aedes communis and Aedes aegypti mosquitoes in children,” International Archives of Allergy and Immunology, vol. 104, no. 4, pp. 366–371, 1994. View at Google Scholar · View at Scopus
  28. F. Remoue, E. Alix, S. Cornelie et al., “IgE and IgG4 antibody responses to Aedes saliva in African children,” Acta Tropica, vol. 104, no. 2-3, pp. 108–115, 2007. View at Publisher · View at Google Scholar · View at Scopus
  29. S. Doucoure, F. Mouchet, A. Cournile et al., “Human antibody response to Aedes aegypti saliva in an urban population in Bolivia: a new biomarker of exposure to Dengue vector bites,” The American Journal of Tropical Medicine and Hygiene, vol. 87, no. 3, pp. 504–510, 2012. View at Google Scholar
  30. S. Doucoure, F. Mouchet, S. Cornelie et al., “Evaluation of the human IgG antibody response to aedes albopictus saliva as a new specific biomarker of exposure to vector bites,” PLoS Neglected Tropical Diseases, vol. 6, no. 2, article e1487, 2012. View at Publisher · View at Google Scholar · View at Scopus