First attempt to validate human IgG antibody response to Nterm-34kDa salivary peptide as biomarker for evaluating exposure to Aedes aegypti bites

PLoS Negl Trop Dis. 2012;6(11):e1905. doi: 10.1371/journal.pntd.0001905. Epub 2012 Nov 15.

Abstract

Background: Much effort is being devoted for developing new indicators to evaluate the human exposure to Aedes mosquito bites and the risk of arbovirus transmission. Human antibody (Ab) responses to mosquito salivary components could represent a promising tool for evaluating the human-vector contact.

Methodology/principal findings: To develop a specific biomarker of human exposure to Aedes aegypti bites, we measured IgG Ab response to Ae. aegypti Nterm-34 kDa salivary peptide in exposed children in 7 villages of Southern Benin (West Africa). Results showed that specific IgG response presented high inter-individual heterogeneity between villages. IgG response was associated with rainfall and IgG level increased from dry (low exposure) to rainy (high exposure) seasons. These findings indicate that IgG Ab to Nterm-34 kDa salivary peptide may represent a reliable biomarker to detect variation in human exposure to Ae. aegypti bites.

Conclusion/significance: This preliminary study highlights the potential use of Ab response to this salivary peptide for evaluating human exposure to Ae. aegypti. This biomarker could represent a new promising tool for assessing the risk of arbovirus transmission and for evaluating the efficacy of vector control interventions.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aedes / immunology*
  • Animals
  • Antibody Formation
  • Benin
  • Biomarkers*
  • Child, Preschool
  • Female
  • Humans
  • Immunoglobulin G / blood*
  • Infant
  • Infant, Newborn
  • Insect Bites and Stings / diagnosis*
  • Insect Proteins / immunology*
  • Male
  • Salivary Proteins and Peptides / immunology

Substances

  • Biomarkers
  • Immunoglobulin G
  • Insect Proteins
  • Salivary Proteins and Peptides

Grants and funding

This work was integrated in the framework of the Project FSP/REFS N° 2006-22 supported by the French Ministry of Foreign Affairs (MAEE). Financial support was also provided by AIRD-CRVOI (Centre de Recherche et Veille en Océan Indien – Projet N° PRAO/AIRD/CRVOI/08/01) funded project and by IRD (Département Expertise et Valorisation). E. Elanga-Ndille and A. Djenontin were supported by a PhD fellowship provided by the IRD (Département des Programmes de Formation au Sud). S. Doucoure and P.M. Drame were supported by a PhD and Post-doc fellowship respectively, provided by the “Infectiopole Sud” Foundation (Marseille, France). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.