Abstract

BackgroundAntibody responses to malaria antigens reflect exposure to parasites, and seroprevalence correlates with malaria transmission intensity. Antibodies are routinely measured in sera or on dried blood spots but a non-invasive method would provide extra utility in sampling general populations. Saliva is already in use in the detection of plasma-derived IgM and IgG to viral infections. In this study, antibodies to Plasmodium falciparum merozoite antigens were compared between blood and saliva samples from the same individuals in unlinked surveys conducted in Tanzania and The Gambia.MethodsIn Tanzania, 53 individuals provided paired fingerprick blood and saliva sample using two commercially available sampling devices. In the Gambia, archived plasma and saliva samples collected from 200 children in the Farafenni area in a cross-sectional survey were analyzed.IgG antibodies against P. falciparum antigens, Merozoite Surface Protein-1 (MSP-119) and Apical membrane Antigen (AMA-1) were measured by ELISA in paired saliva and blood samples from both sites. Antibody levels were compared as continuous optical density (OD) values and by sero-positivity.ResultsSignificant correlations between saliva and plasma antibody levels were seen in Tanzania for both antigens, AMA-1(r2 range 0.93 to 0.89, p < 0.001) and MSP-119 (r2 range 0.93 to 0.75, p < 0.001), with a weaker correlation for results from The Gambia (r2range 0.64 to 0.63, p < 0.01). When assessed as seropositivity and compared with plasma, sensitivity and specificity were good with saliva antibody levels to both AMA-1 and MSP-119 (sensitivity range 64-77% and specificity range 91-100% & 47-67% and 90-97% respectively) over the different sample sets.ConclusionsThese data demonstrate anti-malarial antibodies can be detected in saliva and correlate strongly with levels in plasma. This non-invasive relatively simple collection method will be potentially useful for general population surveys, and particularly in migratory populations or those with infrequent contact with health services or opposed to blood withdrawal. Further studies will be needed to optimize collection methods, standardize volumes and content and develop controls.

Highlights

  • Antibody responses to malaria antigens reflect exposure to parasites, and seroprevalence correlates with malaria transmission intensity

  • Matched filter paper or plasma samples and saliva were available from 53 Tanzanian participants and 200 Gambian participants

  • Similar results were seen for antibodies against MSP-119 (r2 Oracol-fingerprick = 0.75, r2Orasure-Fingerprick = 0.94, both p < 0.001, figure 1c &1d, Table 1)

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Summary

Introduction

Antibody responses to malaria antigens reflect exposure to parasites, and seroprevalence correlates with malaria transmission intensity. Antibodies to Plasmodium falciparum merozoite antigens were compared between blood and saliva samples from the same individuals in unlinked surveys conducted in Tanzania and The Gambia. Parasite rate (PR) and the entomological inoculation rate (EIR) are the measures widely used to estimate the transmission intensity for malaria, but these have poor precision at low transmission levels [6]. Antibodies can persist for months or years after infection and, may have particular utility as a proxy measure of malaria transmission in low transmission settings [6]. Samples for both PR and serological estimations are typically collected as blood by finger prick. Commercial saliva-based kits for HIV and illicit drugs are already available for the detection of human antibodies for population-based studies [12,14]

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