Serology reveals heterogeneity of Plasmodium falciparum transmission in northeastern South Africa: implications for malaria elimination. (December 2017)

• Record Type: Journal Article
• Authors: Biggs, Joseph; Raman, Jaishree; Cook, Jackie; Hlongwana, Khumbulani; Drakeley, Chris; Morris, Natashia; Serocharan, Ishen; Agubuzo, Eunice; Kruger, Philip; Mabuza, Aaron; Zitha, Alpheus; Machaba, Elliot; Coetzee, Maureen; Kleinschmidt, Immo
• Is Part Of: Malaria journal. Volume 16:Number 1(2017)
• Page Start: 1
• Page End: 13
• Publication Date: 2017-12
• Subjects: Malaria -- Elimination -- Serology -- PfAMA-1 -- PfMSP-119 -- Transmission -- Heterogeneity -- Hotspot -- South Africa; Malaria -- Periodicals; 616.9362
• DOI: 10.1186/s12936-017-1701-7
• Languages: English
• ISSNs: 1475-2875

Abstract

Abstract Background It is widely acknowledged that modifications to existing control interventions are required if South Africa is to achieve malaria elimination. Targeting indoor residual spraying (IRS) to areas where cases have been detected is one strategy currently under investigation in northeastern South Africa. This seroprevalence baseline study, nested within a targeted IRS trial, was undertaken to provide insights into malaria transmission dynamics in South Africa and evaluate whether sero-epidemiological practices have the potential to be routinely incorporated into elimination programmes. Methods Filter-paper blood spots, demographic and household survey data were collected from 2710 randomly selected households in 56 study wards located in the municipalities of Ba-Phalaborwa and Bushbuckridge. Blood spots were assayed forPlasmodium falciparum apical membrane antigen-1 and merozoite surface protein-119 blood-stage antigens using an enzyme linked immunosorbent assay. Seroprevalence data were analysed using a reverse catalytic model to determine malaria seroconversion rates (SCR). Geospatial cluster analysis was used to investigate transmission heterogeneity while random effects logistic regression identified risk factors associated with malaria exposure. Results The overall SCR across the entire study site was 0.012 (95% CI 0.008–0.017) per year. Contrasting SCRs, corresponding to distinct geographical regions across the study site, ranging from <0.001 (95% CI <0.001–0.005) to 0.022 (95% CI 0.008–0.062) per annum revealed prominent transmission heterogeneity. Geospatial cluster analysis of household seroprevalence and age-adjusted antibody responses detected statistically significant (p < 0.05) spatial clusters ofP. falciparum exposure. Formal secondary education was associated with lower malaria exposure in the sampled population (AOR 0.72, 95% CI 0.56–0.95, p = 0.018). Conclusions Although overall transmission intensity and exposure to malaria was low across both study sites, malaria transmission intensity was highly heterogeneous and associated with low socio-economic status in the region. Findings suggest focal targeting of interventions has the potential to be an appropriate strategy to deploy in South Africa. Furthermore, routinely incorporating sero-epidemiological practices into elimination programmes may prove useful in monitoring malaria transmission intensity in South Africa, and other countries striving for malaria elimination.