Publication:
Anopheles salivary biomarker as a proxy for estimating plasmodium falciparum malaria exposure on the Thailand-Myanmar border

dc.contributor.authorPhubeth Ya-Umphanen_US
dc.contributor.authorDominique Cerqueiraen_US
dc.contributor.authorGilles Cottrellen_US
dc.contributor.authorDaniel M. Parkeren_US
dc.contributor.authorFreya J.I. Fowkesen_US
dc.contributor.authorFrancois Nostenen_US
dc.contributor.authorVincent Corbelen_US
dc.contributor.otherMelbourne School of Population and Global Healthen_US
dc.contributor.otherUniversite Paris Descartesen_US
dc.contributor.otherIRD Centre de Montpellieren_US
dc.contributor.otherMonash Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherNuffield Department of Clinical Medicineen_US
dc.contributor.otherUniversity of California, Irvineen_US
dc.contributor.otherBurnet Instituteen_US
dc.date.accessioned2019-08-23T11:25:13Z
dc.date.available2019-08-23T11:25:13Z
dc.date.issued2018-01-01en_US
dc.description.abstractCopyright © 2018 by The American Society of Tropical Medicine and Hygiene. Timely identification and treatment of malaria transmission “hot spots” is essential to achieve malaria elimination. Here we investigate the relevance of using an Anopheles salivary biomarker to estimate Plasmodium falciparum malaria exposure risk along the Thailand-Myanmar border to guide malaria control. Between May 2013 and December 2014, > 9,000 blood samples collected in a cluster randomized control trial were screened with serological assays to measure the antibody responses to Anopheles salivary antigen (gSG6-P1) and P. falciparum malaria antigens (circumsporozoite protein, merozoite surface protein 119 [MSP-119]). Plasmodium falciparum infections were monitored through passive and active case detection. Seroprevalence to gSG6-P1, MSP-119, and CSP were 71.8% (95% Confidence interval [CI]: 70.9, 72.7), 68.6% (95% CI: 67.7, 69.5), and 8.6% (95% CI: 8.0, 9.2), respectively. Multivariate analysis showed that individuals with the highest Ab response to gSG6-P1 had six times the odds of being positive to CSP antigens (P < 0.001) and two times the odds of P. falciparum infection compared with low gSG6-P1 responders (P = 0.004). Spatial scan statistics revealed the presence of clusters of gSG6-P1 that partially overlapped P. falciparum infections. The gSG6-P1 salivary biomarker represents a good proxy for estimating P. falciparum malaria risk and could serve to implement hot spot-targeted vector control interventions to achieve malaria elimination.en_US
dc.identifier.citationAmerican Journal of Tropical Medicine and Hygiene. Vol.99, No.2 (2018), 350-356en_US
dc.identifier.doi10.4269/ajtmh.18-0081en_US
dc.identifier.issn00029637en_US
dc.identifier.other2-s2.0-85051075259en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/46080
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85051075259&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleAnopheles salivary biomarker as a proxy for estimating plasmodium falciparum malaria exposure on the Thailand-Myanmar borderen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85051075259&origin=inwarden_US

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