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Geospatial joint modeling of vector and parasite serology to microstratify malaria transmission.
Kearney, Ellen A; Amratia, Punam; Kang, Su Yun; Agius, Paul A; Alene, Kefyalew Addis; O'Flaherty, Katherine; Oo, Win Han; Cutts, Julia C; Htike, Win; Da Silva Goncalves, Daniela; Razook, Zahra; Barry, Alyssa E; Drew, Damien; Thi, Aung; Aung, Kyaw Zayar; Thu, Htin Kyaw; Thein, Myat Mon; Zaw, Nyi Nyi; Htay, Wai Yan Min; Soe, Aung Paing; Beeson, James G; Simpson, Julie A; Gething, Peter W; Cameron, Ewan; Fowkes, Freya J I.
Afiliação
  • Kearney EA; Disease Elimination Program, Burnet Institute, Melbourne, VIC 3004, Australia.
  • Amratia P; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC 3010, Australia.
  • Kang SY; Malaria Atlas Project, Telethon Kids Institute, Perth, WA 6009, Australia.
  • Agius PA; Malaria Atlas Project, Telethon Kids Institute, Perth, WA 6009, Australia.
  • Alene KA; Disease Elimination Program, Burnet Institute, Melbourne, VIC 3004, Australia.
  • O'Flaherty K; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC 3010, Australia.
  • Oo WH; Biostatistics Unit, Faculty of Health, Deakin University, Melbourne, VIC 3125, Australia.
  • Cutts JC; Malaria Atlas Project, Telethon Kids Institute, Perth, WA 6009, Australia.
  • Htike W; Faculty of Health Sciences, Curtin University, Perth, WA 6102, Australia.
  • Da Silva Goncalves D; Disease Elimination Program, Burnet Institute, Melbourne, VIC 3004, Australia.
  • Razook Z; Health Security and Malaria Program, Burnet Institute Myanmar, Yangon 11201, Myanmar.
  • Barry AE; Disease Elimination Program, Burnet Institute, Melbourne, VIC 3004, Australia.
  • Drew D; Department of Medicine at the Doherty Institute, The University of Melbourne, Melbourne, VIC 3000, Australia.
  • Thi A; Health Security and Malaria Program, Burnet Institute Myanmar, Yangon 11201, Myanmar.
  • Aung KZ; Disease Elimination Program, Burnet Institute, Melbourne, VIC 3004, Australia.
  • Thu HK; Disease Elimination Program, Burnet Institute, Melbourne, VIC 3004, Australia.
  • Thein MM; Institute for Physical and Mental Health and Clinical Translation, School of Medicine, Deakin University, Geelong, VIC 3216, Australia.
  • Zaw NN; Disease Elimination Program, Burnet Institute, Melbourne, VIC 3004, Australia.
  • Htay WYM; Institute for Physical and Mental Health and Clinical Translation, School of Medicine, Deakin University, Geelong, VIC 3216, Australia.
  • Soe AP; Disease Elimination Program, Burnet Institute, Melbourne, VIC 3004, Australia.
  • Beeson JG; Department of Public Health, Myanmar Ministry of Health and Sports, Nay Pyi Taw 15011, Myanmar.
  • Simpson JA; Health Security and Malaria Program, Burnet Institute Myanmar, Yangon 11201, Myanmar.
  • Gething PW; Health Security and Malaria Program, Burnet Institute Myanmar, Yangon 11201, Myanmar.
  • Cameron E; Health Security and Malaria Program, Burnet Institute Myanmar, Yangon 11201, Myanmar.
  • Fowkes FJI; Health Security and Malaria Program, Burnet Institute Myanmar, Yangon 11201, Myanmar.
Proc Natl Acad Sci U S A ; 121(24): e2320898121, 2024 Jun 11.
Article em En | MEDLINE | ID: mdl-38833464
ABSTRACT
The World Health Organization identifies a strong surveillance system for malaria and its mosquito vector as an essential pillar of the malaria elimination agenda. Anopheles salivary antibodies are emerging biomarkers of exposure to mosquito bites that potentially overcome sensitivity and logistical constraints of traditional entomological surveys. Using samples collected by a village health volunteer network in 104 villages in Southeast Myanmar during routine surveillance, the present study employs a Bayesian geostatistical modeling framework, incorporating climatic and environmental variables together with Anopheles salivary antigen serology, to generate spatially continuous predictive maps of Anopheles biting exposure. Our maps quantify fine-scale spatial and temporal heterogeneity in Anopheles salivary antibody seroprevalence (ranging from 9 to 99%) that serves as a proxy of exposure to Anopheles bites and advances current static maps of only Anopheles occurrence. We also developed an innovative framework to perform surveillance of malaria transmission. By incorporating antibodies against the vector and the transmissible form of malaria (sporozoite) in a joint Bayesian geostatistical model, we predict several foci of ongoing transmission. In our study, we demonstrate that antibodies specific for Anopheles salivary and sporozoite antigens are a logistically feasible metric with which to quantify and characterize heterogeneity in exposure to vector bites and malaria transmission. These approaches could readily be scaled up into existing village health volunteer surveillance networks to identify foci of residual malaria transmission, which could be targeted with supplementary interventions to accelerate progress toward elimination.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Teorema de Bayes / Mosquitos Vetores / Malária / Anopheles Limite: Animals / Humans Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Teorema de Bayes / Mosquitos Vetores / Malária / Anopheles Limite: Animals / Humans Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Austrália