Benjamin L Rice1,2,3, Christopher D Golden4,5, Hervet J Randriamady4,5, Anjaharinony Andry Ny Aina Rakotomalala4,6, Miadana Arisoa Vonona4, Evelin Jean Gasta Anjaranirina4, James Hazen7, Marcia C Castro8, C Jessica E Metcalf9, Daniel L Hartl10. 1. Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, USA. b.rice@princeton.edu. 2. Madagascar Health and Environmental Research (MAHERY), Maroantsetra, Madagascar. b.rice@princeton.edu. 3. Department of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ, USA. b.rice@princeton.edu. 4. Madagascar Health and Environmental Research (MAHERY), Maroantsetra, Madagascar. 5. Department of Nutrition, Harvard TH Chan School of Public Health, Boston, MA, USA. 6. Department of Entomology, University of Antananarivo, Antananarivo, Madagascar. 7. Catholic Relief Services (CRS) Madagascar, Antananarivo, Madagascar. 8. Department of Global Health and Population, Harvard TH Chan School of Public Health, Boston, MA, USA. 9. Department of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ, USA. 10. Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, USA.
Abstract
BACKGROUND: Large-scale variation in ecological parameters across Madagascar is hypothesized to drive varying spatial patterns of malaria infection. However, to date, few studies of parasite prevalence with resolution at finer, sub-regional spatial scales are available. As a result, there is a poor understanding of how Madagascar's diverse local ecologies link with variation in the distribution of infections at the community and household level. Efforts to preserve Madagascar's ecological diversity often focus on improving livelihoods in rural communities near remaining forested areas but are limited by a lack of data on their infectious disease burden. METHODS: To investigate spatial variation in malaria prevalence at the sub-regional scale in Madagascar, we sampled 1476 households (7117 total individuals, all ages) from 31 rural communities divided among five ecologically distinct regions. The sampled regions range from tropical rainforest to semi-arid, spiny forest and include communities near protected areas including the Masoala, Makira, and Mikea forests. Malaria prevalence was estimated by rapid diagnostic test (RDT) cross-sectional surveys performed during malaria transmission seasons over 2013-2017. RESULTS: Indicative of localized hotspots, malaria prevalence varied more than 10-fold between nearby (< 50 km) communities in some cases. Prevalence was highest on average in the west coast region (Morombe district, average community prevalence 29.4%), situated near protected dry deciduous forest habitat. At the household level, communities in southeast Madagascar (Mananjary district) were observed with over 50% of households containing multiple infected individuals at the time of sampling. From simulations accounting for variation in household size and prevalence at the community level, we observed a significant excess of households with multiple infections in rural communities in southwest and southeast Madagascar, suggesting variation in risk within communities. CONCLUSIONS: Our data suggest that the malaria infection burden experienced by rural communities in Madagascar varies greatly at smaller spatial scales (i.e., at the community and household level) and that the southeast and west coast ecological regions warrant further attention from disease control efforts. Conservation and development efforts in these regions may benefit from consideration of the high, and variable, malaria prevalences among communities in these areas.
BACKGROUND: Large-scale variation in ecological parameters across Madagascar is hypothesized to drive varying spatial patterns of malaria infection. However, to date, few studies of parasite prevalence with resolution at finer, sub-regional spatial scales are available. As a result, there is a poor understanding of how Madagascar's diverse local ecologies link with variation in the distribution of infections at the community and household level. Efforts to preserve Madagascar's ecological diversity often focus on improving livelihoods in rural communities near remaining forested areas but are limited by a lack of data on their infectious disease burden. METHODS: To investigate spatial variation in malaria prevalence at the sub-regional scale in Madagascar, we sampled 1476 households (7117 total individuals, all ages) from 31 rural communities divided among five ecologically distinct regions. The sampled regions range from tropical rainforest to semi-arid, spiny forest and include communities near protected areas including the Masoala, Makira, and Mikea forests. Malaria prevalence was estimated by rapid diagnostic test (RDT) cross-sectional surveys performed during malaria transmission seasons over 2013-2017. RESULTS: Indicative of localized hotspots, malaria prevalence varied more than 10-fold between nearby (< 50 km) communities in some cases. Prevalence was highest on average in the west coast region (Morombe district, average community prevalence 29.4%), situated near protected dry deciduous forest habitat. At the household level, communities in southeast Madagascar (Mananjary district) were observed with over 50% of households containing multiple infected individuals at the time of sampling. From simulations accounting for variation in household size and prevalence at the community level, we observed a significant excess of households with multiple infections in rural communities in southwest and southeast Madagascar, suggesting variation in risk within communities. CONCLUSIONS: Our data suggest that the malaria infection burden experienced by rural communities in Madagascar varies greatly at smaller spatial scales (i.e., at the community and household level) and that the southeast and west coast ecological regions warrant further attention from disease control efforts. Conservation and development efforts in these regions may benefit from consideration of the high, and variable, malaria prevalences among communities in these areas.
Entities:
Keywords:
Community health; Ecology; Madagascar; Malaria; Spatial variation
Authors: M E Woolhouse; C Dye; J F Etard; T Smith; J D Charlwood; G P Garnett; P Hagan; J L Hii; P D Ndhlovu; R J Quinnell; C H Watts; S K Chandiwana; R M Anderson Journal: Proc Natl Acad Sci U S A Date: 1997-01-07 Impact factor: 11.205
Authors: C Schwitzer; R A Mittermeier; S E Johnson; G Donati; M Irwin; H Peacock; J Ratsimbazafy; J Razafindramanana; E E Louis; L Chikhi; I C Colquhoun; J Tinsman; R Dolch; M LaFleur; S Nash; E Patel; B Randrianambinina; T Rasolofoharivelo; P C Wright Journal: Science Date: 2014-02-21 Impact factor: 47.728
Authors: Amy Yomiko Vittor; Robert H Gilman; James Tielsch; Gregory Glass; Tim Shields; Wagner Sánchez Lozano; Viviana Pinedo-Cancino; Jonathan A Patz Journal: Am J Trop Med Hyg Date: 2006-01 Impact factor: 2.345
Authors: Su Yun Kang; Katherine E Battle; Harry S Gibson; Arsène Ratsimbasoa; Milijaona Randrianarivelojosia; Stéphanie Ramboarina; Peter A Zimmerman; Daniel J Weiss; Ewan Cameron; Peter W Gething; Rosalind E Howes Journal: BMC Med Date: 2018-05-23 Impact factor: 8.775
Authors: Gillian H Stresman; Julia Mwesigwa; Jane Achan; Emanuele Giorgi; Archibald Worwui; Musa Jawara; Gian Luca Di Tanna; Teun Bousema; Jean-Pierre Van Geertruyden; Chris Drakeley; Umberto D'Alessandro Journal: BMC Med Date: 2018-09-14 Impact factor: 8.775
Authors: Sarah Zohdy; Kristin Derfus; Emily G Headrick; Mbolatiana Tovo Andrianjafy; Patricia C Wright; Thomas R Gillespie Journal: Malar J Date: 2016-02-24 Impact factor: 2.979
Authors: Felana A Ihantamalala; Feno M J Rakotoarimanana; Tanjona Ramiadantsoa; Jean Marius Rakotondramanga; Gwenaëlle Pennober; Fanjasoa Rakotomanana; Simon Cauchemez; Charlotte J E Metcalf; Vincent Herbreteau; Amy Wesolowski Journal: Malar J Date: 2018-02-01 Impact factor: 2.979