Seasonal Variation in the Epidemiology of Asymptomatic Plasmodium falciparum Infections across Two Catchment Areas in Bongo District, Ghana
Understanding the epidemiology of asymptomatic infections is critical for countries to move toward malaria elimination. Using different methods for parasite detection, we evaluated how seasonality, spatial location, and other factors affect the age-specific epidemiology of asymptomatic malaria in Bo...
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Published in | The American journal of tropical medicine and hygiene Vol. 97; no. 1; pp. 199 - 212 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
The American Society of Tropical Medicine and Hygiene
01.07.2017
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Subjects | |
Online Access | Get full text |
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Summary: | Understanding the epidemiology of asymptomatic
infections is critical for countries to move toward malaria elimination. Using different methods for parasite detection, we evaluated how seasonality, spatial location, and other factors affect the age-specific epidemiology of asymptomatic malaria in Bongo District, Ghana. Asymptomatic prevalence by microscopy decreased significantly from 42.5% at the end of the wet to 27.5% at the end of the dry season (
< 0.001). Using the
polymerase chain reactions (PCRs), all microscopy-negative samples were screened and prevalence of submicroscopic infections also decreased significantly from the wet (55.4%) to the dry (20.7%) season (
< 0.001). Combining detection methods, 74.4% and 42.5% of the population in the wet and dry seasons, respectively, had evidence of a
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infection. Interestingly in those > 20 years of age, we found evidence of infection in 64.3% of the population in the wet and 27.0% in the dry season. Using both microscopy and PCR, the asymptomatic
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reservoir peaks at the end of the wet season and infections in all age groups constitute the reservoir of malaria infection. At the end of the wet season, spatial heterogeneity in the prevalence and density of
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infections was observed between the two catchment areas surveyed in Bongo District. These results indicate that if elimination is to succeed, interventions will need to target not just
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infections in children but also in adults, and be implemented toward the end of the dry season in this area of West Africa. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Financial support: This research was supported by the Fogarty International Center at National Institutes of Health (Program on the Ecology and Evolution of Infectious Diseases (EEID), Grant number: R01-TW009670); and the National Institute of Allergy and Infectious Disease, National Institutes of Health (Grant number: R01-AI084156). Authors' addresses: Kathryn E. Tiedje, School of BioSciences, Bio21 Institute/University of Melbourne, Melbourne, Australia, E-mail: kathryn.tiedje@unimelb.edu.au. Abraham R. Oduro, Godfred Agongo, Thomas Anyorigiya, Daniel Azongo, and Timothy Awine, Navrongo Health Research Center, Navrongo, Ghana, E-mails: abraham.oduro@navrongo-hrc.org, godfred.agongo@navrongo-hrc.org, thomas.anyorigiya@navrongo-hrc.org, daniel.azongo@navrongo-hrc.org, and timothy.awine@navrongo-hrc.org. Anita Ghansah, Noguchi Memorial Institute for Medical Research, University of Ghana, Legon, Ghana, E-mail: aghansah@noguchi.ug.edu.gh. Mercedes Pascual, Department of Ecology and Evolution, University of Chicago, Chicago, IL, E-mail: pascualmm@uchicago.edu. Kwadwo A. Koram, Noguchi Memorial Institute for Medical Research, University of Ghana, Legon, Ghana, E-mail: kkoram@noguchi.ug.edu.gh. Karen P. Day, School of Biosciences, University of Melbourne, Melbourne, Australia, E-mail: karen.day@unimelb.edu.au. |
ISSN: | 0002-9637 1476-1645 |
DOI: | 10.4269/ajtmh.16-0959 |