Despite remarkable advances in our understanding of the biology of malaria in the last 30 years, malaria elimination, or even control, remains on the distant horizon in most of sub-Saharan Africa. In this proposal, we will define the burden of malaria disease and infection in Malawi and bring to control and elimination efforts the most advanced scientific methods available to apply new interventions, target established ones and assess their impact rapidly and accurately. Malawi is a country hit hard by malaria, it has an excellent collaborative relationship between policy-makers and investigators and the physical and scientific infrastructure to support the novel approaches proposed in this application. The overall goal of Project 1 is to characterize the changing epidemiology of malaria in response to control and elimination efforts in diverse epidemiological settings within Malawi, and to understand how this changing epidemiology affects the burden of malaria disease, the reservoir of malaria infection, and the emergence and spread (or reversal) of resistance to antimalarial drugs. These goals will be accomplished through the following three specific aims: 1) to evaluate the burden of malaria infection and disease in diverse eco-geographic regions of Malawi and in relation to control and elimination interventions, 2) to characterize the parasite population genetics in diverse eco-geographic regions of Malawi and in response to malaria control and elimination interventions and 3) to measure the effect of changes in antimalarial drug policy on the prevalence of drug-resistant parasites.
These aims will be accomplished through cross-sectional studies, health facility-based surveillance and small but detailed cohort studies in Blantyre, Thyolo and Chikwawa districts to accurately define the burden of disease and infection and detect sources of transmission. Specimens collected from these sources will undergo genomic analysis for the purposes of assessing the effect of transmission intensity on population genetics, the development of field-appropriate genetic tools for Malawi and for detecting changes in drug-resistance patterns as a result of new drug policies.

Public Health Relevance

The results of the studies described in this proposal will answer several long-standing but unresolved questions about malaria control and elimination: Do malaria control efforts shift the burden of disease to different age groups? Are there people who are important sources of disease transmission but who are not symptomatic? If malaria transmission decreases, will drug resistant parasites become fixed in the population?

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program--Cooperative Agreements (U19)
Project #
5U19AI089683-04
Application #
8499218
Study Section
Special Emphasis Panel (ZAI1-AWA-M)
Project Start
Project End
Budget Start
2013-07-01
Budget End
2014-06-30
Support Year
4
Fiscal Year
2013
Total Cost
$738,481
Indirect Cost
$38,807
Name
Michigan State University
Department
Type
DUNS #
193247145
City
East Lansing
State
MI
Country
United States
Zip Code
48824
Dear, Nicole F; Kadangwe, Chifundo; Mzilahowa, Themba et al. (2018) Household-level and surrounding peri-domestic environmental characteristics associated with malaria vectors Anopheles arabiensis and Anopheles funestus along an urban-rural continuum in Blantyre, Malawi. Malar J 17:229
Coalson, Jenna E; Cohee, Lauren M; Buchwald, Andrea G et al. (2018) Simulation models predict that school-age children are responsible for most human-to-mosquito Plasmodium falciparum transmission in southern Malawi. Malar J 17:147
Ducati, Rodrigo G; Namanja-Magliano, Hilda A; Harijan, Rajesh K et al. (2018) Genetic resistance to purine nucleoside phosphorylase inhibition in Plasmodium falciparum. Proc Natl Acad Sci U S A 115:2114-2119
Gupta-Wright, Ankur; Tembo, Dumizulu; Jambo, Kondwani C et al. (2017) Functional Analysis of Phagocyte Activity in Whole Blood from HIV/Tuberculosis-Infected Individuals Using a Novel Flow Cytometry-Based Assay. Front Immunol 8:1222
Mohanty, Sanjib; Benjamin, Laura A; Majhi, Megharay et al. (2017) Magnetic Resonance Imaging of Cerebral Malaria Patients Reveals Distinct Pathogenetic Processes in Different Parts of the Brain. mSphere 2:
Buchwald, Andrea G; Coalson, Jenna E; Cohee, Lauren M et al. (2017) Insecticide-treated net effectiveness at preventing Plasmodium falciparum infection varies by age and season. Malar J 16:32
Coalson, Jenna E; Walldorf, Jenny A; Cohee, Lauren M et al. (2016) High prevalence of Plasmodium falciparum gametocyte infections in school-age children using molecular detection: patterns and predictors of risk from a cross-sectional study in southern Malawi. Malar J 15:527
Feintuch, Catherine Manix; Saidi, Alex; Seydel, Karl et al. (2016) Activated Neutrophils Are Associated with Pediatric Cerebral Malaria Vasculopathy in Malawian Children. MBio 7:e01300-15
Buchwald, Andrea G; Walldorf, Jenny A; Cohee, Lauren M et al. (2016) Bed net use among school-aged children after a universal bed net campaign in Malawi. Malar J 15:127
Mathanga, Don P; Tembo, Atupele Kapito; Mzilahowa, Themba et al. (2016) Patterns and determinants of malaria risk in urban and peri-urban areas of Blantyre, Malawi. Malar J 15:590

Showing the most recent 10 out of 25 publications