Malaria Transmission Dynamics in a High-Transmission Setting of Western Kenya and the Inadequate Treatment Response to Artemether-Lumefantrine in an Asymptomatic Population

Author:

Andagalu Ben1,Watson Oliver J2,Onyango Irene1,Opot Benjamin1,Okoth Raphael1,Chemwor Gladys1,Sifuna Peter1,Juma Dennis1,Cheruiyot Agnes1,Yeda Redemptah1,Okudo Charles1,Wafubwa Jackline1,Yalwala Santos1,Abuom David1,Ogutu Bernhards3,Cowden Jessica1,Akala Hoseah M1,Kamau Edwin145ORCID

Affiliation:

1. Department of Emerging and Infectious Diseases (DEID), US Army Medical Research Directorate-Africa (USAMRD-A), Kenya Medical Research Institute (KEMRI)/Walter Reed Project , Kisumu , Kenya

2. Medical Research Council, Centre for Global Infectious Disease Analysis, Department of Infectious Disease Epidemiology, Imperial College London , London , United Kingdom

3. Kenya Medical Research Institute (KEMRI) , Nairobi , Kenya

4. US Military HIV Research Program, Walter Reed Army Institute of Research , Silver Spring, Maryland , USA

5. Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles , Los Angeles, California , USA

Abstract

Abstract Background Assessing the infectious reservoir is critical in malaria control and elimination strategies. We conducted a longitudinal epidemiological study in a high-malaria-burden region in Kenya to characterize transmission in an asymptomatic population. Methods 488 study participants encompassing all ages in 120 households within 30 clusters were followed for 1 year with monthly sampling. Malaria was diagnosed by microscopy and molecular methods. Transmission potential in gametocytemic participants was assessed using direct skin and/or membrane mosquito feeding assays, then treated with artemether-lumefantrine. Study variables were assessed using mixed-effects generalized linear models. Results Asexual and sexual parasite data were collected from 3792 participant visits, with 903 linked with feeding assays. Univariate analysis revealed that the 6–11-year-old age group was at higher risk of harboring asexual and sexual infections than those <6 years old (odds ratio [OR] 1.68, P < .001; and OR 1.81, P < .001), respectively. Participants with submicroscopic parasitemia were at a lower risk of gametocytemia compared with microscopic parasitemia (OR 0.04, P < .001), but they transmitted at a significantly higher rate (OR 2.00, P = .002). A large proportion of the study population who were infected at least once remained infected (despite treatment) with asexual (71.7%, 291/406) or sexual (37.4%, 152/406) parasites. 88.6% (365/412) of feeding assays conducted in individuals who failed treatment the previous month resulted in transmissions. Conclusions Individuals with asymptomatic infection sustain the transmission cycle, with the 6–11-year age group serving as an important reservoir. The high rates of artemether-lumefantrine treatment failures suggest surveillance programs using molecular methods need to be expanded for accurate monitoring and evaluation of treatment outcomes.

Funder

Malaria Vaccine Branch of the Walter Reed Army Institute of Research

Rhodes Trust

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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