Higher gametocyte production and mosquito infectivity in chronic compared to incident Plasmodium falciparum infections

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作者
Aissata Barry
John Bradley
Will Stone
Moussa W. Guelbeogo
Kjerstin Lanke
Alphonse Ouedraogo
Issiaka Soulama
Issa Nébié
Samuel S. Serme
Lynn Grignard
Catriona Patterson
Lindsey Wu
Jessica J. Briggs
Owen Janson
Shehu S. Awandu
Mireille Ouedraogo
Casimire W. Tarama
Désiré Kargougou
Soumanaba Zongo
Sodiomon B. Sirima
Matthias Marti
Chris Drakeley
Alfred B. Tiono
Teun Bousema
机构
[1] Centre National de Recherche et de Formation sur le Paludisme (CNRFP),Radboud Institute for Health Sciences and Radboud Center for Infectious Diseases
[2] Radboud University Medical Centre,Department of Immunology and Infection
[3] MRC International Statistics and Epidemiology Group,Department of Medicine
[4] London School of Hygiene and Tropical Medicine,undefined
[5] London School of Hygiene and Tropical Medicine,undefined
[6] University of California San Francisco,undefined
[7] Wellcome Centre for Integrative Parasitology,undefined
[8] University of Glasgow,undefined
来源
Nature Communications | / 12卷
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摘要
Plasmodium falciparum gametocyte kinetics and infectivity may differ between chronic and incident infections. In the current study, we assess parasite kinetics and infectivity to mosquitoes among children (aged 5–10 years) from Burkina Faso with (a) incident infections following parasite clearance (n = 48) and (b) chronic asymptomatic infections (n = 60). In the incident infection cohort, 92% (44/48) of children develop symptoms within 35 days, compared to 23% (14/60) in the chronic cohort. All individuals with chronic infection carried gametocytes or developed them during follow-up, whereas only 35% (17/48) in the incident cohort produce gametocytes before becoming symptomatic and receiving treatment. Parasite multiplication rate (PMR) and the relative abundance of ap2-g and gexp-5 transcripts are positively associated with gametocyte production. Antibody responses are higher and PMR lower in chronic infections. The presence of symptoms and sexual stage immune responses are associated with reductions in gametocyte infectivity to mosquitoes. We observe that most incident infections require treatment before the density of mature gametocytes is sufficient to infect mosquitoes. In contrast, chronic, asymptomatic infections represent a significant source of mosquito infections. Our observations support the notion that malaria transmission reduction may be expedited by enhanced case management, involving both symptom-screening and infection detection.
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