Genetic Analysis of Circulating and Sequestered Populations ofPlasmodium falciparumin Fatal Pediatric Malaria
Author(s) -
Jacqui Montgomery,
Danny A. Milner,
Man Tsuey Tse,
Alfred Njobvu,
K Kayira,
Charles P. Dzamalala,
Terrie E. Taylor,
Stephen J. Rogerson,
Alister Craig,
Malcolm E. Molyneux
Publication year - 2006
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/504689
Subject(s) - parasitemia , malaria , plasmodium falciparum , cerebral malaria , genotype , biology , parasite hosting , immunology , plasmodium (life cycle) , virology , gene , genetics , world wide web , computer science
Falciparum malaria is characterized by cytoadherence of host erythrocytes containing mature asexual-stage parasites and the consequent sequestration of these forms in tissue microvasculature. A postmortem study of pediatric malaria provided us with the opportunity to compare the genetic complexity of circulating and sequestered Plasmodium falciparum populations, in patients with fatal cerebral malaria (CM) versus control subjects with incidental P. falciparum parasitemia who died of causes other than malaria. Parasite genotypes identified in peripheral blood collected at the time of admission to the hospital constituted a subset of those detected in the tissues at death. Despite a higher tissue burden of parasitized erythrocytes in patients with CM than in parasitemic control subjects, parasite populations in tissues from patients with CM were less genetically complex, and the genotypes were more homogeneously distributed throughout the body, than in patients with incidental infection. Our findings support the notion that CM is associated with the emergence of a small number of dominant genotypes in an infected individual.
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