Expression of Merozoite Surface Protein Markers by Plasmodium falciparum-Infected Erythrocytes in Peripheral Blood and Tissues of Children with Fatal Malaria

• Published in: Infection and Immunity 2007-02, Vol.75 (2), p.643-652
• Main Authors: Dobaño, Carlota, Rogerson, Stephen J, Taylor, Terrie E, McBride, Jana S, Molyneux, Malcolm E
• Format: Article
• Language: English
• Subjects: Animals; Antigens, Protozoan - analysis; Antigens, Protozoan - immunology; Biological and medical sciences; Biomarkers - analysis; Brain - parasitology; Child; Child, Preschool; Erythrocytes - chemistry; Erythrocytes - parasitology; Fundamental and applied biological sciences. Psychology; Fungal and Parasitic Infections; Human protozoal diseases; Humans; Immunohistochemistry; Infectious diseases; Liver - parasitology; Lung - parasitology; Malaria; Malaria, Cerebral - parasitology; Malaria, Falciparum - parasitology; Malawi; Medical sciences; Merozoite Surface Protein 1 - analysis; Merozoite Surface Protein 1 - immunology; Microbiology; Microscopy, Fluorescence; Parasitic diseases; Plasmodium; Plasmodium falciparum; Plasmodium falciparum - classification; Plasmodium falciparum - isolation & purification; Protozoal diseases; Protozoan Proteins - analysis; Protozoan Proteins - immunology; Serotyping; Spleen - parasitology
• ISSN: 0019-9567; 1098-5522
• DOI: 10.1128/IAI.01527-06

Sequestration of Plasmodium falciparum-infected erythrocytes is a pathological feature of fatal cerebral malaria. P. falciparum is genetically diverse among, and often within, patients. Preferential sequestration of certain genotypes might be important in pathogenesis. We compared circulating parasites with parasites sequestered in the brain, spleen, liver, and lung in the same Malawian children with fatal malaria, classifying serotypes using antibodies to merozoite surface proteins 1 and 2 and immunofluorescence in order to differentiate parasites and to quantify the proportions of each serotype. We found (i) similar distributions of various serotypes in different tissues and (ii) concordance between parasite serotypes in peripheral blood and parasite serotypes in tissues. No serotypes predominated in the brain in cerebral malaria, and parasites belonging to a single serotype did not cluster within individual vessels or within single tissues. These findings do not support the hypothesis that cerebral malaria is caused by cerebral sequestration of certain virulent types.