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Rheopathologic Consequence of Plasmodium vivax Rosette Formation
Author(s) -
Rou Zhang,
Wenn-Chyau Lee,
Yee Ling Lau,
Letusa Albrecht,
Stefanie Costa Pinto Lopes,
Fábio Trindade Maranhão Costa,
Rossarin Suwanarusk,
François Nosten,
Brian M. Cooke,
Laurent Rénia,
Bruce Russell
Publication year - 2016
Publication title -
plos neglected tropical diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.99
H-Index - 135
eISSN - 1935-2735
pISSN - 1935-2727
DOI - 10.1371/journal.pntd.0004912
Subject(s) - rosette (schizont appearance) , plasmodium vivax , malaria , adhesion , spleen , biology , plasmodium (life cycle) , parasite hosting , microbiology and biotechnology , plasmodium falciparum , biophysics , immunology , virology , chemistry , computer science , organic chemistry , world wide web
Malaria parasites dramatically alter the rheological properties of infected red blood cells. In the case of Plasmodium vivax , the parasite rapidly decreases the shear elastic modulus of the invaded RBC, enabling it to avoid splenic clearance. This study highlights correlation between rosette formation and altered membrane deformability of P . vivax -infected erythrocytes, where the rosette-forming infected erythrocytes are significantly more rigid than their non-rosetting counterparts. The adhesion of normocytes to the Pv IRBC is strong (mean binding force of 440pN) resulting in stable rosette formation even under high physiological shear flow stress. Rosetting may contribute to the sequestration of Pv IRBC schizonts in the host microvasculature or spleen.

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