In Vivo and In Vitro Model of Plasmodium falciparum Rosetting and Autoagglutination Mediated by varO, a Group A var Gene Encoding a Frequent Serotype

In the Saimiri sciureus monkey, erythrocytes infected with the varO antigenic variant of the Plasmodium falciparum Palo Alto 89F5 clone bind uninfected red blood cells (rosetting), form autoagglutinates, and have a high multiplication rate, three phenotypic characteristics that are associated with s...

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Published in:Infection and Immunity Vol. 76; no. 12; pp. 5565 - 5580
Main Authors: Vigan-Womas, Inès, Guillotte, Micheline, Le Scanf, Cécile, Igonet, Sébastien, Petres, Stéphane, Juillerat, Alexandre, Badaut, Cyril, Nato, Farida, Schneider, Achim, Lavergne, Anne, Contamin, Hugues, Tall, Adama, Baril, Laurence, Bentley, Graham A, Mercereau-Puijalon, Odile
Format: Journal Article
Language:English
Published: Washington, DC American Society for Microbiology 01-12-2008
American Society for Microbiology (ASM)
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Summary:In the Saimiri sciureus monkey, erythrocytes infected with the varO antigenic variant of the Plasmodium falciparum Palo Alto 89F5 clone bind uninfected red blood cells (rosetting), form autoagglutinates, and have a high multiplication rate, three phenotypic characteristics that are associated with severe malaria in human patients. We report here that varO parasites express a var gene having the characteristics of group A var genes, and we show that the varO Duffy binding-like 1α₁ (DBL1α₁) domain is implicated in the rosetting of both S. sciureus and human erythrocytes. The soluble varO N-terminal sequence (NTS)-DBL1α₁ recombinant domain, produced in a baculovirus-insect cell system, induced high titers of antibodies that reacted with varO-infected red blood cells and disrupted varO rosettes. varO parasites were culture adapted in vitro using human erythrocytes. They formed rosettes and autoagglutinates, and they had the same surface serotype and expressed the same varO gene as the monkey-propagated parasites. To develop an in vitro model with highly homogeneous varO parasites, rosette purification was combined with positive selection by panning with a varO NTS-DBL1α₁-specific mouse monoclonal antibody. The single-variant, clonal parasites were used to analyze seroprevalence for varO at the village level in a setting where malaria is holoendemic (Dielmo, Senegal). We found 93.6% (95% confidence interval, 89.7 to 96.4%) seroprevalence for varO surface-reacting antibodies and 86.7% (95% confidence interval, 82.8 to 91.6%) seroprevalence for the recombinant NTS-DBL1α₁ domain, and virtually all permanent residents had seroconverted by the age of 5 years. These data imply that the varO model is a relevant in vivo and in vitro model for rosetting and autoagglutination that can be used for rational development of vaccine candidates and therapeutic strategies aimed at preventing malaria pathology.
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PMCID: PMC2583593
Corresponding author. Mailing address: Institut Pasteur, Unité d'Immunologie Moléculaire des Parasites, CNRS URA 2581, 25 rue du Dr Roux, F-75724 Paris, France. Phone: 33 1 45 68 82 19. Fax: 33 1 45 68 85 88. E-mail: ines.vigan-womas@pasteur.fr
Editor: W. A. Petri, Jr.
ISSN:0019-9567
1098-5522
DOI:10.1128/IAI.00901-08