MEM INST OSWALDO CRUZ, RIO DE JANEIRO, 112(12) December 2017
PAGES: 850-856 DOI: 10.1590/0074-02760170041 Short communication
Immunoproteomics of Plasmodium falciparum-infected red blood cell membrane fractions

Fernanda J Cabral1,2+, Luciana G Vianna3, Marcia M Medeiros2,6, Bianca Cechetto Carlos2, Rosimeire D Martha4, Nadia Maria Silva1, Luiz Hildebrando P da Silva4,†, Rodrigo G Stabeli5, Gerhard Wunderlich2

1Universidade Estadual de Campinas, Instituto de Biologia, Departamento de Biologia Animal, Campinas, SP, Brasil
2Universidade de São Paulo, Instituto de Ciências Biomédicas, Departamento de Parasitologia, São Paulo, SP, Brasil
3Instituto Butantan, São Paulo, SP, Brasil
4Centro de Pesquisa em Medicina Tropical, Porto Velho, RO, Brasil
5Fundação Oswaldo Cruz-Fiocruz, Rio de Janeiro, RJ, Brasil
6Universidade Nova de Lisboa, Instituto de Higiene e Medicina Tropical, Lisboa, Portugal

Abstract

BACKGROUND The surface of infected red blood cells (iRBCs) has been widely investigated because of the molecular complexity and pathogenesis mechanisms involved. Asymptomatic individuals are important in the field because they can perpetuate transmission as natural reservoirs and present a challenge for diagnosing malaria because of their low levels of circulating parasites. Recent studies of iRBC antibody recognition have shown that responses are quantitatively similar in symptomatic and asymptomatic infections, but no studies have characterised the plasmodial proteins targeted by this response.

OBJECTIVES Our main objective was to identify Plasmodium falciparum proteins associated with iRBC ghosts recognised by antibodies in the sera of symptomatic and asymptomatic individuals in the Brazilian Amazon.

METHODS We collected symptomatic and asymptomatic sera from patients residing in the Brazilian Amazon and P. falciparum iRBC ghosts to identify the proteins involved in natural antibody recognition by 2D-electrophoresis, western blotting, and high-resolution mass spectrometry.

FINDINGS 2D gel-based immunoproteome analysis using symptomatic and asymptomatic sera identified 11 proteins with at least one unique peptide, such as chaperones HSP70-1 and HSP70-x, which likely are components of the secretion machinery/PTEX translocon. PfEMP1 is involved in antigenic variation in symptomatic infections and we found putative membrane proteins whose functions are unknown.

MAIN FINDINGS Our results suggest a potential role of old and new proteins, such as antigenic variation proteins, iRBC remodelling, and membrane proteins, with no assigned functions related to the immune response against P. falciparum, providing insights into the pathogenesis, erythrocyte remodelling, and secretion machinery important for alternative diagnosis and/or malaria therapy.

Financial support: CAPES, CNPq, FAPESP
FJC was a Pos-Doc NanoCAPES fellow, GW is a CNPq research fellow and supported by FAPESP (grant 2012/23306-5).
+ Corresponding author: This e-mail address is being protected from spambots. You need JavaScript enabled to view it.
† In memoriam
Received 1 February 2017
Accepted 30 June 2017

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