Login / Signup

A simple, ex vivo phagocytosis assay of Plasmodium vivax merozoites by flow cytometry.

Elizangela FariasFhabiane BezerraDjane Clarys Baia-da-SilvaYury Oliveira ChavesTatiana Bacry CardozaMaria Edilene Martins de AlmeidaLucas Barbosa OliveiraPritesh LalwaniPatrícia Puccinelli OrlandiMarcus Vinicius Guimaraes LacerdaStefanie Costa Pinto LopesPaulo Afonso Nogueira
Published in: Memorias do Instituto Oswaldo Cruz (2019)
As phagocytosis is the first line of defense against malaria, we developed a phagocytosis assay with Plasmodium vivax (P. vivax) merozoites that can be applied to evaluate vaccine candidates. Briefly, after leukocyte removal with loosely packed cellulose powder in a syringe, P. vivax trophozoites matured to the merozoite-rich schizont stages in the presence of the E64 protease inhibitor. The Percoll gradient-enriched schizonts were chemically disrupted to release merozoites that were submitted to merozoite opsonin-dependent phagocytosis in two phagocytic lines with human and mouse antibodies against the N- and C-terminus of P. vivax Merozoite Surface Protein-1 (Nterm-PvMSP1 and MSP119). The resulting assay is simple and efficient for use as a routine phagocytic assay for the evaluation of merozoite stage vaccine candidates.
Keyphrases
  • plasmodium falciparum
  • high throughput
  • flow cytometry
  • endothelial cells
  • clinical practice
  • peripheral blood
  • single cell
  • induced pluripotent stem cells