Unveiling P. vivax invasion pathways in Duffy-negative individuals.

Cell Host Microbe

Malaria Genetics and Resistance Unit, INSERM U1201, Institut Pasteur, Université Paris Cité, 75015 Paris, France; Malaria Parasite Biology and Vaccines Unit, Institut Pasteur, Université Paris Cité, 75015 Paris, France; Institute of Parasitology and Tropical Diseases, UR7292 Dynamics of Host-Pathogen Interactions, Université de Strasbourg, 67000 Strasbourg, France; Laboratory of Parasitology and Medical Mycology, CHU Strasbourg, 67000 Strasbourg, France. Electronic address:

Published: December 2023

AI Article Synopsis

  • Vivax malaria was previously thought to be absent in sub-Saharan Africa because many people lack the Duffy antigen receptor (DARC), which is key for the malaria parasite P. vivax to invade red blood cells.
  • New research has found that some Duffy-negative individuals can temporarily express DARC during the development of their red blood cells, allowing P. vivax to invade these cells.
  • This indicates that there may be many Duffy-negative individuals silently harboring P. vivax infections, potentially leading to underreported health issues in the region.

Article Abstract

Vivax malaria has long been thought to be absent from sub-Saharan Africa owing to the high proportion of individuals lacking the Duffy antigen receptor for chemokines (DARC) in their erythrocytes. The interaction between P. vivax Duffy-binding protein (PvDBP) and DARC is assumed to be the main pathway used by merozoites to invade reticulocytes. However, the increasing number of reports of vivax malaria cases in genotypically Duffy-negative (DN) individuals has raised questions regarding the P. vivax invasion pathway(s). Here, we show that a subset of DN erythroblasts transiently express DARC during terminal erythroid differentiation and that P. vivax merozoites, irrespective of their origin, can invade DARC+ DN erythroblasts. These findings reveal that a large number of DN individuals may represent a silent reservoir of deep P. vivax infections at the sites of active erythropoiesis with low or no parasitemia, and it may represent an underestimated biological problem with potential clinical consequences in sub-Saharan Africa.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10727064PMC
http://dx.doi.org/10.1016/j.chom.2023.11.007DOI Listing

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