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Potential hidden Plasmodium vivax malaria reservoirs from low parasitemia Duffy-negative Ethiopians: Molecular evidence
Journal article   Open access   Peer reviewed

Potential hidden Plasmodium vivax malaria reservoirs from low parasitemia Duffy-negative Ethiopians: Molecular evidence

Abnet Abebe, Isabelle Bouyssou, Solenne Mabilotte, Sisay L. Dugassa, Ashenafi Assefa, Jonathan L. Juliano, Eugenia Lo, Didier L. Menard and Lemu Golassa
PLoS neglected tropical diseases, v 17(7), pe0011326
03 Jul 2023
DOI: https://doi.org/10.1371/journal.pntd.0011326
PMID: 37399221
Featured in Collection :   UN Sustainable Development Goals @ Drexel
url
https://doi.org/10.1371/journal.pntd.0011326View
Published, Version of Record (VoR) Open

Abstract

Infectious Diseases Life Sciences & Biomedicine Parasitology Science & Technology Tropical Medicine
BackgroundThe interaction between the Plasmodium vivax Duffy-binding protein and the corresponding Duffy Antigen Receptor for Chemokines (DARC) is primarily responsible for the invasion of reticulocytes by P. vivax. The Duffy-negative host phenotype, highly prevalent in sub-Saharan Africa, is caused by a single point mutation in the GATA-1 transcription factor binding site of the DARC gene promoter. The aim of this study was to assess the Duffy status of patients with P. vivax infection from different study sites in Ethiopia. MethodsA cross-sectional study was conducted from February 2021 to September 2022 at five varying eco-epidemiological malaria endemic sites in Ethiopia. Outpatients who were diagnosed with P. vivax infection (pure and mixed P. vivax/P. falciparum) by microscopy and Rapid Diagnostic Test (RDT) were subjected to PCR genotyping at the DARC promoter. The associations between P. vivax infection, host genotypes and other factors were evaluated. ResultIn total, 361 patients with P. vivax infection were included in the study. Patients with pure P. vivax infections accounted for 89.8% (324/361), while the remaining 10.2% (37/361) had mixed P. vivax/P. falciparum infections. About 95.6% (345/361) of the participants were Duffy-positives (21.2% homozygous and 78.8%, heterozygous) and 4.4% (16/361) were Duffy-negatives. The mean asexual parasite density in homozygous and heterozygous Duffy-positives was 12,165 p/& mu;l (IQR25-75: 1,640-24,234 p/& mu;l) and11,655 p/& mu;l (IQR25-75: 1,676-14,065 p/& mu;l), respectively, significantly higher than that in Duffy-negatives (1,227p/& mu;l; IQR25-75: 539-1,732p/& mu;l). ConclusionThis study confirms that Duffy-negativity does not provide complete protection against P. vivax infection. The development of P. vivax-specific elimination strategies, including alternative antimalarial vaccines should be facilitated by a better understanding of the epidemiological landscape of vivax malaria in Africa. More importantly, low parasitemia associated with P. vivax infections in Duffy-negative patients may represent hidden reservoirs of transmission in Ethiopia. Author summaryPlasmodium vivax generally receives less attention than P. falciparum and was neglected in sub-Saharan Africa. However, the characteristics of P. vivax infection in Duffy-negative individuals, and the distribution of Duffy blood group in different eco-epidemiological zones and ethnic groups of Ethiopia are not well documented. Here, we determined the Duffy genotypes of P. vivax infected patients across broad regions of Ethiopia. It is clear that Duffy negative individuals in Ethiopia are not fully protected against P. vivax infection, and that these infections in Duffy negatives are often associated with low parasitemia. Our findings lend support to the notion that P. vivax may have developed a Duffy-independent erythrocyte invasion pathway and/or evolution in host immune responses.

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Infectious Diseases
Parasitology
Tropical Medicine
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