Evidence map›Paper›PMID 30346980›Full record

ArticlePLoS neglected tropical diseases2018

Genetic diversity in two Plasmodium vivax protein ligands for reticulocyte invasion.

Camille Roesch, Jean Popovici, Sophalai Bin, Vorleak Run, Saorin Kim, Stéphanie Ramboarina, Emma Rakotomalala, Rado Lalaina Rakotoarison, Tsikiniaina Rasoloharimanana, Zo Andriamanantena and 7 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.9field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 55 citations in OpenAlex.

  1. Trial
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  7. Natural genetic diversity of the DBL domain of a novel member of the Plasmodium vivax erythrocyte binding-like proteins (EBP2) in the Amazon rainforest.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2024
    Article
  8. Complement receptor 1 is the human erythrocyte receptor forProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Relationship between Duffy Genotype/Phenotype and Prevalence ofTropical medicine and infectious disease · 2023
    Review
  14. Article
  15. Article
  16. Article
  17. Naturally-acquired and Vaccine-induced Human Monoclonal Antibodies tobioRxiv : the preprint server for biology · 2023
    Article
  18. Article
  19. Evolution ofLe infezioni in medicina · 2023
    Review
  20. The Black Box of Cellular and Molecular Events ofInternational journal of molecular sciences · 2022
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 5 institutions in 5 countries.

Camille RoeschMalaria Molecular Epidemiology Unit, Institut Pasteur in Cambodia, Phnom Penh, Cambodia.
Jean PopoviciMalaria Molecular Epidemiology Unit, Institut Pasteur in Cambodia, Phnom Penh, Cambodia.ORCID 0000-0002-3135-1175
Sophalai BinMalaria Molecular Epidemiology Unit, Institut Pasteur in Cambodia, Phnom Penh, Cambodia.
Vorleak RunMalaria Molecular Epidemiology Unit, Institut Pasteur in Cambodia, Phnom Penh, Cambodia.
Saorin KimMalaria Molecular Epidemiology Unit, Institut Pasteur in Cambodia, Phnom Penh, Cambodia.
Stéphanie RamboarinaImmunology of Infectious Diseases Unit, Institut Pasteur de Madagascar, Antananarivo, Madagascar.
Emma RakotomalalaImmunology of Infectious Diseases Unit, Institut Pasteur de Madagascar, Antananarivo, Madagascar.
Rado Lalaina RakotoarisonImmunology of Infectious Diseases Unit, Institut Pasteur de Madagascar, Antananarivo, Madagascar.ORCID 0000-0002-7325-9238
Tsikiniaina RasoloharimananaImmunology of Infectious Diseases Unit, Institut Pasteur de Madagascar, Antananarivo, Madagascar.
Zo AndriamanantenaImmunology of Infectious Diseases Unit, Institut Pasteur de Madagascar, Antananarivo, Madagascar.
Anuj KumarInternational Centre for Genetic Engineering and Biotechnology (ICGEB), New Delhi, India.ORCID 0000-0002-8814-3625
Micheline Guillotte-BlisnickMalaria Parasite Biology and Vaccines Unit, Institut Pasteur, Paris, France.
Christèle HuonMalaria Parasite Biology and Vaccines Unit, Institut Pasteur, Paris, France.
David SerreInstitute for Genome Sciences, University of Maryland, Baltimore, Maryland, United States of America.
Chetan E ChitnisInternational Centre for Genetic Engineering and Biotechnology (ICGEB), New Delhi, India.
Inès Vigan-WomasImmunology of Infectious Diseases Unit, Institut Pasteur de Madagascar, Antananarivo, Madagascar.
Didier MenardMalaria Molecular Epidemiology Unit, Institut Pasteur in Cambodia, Phnom Penh, Cambodia.ORCID 0000-0003-1357-4495
Institut Pasteur de Madagascar · MGInstitut Pasteur du Cambodge · KHInstitut Pasteur · FRInternational Centre for Genetic Engineering and Biotechnology · INUniversity of Maryland, Baltimore · US

Funding

Genomic Analyses of Plasmodium vivax Responses to Antimalarial Drugs in CambodiaR01AI103228 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI SERRE, DAVID · 2013 to 2017
$1.8M
NIAID NIH HHS R01 AI103228
6 · The paper itself

Abstract

The interaction between Plasmodium vivax Duffy binding protein (PvDBP) and Duffy antigen receptor for chemokines (DARC) has been described as critical for the invasion of human reticulocytes, although increasing reports of P. vivax infections in Duffy-negative individuals questions its unique role. To investigate the genetic diversity of the two main protein ligands for reticulocyte invasion, PvDBP and P. vivax Erythrocyte Binding Protein (PvEBP), we analyzed 458 isolates collected in Cambodia and Madagascar from individuals genotyped as Duffy-positive. First, we observed a high proportion of isolates with multiple copies PvEBP from Madagascar (56%) where Duffy negative and positive individuals coexist compared to Cambodia (19%) where Duffy-negative population is virtually absent. Whether the gene amplification observed is responsible for alternate invasion pathways remains to be tested. Second, we found that the PvEBP gene was less diverse than PvDBP gene (12 vs. 33 alleles) but provided evidence for an excess of nonsynonymous mutations with the complete absence of synonymous mutations. This finding reveals that PvEBP is under strong diversifying selection, and confirms the importance of this protein ligand in the invasion process of the human reticulocytes and as a target of acquired immunity. These observations highlight how genomic changes in parasite ligands improve the fitness of P. vivax isolates in the face of immune pressure and receptor polymorphisms.

Indexed as

Genetic VariationAntigens, ProtozoanCambodiaCross-Sectional StudiesGenotypeHumansMadagascarMalaria, VivaxPlasmodium vivaxProtozoan ProteinsReceptors, Cell SurfaceAntigens, ProtozoanDuffy antigen binding protein, PlasmodiumProtozoan ProteinsReceptors, Cell Surface

Identifiers

PMID30346980
PMCPMC6211765
OpenAlexW2803598103

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.