Evidence map›Paper›PMID 37821878›Full record

ArticleBMC genomics2023

A new Plasmodium vivax reference genome for South American isolates.

Katlijn De Meulenaere, Bart Cuypers, Dionicia Gamboa, Kris Laukens, Anna Rosanas-Urgell

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Methylation-associated mutagenesis underlies variation in the mutation spectrum across eukaryotes.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  3. Exploring Genetic Polymorphism ofJournal of tropical medicine · 2026
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  4. Article
  5. Parasitology · 2025
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  6. Article
  7. Article
  8. Assembled genome of an EthiopianMicrobiology resource announcements · 2024
    Article
  9. Article
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

5 authors at 3 institutions in 2 countries.

Katlijn De MeulenaereDepartment of Biomedical Sciences, Institute of Tropical Medicine Antwerp, Antwerp, Belgium. kdemeulenaere@itg.be.
Bart CuypersDepartment of Computer Science, University of Antwerp, Antwerp, Belgium.
Dionicia GamboaInstituto de Medicina Tropical Alexander von Humboldt, Universidad Peruana Cayetano Heredia, Lima, Peru.
Kris LaukensDepartment of Computer Science, University of Antwerp, Antwerp, Belgium.
Anna Rosanas-UrgellDepartment of Biomedical Sciences, Institute of Tropical Medicine Antwerp, Antwerp, Belgium. arosanas@itg.be.
Instituut voor Tropische Geneeskunde · BEUniversity of Antwerp · BEUniversidad Peruana Cayetano Heredia · PE

Funding

Belgium Development Cooperation (DGD) FA4 Peru 2017-2021Departement Economie, Wetenschap en Innovatie SOFIFonds Wetenschappelijk Onderzoek 1S48419NUniversiteit Antwerpen Biomina core facility
6 · The paper itself

Abstract

backgroundPlasmodium vivax is the second most important cause of human malaria worldwide, and accounts for the majority of malaria cases in South America. A high-quality reference genome exists for Papua Indonesia (PvP01) and Thailand (PvW1), but is lacking for South America. A reference genome specifically for South America would be beneficial though, as P. vivax is a genetically diverse parasite with geographical clustering.

resultsThis study presents a new high-quality assembly of a South American P. vivax isolate, referred to as PvPAM (P. vivax Peruvian AMazon). The genome was obtained from a low input patient sample from the Peruvian Amazon and sequenced using PacBio technology, resulting in a highly complete assembly with 6497 functional genes. Telomeric ends were present in 17 out of 28 chromosomal ends, and additional (sub)telomeric regions are present in 12 unassigned contigs. A comparison of multigene families between PvPAM and the PvP01 genome revealed remarkable variation in vir genes, and the presence of merozoite surface proteins (MSP) 3.6 and 3.7. Three dhfr and dhps drug resistance associated mutations are present in PvPAM, similar to those found in other Peruvian isolates. Mapping of publicly available South American whole genome sequencing (WGS) data to PvPAM resulted in significantly fewer variants and truncated reads compared to the use of PvP01 or PvW1 as reference genomes. To minimize the number of core genome variants in non-South American samples, PvW1 is most suited for Southeast Asian isolates, both PvPAM and PvW1 are suited for South Asian isolates, and PvPAM is recommended for African isolates. Interestingly, non-South American samples still contained the least subtelomeric variants when mapped to PvPAM, indicating high quality of the PvPAM subtelomeric regions.

conclusionsOur findings show that the PvPAM reference genome more accurately represents South American P. vivax isolates in comparison to PvP01 and PvW1. In addition, PvPAM has a high level of completeness, and contains a similar number of annotated genes as PvP01 or PvW1. The PvPAM genome therefore will be a valuable resource to improve future genomic analyses on P. vivax isolates from the South American continent.

Indexed as

MalariaMalaria, VivaxHumansMutationPlasmodium vivaxProtozoan ProteinsSouth AmericaWhole Genome SequencingProtozoan ProteinsGenome assemblyPacBio sequencingPlasmodium vivaxReference genome

Identifiers

PMID37821878
PMCPMC10568799
OpenAlexW4387540959

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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.