Evidence map›Paper›PMID 25874894›Full record

ArticlePLoS neglected tropical diseases2015

Plasmodium vivax populations are more genetically diverse and less structured than sympatric Plasmodium falciparum populations.

Charlie Jennison, Alicia Arnott, Natacha Tessier, Livingstone Tavul, Cristian Koepfli, Ingrid Felger, Peter M Siba, John C Reeder, Melanie Bahlo, Ivo Mueller and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
14.2field-weighted citation impact, top 1% 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

54 citing papers in PubMed, 97 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Population genetics ofFrontiers in genetics · 2025
    Article
  5. Article
  6. Review
  7. Retrospective analysis ofFrontiers in microbiology · 2023
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

11 authors at 5 institutions in 4 countries.

Charlie JennisonDivision of Infection and Immunity, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia; Department of Medical Biology, University of Melbourne, Parkville, Victoria, Australia.
Alicia ArnottDivision of Infection and Immunity, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia; Department of Medical Biology, University of Melbourne, Parkville, Victoria, Australia.
Natacha TessierDivision of Infection and Immunity, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Livingstone TavulPapua New Guinea Institute for Medical Research, Goroka, Eastern Highlands Province, Papua New Guinea.
Cristian KoepfliDivision of Infection and Immunity, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia; Department of Medical Biology, University of Melbourne, Parkville, Victoria, Australia.
Ingrid FelgerSwiss Tropical and Public Health Institute, Basel, Switzerland.
Peter M SibaPapua New Guinea Institute for Medical Research, Goroka, Eastern Highlands Province, Papua New Guinea.
John C ReederCentre for Population Health, Burnet Institute, Melbourne, Victoria, Australia.
Melanie BahloDivision of Infection and Immunity, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia; Department of Medical Biology, University of Melbourne, Parkville, Victoria, Australia; Department of Mathematics and Statistics, University of Melbourne, Parkville, Victoria, Australia.
Ivo MuellerDivision of Infection and Immunity, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia; Barcelona Centre for International Health Research, Barcelona, Spain.
Alyssa E BarryDivision of Infection and Immunity, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia; Department of Medical Biology, University of Melbourne, Parkville, Victoria, Australia.
Walter and Eliza Hall Institute of Medical Research · AUPapua New Guinea Institute of Medical Research · PGBurnet Institute · AUSwiss Tropical and Public Health Institute · CHUniversity of Melbourne · AU

Funding

TransmissionU19AI089686 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI KAZURA, JAMES WALTER · 2010 to 2016
$9.9M
NIAID NIH HHS U19 AI089686
6 · The paper itself

Abstract

introductionThe human malaria parasite, Plasmodium vivax, is proving more difficult to control and eliminate than Plasmodium falciparum in areas of co-transmission. Comparisons of the genetic structure of sympatric parasite populations may provide insight into the mechanisms underlying the resilience of P. vivax and can help guide malaria control programs. METHODOLOGY/PRINCIPLE

findingsP. vivax isolates representing the parasite populations of four areas on the north coast of Papua New Guinea (PNG) were genotyped using microsatellite markers and compared with previously published microsatellite data from sympatric P. falciparum isolates. The genetic diversity of P. vivax (He = 0.83-0.85) was higher than that of P. falciparum (He = 0.64-0.77) in all four populations. Moderate levels of genetic differentiation were found between P. falciparum populations, even over relatively short distances (less than 50 km), with 21-28% private alleles and clear geospatial genetic clustering. Conversely, very low population differentiation was found between P. vivax catchments, with less than 5% private alleles and no genetic clustering observed. In addition, the effective population size of P. vivax (30353; 13043-69142) was larger than that of P. falciparum (18871; 8109-42986). CONCLUSIONS/SIGNIFICANCE: Despite comparably high prevalence, P. vivax had higher diversity and a panmictic population structure compared to sympatric P. falciparum populations, which were fragmented into subpopulations. The results suggest that in comparison to P. falciparum, P. vivax has had a long-term large effective population size, consistent with more intense and stable transmission, and limited impact of past control and elimination efforts. This underlines suggestions that more intensive and sustained interventions will be needed to control and eventually eliminate P. vivax. This research clearly demonstrates how population genetic analyses can reveal deeper insight into transmission patterns than traditional surveillance methods.

Indexed as

Genetic VariationAllelesGenetics, PopulationGenotypeHumansMalariaMaleMicrosatellite RepeatsPapua New GuineaPlasmodium falciparumPlasmodium vivaxPrevalence

Identifiers

PMID25874894
PMCPMC4398418
OpenAlexW2052410578

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.