Evidence map›Paper›PMID 23535659›Full record

ArticleNature communications2013

Expansion of host cellular niche can drive adaptation of a zoonotic malaria parasite to humans.

Caeul Lim, Elsa Hansen, Tiffany M DeSimone, Yovany Moreno, Klara Junker, Amy Bei, Carlo Brugnara, Caroline O Buckee, Manoj T Duraisingh

Open access · bronzeAbstract read
In one paragraph

Article in Nature communications, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 1 pooled it
7.5field-weighted citation impact, top 3% 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

78 citing papers in PubMed, 1 synthesis or guideline pooled it, 123 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Article
  7. The essential genome ofScience (New York, N.Y.) · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Tropical medicine and infectious disease · 2023
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Targeting malaria parasites with novel derivatives of azithromycin.Frontiers in cellular and infection microbiology · 2022
    Article
  18. Review
  19. Review
  20. Gliding motility ofProceedings of the National Academy of Sciences of the United States of America · 2021
    Article

18 more citing papers are in PubMed but not listed here.

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

9 authors at 2 institutions in 1 country.

Caeul Lim *Department of Immunology & Infectious Diseases, Harvard School of Public Health, Boston, MA 02115, USA.
Elsa Hansen *Center for Communicable Disease Dynamics, Harvard School of Public Health, MA, 02115, USA.
Tiffany M DeSimoneDepartment of Immunology & Infectious Diseases, Harvard School of Public Health, Boston, MA 02115, USA.
Yovany MorenoDepartment of Immunology & Infectious Diseases, Harvard School of Public Health, Boston, MA 02115, USA.
Klara JunkerDepartment of Immunology & Infectious Diseases, Harvard School of Public Health, Boston, MA 02115, USA.
Amy BeiDepartment of Immunology & Infectious Diseases, Harvard School of Public Health, Boston, MA 02115, USA.
Carlo BrugnaraDepartment of Laboratory Medicine, Children's Hospital Boston, Boston, MA 02115, USA.
Caroline O BuckeeCenter for Communicable Disease Dynamics, Harvard School of Public Health, MA, 02115, USA.
Manoj T DuraisinghDepartment of Immunology & Infectious Diseases, Harvard School of Public Health, Boston, MA 02115, USA.
Boston Children's Hospital · USHarvard University · US

Funding

Understanding and controlling antibiotic resistanceU54GM088558 · NIGMS · HARVARD SCHOOL OF PUBLIC HEALTH · PI LIPSITCH, MARC · 2009 to 2018
$26.4M
Functional analysis of erythrocyte determinants of malaria infectionR01AI091787 · NIAID · HARVARD SCHOOL OF PUBLIC HEALTH · PI DURAISINGH, MANOJ T · 2011 to 2015
$2.0M
NIAID NIH HHS R01 AI091787NIAID NIH HHS R01AI091787NIGMS NIH HHS U54 GM088558NIGMS NIH HHS U54GM088558
6 · The paper itself

Abstract

The macaque malaria parasite Plasmodium knowlesi has recently emerged as an important zoonosis in Southeast Asia. Infections are typically mild but can cause severe disease, achieving parasite densities similar to fatal Plasmodium falciparum infections. Here we show that a primate-adapted P. knowlesi parasite proliferates poorly in human blood due to a strong preference for young red blood cells (RBCs). We establish a continuous in vitro culture system by using human blood enriched for young cells. Mathematical modelling predicts that parasite adaptation for invasion of older RBCs is a likely mechanism leading to high parasite densities in clinical infections. Consistent with this model, we find that P. knowlesi can adapt to invade a wider age range of RBCs, resulting in proliferation in normal human blood. Such cellular niche expansion may increase pathogenesis in humans and will be a key feature to monitor as P. knowlesi emerges in human populations.

Indexed as

Adaptation, PhysiologicalZoonosesAnimalsErythrocytesHumansMacaca mulattaPlasmodium knowlesi

Identifiers

PMID23535659
PMCPMC3762474
OpenAlexW1967299387

What OpenQuestion holds

Textmetadata
LicenceTDM
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.