Evidence map›Paper›PMID 39209862›Full record

ArticleNature communications2024

The artemisinin-induced dormant stages of Plasmodium falciparum exhibit hallmarks of cellular quiescence/senescence and drug resilience.

Jaishree Tripathi, Michal Stoklasa, Sourav Nayak, Kay En Low, Erica Qian Hui Lee, Quang Huy Duong Tien, Laurent Rénia, Benoit Malleret, Zbynek Bozdech

Erratum issuedAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Article
  2. Identification of an Orally Efficacious Imidazo[4,5-Journal of medicinal chemistry · 2026
    Article
  3. Double Mutations inbioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. High throughput quantitative tracking ofbioRxiv : the preprint server for biology · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Isolation and characterization ofAntimicrobial agents and chemotherapy · 2025
    Article
  13. Article
  14. The Antiviral and Antimalarial Prodrug Artemisinin from theCurrent issues in molecular biology · 2024
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Jaishree Tripathi *School of Biological Sciences, Nanyang Technological University (NTU), Singapore, 637551, Singapore. jtmic@nus.edu.sg.ORCID 0000-0003-3461-4767
Michal Stoklasa *School of Biological Sciences, Nanyang Technological University (NTU), Singapore, 637551, Singapore.
Sourav NayakSchool of Biological Sciences, Nanyang Technological University (NTU), Singapore, 637551, Singapore.
Kay En LowElectron Microscopy Unit, Yong Loo Lin School of Medicine, National University of Singapore (NUS), Singapore, 117597, Singapore.
Erica Qian Hui LeeDepartment of Microbiology and Immunology, Immunology Translational Research Programme, Yong Loo Lin School of Medicine, National University of Singapore (NUS), Singapore, 117597, Singapore.
Quang Huy Duong TienSchool of Biological Sciences, Nanyang Technological University (NTU), Singapore, 637551, Singapore.ORCID 0009-0004-6051-3200
Laurent RéniaSchool of Biological Sciences, Nanyang Technological University (NTU), Singapore, 637551, Singapore.
Benoit MalleretElectron Microscopy Unit, Yong Loo Lin School of Medicine, National University of Singapore (NUS), Singapore, 117597, Singapore.ORCID 0000-0001-9658-7528
Zbynek BozdechSchool of Biological Sciences, Nanyang Technological University (NTU), Singapore, 637551, Singapore. zbozdech@ntu.edu.sg.ORCID 0000-0002-9830-8446

Funding

Ministry of Education - Singapore (MOE) MOE2019-T3-1-007Ministry of Health -Singapore (MOH) OFIRG21nov-0014
6 · The paper itself

Abstract

Recrudescent infections with the human malaria parasite, Plasmodium falciparum, presented traditionally the major setback of artemisinin-based monotherapies. Although the introduction of artemisinin combination therapies (ACT) largely solved the problem, the ability of artemisinin to induce dormant parasites still poses an obstacle for current as well as future malaria chemotherapeutics. Here, we use a laboratory model for induction of dormant P. falciparum parasites and characterize their transcriptome, drug sensitivity profile, and cellular ultrastructure. We show that P. falciparum dormancy requires a ~ 5-day maturation process during which the genome-wide gene expression pattern gradually transitions from the ring-like state to a unique form. The transcriptome of the mature dormant stage carries hallmarks of both cellular quiescence and senescence, with downregulation of most cellular functions associated with growth and development and upregulation of selected metabolic functions and DNA repair. Moreover, the P. falciparum dormant stage is considerably more resistant to antimalaria drugs compared to the fast-growing asexual stages. Finally, the irregular cellular ultrastructure further suggests unique properties of this developmental stage of the P. falciparum life cycle that should be taken into consideration by malaria control strategies.

Indexed as

AntimalarialsArtemisininsCellular SenescenceMalaria, FalciparumPlasmodium falciparumDrug ResistanceHumansLife Cycle StagesTranscriptomeAntimalarialsartemisininArtemisinins

Identifiers

PMID39209862
PMCPMC11362153

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.