Evidence map›Paper›PMID 32488076›Full record

ArticleNature communications2020

Malaria parasites regulate intra-erythrocytic development duration via serpentine receptor 10 to coordinate with host rhythms.

Amit K Subudhi, Aidan J O'Donnell, Abhinay Ramaprasad, Hussein M Abkallo, Abhinav Kaushik, Hifzur R Ansari, Alyaa M Abdel-Haleem, Fathia Ben Rached, Osamu Kaneko, Richard Culleton and 2 more

Abstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing 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

40 citing papers in PubMed.

  1. Article
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  3. Revisiting Glutathione Transferases ofPharmaceuticals (Basel, Switzerland) · 2026
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  6. Article
  7. Review
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  9. Phenotypic and fitness consequences of plasticity in the rhythmic replication of malaria parasites.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Article
  10. Circadian rhythms: pervasive, and often times evasive.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  11. Immune regulation of host energy metabolism and periodicity of malaria parasites.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  12. Article
  13. Identification of a divalent metal transporter required for cellular iron metabolism in malaria parasites.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  14. Review
  15. AeLife · 2024
    Article
  16. Melatonin as a Circadian Marker forInternational journal of molecular sciences · 2024
    Review
  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

12 authors.

Amit K SubudhiPathogen Genomics Group, BESE Division, King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Kingdom of Saudi Arabia.
Aidan J O'Donnell *Institute of Evolutionary Biology, and Institute of Immunology and Infection Research, University of Edinburgh, Edinburgh, EH9 3FL, UK.
Abhinay Ramaprasad *Pathogen Genomics Group, BESE Division, King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Kingdom of Saudi Arabia.
Hussein M AbkalloMalaria Unit, Department of Pathology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, 1-12-4 Sakamoto, Nagasaki, 852-8523, Japan.ORCID http://orcid.org/0000-0002-5594-4418
Abhinav KaushikPathogen Genomics Group, BESE Division, King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Kingdom of Saudi Arabia.ORCID http://orcid.org/0000-0001-5682-0209
Hifzur R AnsariPathogen Genomics Group, BESE Division, King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Kingdom of Saudi Arabia.ORCID http://orcid.org/0000-0002-0646-1743
Alyaa M Abdel-HaleemPathogen Genomics Group, BESE Division, King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Kingdom of Saudi Arabia.
Fathia Ben RachedPathogen Genomics Group, BESE Division, King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Kingdom of Saudi Arabia.ORCID http://orcid.org/0000-0001-6601-3080
Osamu KanekoDepartment of Protozoology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, 1-12-4 Sakamoto, Nagasaki, 852-8523, Japan.ORCID http://orcid.org/0000-0003-0675-8296
Richard CulletonMalaria Unit, Department of Pathology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, 1-12-4 Sakamoto, Nagasaki, 852-8523, Japan. richard@nagasaki-u.ac.jp.ORCID http://orcid.org/0000-0001-8808-5771
Sarah E ReeceInstitute of Evolutionary Biology, and Institute of Immunology and Infection Research, University of Edinburgh, Edinburgh, EH9 3FL, UK. sarah.reece@ed.ac.uk.ORCID http://orcid.org/0000-0001-6716-6732
Arnab PainPathogen Genomics Group, BESE Division, King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Kingdom of Saudi Arabia. arnab.pain@kaust.edu.sa.ORCID http://orcid.org/0000-0002-1755-2819

Funding

Wellcome TrustWellcome Trust 202769/Z/16/ZWellcome Trust 204511/Z/16/Z
6 · The paper itself

Abstract

Malaria parasites complete their intra-erythrocytic developmental cycle (IDC) in multiples of 24 h suggesting a circadian basis, but the mechanism controlling this periodicity is unknown. Combining in vivo and in vitro approaches utilizing rodent and human malaria parasites, we reveal that: (i) 57% of Plasmodium chabaudi genes exhibit daily rhythms in transcription; (ii) 58% of these genes lose transcriptional rhythmicity when the IDC is out-of-synchrony with host rhythms; (iii) 6% of Plasmodium falciparum genes show 24 h rhythms in expression under free-running conditions; (iv) Serpentine receptor 10 (SR10) has a 24 h transcriptional rhythm and disrupting it in rodent malaria parasites shortens the IDC by 2-3 h; (v) Multiple processes including DNA replication, and the ubiquitin and proteasome pathways, are affected by loss of coordination with host rhythms and by disruption of SR10. Our results reveal malaria parasites are at least partly responsible for scheduling the IDC and coordinating their development with host daily rhythms.

Indexed as

AnimalsCaenorhabditis elegans ProteinsCircadian RhythmDisease Models, AnimalErythropoiesisFemaleGene ExpressionHost-Parasite InteractionsHumansMalariaMiceMice, KnockoutPlasmodium chabaudiPlasmodium falciparumProtozoan ProteinsReceptors, G-Protein-CoupledCaenorhabditis elegans ProteinsProtozoan ProteinsReceptors, G-Protein-CoupledSecologanin Tryptamine Alkaloidsserpentine (alkaloid)SRD-1 protein, C elegans

Identifiers

PMID32488076
PMCPMC7265539

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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.