Evidence map›Paper›PMID 28810863›Full record

ArticleBMC biology2017

Multiple essential functions of Plasmodium falciparum actin-1 during malaria blood-stage development.

Sujaan Das, Leandro Lemgruber, Chwen L Tay, Jake Baum, Markus Meissner

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
6.7field-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

46 citing papers in PubMed, 69 citations in OpenAlex.

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  12. Luminal acetylation of microtubules is not essential forMicrobial cell (Graz, Austria) · 2025
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  16. Detailing organelle division and segregation inbioRxiv : the preprint server for biology · 2024
    Article
  17. Article
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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 2 institutions in 2 countries.

Sujaan DasWellcome Centre for Molecular Parasitology, Institute of Infection, Immunity & Inflammation, Glasgow Biomedical Research Centre, University of Glasgow, 120 University Place, Glasgow, G12 8TA, UK. Sujaan.Das@glasgow.ac.uk.
Leandro LemgruberWellcome Centre for Molecular Parasitology, Institute of Infection, Immunity & Inflammation, Glasgow Biomedical Research Centre, University of Glasgow, 120 University Place, Glasgow, G12 8TA, UK.
Chwen L TayDepartment of Life Sciences, Imperial College London, South Kensington, London, SW7 2AZ, UK.
Jake BaumDepartment of Life Sciences, Imperial College London, South Kensington, London, SW7 2AZ, UK.
Markus MeissnerWellcome Centre for Molecular Parasitology, Institute of Infection, Immunity & Inflammation, Glasgow Biomedical Research Centre, University of Glasgow, 120 University Place, Glasgow, G12 8TA, UK. Markus.Meissner@glasgow.ac.uk.ORCID 0000-0002-4816-5221
Wellcome Centre for Molecular Parasitology · GBImperial College London · GB

Funding

Wellcome Trust 085349Wellcome Trust 087582/Z/08/ZWellcome Trust 100993/Z/13/Z
6 · The paper itself

Abstract

backgroundThe phylum Apicomplexa includes intracellular parasites causing immense global disease burden, the deadliest of them being the human malaria parasite Plasmodium falciparum, which invades and replicates within erythrocytes. The cytoskeletal protein actin is well conserved within apicomplexans but divergent from mammalian actins, and was primarily reported to function during host cell invasion. However, novel invasion mechanisms have been described for several apicomplexans, and specific functions of the acto-myosin system are being reinvestigated. Of the two actin genes in P. falciparum, actin-1 (pfact1) is ubiquitously expressed in all life-cycle stages and is thought to be required for erythrocyte invasion, although its functions during parasite development are unknown, and definitive in vivo characterisation during invasion is lacking.

resultsHere we have used a conditional Cre-lox system to investigate the functions of PfACT1 during P. falciparum blood-stage development and host cell invasion. We demonstrate that PfACT1 is crucially required for segregation of the plastid-like organelle, the apicoplast, and for efficient daughter cell separation during the final stages of cytokinesis. Surprisingly, we observe that egress from the host cell is not an actin-dependent process. Finally, we show that parasites lacking PfACT1 are capable of microneme secretion, attachment and formation of a junction with the erythrocyte, but are incapable of host cell invasion.

conclusionsThis study provides important mechanistic insights into the definitive essential functions of PfACT1 in P. falciparum, which are not only of biological interest, but owing to functional divergence from mammalian actins, could also form the basis for the development of novel therapeutics against apicomplexans.

Indexed as

ActinsErythrocytesHost-Parasite InteractionsHumansMalaria, FalciparumPlasmodium falciparumProtozoan ProteinsActinsProtozoan ProteinsActinActomyosinApicomplexaApicoplastConditional gene disruptionCytokinesisCytoskeletonEgressInvasionMalariaMerozoitePlasmodiumPlasmodium falciparum

Identifiers

PMID28810863
PMCPMC5557482
OpenAlexW2747446496

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.