Evidence map›Paper›PMID 29343745›Full record

ArticleScientific reports2018

Malaria infected red blood cells release small regulatory RNAs through extracellular vesicles.

Kehinde Adebayo Babatunde, Smart Mbagwu, María Andrea Hernández-Castañeda, Swamy R Adapa, Michael Walch, Luis Filgueira, Laurent Falquet, Rays H Y Jiang, Ionita Ghiran, Pierre-Yves Mantel

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

52 citing papers in PubMed, 84 citations in OpenAlex.

  1. Review
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  12. Drug-induced stress mediatesMicrobiology spectrum · 2024
    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

10 authors at 3 institutions in 2 countries.

Kehinde Adebayo BabatundeDepartment of Medicine, University of Fribourg, 1700, Fribourg, Switzerland.
Smart MbagwuDepartment of Medicine, University of Fribourg, 1700, Fribourg, Switzerland.
María Andrea Hernández-CastañedaDepartment of Medicine, University of Fribourg, 1700, Fribourg, Switzerland.
Swamy R AdapaDepartment of Global Health (GH) & Center for Drug Discovery and Innovation (CDDI), College of Public Health, University of South Florida, Tampa, FL, 33612, USA.ORCID http://orcid.org/0000-0003-3313-2782
Michael WalchDepartment of Medicine, University of Fribourg, 1700, Fribourg, Switzerland.
Luis FilgueiraDepartment of Medicine, University of Fribourg, 1700, Fribourg, Switzerland.
Laurent FalquetDepartment of Medicine, University of Fribourg, 1700, Fribourg, Switzerland.ORCID http://orcid.org/0000-0001-8102-7579
Rays H Y JiangDepartment of Global Health (GH) & Center for Drug Discovery and Innovation (CDDI), College of Public Health, University of South Florida, Tampa, FL, 33612, USA.ORCID http://orcid.org/0000-0001-8982-4169
Ionita GhiranDivision of Allergy and Infection, Beth Israel Deaconess Medical Center, Boston, MA, 02115, USA.
Pierre-Yves MantelDepartment of Medicine, University of Fribourg, 1700, Fribourg, Switzerland. Pierre-Yves.mantel@unifr.ch.
University of Fribourg · CHUniversity of South Florida · USBeth Israel Deaconess Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The parasite Plasmodium falciparum causes the most severe form of malaria. Cell communication between parasites is an important mechanism to control population density and differentiation. The infected red blood cells (iRBCs) release small extracellular vesicles (EVs) that transfer cargoes between cells. The EVs synchronize the differentiation of the asexual parasites into gametocytes to initiate the transmission to the mosquito. Beside their role in parasite communication, EVs regulate vascular function. So far, the exact cargoes responsible for cellular communication remain unknown. We isolated EVs from cultured iRBCs to determine their small RNA content. We identified several types of human and plasmodial regulatory RNAs. While the miRNAs and tRNA-derived fragments were the most abundant human RNAs, we also found Y-RNAs, vault RNAs, snoRNAs and piRNAs. Interestingly, we found about 120 plasmodial RNAs, including mRNAs coding for exported proteins and proteins involved in drug resistance, as well as non-coding RNAs, such as rRNAs, small nuclear (snRNAs) and tRNAs. These data show, that iRBC-EVs carry small regulatory RNAs. A role in cellular communication is possible since the RNAs were transferred to endothelial cells. Furthermore, the presence of Plasmodium RNAs, in EVs suggests that they may be used as biomarker to track and detect disease.

Indexed as

Cell CommunicationCell DifferentiationCells, CulturedEndothelial CellsErythrocyte CountErythrocytesExtracellular VesiclesHumansMalariaPlasmodium falciparumRNARNA

Identifiers

PMID29343745
PMCPMC5772623
OpenAlexW2784008255

What OpenQuestion holds

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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.