Evidence map›Paper›PMID 33253209›Full record

ArticlePLoS neglected tropical diseases2020

Extracellular non-coding RNA signatures of the metacestode stage of Echinococcus multilocularis.

María Eugenia Ancarola, Gabriel Lichtenstein, Johannes Herbig, Nancy Holroyd, Mara Mariconti, Enrico Brunetti, Matthew Berriman, Krystyna Albrecht, Antonio Marcilla, Mara Cecilia Rosenzvit and 3 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  5. Genome-wide transcriptome analysis ofFrontiers in cellular and infection microbiology · 2024
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  8. Transforming growth factor-β signalling regulates protoscolex formation in theFrontiers in cellular and infection microbiology · 2023
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  10. Review
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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

13 authors at 5 institutions in 5 countries.

María Eugenia AncarolaDepartament of Microbiology, School of Medicine, University of Buenos Aires, Buenos Aires, Argentina.ORCID 0000-0001-6971-7147
Gabriel LichtensteinDepartament of Microbiology, School of Medicine, University of Buenos Aires, Buenos Aires, Argentina.ORCID 0000-0002-2974-6717
Johannes HerbigDepartment of Functional Materials in Medicine and Dentistry and Bavarian Polymer Institute, University of Würzburg, Würzburg, Germany.
Nancy HolroydWellcome Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom.ORCID 0000-0003-2608-7151
Mara MaricontiUnit of Infectious and Tropical Diseases, San Matteo Hospital Foundation, Pavia, Italy.ORCID 0000-0003-4154-930X
Enrico BrunettiUnit of Infectious and Tropical Diseases, San Matteo Hospital Foundation, Pavia, Italy.
Matthew BerrimanWellcome Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom.ORCID 0000-0002-9581-0377
Krystyna AlbrechtDepartment of Functional Materials in Medicine and Dentistry and Bavarian Polymer Institute, University of Würzburg, Würzburg, Germany.
Antonio MarcillaDepartament de Farmàcia i Tecnologia Farmacéutica i Parasitologia, Universitat de València, València, Spain.ORCID 0000-0003-0004-0531
Mara Cecilia RosenzvitDepartament of Microbiology, School of Medicine, University of Buenos Aires, Buenos Aires, Argentina.
Laura KamenetzkyDepartament of Microbiology, School of Medicine, University of Buenos Aires, Buenos Aires, Argentina.
Klaus BrehmInstitute for Hygiene and Microbiology, University of Würzburg, Würzburg, Germany.ORCID 0000-0001-6768-824X
Marcela CucherDepartament of Microbiology, School of Medicine, University of Buenos Aires, Buenos Aires, Argentina.ORCID 0000-0003-1357-9210
Consejo Nacional de Investigaciones Científicas y Técnicas · ARUniversity of Würzburg · DEWellcome Sanger Institute · GBUniversitat de València · ESUniversity of Pavia · IT

Funding

Wellcome TrustWellcome Trust 107475/Z/15/ZWellcome Trust 206194Wellcome Trust WT 098051
6 · The paper itself

Abstract

Extracellular RNAs (ex-RNAs) are secreted by cells through different means that may involve association with proteins, lipoproteins or extracellular vesicles (EV). In the context of parasitism, ex-RNAs represent new and exciting communication intermediaries with promising potential as novel biomarkers. In the last years, it was shown that helminth parasites secrete ex-RNAs, however, most work mainly focused on RNA secretion mediated by EV. Ex-RNA study is of special interest in those helminth infections that still lack biomarkers for early and/or follow-up diagnosis, such as echinococcosis, a neglected zoonotic disease caused by cestodes of the genus Echinococcus. In this work, we have characterised the ex-RNA profile secreted by in vitro grown metacestodes of Echinococcus multilocularis, the casuative agent of alveolar echinococcosis. We have used high throughput RNA-sequencing together with RT-qPCR to characterise the ex-RNA profile secreted towards the extra- and intra-parasite milieus in EV-enriched and EV-depleted fractions. We show that a polarized secretion of small RNAs takes place, with microRNAs mainly secreted to the extra-parasite milieu and rRNA- and tRNA-derived sequences mostly secreted to the intra-parasite milieu. In addition, we show by nanoparticle tracking analyses that viable metacestodes secrete EV mainly into the metacestode inner vesicular fluid (MVF); however, the number of nanoparticles in culture medium and MVF increases > 10-fold when metacestodes show signs of tegument impairment. Interestingly, we confirm the presence of host miRNAs in the intra-parasite milieu, implying their internalization and transport through the tegument towards the MVF. Finally, our assessment of the detection of Echinococcus miRNAs in patient samples by RT-qPCR yielded negative results suggesting the tested miRNAs may not be good biomarkers for this disease. A comprehensive study of the secretion mechanisms throughout the life cycle of these parasites will help to understand parasite interaction with the host and also, improve current diagnostic tools.

Indexed as

AnimalsBiomarkersCulture Media, ConditionedEchinococcus multilocularisExtracellular VesiclesHigh-Throughput Nucleotide SequencingHost-Parasite InteractionsHumansMiceMicroRNAsNanoparticlesReal-Time Polymerase Chain ReactionSequence Analysis, RNABiomarkersCulture Media, ConditionedMicroRNAs

Identifiers

PMID33253209
PMCPMC7728270
OpenAlexW3110590014

What OpenQuestion holds

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LicenceCC BY
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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.