Evidence map›Paper›PMID 29222644›Full record

ArticleCellular and molecular life sciences : CMLS2018

Membrane-shed vesicles from the parasite Trichomonas vaginalis: characterization and their association with cell interaction.

Yesica R Nievas, Veronica M Coceres, Victor Midlej, Wanderley de Souza, Marlene Benchimol, Antonio Pereira-Neves, Ajay A Vashisht, James A Wohlschlegel, Patricia J Johnson, Natalia de Miguel

Open access · bronzeAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2018. 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
1.6field-weighted citation impact, top 17% 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

40 citing papers in PubMed, 73 citations in OpenAlex.

  1. Trichomonas vaginalis cathepsin D-like aspartic proteinase (Tv-CatD) is regulated by iron at different levels.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2026
    Article
  2. Extracellular Vesicles ofJournal of extracellular biology · 2026
    Article
  3. Review
  4. Article
  5. Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Viruses · 2025
    Review
  7. Article
  8. Iron triggersmBio · 2025
    Article
  9. Article
  10. Article
  11. Pathogens (Basel, Switzerland) · 2024
    Article
  12. Review
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  15. 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 4 institutions in 3 countries.

Yesica R NievasLaboratorio de Parásitos Anaerobios Instituto de Investigaciones Biotecnológicas-Instituto Tecnológico Chascomús (IIB-INTECH), CONICET-UNSAM, Intendente Marino KM 8.200 Chascomús, B7130IWA, Chascomús, Provincia de Buenos Aires, Argentina.
Veronica M CoceresLaboratorio de Parásitos Anaerobios Instituto de Investigaciones Biotecnológicas-Instituto Tecnológico Chascomús (IIB-INTECH), CONICET-UNSAM, Intendente Marino KM 8.200 Chascomús, B7130IWA, Chascomús, Provincia de Buenos Aires, Argentina.
Victor MidlejInstituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio De Janeiro, Brazil.
Wanderley de SouzaInstituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio De Janeiro, Brazil.
Marlene BenchimolInstituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio De Janeiro, Brazil.
Antonio Pereira-NevesDepartamento de Microbiologia, Instituto Aggeu Magalhães, Fiocruz, Recife, Pernambuco, Brazil.
Ajay A VashishtDepartment of Biological Chemistry, University of California, Los Angeles, CA, 90095-1489, USA.
James A WohlschlegelDepartment of Biological Chemistry, University of California, Los Angeles, CA, 90095-1489, USA.
Patricia J JohnsonDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, CA, 90095-1489, USA.
Natalia de MiguelLaboratorio de Parásitos Anaerobios Instituto de Investigaciones Biotecnológicas-Instituto Tecnológico Chascomús (IIB-INTECH), CONICET-UNSAM, Intendente Marino KM 8.200 Chascomús, B7130IWA, Chascomús, Provincia de Buenos Aires, Argentina. ndemiguel@intech.gov.ar.ORCID 0000-0002-3864-0703
Consejo Nacional de Investigaciones Científicas y Técnicas · ARUniversidade Federal do Rio de Janeiro · BRUniversity of California, Los Angeles · USFundação Oswaldo Cruz · BR

Funding

Trichomonas vaginalis exosomes: Mediators of host:pathogen interactionsR01AI103182 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI JOHNSON, PATRICIA JEAN · 2013 to 2017
$2.9M
Consejo Nacional de Investigaciones Científicas y Técnicas CONICET-FAPERJFondo para la Investigación Científica y Tecnológica PICT 2013- 1184National Institute of Allergy and Infectious Diseases AI103182NIAID NIH HHS R01 AI103182
6 · The paper itself

Abstract

Trichomonas vaginalis is a common sexually transmitted parasite that colonizes the human urogenital tract, where it remains extracellular and adheres to epithelial cells. Infections range from asymptomatic to highly inflammatory, depending on the host and the parasite strain. Despite the serious consequences associated with trichomoniasis disease, little is known about parasite or host factors involved in attachment of the parasite-to-host epithelial cells. Here, we report the identification of microvesicle-like structures (MVs) released by T. vaginalis. MVs are considered universal transport vehicles for intercellular communication as they can incorporate peptides, proteins, lipids, miRNA, and mRNA, all of which can be transferred to target cells through receptor-ligand interactions, fusion with the cell membrane, and delivery of a functional cargo to the cytoplasm of the target cell. In the present study, we demonstrated that T. vaginalis release MVs from the plasma and the flagellar membranes of the parasite. We performed proteomic profiling of these structures demonstrating that they possess physical characteristics similar to mammalian extracellular vesicles and might be selectively charged with specific protein content. In addition, we demonstrated that viable T. vaginalis parasites release large vesicles (LVs), membrane structures larger than 1 µm that are able to interact with other parasites and with the host cell. Finally, we show that both populations of vesicles present on the surface of T vaginalis are induced in the presence of host cells, consistent with a role in modulating cell interactions.

Indexed as

Host-Parasite InteractionsCell CommunicationExtracellular VesiclesFemaleHeLa CellsHumansProteomicsProtozoan ProteinsTrichomonas vaginalisTrichomonas VaginitisProtozoan ProteinsCellular communicationLarge vesiclesMicrovesiclesParasiteTrichomonas vaginalis

Identifiers

PMID29222644
PMCPMC11105416
OpenAlexW2775016312

What OpenQuestion holds

Textmetadata
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.