Evidence map›Paper›PMID 29157281›Full record

ArticleParasites & vectors2017

Identification of immunogenic proteins of the cysticercoid of Hymenolepis diminuta.

Anna Sulima, Justyna Bień, Kirsi Savijoki, Anu Näreaho, Rusłan Sałamatin, David Bruce Conn, Daniel Młocicki

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2017. 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
2.2field-weighted citation impact, top 12% 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, 18 citations in OpenAlex.

  1. Review
  2. The TapewormPathogens (Basel, Switzerland) · 2022
    Review
  3. Article
  4. Immunoproteomic Analysis ofPathogens (Basel, Switzerland) · 2021
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Selected Molecular Mechanisms Involved in the Parasite⁻Host SystemInternational journal of molecular sciences · 2018
    Review
  11. Article
  12. Comparative Proteomic Analysis ofFrontiers in microbiology · 2017
    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

7 authors at 6 institutions in 3 countries.

Anna SulimaDepartment of General Biology and Parasitology, Medical University of Warsaw, Warsaw, Poland.
Justyna BieńWitold Stefański Institute of Parasitology, Polish Academy of Sciences, Warsaw, Poland.
Kirsi SavijokiDepartment of Food and Environmental Sciences, University of Helsinki, Helsinki, Finland.
Anu NäreahoDepartment of Veterinary Biosciences, University of Helsinki, Helsinki, Finland.
Rusłan SałamatinDepartment of General Biology and Parasitology, Medical University of Warsaw, Warsaw, Poland.
David Bruce ConnOne Health Center, Berry College, Mount Berry, GA, USA.
Daniel MłocickiDepartment of General Biology and Parasitology, Medical University of Warsaw, Warsaw, Poland. danmlo@twarda.pan.pl.
University of Helsinki · FIHarvard University · USMedical University of Warsaw · PLNational Institute of Public Health · PLPolish Academy of Sciences · PLWitold Stefański Institute of Parasitology · PL

Funding

Narodowe Centrum Nauki 2012/05/B/NZ6/00769
6 · The paper itself

Abstract

backgroundA wide range of molecules are used by tapeworm metacestodes to establish successful infection in the hostile environment of the host. Reports indicating the proteins in the cestode-host interactions are limited predominantly to taeniids, with no previous data available for non-taeniid species. A non-taeniid, Hymenolepis diminuta, represents one of the most important model species in cestode biology and exhibits an exceptional developmental plasticity in its life-cycle, which involves two phylogenetically distant hosts, arthropod and vertebrate.

resultsWe identified H. diminuta cysticercoid proteins that were recognized by sera of H. diminuta-infected rats using two-dimensional gel electrophoresis (2DE), 2D-immunoblotting, and LC-MS/MS mass spectrometry. Proteomic analysis of 42 antigenic spots revealed 70 proteins. The largest number belonged to structural proteins and to the heat-shock protein (HSP) family. These results show a number of the antigenic proteins of the cysticercoid stage, which were present already in the insect host prior to contact with the mammal host. These are the first parasite antigens that the mammal host encounters after the infection, therefore they may represent some of the molecules important in host-parasite interactions at the early stage of infection.

conclusionsThese results could help in understanding how H. diminuta and other cestodes adapt to their diverse and complex parasitic life-cycles and show universal molecules used among diverse groups of cestodes to escape the host response to infection.

Indexed as

Host-Parasite InteractionsAnimalsElectrophoresis, Gel, Two-DimensionalHelminth ProteinsHymenolepiasisHymenolepis diminutaLife Cycle StagesMass SpectrometryProteomicsRatsHelminth ProteinsHymenolepis diminutaImmunogenic proteinsMass spectrometryTwo-dimensional electrophoresis

Identifiers

PMID29157281
PMCPMC5697066
OpenAlexW2770362391

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.