Evidence map›Paper›PMID 28578460›Full record

ArticleParasitology research2017

Genetic variation in potential Giardia vaccine candidates cyst wall protein 2 and α1-giardin.

Matej Radunovic, Christian Klotz, Christina Skår Saghaug, Hans-Richard Brattbakk, Toni Aebischer, Nina Langeland, Kurt Hanevik

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Article in Parasitology research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Extracellular Vesicles ofJournal of extracellular biology · 2026
    Article
  2. Parasitology · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. A hybrid sequencing and assembly strategy for generating culture freeCurrent research in microbial sciences · 2022
    Article
  7. "Immunoinformatic Identification of T-Cell and B-Cell Epitopes FromFrontiers in cellular and infection microbiology · 2021
    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.

Matej RadunovicDepartment of Clinical Science, University of Bergen, 8th floor, Lab-building, N-5021, Bergen, Norway.
Christian KlotzDepartment of Infectious Diseases, Unit 16 Mycotic and Parasitic Agents and Mycobacteria, Robert Koch-Institute, Berlin, Germany.
Christina Skår SaghaugDepartment of Clinical Science, University of Bergen, 8th floor, Lab-building, N-5021, Bergen, Norway.
Hans-Richard BrattbakkDepartment of Clinical Science, University of Bergen, 8th floor, Lab-building, N-5021, Bergen, Norway.
Toni AebischerDepartment of Infectious Diseases, Unit 16 Mycotic and Parasitic Agents and Mycobacteria, Robert Koch-Institute, Berlin, Germany.
Nina LangelandDepartment of Clinical Science, University of Bergen, 8th floor, Lab-building, N-5021, Bergen, Norway.
Kurt HanevikDepartment of Clinical Science, University of Bergen, 8th floor, Lab-building, N-5021, Bergen, Norway. kurt.hanevik@med.uib.no.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Giardia is a prevalent intestinal parasitic infection. The trophozoite structural protein a1-giardin (a1-g) and the cyst protein cyst wall protein 2 (CWP2) have shown promise as Giardia vaccine antigen candidates in murine models. The present study assesses the genetic diversity of a1-g and CWP2 between and within assemblages A and B in human clinical isolates. a1-g and CWP2 sequences were acquired from 15 Norwegian isolates by PCR amplification and 20 sequences from German cultured isolates by whole genome sequencing. Sequences were aligned to reference genomes from assemblage A2 and B to identify genetic variance. Genetic diversity was found between assemblage A and B reference sequences for both a1-g (90.8% nucleotide identity) and CWP2 (82.5% nucleotide identity). However, for a1-g, this translated into only 3 amino acid (aa) substitutions, while for CWP2 there were 41 aa substitutions, and also one aa deletion. Genetic diversity within assemblage B was larger; nucleotide identity 92.0% for a1-g and 94.3% for CWP2, than within assemblage A (nucleotide identity 99.0% for a1-g and 99.7% for CWP2). For CWP2, the diversity on both nucleotide and protein level was higher in the C-terminal end. Predicted antigenic epitopes were not affected for a1-g, but partially for CWP2. Despite genetic diversity in a1-g, we found aa sequence, characteristics, and antigenicity to be well preserved. CWP2 showed more aa variance and potential antigenic differences. Several CWP2 antigens might be necessary in a future Giardia vaccine to provide cross protection against both Giardia assemblages infecting humans.

Indexed as

Genetic VariationAmino Acid SequenceAnimalsCytoskeletal ProteinsGenotypeGiardia lambliaHumansNorwayPolymerase Chain ReactionProtozoan ProteinsProtozoan VaccinesTrophozoitesCytoskeletal Proteinsgiardin protein, Giardia lambliaProtozoan ProteinsProtozoan VaccinesAlpha1-giardinCyst wall protein 2Genetic diversityGiardiaVaccine

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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.