Evidence map›Paper›PMID 25077614›Full record

ArticlePloS one2014

Cell cycle-dependent phosphorylation of Theileria annulata schizont surface proteins.

Olga Wiens, Dong Xia, Conrad von Schubert, Jonathan M Wastling, Dirk A E Dobbelaere, Volker T Heussler, Kerry L Woods

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Investigation of carbohydrate-based molecules ofFrontiers in veterinary science · 2026
    Article
  3. Article
  4. Parasitology · 2021
    Article
  5. Frontiers in cell and developmental biology · 2021
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. 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 3 institutions in 2 countries.

Olga WiensDivision of Molecular Pathobiology, Vetsuisse Faculty, University of Bern, Bern, Switzerland.
Dong XiaDepartment of Infection Biology, Institute of Infection and Global Health & School of Veterinary Science, University of Liverpool, Liverpool, England.
Conrad von SchubertDivision of Molecular Pathobiology, Vetsuisse Faculty, University of Bern, Bern, Switzerland.
Jonathan M WastlingDepartment of Infection Biology, Institute of Infection and Global Health & School of Veterinary Science, University of Liverpool, Liverpool, England; The National Institute for Health Research Health Protection Research Unit in Emerging and Zoonotic Infections, University of Liverpool, Liverpool, England.
Dirk A E DobbelaereDivision of Molecular Pathobiology, Vetsuisse Faculty, University of Bern, Bern, Switzerland.
Volker T HeusslerInstitute of Cell Biology, University of Bern, Bern, Switzerland.
Kerry L WoodsDivision of Molecular Pathobiology, Vetsuisse Faculty, University of Bern, Bern, Switzerland.
University of Bern · CHNational Institute for Health Research · GBUniversity of Liverpool · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The invasion of Theileria sporozoites into bovine leukocytes is rapidly followed by the destruction of the surrounding host cell membrane, allowing the parasite to establish its niche within the host cell cytoplasm. Theileria infection induces host cell transformation, characterised by increased host cell proliferation and invasiveness, and the activation of anti-apoptotic genes. This process is strictly dependent on the presence of a viable parasite. Several host cell kinases, including PI3-K, JNK, CK2 and Src-family kinases, are constitutively activated in Theileria-infected cells and contribute to the transformed phenotype. Although a number of host cell molecules, including IkB kinase and polo-like kinase 1 (Plk1), are recruited to the schizont surface, very little is known about the schizont molecules involved in host-parasite interactions. In this study we used immunofluorescence to detect phosphorylated threonine (p-Thr), serine (p-Ser) and threonine-proline (p-Thr-Pro) epitopes on the schizont during host cell cycle progression, revealing extensive schizont phosphorylation during host cell interphase. Furthermore, we established a quick protocol to isolate schizonts from infected macrophages following synchronisation in S-phase or mitosis, and used mass spectrometry to detect phosphorylated schizont proteins. In total, 65 phosphorylated Theileria proteins were detected, 15 of which are potentially secreted or expressed on the surface of the schizont and thus may be targets for host cell kinases. In particular, we describe the cell cycle-dependent phosphorylation of two T. annulata surface proteins, TaSP and p104, both of which are highly phosphorylated during host cell S-phase. TaSP and p104 are involved in mediating interactions between the parasite and the host cell cytoskeleton, which is crucial for the persistence of the parasite within the dividing host cell and the maintenance of the transformed state.

Indexed as

Protein Processing, Post-TranslationalAmino Acid SequenceAnimalsAntigens, ProtozoanCattleCell LineCytokinesisHost-Parasite InteractionsInterphaseMembrane ProteinsPhosphorylationProtozoan ProteinsSchizontsTheileria annulataAntigens, ProtozoanMembrane ProteinsProtozoan Proteins

Identifiers

PMID25077614
PMCPMC4117643
OpenAlexW1969831688

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.