Evidence map›Paper›PMID 33666550›Full record

ArticleParasite (Paris, France)2021

iTRAQ-based comparative proteomic analysis in different developmental stages of Echinococcus granulosus.

Xin Li, Song Jiang, Xuhai Wang, Wenqiao Hui, Bin Jia

Open access · goldAbstract read
In one paragraph

Article in Parasite (Paris, France), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. First comparative proteomic andFrontiers in veterinary science · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Comparative proteomics analysis of adultFrontiers in cellular and infection microbiology · 2023
    Article
  9. 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

5 authors at 2 institutions in 1 country.

Xin LiCollege of Life Sciences, Shihezi University, Road Beisi, Shihezi 832003, Xinjiang, PR China - College of Animal Science and Technology, Shihezi University, Road Beisi, Shihezi 832003, Xinjiang, PR China.ORCID 0000-0002-3039-2389
Song JiangCollege of Animal Science and Technology, Shihezi University, Road Beisi, Shihezi 832003, Xinjiang, PR China.ORCID 0000-0003-3751-7321
Xuhai WangCollege of Animal Science and Technology, Shihezi University, Road Beisi, Shihezi 832003, Xinjiang, PR China.ORCID 0000-0003-3478-3712
Wenqiao HuiAnhui Province Key Laboratory of Livestock and Poultry Product Safety Engineering, Institute of Animal Husbandry and Veterinary Medicine, Anhui Academy of Agriculture Sciences, Road Nongkenan, Hefei 230031, Anhui, PR China.ORCID 0000-0002-1645-1311
Bin JiaCollege of Animal Science and Technology, Shihezi University, Road Beisi, Shihezi 832003, Xinjiang, PR China.ORCID 0000-0002-4355-9862
Shihezi University · CNAnimal Science Research Institute · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cystic echinococcosis, caused by infection with the larval stage of the cestode Echinococcus granulosus, is a chronic zoonosis. The lifecycle of the E. granulosus parasite includes three consecutive stages that require specific gene regulation or protein expression to survive environmental shifts between definitive hosts and intermediate hosts. The aim of the present study is to screen and analyze the stage differential antigens to be considered for vaccine development against E. granulosus. By using the iTRAQ (isobaric tags for relative and absolute quantification) method, the differentially expressed proteins were selected from the three consecutive developmental stages of E. granulosus: oncosphere, adult tapeworms, and protoscolex. Through a bioinformatics analysis including Clusters of Orthologous Groups (COG), Gene Ontology (GO), and pathway metabolic annotation, we identified some proteins of interest from each stage. The results showed that a large number of differentially expressed proteins (375: oncosphere vs. adult, 346: oncosphere vs. protoscolex, and 391: adult vs. protoscolex) were identified from the three main lifecycle stages. Analysis of the differential protein pathways showed that these differential proteins are mainly enriched in metabolic pathways, Huntington's diseases, Alzheimer's diseases, and ribosome metabolic pathways. Interestingly, among these differential proteins, expression levels of paramyosin, HSP60, HSP70, HSP90, cathepsin L1, cathepsin D, casein kinase, and calmodulin were significantly higher in the oncosphere than in the adult or protoscolex (p < 0.05). We hope our findings will help to identify potential targets for diagnosis or for therapeutic and prophylactic intervention.

Indexed as

Echinococcus granulosusProteomicsAnimalsAntigens, HelminthComputational BiologyEchinococcosisLife Cycle StagesAntigens, HelminthCandidate targets for diagnosis or therapeuticsDifferential expression proteinsE. granulosusiTRAQ

Identifiers

PMID33666550
PMCPMC7934609
OpenAlexW3133673628

What OpenQuestion holds

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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.