Evidence map›Paper›PMID 26141436›Full record

ArticleParasitology research2015

MIC3, a novel cross-protective antigen expressed in Toxoplasma gondii and Neospora caninum.

Daoyu Yang, Jing Liu, Pan Hao, Jing Wang, Tao Lei, Dan Shan, Qun Liu

Abstract read
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In one paragraph

Article in Parasitology research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–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

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. A systematic review on efficiency of microneme proteins to induce protective immunity against Toxoplasma gondii.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2019
    Pooled it
  2. HarnessingAnnals of medicine · 2026
    Review
  3. NcROP2 deletion reducesFrontiers in immunology · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Microneme Protein 6 Is Involved in Invasion and Egress byPathogens (Basel, Switzerland) · 2021
    Article
  8. Article
  9. Characterization ofFrontiers in veterinary science · 2020
    Article
  10. Assessment of DNA vaccine encodingIranian journal of basic medical sciences · 2019
    Article
  11. Recent progress in microneme-based vaccines development againstClinical and experimental vaccine research · 2018
    Review
  12. Article
  13. Activation of aFrontiers in microbiology · 2017
    Article
  14. 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.

Daoyu YangKey Laboratory of Animal Epidemiology and Zoonosis, Ministry of Agriculture, Beijing, China.
Jing Liu
Pan Hao
Jing Wang
Tao Lei
Dan Shan
Qun Liu

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microneme protein 3 (MIC3) is an important adhesion molecule expressed by Toxoplasma gondii and Neospora caninum that plays a crucial role in invasion. In our study, we found that recombinant TgMIC3 (rTgMIC3) was recognized by both T. gondii-reactive sera and hyper-immune serum against N. caninum. Polyclonal antibodies against TgMIC3 reacted with N. caninum by western blot and immunofluorescence assay (IFA). These results indicate that MIC3 is a novel cross-reactive antigen expressed in N. caninum and T. gondii. To evaluate the immune-protective effect of TgMIC3, we created the eukaryotic expression vector pcDNA3.1-TgMIC3, transfected this vector into HEK293T cells by lipofection, and evaluated TgMIC3 expression in HEK293T cells using western blot and IFA. Then, groups of BALB/c mice were immunized with recombinant TgMIC3 protein, pcDNA3.1-TgMIC3, or two-vaccine immunization. The mice were challenged with T. gondii RH or N. caninum Nc-1 tachyzoites 14 days after the final immunization. The survival time of T. gondii-infected mice was recorded, and the parasite burden in the brain of N. caninum-infected mice 30 days post-infection was measured using real-time PCR. The results demonstrated that mice immunized with TgMIC3-based vaccines elicited high antibody titers. After parasitic challenge, mice immunized with pcDNA-TgMIC3 exhibited prolonged survival when infected with T. gondii tachyzoites and a lower parasitic burden in the brains of mice challenged with N. caninum tachyzoites. These results demonstrate that TgMIC3 is a cross-protective antigen expressed in T. gondii and N. caninum and could elicit some protection against toxoplasmosis and neosporosis.

Indexed as

AnimalsAntigens, ProtozoanBlotting, WesternBrainCross ReactionsCytokinesFemaleHEK293 CellsHumansImmunizationMiceMice, Inbred BALB CNeosporaProtozoan ProteinsProtozoan VaccinesReal-Time Polymerase Chain ReactionAntigens, ProtozoanCytokinesMIC3 protein, Toxoplasma gondiiProtozoan ProteinsProtozoan VaccinesRecombinant Proteins

Identifiers

What OpenQuestion holds

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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.