Evidence map›Paper›PMID 36366505›Full record

ArticleViruses2022

Interferon-Inducible Transmembrane Protein 3 (IFITM3) Restricts Rotavirus Infection.

Zhaoxia Pang, Pengfei Hao, Qiaoqiao Qu, Letian Li, Yuhang Jiang, Shuqi Xiao, Ningyi Jin, Chang Li

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
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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

8 authors at 2 institutions in 1 country.

Zhaoxia PangCollege of Veterinary Medicine, Northwest A&F University, Yangling, Xianyang 712100, China.ORCID 0000-0001-9847-1940
Pengfei HaoChinese Academy of Medical Sciences, Changchun Institute of Veterinary Medicine, Changchun 130122, China.
Qiaoqiao QuChinese Academy of Medical Sciences, Changchun Institute of Veterinary Medicine, Changchun 130122, China.
Letian LiChinese Academy of Medical Sciences, Changchun Institute of Veterinary Medicine, Changchun 130122, China.
Yuhang JiangChinese Academy of Medical Sciences, Changchun Institute of Veterinary Medicine, Changchun 130122, China.
Shuqi XiaoCollege of Veterinary Medicine, Northwest A&F University, Yangling, Xianyang 712100, China.
Ningyi JinCollege of Veterinary Medicine, Northwest A&F University, Yangling, Xianyang 712100, China.
Chang LiChinese Academy of Medical Sciences, Changchun Institute of Veterinary Medicine, Changchun 130122, China.ORCID 0000-0002-3267-1859
Chinese Academy of Medical Sciences & Peking Union Medical College · CNNorthwest A&F University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rotavirus (RV) is a non-enveloped icosahedral virus with an 11-segment double-stranded RNA genome, belonging to the family of rotaviruses. RV is one of the pathogens causing diarrhea in infants and young animals, and it induces the production of type I interferons (IFNs), which can trigger antiviral function by inducing the production of interferon-stimulated genes (ISGs). Although IFITM3, an ISG localizing to late endosomes, can limit many viral infections, whether or not it restricts the infection of RV is still unknown. Therefore, we attempted to determine whether IFITM3 also restricts RV infection by using over-expression and knockout cell strains. It was found that IFITM3-expressing cell strains were less susceptible to RV infection, as the replication of RV in over-expressing cells was significantly less than in control group cells. Correspondingly, IFITM3-knockout cells were significantly susceptible compared to the normal cells. Furthermore, the IFN-induced antiviral effect was significantly attenuated in the absence of IFITM3, and IFITM3 delayed RV escape from endosomes in the presence of IFITM3, suggesting that endogenous IFITM3 is of great importance in type I IFN-mediated antiviral responses and may restrict infection by affecting the function of the late endosomal compartment. In conclusion, these data provide the first evidence that IFITM3 limits RV infection in vitro and delays RV escape from late endosomes into the cytoplasm.

Indexed as

Interferon Type IRotavirusRotavirus InfectionsAnimalsAntiviral AgentsMembrane ProteinsVirus ReplicationAntiviral AgentsInterferon Type IMembrane Proteinscell entrycell infectionIFITM3rotavirus

Identifiers

PMID36366505
PMCPMC9696312
OpenAlexW4307943171

What OpenQuestion holds

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LicenceCC BY
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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.