Evidence map›Paper›PMID 30333168›Full record

ArticleJournal of virology2019

Human MxB Inhibits the Replication of Hepatitis C Virus.

Dong-Rong Yi, Ni An, Zhen-Long Liu, Feng-Wen Xu, Kavita Raniga, Quan-Jie Li, Rui Zhou, Jing Wang, Yong-Xin Zhang, Jin-Ming Zhou and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

40 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
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  17. Review
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  19. Article
  20. Polymorphisms of theFrontiers in cellular and infection microbiology · 2023
    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

17 authors at 4 institutions in 2 countries.

Dong-Rong Yi *Institute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing, China.
Ni An *Institute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing, China.
Zhen-Long Liu *Lady Davis Institute for Medical Research and McGill AIDS Centre, Jewish General Hospital, Montreal, Quebec, Canada.
Feng-Wen XuInstitute of Pathogen Biology, Chinese Academy of Medical Science, Beijing, China.
Kavita RanigaLady Davis Institute for Medical Research and McGill AIDS Centre, Jewish General Hospital, Montreal, Quebec, Canada.
Quan-Jie LiInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing, China.
Rui ZhouInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing, China.
Jing WangInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing, China.
Yong-Xin ZhangInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing, China.
Jin-Ming ZhouInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing, China.
Lei-Liang ZhangInstitute of Pathogen Biology, Chinese Academy of Medical Science, Beijing, China.
Jing AnDepartment of Microbiology and Parasitology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Cheng-Feng QinDepartment of Virology, Beijing Institute of Microbiology and Epidemiology, Beijing, China.ORCID 0000-0002-0632-2807
Fei GuoInstitute of Pathogen Biology, Chinese Academy of Medical Science, Beijing, China.
Xiao-Yu LiInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing, China.
Chen LiangLady Davis Institute for Medical Research and McGill AIDS Centre, Jewish General Hospital, Montreal, Quebec, Canada chen.liang@mcgill.ca shancen@imb.pumc.edu.cn.
Shan CenInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing, China chen.liang@mcgill.ca shancen@imb.pumc.edu.cn.
Chinese Academy of Medical Sciences & Peking Union Medical College · CNJewish General Hospital · CACapital Medical University · CNInstitute of Microbiology · CN

Funding

CIHR HOP-143171
6 · The paper itself

Abstract

Type I interferon (IFN) inhibits viruses by inducing the expression of antiviral proteins. The IFN-induced myxovirus resistance B (MxB) protein has been reported to inhibit a limited number of viruses, including HIV-1 and herpesviruses, but its antiviral coverage remains to be explored further. Here we show that MxB interferes with RNA replication of hepatitis C virus (HCV) and significantly inhibits viral replication in a cyclophilin A (CypA)-dependent manner. Our data further show that MxB interacts with the HCV protein NS5A, thereby impairing NS5A interaction with CypA and NS5A localization to the endoplasmic reticulum, two events essential for HCV RNA replication. Interestingly, we found that MxB significantly inhibits two additional CypA-dependent viruses of the

Indexed as

AnimalsCell LineChlorocebus aethiopsCyclophilin ACyclosporineEndoplasmic ReticulumGene Knockdown TechniquesHEK293 CellsHepacivirusHumansInterferonsMyxovirus Resistance ProteinsProtein BindingRNA-Dependent RNA PolymeraseVero CellsViral Nonstructural ProteinsCyclophilin ACyclosporineInterferonsMX2 protein, humanMyxovirus Resistance ProteinsNS-5 protein, hepatitis C virusRNA-Dependent RNA PolymeraseViral Nonstructural ProteinsCypAFlaviviridaehepatitis C virusMxBNS5A

Identifiers

PMID30333168
PMCPMC6288330
OpenAlexW2896579627

What OpenQuestion holds

Textmetadata
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.