Evidence map›Paper›PMID 20526602›Full record

ArticleCurrent microbiology2011

Characterization of the antiviral activity for influenza viruses M1 zinc finger peptides.

Yongjin Wang, Huihui Xiao, Nannan Wu, Huiling Shi, Hongwei Xu, Lichen Zhou, Xu-Guang Xi, Tianhou Wang, Xiaoming Wang

Abstract read
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In one paragraph

Article in Current microbiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

1 citing paper in PubMed.

  1. 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

9 authors.

Yongjin WangLaboratory of Wildlife Epidemic Diseases, East China Normal University, Shanghai, 200062, China. yjwang@ecnu.edu.cn
Huihui Xiao
Nannan Wu
Huiling Shi
Hongwei Xu
Lichen Zhou
Xu-Guang Xi
Tianhou Wang
Xiaoming Wang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We sought to investigate the cellular uptake and antiviral activity for the M1 zinc finger peptides derived from influenza A and influenza B viruses in vitro. No cellular uptake was detected by fluorescent microscopy for the synthetic zinc finger peptides. When flanked to a cell permeable peptide Tp10, the zinc finger recombinant proteins were efficiently internalized by MDCK cells. However, no antiviral activity was detected against homologous or heterologous virus infections for the synthetic peptides or the Tp10-flanked recombinant proteins, regardless treated with or without Zn(2+). Nevertheless, MDCK cell constitutively expressing the M1 zinc finger peptides in cell nuclei potently inhibited replication of homologous, but not heterologous influenza viruses. Adenoviral vector delivered M1 zinc finger peptides also exhibited potent antiviral activity against homologous viruses challenge. Transduction at 100 PFU dose of recombinant adenovirus efficiently protected 99% of the cells from 100 TCID(50) of different virus infections for both peptides. These results brought new insight to the antiviral researches against influenza virus infections.

Indexed as

Zinc FingersAdenoviridaeAnimalsAntiviral AgentsCell LineDogsGenetic VectorsOrthomyxoviridaePeptidesViral Matrix ProteinsVirus ReplicationAntiviral AgentsM1 matrix protein, influenza B virusM1 protein, Influenza A virusPeptidesViral Matrix Proteins

Identifiers

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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.