Evidence map›Paper›PMID 27128943›Full record

ArticleToxins2016

A Scorpion Defensin BmKDfsin4 Inhibits Hepatitis B Virus Replication in Vitro.

Zhengyang Zeng, Qian Zhang, Wei Hong, Yingqiu Xie, Yun Liu, Wenxin Li, Yingliang Wu, Zhijian Cao

Open access · goldAbstract read
In one paragraph

Article in Toxins, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

  1. Scorpion Peptides in Antiviral Drug Discovery: An In-depth Review.Probiotics and antimicrobial proteins · 2026
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  12. Peptide OPTX-1 FromFrontiers in microbiology · 2021
    Article
  13. Review
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  15. Article
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  18. 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

8 authors at 2 institutions in 2 countries.

Zhengyang ZengState Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan 430072, China. zzybio@126.com.
Qian ZhangState Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan 430072, China. white2459533@163.com.
Wei HongState Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan 430072, China. whong1@partners.org.
Yingqiu XieDepartment of Biology, Nazarbayev University School of Science and Technology, Astana 010000, Republic of Kazakhstan. yingqiu.xie@nu.edu.kz.
Yun LiuState Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan 430072, China. 2013301580085@whu.edu.cn.
Wenxin LiState Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan 430072, China. liwxlab@whu.edu.cn.
Yingliang WuState Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan 430072, China. ylwu@whu.edu.cn.
Zhijian CaoState Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan 430072, China. zjcao@whu.edu.cn.
Wuhan University · CNNazarbayev University · KZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatitis B virus (HBV) infection is a major worldwide health problem which can cause acute and chronic hepatitis and can significantly increase the risk of liver cirrhosis and primary hepatocellular carcinoma (HCC). Nowadays, clinical therapies of HBV infection still mainly rely on nucleotide analogs and interferons, the usage of which is limited by drug-resistant mutation or side effects. Defensins had been reported to effectively inhibit the proliferation of bacteria, fungi, parasites and viruses. Here, we screened the anti-HBV activity of 25 scorpion-derived peptides most recently characterized by our group. Through evaluating anti-HBV activity and cytotoxicity, we found that BmKDfsin4, a scorpion defensin with antibacterial and Kv1.3-blocking activities, has a comparable high inhibitory rate of both HBeAg and HBsAg in HepG2.2.15 culture medium and low cytotoxicity to HepG2.2.15. Then, our experimental results further showed that BmKDfsin4 can dose-dependently decrease the production of HBV DNA and HBV viral proteins in both culture medium and cell lysate. Interestingly, BmKDfsin4 exerted high serum stability. Together, this study indicates that the scorpion defensin BmKDfsin4 also has inhibitory activity against HBV replication along with its antibacterial and potassium ion channel Kv1.3-blocking activities, which shows that BmKDfsin4 is a uniquely multifunctional defensin molecule. Our work also provides a good molecule material which will be used to investigate the link or relationship of its antiviral, antibacterial and ion channel-modulating activities in the future.

Indexed as

ScorpionsAnimalsAntiviral AgentsCell SurvivalDefensinsDNA, ViralErythrocytesHemolysisHepatitis B e AntigensHepatitis B Surface AntigensHepatitis B virusHep G2 CellsHumansVirus ReplicationAntiviral AgentsDefensinsDNA, ViralHepatitis B e AntigensHepatitis B Surface Antigensantiviral peptideHBVmultifunctionscorpion defensin

Identifiers

PMID27128943
PMCPMC4885039
OpenAlexW2345245005

What OpenQuestion holds

Textmetadata
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.