Evidence map›Paper›PMID 31253850›Full record

ArticleScientific reports2019

Manassantin B shows antiviral activity against coxsackievirus B3 infection by activation of the STING/TBK-1/IRF3 signalling pathway.

Jae-Hyoung Song, Jae-Hee Ahn, Seong-Ryeol Kim, Sungchan Cho, Eun-Hye Hong, Bo-Eun Kwon, Dong-Eun Kim, Miri Choi, Hwa-Jung Choi, Younggil Cha and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

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  13. [Mitochondrial DNA and cGAS-STING Innate Immune Signaling Pathway: Latest Research Progress].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2021
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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

12 authors at 4 institutions in 1 country.

Jae-Hyoung SongCollege of Pharmacy, Kangwon National University, Chuncheon, South Korea.
Jae-Hee AhnCollege of Pharmacy, Kangwon National University, Chuncheon, South Korea.
Seong-Ryeol KimCollege of Pharmacy, Kangwon National University, Chuncheon, South Korea.
Sungchan ChoAnticancer Agent Research Center, Korea Research Institute of Bioscience & Biotechnology, Ochang, South Korea.
Eun-Hye HongCollege of Pharmacy, Kangwon National University, Chuncheon, South Korea.
Bo-Eun KwonCollege of Pharmacy, Kangwon National University, Chuncheon, South Korea.ORCID http://orcid.org/0000-0002-8748-1171
Dong-Eun KimAnticancer Agent Research Center, Korea Research Institute of Bioscience & Biotechnology, Ochang, South Korea.
Miri ChoiAnticancer Agent Research Center, Korea Research Institute of Bioscience & Biotechnology, Ochang, South Korea.
Hwa-Jung ChoiDepartment of Beauty Science, Kwangju Women's University, Gwangju, South Korea.
Younggil ChaCollege of Pharmacy, Kangwon National University, Chuncheon, South Korea.
Sun-Young ChangResearch Institute of Pharmaceutical Science and Technology (RIPST), College of Pharmacy, Ajou University, Suwon, South Korea. sychang@ajou.ac.kr.ORCID http://orcid.org/0000-0001-7336-9245
Hyun-Jeong KoCollege of Pharmacy, Kangwon National University, Chuncheon, South Korea. hjko@kangwon.ac.kr.
Kangwon National University · KRKorea Research Institute of Bioscience and Biotechnology · KRAjou University · KRKwangju Women's University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coxsackievirus B3 (CVB3) is an important human pathogen associated with the development of acute pancreatitis, myocarditis, and type 1 diabetes. Currently, no vaccines or antiviral therapeutics are approved for the prevention and treatment of CVB3 infection. We found that Saururus chinensis Baill extract showed critical antiviral activity against CVB3 infection in vitro. Further, manassantin B inhibited replication of CVB3 and suppressed CVB3 VP1 protein expression in vitro. Additionally, oral administration of manassantin B in mice attenuated CVB3 infection-associated symptoms by reducing systemic production of inflammatory cytokines and chemokines including TNF-α, IL-6, IFN-γ, CCL2, and CXCL-1. We found that the antiviral activity of manassantin B is associated with increased levels of mitochondrial ROS (mROS). Inhibition of mROS generation attenuated the antiviral activity of manassantin B in vitro. Interestingly, we found that manassantin B also induced cytosolic release of mitochondrial DNA based on cytochrome C oxidase DNA levels. We further confirmed that STING and IRF-3 expression and STING and TBK-1 phosphorylation were increased by manassantin B treatment in CVB3-infected cells. Collectively, these results suggest that manassantin B exerts antiviral activity against CVB3 through activation of the STING/TKB-1/IRF3 antiviral pathway and increased production of mROS.

Indexed as

AnimalsAntiviral AgentsChlorocebus aethiopsCoxsackievirus InfectionsCytokinesElectron Transport Chain Complex ProteinsEnterovirus B, HumanFemaleFuransHumansInflammation MediatorsInterferon Regulatory Factor-3Membrane ProteinsMiceMitochondriaPlant ExtractsAntiviral AgentsCytokinesElectron Transport Chain Complex ProteinsFuransInflammation MediatorsInterferon Regulatory Factor-3Irf3 protein, mousemanassantin BMembrane ProteinsPlant ExtractsProtein Serine-Threonine KinasesSting1 protein, mouseSTING ProteinTbk1 protein, mouse

Identifiers

PMID31253850
PMCPMC6599049
OpenAlexW2954710562

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.