Evidence map›Paper›PMID 32130467›Full record

ArticleApplied microbiology and biotechnology2020

Targeting staphylocoagulase with isoquercitrin protects mice from Staphylococcus aureus-induced pneumonia.

Zeyuan Gao, Yongxin Luan, Panpan Yang, Li Wang, Haitao Zhang, Shisong Jing, Lin Wang, Tiedong Wang, Dacheng Wang

Abstract read
PubMed Publisher
In one paragraph

Article in Applied microbiology and biotechnology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.3field-weighted citation impact, top 28% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. DisarmingPathogens (Basel, Switzerland) · 2025
    Review
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  6. Antibacterial and antibiofilm activities and mechanisms ofCurrent research in food science · 2025
    Article
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  10. PhytoestrogenVaccines · 2023
    Article
  11. Article
  12. Article
  13. Isovitexin Is a Direct Inhibitor ofJournal of microbiology and biotechnology · 2021
    Article
  14. Article
  15. Article
  16. Polyphenol-RichAntibiotics (Basel, Switzerland) · 2021
    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 at 1 institution in 1 country.

Zeyuan Gao *College of Animal Science, Jilin University, Changchun, 130062, China.
Yongxin Luan *Department of Neurosurgery, First Hospital of Jilin University, Jilin University, Changchun, China.
Panpan YangDepartment of Pharmacology, College of Basic Medical Science, Jilin University, Changchun, China.
Li WangCollege of Animal Science, Jilin University, Changchun, 130062, China.
Haitao ZhangCollege of Animal Science, Jilin University, Changchun, 130062, China.
Shisong JingCollege of Animal Science, Jilin University, Changchun, 130062, China.
Lin WangKey Laboratory of Zoonosis Research, Ministry of Education/Institute of Zoonosis/College of Veterinary Medicine, Jilin University, Changchun, China.
Tiedong WangCollege of Animal Science, Jilin University, Changchun, 130062, China. wangtd@jlu.edu.cn.
Dacheng WangCollege of Animal Science, Jilin University, Changchun, 130062, China. wangdc@jlu.edu.cn.
Jilin University · CN

Funding

Jilin Province Scientific and Technological Development Program 20180520043JHNational Key Research and Development Program of China 2018YFD0500300National Key Technology R & D Program No. 2016YFD05013Science Foundation of Jilin Province, China No. 20180101276JC
6 · The paper itself

Abstract

Staphylocoagulase (Coa) is a virulence factor of Staphylococcus aureus (S. aureus) that promotes blood coagulation by activating prothrombin to convert fibrinogen to fibrin. Coa plays a crucial role in disease pathogenesis and is a promising target for the treatment of S. aureus infections. Here, we identified that isoquercitrin, a natural flavonol compound, can markedly reduce the activity of Coa at concentrations that have no effect on bacterial growth. Mechanistic studies employing molecular dynamics simulation revealed that isoquercitrin binds to Coa by interacting with Asp-181 and Tyr-188, thereby affecting the binding of Coa to prothrombin. Importantly, in vivo studies showed that isoquercitrin treatment significantly reduced the bacterial burden, pathological damage, and inflammation of lung tissue and improved the percentage of survival of mice infected with S. aureus Newman strain. These data suggest that isoquercitrin is a promising inhibitor of Coa that can be used for the development of therapeutic drugs to combat S. aureus infections.Key Points• Staphylocoagulase plays a key role in the pathogenesis of S. aureus infection.• We identified that isoquercitrin is a direct inhibitor of staphylocoagulase.• Isoquercitrin treatment can significantly attenuate S. aureus virulence in vivo.

Indexed as

AnimalsCoagulaseMiceMice, Inbred C57BLPneumonia, StaphylococcalProthrombinQuercetinStaphylococcal InfectionsStaphylococcus aureusVirulenceVirulence FactorsCoagulaseisoquercitrinProthrombinQuercetinVirulence FactorsCoaInhibitorIsoquercitrinPneumoniaStaphylococcus aureus

Identifiers

PMID32130467
OpenAlexW3009958993

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.