Evidence map›Paper›PMID 32506158›Full record

ArticleApplied microbiology and biotechnology2020

Therapeutic potential of a designed CSαβ peptide ID13 in Staphylococcus aureus-induced endometritis of mice.

Bing Li, Na Yang, Yuxue Shan, Xiumin Wang, Ya Hao, Ruoyu Mao, Da Teng, Huan Fan, Jianhua Wang

Open access · bronzeAbstract read
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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  5. Review
  6. Animals : an open access journal from MDPI · 2022
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  7. Article
  8. Active components and molecular mechanism ofFrontiers in veterinary science · 2022
    Article
  9. Article
  10. Article
  11. The Pharmacodynamics Study of Insect Defensin DLP4 Against ToxigenicFrontiers in cellular and infection microbiology · 2021
    Article
  12. Article
  13. Mangiferin Inhibits Apoptosis and Autophagy Induced byJournal of inflammation research · 2020
    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 2 institutions in 1 country.

Bing LiTeam of Alternatives to Antibiotics, Gene Engineering Lab, Feed Research Institute, Chinese Academy of Agricultural Science, Beijing, 100081, People's Republic of China.
Na YangTeam of Alternatives to Antibiotics, Gene Engineering Lab, Feed Research Institute, Chinese Academy of Agricultural Science, Beijing, 100081, People's Republic of China.
Yuxue ShanTeam of Alternatives to Antibiotics, Gene Engineering Lab, Feed Research Institute, Chinese Academy of Agricultural Science, Beijing, 100081, People's Republic of China.
Xiumin WangTeam of Alternatives to Antibiotics, Gene Engineering Lab, Feed Research Institute, Chinese Academy of Agricultural Science, Beijing, 100081, People's Republic of China.
Ya HaoTeam of Alternatives to Antibiotics, Gene Engineering Lab, Feed Research Institute, Chinese Academy of Agricultural Science, Beijing, 100081, People's Republic of China.
Ruoyu MaoTeam of Alternatives to Antibiotics, Gene Engineering Lab, Feed Research Institute, Chinese Academy of Agricultural Science, Beijing, 100081, People's Republic of China. maoruoyu@caas.cn.
Da TengTeam of Alternatives to Antibiotics, Gene Engineering Lab, Feed Research Institute, Chinese Academy of Agricultural Science, Beijing, 100081, People's Republic of China. tengda@caas.cn.
Huan FanTianjin Animal Science and Veterinary Research Institute, Tianjin, 300381, People's Republic of China.
Jianhua WangTeam of Alternatives to Antibiotics, Gene Engineering Lab, Feed Research Institute, Chinese Academy of Agricultural Science, Beijing, 100081, People's Republic of China. wangjianhua@caas.cn.ORCID http://orcid.org/0000-0002-4048-6055
Feed Research Institute · CNTianjin Academy of Agricultural Sciences · CN

Funding

Key Project of Alternatives to Antibiotics for Feed Usages CAAS-ZDXT2018008National Innovation Program of Agricultural Science and Technology CAAS-ASTIP-2013-FRI-02National Natural Science Foundation of China 31702146National Natural Science Foundation of China 31772640National Natural Science Foundation of China (CN) 31872393
6 · The paper itself

Abstract

Staphylococcus aureus is a common pathogen that can cause clinical and subclinical endometritis in humans and animals. In this study, a designed CSαβ peptide ID13 from DLP4 exhibited high stable antibacterial activity in simulated gastric fluid (90.79%), serum (99.54%), and different pH buffers (> 99%) against S. aureus CVCC 546 and lower cytotoxicity (89.62% viability) than its parent peptide DLP4 (74.14% viability) toward mouse endometrial epithelial cells (MEECs). ID13 caused a depolarization of bacterial membrane and downregulation of the expression of genes involved in membrane potential maintenance and biofilm formation. The in vitro efficacy analysis of ID13 showed a synergistic effect with vancomycin, ampicillin, rifampin, and ciprofloxacin; intracellular antimicrobial activity against S. aureus CVCC 546 in MEECs; and the ability to inhibit lipoteichoic acid-induced pro-inflammatory cytokines from RAW 264.7. In the S. aureus-induced endometritis of mice, similar to vancomycin, ID13 remarkably alleviated pathological conditions, inhibited the production of cytokines (TNF-α, IL-1ß, IL-6, and IL-10), and suppressed the TLR2-NF-κB signal pathway. Collectively, these results suggest that ID13 could be a potential candidate peptide for therapeutic application in S. aureus-induced endometritis. Key Points •Higher antibacterial activity and lower hemolysis of ID13 than DLP4. •ID13 could downregulate the genes of bacterial survival and infection. •ID13 could alleviate the S. aureus-induced endometritis of mice. •ID13 could regulate the cytokines and suppress the TLR2-NF-κB signal pathway.

Indexed as

AnimalsAnti-Bacterial AgentsDrug SynergismEndometritisEndometriumEpithelial CellsFemaleMicePore Forming Cytotoxic ProteinsSignal TransductionStaphylococcal InfectionsStaphylococcus aureusAnti-Bacterial AgentsPore Forming Cytotoxic ProteinsCSαβ peptideEndometritisStaphylococcus aureusTherapeutic potentialTranscriptome sequencing

Identifiers

PMID32506158
PMCPMC7275135
OpenAlexW3033501487

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.