Evidence map›Paper›PMID 36071151›Full record

ArticleCommunications biology2022

The antimicrobial peptide LI14 combats multidrug-resistant bacterial infections.

Jingru Shi, Chen Chen, Dejuan Wang, Zhiqiang Wang, Yuan Liu

Abstract read
In one paragraph

Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed, 1 pooled it
–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

62 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. From screening to treatment:Microbiology spectrum · 2026
    Article
  7. Review
  8. Article
  9. Multidrug-ResistantPolish journal of microbiology · 2026
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Microorganisms · 2026
    Review
  16. Recombinant Molecules as a New Frontier in Mucositis Therapy.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
    Review
  17. Review
  18. Article
  19. Review
  20. Article

2 more citing papers are in PubMed but not listed here.

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

5 authors.

Jingru ShiCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, China.
Chen ChenCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, China.
Dejuan WangCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, China.
Zhiqiang WangCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, China. zqwang@yzu.edu.cn.ORCID 0000-0001-6486-9600
Yuan LiuCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, China. liuyuan2018@yzu.edu.cn.ORCID 0000-0002-9622-6471

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prevalence of multidrug-resistant (MDR) pathogens raises public fears of untreatable infections and represents a huge health risk. There is an urgent need to exploit novel antimicrobial agents. Due to the unique mechanisms, antimicrobial peptides (AMPs) with a low probability to achieve resistance are regarded as potential antibiotic alternatives to address this issue. Herein, we develop a panel of synthetic peptide compounds with novel structures based on the database filters technology (DFT), and the lead peptide LI14 shows potent antibacterial activity against all tested drug-resistant bacteria. LI14 exhibits rapid bactericidal activity and excellent anti-biofilm and -persisters activity, simultaneously showing a low propensity to induce resistance. Moreover, LI14 shows tolerance against pH, temperatures, and pepsin treatment, and no detectable toxicity both in vitro and in vivo. Mechanistic studies revealed that LI14 induces membrane damage by targeting bacterial-specific membrane components and dissipates the proton motive force (PMF), thereby resulting in metabolic perturbations and the accumulation of toxic metabolic products. Furthermore, LI14 sensitizes clinically relevant antibiotics against MDR bacteria. In animal models of infection, LI14 or combined with antibiotics are effective against drug-resistant pathogens. These findings suggest that LI14 is a promising antibiotic candidate to tackle MDR bacterial infections.

Indexed as

Antimicrobial PeptidesBacterial InfectionsAnimalsAnti-Bacterial AgentsBacteriaMicrobial Sensitivity TestsPeptidesAnti-Bacterial AgentsAntimicrobial PeptidesPeptides

Identifiers

PMID36071151
PMCPMC9452538

What OpenQuestion holds

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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.