ArticleProbiotics and antimicrobial proteins2026
Anti-Pseudomonas aeruginosa Activity of the Scorpion-Derived Peptide GK8.
Article in Probiotics and antimicrobial proteins, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
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.
Who cites it
2 citing papers in PubMed.
- FOXM1 inhibitor, RCM‑1, enhances venetoclax mediated apoptosis through downregulation of ATP2B4 in rhabdomyosarcoma.International journal of oncology · 2026Article
- Scorpion venom as a source of new antimicrobial agents.Frontiers in microbiology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
Abstract
The increasing infection and antibiotic resistance of Pseudomonas aeruginosa has become a major threat to public health, making exploring new and effective antimicrobial agents particularly important. In this study, the scorpion-derived cationic peptide GK8 was designed, which showed effectiveness against P. aeruginosa including clinical resistance strains with low hemolytic activity. In the mouse skin subcutaneous infection model, GK8 significantly decreased the number of P. aeruginosa cells and inflammatory infiltration in the infected area. Mechanism research showed that GK8 killed P. aeruginosa in a concentration- and time-dependent manner, damaging the membrane integrity and membrane potential, inducing ROS accumulation, and interacting with nucleic acids. Moreover, GK8 could inhibit the pathogenic factors of P. aeruginosa, including inhibiting adhesion, motility, pyocyanin production, protease and elastase activities, and biofilm formation. Taken together, GK8 could be a potential alternative anti-infective agent against skin infection caused by P. aeruginosa.
Indexed as
Identifiers
40608284What OpenQuestion holds
Registered trials
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.