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ORIGINAL RESEARCH article

Front. Vet. Sci.

Sec. Veterinary Pharmacology and Toxicology

This article is part of the Research TopicInnovations in Pharmacotherapy: Developing Novel Medicines for the Treatment of Animal DiseasesView all 4 articles

PFK-158 Enhances Colistin Efficacy Against Resistant Edwardsiella piscicida Through Synergistic Mechanisms

Provisionally accepted
Jinfang  LuJinfang Lu1*雅靖  潘雅靖 潘1Yuepeng  ZhangYuepeng Zhang2Zubair  Ahmed LaghariZubair Ahmed Laghari3Yangbin  ShiYangbin Shi1Hans-Peter  GrossartHans-Peter Grossart4Yelin  JiangYelin Jiang1Wu  SihongWu Sihong1DAN-LI  XIEDAN-LI XIE1Wanchun  GuanWanchun Guan1He  ZhangHe Zhang5Yong-Liang  LouYong-Liang Lou1
  • 1School of Laboratory Medicine and Life Science, Wenzhou Medical University, Wenzhou, China
  • 2Wenzhou Cangnan Ecological Environmental Monitoring Station, Wenzhou, China
  • 3Sindh Agriculture University, Tando Jam, Pakistan
  • 4Leibniz-Institute of Freshwater Ecology and Inland Fisheries, Stechlin, Germany
  • 5Wenzhou University, Wenzhou, China

The final, formatted version of the article will be published soon.

Edwardsiella piscicida (E. piscicida) is a well-known bacterial pathogen that causes severe diseases in various cultured fish species, posing a significant threat to the global aquaculture industry. The increasing incidence of multidrug resistant (MDR) E. piscicida has greatly limited the efficacy of conventional antibiotics, highlighting the urgent need for new and effective therapeutic strategies. In the current study, several potential non-antibiotic adjuvants were screened, and PFK-158 was identified as promising compound that synergistically decreased the minimum inhibitory concentration (MIC) of colistin resistant E. piscicida, and significantly enhanced colistin's bactericidal activity against E. piscicida and other fish pathogens (e.g., Vibrio parahaemolyticus). Mechanistic characterization revealed that the combined treatment with PFK-158 and colistin increased bacterial membrane permeability, inhibited efflux pump activity and biofilm formation, promoted colistin accumulation, and induced the overproduction of reactive oxygen species (ROS). Transcriptomic analysis further demonstrated that PFK-158 in combination with colistin significantly downregulated genes associated with bacterial secretion systems, virulence, and lipopolysaccharide modification. Moreover, the co-administration of colistin and PFK-158 efficiently reduced bacterial loads in vivo and improved survival rates in infected fish. These results indicate that PFK-158 may serve as a safe and effective colistin adjuvant to synergistically combat MDR E. piscicida infections. This study provides valuable insights for the development of non-antibiotic adjuvants to manage diseases caused by Edwardsiella and other colistin-resistant pathogens in aquaculture.

Keywords: Aquaculture, Edwardsiella piscicida, non-antibiotic adjuvant, PFK-, synergistic effect

Received: 18 Nov 2025; Accepted: 19 Jan 2026.

Copyright: © 2026 Lu, 潘, Zhang, Laghari, Shi, Grossart, Jiang, Sihong, XIE, Guan, Zhang and Lou. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Jinfang Lu

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