Prodigiosin as an Antibiofilm Agent against the Bacterial Biofilm-Associated Infection of .

Zhiwen Ma, Hong Xiao, Hailin Li, Xiaoling Lu, Jing Yan, Hao Nie, Qi Yin
Author Information
  1. Zhiwen Ma: Department of Health Laboratory Technology, School of Public Health, Chongqing Medical University, No. 61 Daxuecheng Middle Road, Shapingba District, Chongqing 401334, China.
  2. Hong Xiao: Department of Health Laboratory Technology, School of Public Health, Chongqing Medical University, No. 61 Daxuecheng Middle Road, Shapingba District, Chongqing 401334, China.
  3. Hailin Li: Department of Health Laboratory Technology, School of Public Health, Chongqing Medical University, No. 61 Daxuecheng Middle Road, Shapingba District, Chongqing 401334, China.
  4. Xiaoling Lu: Department of Health Laboratory Technology, School of Public Health, Chongqing Medical University, No. 61 Daxuecheng Middle Road, Shapingba District, Chongqing 401334, China.
  5. Jing Yan: Department of Health Laboratory Technology, School of Public Health, Chongqing Medical University, No. 61 Daxuecheng Middle Road, Shapingba District, Chongqing 401334, China.
  6. Hao Nie: Department of Health Laboratory Technology, School of Public Health, Chongqing Medical University, No. 61 Daxuecheng Middle Road, Shapingba District, Chongqing 401334, China.
  7. Qi Yin: Department of Health Laboratory Technology, School of Public Health, Chongqing Medical University, No. 61 Daxuecheng Middle Road, Shapingba District, Chongqing 401334, China.

Abstract

is known to generate bacterial biofilms that increase antibiotic resistance. With the increase of multi-drug resistance in recent years, the formulation of a new therapeutic strategy has seemed urgent. Preliminary findings show that Prodigiosin (PG), derived from chromium-resistant , exhibited efficient anti-biofilm activity against . However, its anti-biofilm activity against remains largely unexplored. The anti-biofilm activity of PG against three clinical single drug-resistant was evaluated using crystal violet staining, and the viability of biofilms and planktonic cells were also assessed. A model of chronic lung Infection was constructed to test the in vivo antibiofilm activity of PG. The results showed that PG inhibited biofilm formation and effectively inhibited the production of pyocyanin and extracellular polysaccharides in vitro, as well as moderated the expression of interleukins (IL-1��, IL-6, IL-10) and tumor necrosis factor (TNF-��) in vivo, which might be attributed to the downregulation of biofilm-related genes such as , , and . These findings suggest that PG could be a potential treatment for drug-resistant and chronic biofilm infections.

Keywords

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Grants

  1. No.32100139/National Natural Science Foundation of China
  2. No.sl202100000725/The Project of Chongqing Science and Technology Bureau

MeSH Term

Biofilms
Pseudomonas aeruginosa
Prodigiosin
Pseudomonas Infections
Anti-Bacterial Agents
Animals
Mice
Humans
Microbial Sensitivity Tests
Serratia marcescens

Chemicals

Prodigiosin
Anti-Bacterial Agents

Word Cloud

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