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Inhibition of the type III secretion system by syringaldehyde protects mice from Salmonella enterica serovar Typhimurium.

Abstract
The invasiveness of Salmonella enterica serovar Typhimurium (S. Typhimurium) is closely associated with the Salmonella pathogenicity island (SPI)-encoded type Ⅲ secretion system (T3SS), which can directly inject a series of effector proteins into eukaryotic cells to enable bacterial infection. In this study, syringaldehyde was identified as an effective inhibitor of the S. Typhimurium T3SS using an effector protein-lactamase fusion reporter system. Syringaldehyde treatment could inhibit the expression of important effector proteins (SipA, SipB and SipC) at a concentration of 0.18 mM without affecting bacterial growth. Additionally, significant inhibition of bacterial invasion and cellular injury was observed following the syringaldehyde treatment in the co-infection system of HeLa cells and S. Typhimurium. Furthermore, treatment with syringaldehyde provided systemic protection to mice infected with S. Typhimurium, reducing mortality (40.00%) and bacterial loads and relieving caecal damage and systemic inflammation. The results presented in this study indicate that syringaldehyde significantly affects T3SS activity and is a potential leading compound for treating S. Typhimurium infections.
AuthorsQianghua Lv, Xiao Chu, Xinyu Yao, Kelong Ma, Yong Zhang, Xuming Deng
JournalJournal of cellular and molecular medicine (J Cell Mol Med) Vol. 23 Issue 7 Pg. 4679-4688 (07 2019) ISSN: 1582-4934 [Electronic] England
PMID31066220 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2019 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine.
Chemical References
  • Bacterial Proteins
  • Benzaldehydes
  • Type III Secretion Systems
  • syringaldehyde
Topics
  • Animals
  • Bacterial Proteins (metabolism)
  • Benzaldehydes (chemistry, pharmacology)
  • Female
  • Gene Expression Regulation, Bacterial (drug effects)
  • HeLa Cells
  • Humans
  • Mice, Inbred BALB C
  • Protein Transport (drug effects)
  • Salmonella Infections, Animal (microbiology, prevention & control)
  • Salmonella typhimurium (drug effects, genetics, growth & development, physiology)
  • Survival Analysis
  • Transcription, Genetic (drug effects)
  • Type III Secretion Systems (antagonists & inhibitors, metabolism)

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