Inhibitory effect of Jingfang mixture on Staphylococcus aureus α-hemolysin

World J Microbiol Biotechnol. 2024 Jul 31;40(9):286. doi: 10.1007/s11274-024-04073-0.

Abstract

Staphylococcus aureus is a gram-positive bacteria, and its virulence factors can cause many kinds of infections, such as pneumonia, sepsis, enteritis and osteomyelitis. Traditional antibiotics can not only kill bacteria, but also easily lead to bacterial resistance. Jingfang Mixture (JFM) has the effects of inducing sweating and relieving the exterior, dispelling wind and eliminating dampness, and is commonly used in clinic to prevent and treat epidemic diseases and infectious diseases. The main purpose of this study is to explore the inhibitory effect of JFM on alpha-hemolysin (Hla) of S. aureus and to alleviate the damage caused by Hla. We found that JFM could inhibit the hemolytic activity, transcription level and neutralizing activity of Hla in a dose-dependent manner at the concentrations of 125, 250 and 500 µg/mL, without affecting the growth of bacteria. In addition, JFM reduced the damage of Hla to A549 cells and the release of lactate dehydrogenase (LDH). We also observed that in the S. aureus - induced pneumonia mouse model, JFM could significantly prolong the life of mice, reduce the bacterial load in the lungs, significantly improve the pathological state of the lungs and alleviate the damage caused by inflammatory factors, and the pathogenicity of gene deletion strain DU 1090 of S. aureus to pneumonia mice was also significantly reduced. In conclusion, this study proved that JFM is a potential drug against S. aureus infection, and this study provided a preliminary study for better guidance of clinical drug use.

Keywords: Staphylococcus aureus; Anti-virulence strategy; DU 1090; Jingfang mixture; Α-hemolysin.

MeSH terms

  • A549 Cells
  • Animals
  • Anti-Bacterial Agents* / pharmacology
  • Bacterial Load / drug effects
  • Bacterial Toxins / genetics
  • Bacterial Toxins / metabolism
  • Disease Models, Animal
  • Drugs, Chinese Herbal / pharmacology
  • Female
  • Hemolysin Proteins* / metabolism
  • Hemolysis / drug effects
  • Humans
  • Lung / drug effects
  • Lung / microbiology
  • Mice
  • Mice, Inbred BALB C
  • Pneumonia, Staphylococcal / drug therapy
  • Pneumonia, Staphylococcal / microbiology
  • Staphylococcal Infections* / drug therapy
  • Staphylococcal Infections* / microbiology
  • Staphylococcus aureus* / drug effects
  • Virulence Factors / genetics

Substances

  • Anti-Bacterial Agents
  • Bacterial Toxins
  • Drugs, Chinese Herbal
  • Hemolysin Proteins
  • staphylococcal alpha-toxin
  • Virulence Factors