Comprehensive Host Cell-Based Screening Assays for Identification of Anti-Virulence Drugs Targeting Pseudomonas aeruginosa and Salmonella Typhimurium.
Julia von AmbürenFynn SchreiberJulia FischerSandra WinterEdeltraud van GumpelAlexander SimonisJan RybnikerPublished in: Microorganisms (2020)
The prevalence of bacterial pathogens being resistant to antibiotic treatment is increasing worldwide, leading to a severe global health challenge. Simultaneously, the development and approval of new antibiotics stagnated in the past decades, leading to an urgent need for novel approaches to avoid the spread of untreatable bacterial infections in the future. We developed a highly comprehensive screening platform based on quantification of pathogen driven host-cell death to detect new anti-virulence drugs targeting Pseudomonas aeruginosa (Pa) and Salmonella enterica serovar Typhimurium (ST), both known for their emerging antibiotic resistance. By screening over 10,000 small molecules we could identify several substances showing promising effects on Pa and ST pathogenicity in our in vitro infection model. Importantly, we could detect compounds potently inhibiting bacteria induced killing of host cells and one novel comipound with impact on the function of the type 3 secretion system (T3SS) of ST. Thus, we provide proof of concept data of rapid and feasible medium- to high-throughput drug screening assays targeting virulence mechanisms of two major Gram-negative pathogens.
Keyphrases
- pseudomonas aeruginosa
- gram negative
- high throughput
- biofilm formation
- escherichia coli
- antimicrobial resistance
- cystic fibrosis
- multidrug resistant
- cell death
- staphylococcus aureus
- global health
- acinetobacter baumannii
- listeria monocytogenes
- cancer therapy
- drug induced
- candida albicans
- cell cycle arrest
- induced apoptosis
- public health
- stem cells
- signaling pathway
- mesenchymal stem cells
- drug resistant
- big data
- diabetic rats
- early onset
- electronic health record