Furan-based Chalcone Annihilates the Multi-Drug-Resistant Pseudomonas aeruginosa and Protects Zebra Fish Against its Infection.
Santosh Pushpa Ramya Ranjan NayakCatharine BastySeenivasan BoopathiLoganathan Sumathi DhivyaKhaloud Mohammed AlarjaniMohamed Ragab Abdel GawwadRaghda HagerMuthu Kumaradoss KathiravanJesu Arockia RajPublished in: Journal of microbiology (Seoul, Korea) (2024)
The emergence of carbapenem-resistant Pseudomonas aeruginosa, a multi-drug-resistant bacteria, is becoming a serious public health concern. This bacterium infects immunocompromised patients and has a high fatality rate. Both naturally and synthetically produced chalcones are known to have a wide array of biological activities. The antibacterial properties of synthetically produced chalcone were studied against P. aeruginosa. In vitro, study of the compound (chalcone derivative named DKO1), also known as (2E)-1-(5-methylfuran-2-yl)-3-(4-nitrophenyl) prop-2-en-1-one, had substantial antibacterial and biofilm disruptive action. DKO1 effectively shielded against P. aeruginosa-induced inflammation, oxidative stress, lipid peroxidation, and apoptosis in zebrafish larvae. In adult zebrafish, the treatment enhanced the chances of survivability and reduced the sickness-like behaviors. Gene expression, biochemical analysis, and histopathology studies found that proinflammatory cytokines (TNF-α, IL-1β, IL-6, iNOS) were down regulated; antioxidant enzymes such as superoxide dismutase (SOD) and catalase (CAT) levels increased, and histoarchitecture was restored in zebrafish. The data indicate that DKO1 is an effective antibacterial agent against P. aeruginosa demonstrated both in vitro and in vivo.
Keyphrases
- drug resistant
- pseudomonas aeruginosa
- oxidative stress
- acinetobacter baumannii
- multidrug resistant
- diabetic rats
- public health
- gene expression
- cystic fibrosis
- biofilm formation
- silver nanoparticles
- end stage renal disease
- anti inflammatory
- newly diagnosed
- ejection fraction
- dna damage
- ischemia reperfusion injury
- chronic kidney disease
- cell death
- transcription factor
- high resolution
- essential oil
- high glucose
- hydrogen peroxide
- endoplasmic reticulum stress
- machine learning
- electronic health record
- high throughput
- intensive care unit
- patient reported outcomes
- smoking cessation
- wound healing
- cell cycle arrest
- nitric oxide
- single cell
- water soluble
- fatty acid
- replacement therapy