Plasma-Generated Nitric Oxide Water Mediates Environmentally Transmitted Pathogenic Bacterial Inactivation via Intracellular Nitrosative Stress.
Shweta B BorkarManorma NegiNeha KaushikAbdul Munnaf ShaikNguyen Nhat LinhEun Ha ChoiNagendra Kumar KaushikPublished in: International journal of molecular sciences (2023)
Over time, the proportion of resistant bacteria will increase. This is a major concern. Therefore, effective and biocompatible therapeutic strategies against these bacteria are urgently needed. Non-thermal plasma has been exhaustively characterized for its antibacterial activity. This study aims to investigate the inactivation efficiency and mechanisms of plasma-generated nitric oxide water (PG-NOW) on pathogenic water, air, soil, and foodborne Gram-negative and Gram-positive bacteria. Using a colony-forming unit assay, we found that PG-NOW treatment effectively inhibited the growth of bacteria. Moreover, the intracellular nitric oxide (NO) accumulation was evaluated by 4-amino-5-methylamino-2',7'-dichlorofluorescein diacetate (DAF-FM DA) staining. The reduction of viable cells unambiguously indicates the anti-microbial effect of PG-NOW. The soxR and soxS genes are associated with nitrosative stress, and oxyR regulation corresponds to oxidative stress in bacterial cells. To support the nitrosative effect mediated by PG-NOW, we have further assessed the soxRS and oxyR gene expressions after treatment. Accordingly, soxRS expression was enhanced, whereas the oxyR expression was decreased following PG-NOW treatment. The disruption of cell morphology was observed using scanning electron microscopy (SEM) analysis. In conclusion, our findings furnish evidence of an initiation point for the further progress and development of PG-NOW-based antibacterial treatments.
Keyphrases
- nitric oxide
- gram negative
- induced apoptosis
- electron microscopy
- oxidative stress
- poor prognosis
- multidrug resistant
- cell cycle arrest
- hydrogen peroxide
- nitric oxide synthase
- genome wide
- endoplasmic reticulum stress
- microbial community
- high throughput
- binding protein
- gene expression
- ischemia reperfusion injury
- high resolution
- mesenchymal stem cells
- genome wide identification
- dna damage
- cell therapy
- mass spectrometry
- stem cells