Published online Jun 16, 2023. doi: 10.12998/wjcc.v11.i17.4026
Peer-review started: March 28, 2023
First decision: April 11, 2023
Revised: April 21, 2023
Accepted: May 12, 2023
Article in press: May 12, 2023
Published online: June 16, 2023
Processing time: 75 Days and 22.4 Hours
Pseudomonas aeruginosa (P. aeruginosa) is an important cause of nosocomial infections, and contributes to high morbidity and mortality, especially in intensive care units. P. aeruginosa is considered a 'critical' category bacterial pathogen by the World Health Organization to encourage an urgent need for research and development of new antibiotics against its infections.
In this study, the anti-bacterial effect of baicalin combined with tobramycin on carbapenem-resistant P. aeruginosa (CRPA) infection was investigated, including the potential synergistic effect of the two drugs against this pathogen.
The objective of this research is to analyze the distribution of CRPA in a specific hospital over a period of time, and to investigate the effectiveness of baicalin combined with tobramycin therapy as a potential treatment method for CRPA infections. The study aims to explore the correlation between biofilm formation and the expression of drug-resistant and biofilm-related genes in CRPA, with the goal of identifying potential targets for effective treatment.
The expression levels of drug-resistant genes and biofilm-related genes in CRPA that confer resistance to tobramycin, baicalin and tobramycin combined with baicalin were detected.
There was a correlation between biofilm formation and the expression of biofilm-related genes. In addition, VIM, IMP, OprD2, algD, pslA and lasR that confer biofilm production under different concentrations in CRPA were significantly correlated. The synergistic effect of baicalin combined with tobramycin was a significant down-regulation of VIM, IMP, algD, pslA and lasR.
Baicalin combined with tobramycin therapy can be an effective treatment method for patients with CRPA infection.
Future research can focus on further investigating the effectiveness of baicalin combined with tobramycin therapy in the treatment of CRPA infections, including exploring optimal dosage and administration methods. Additionally, further studies can explore the mechanisms underlying the down-regulation of drug-resistant and biofilm-related genes by baicalin and tobramycin, as well as potential side effects or limitations of this treatment method. Moreover, more research could be conducted to investigate other potential treatments for CRPA infections and to evaluate their clinical efficacy. Finally, efforts can be made to develop new approaches for preventing and controlling the spread of CRPA in hospitals and healthcare settings.