Online ISSN: 2515-8260

Keywords : Bacteriophages


Effect of Bacteriophage and Sub-inhibitory concentration of Imipenemon Biofilm Production by Pseudomonas aeruginosa on Endotracheal tubing - An in-vitro model system

KENJAR, APOORVA; J, UDAYALAXMI; SUMAN, ETHEL; KOTIAN, SHASHIDHAR M; SAMSON, HARSHA PAUL

European Journal of Molecular & Clinical Medicine, 2021, Volume 8, Issue 2, Pages 1998-2008

Aim: To studybiofilm production by Pseudomonas aeruginosaon endotracheal tubing in the presence of bacteriophage and sub-inhibitory concentration of imipenem.Methods and Results: A total of 20 clinical isolates of P.aeruginosa obtained from endotracheal samples were taken for this study. Bacteriophages were obtained from sewage samples from sewage water treatment plant. Biofilm assay was performed by modified O’Toole and Kolter method wherein a piece of sterile 0.5cm2 ETTwas incorporated into the microtitre plate wells. Student’s unpaired t test, Kruskal Wallis, ANOVA and HSD Tukey’s test were used to analyse data with SPSS 17.0 software. P value of ˂0.05 was considered statistically significant.Of the 20 isolates, only four (20%) of the isolates were resistant to imipenem. In the presence of bacteriophage, the biofilm production was very less in comparison to biofilm production in the presence of sub-inhibitory concentration of imipenem or in plain broth (p = 0.004). Conclusions: Bacteriophages effectively reduced the biofilm production by P. aeruginosa on catheter tip. Significance and Impact:The present study demonstrates the effectiveness of using bacteriophage as a biofilm reducing agent. Further studies are required to prove the use of bacteriophage coated ETT to curb hospital acquired infections

A NEW APPROACH TO THE TREATMENT AND PREVENTION OF ATOPIC DERMATITIS. POSSIBLE WAY OF CRISIS RESOLUTION.

Sergey F. Gladkov; Nina K. Perevoshchikova; Yulia S. Pichugina; Marina A. Surkova

European Journal of Molecular & Clinical Medicine, 2020, Volume 7, Issue 2, Pages 2689-2698

Abstract
Nowadays, in the absence of a common doctrine and conceptual schemes, both of
treatment and prevention of atopic diseases, we have practically uncontrolled growth of
this pathology. This dead-end situation can only be changed, if there are clinical atopy
biomarkers, thus making preventive therapy possible. The article presents the program
development and implementation results for primary prevention of atopic dermatitis
based on identified biomarkers. A preventive treatment method, based on the correction 
of intestinal microbiota through selective decontamination of opportunistic microflora
using bacteriophages has been substantiated. The results of ten-year experience in
secondary and primary prevention of atopic diseases are presented