Affiliation:
1. Department of Food Engineering, Engineering Faculty, Çukurova University, Adana, Turkey
2. Faculty of Education
and Arts, Sohar University, Sohar, 311, Sultanate of Oman
3. Department of Biotechnology, Institute of Natural and Applied
Sciences (Fen Bilimleri Enstitüsü) Çukurova University, Adana, Turkey
Abstract
Introduction:
Salmonellosis, which is typically distinguished by an immediate onset of
fever, abdominal pain, diarrhea, nausea, and vomiting, is a bacterial infection caused by Salmonella.
The rising incidence of antibiotic resistance in Salmonella Typhimurium is a major worldwide
problem, and a better knowledge of the distribution of antibiotic resistance patterns in Salmonella
Typhimurium is critical for selecting the best antibiotic for infection treatment. In this work, the efficiency
of bacteriophage therapy of vegetative cells and biofilms of S. Typhimurium was investigated.
Methods:
Based on their host ranges, five Bacteriophages were chosen for therapy against 22 Salmonella
isolates collected from various sources. PSCs1, PSDs1, PSCs2, PSSr1, and PSMc1 phages
were found to exhibit potent anti-S. Typhimurium properties. In a 96-well microplate, the efficacy
of bacteriophage therapy (105-1011 PFU/mL) against S. Typhimurium biofilm formers was first tested.
A bacteriophage treatment (109 PFU/mL) was subsequently applied in the laboratory for 24
hours to minimize Salmonella adhering to the surfaces of gallstones and teeth. In 96-well microplate
experiments, bacteriophage treatment inhibited biofilm development and reduced biofilm by
up to 63.6% (P ≤ 0.05).
Result:
When compared to controls, bacteriophages (PSCs1, PSDs1, PSCs2, PSSr1, PSMc1) demonstrated
a rapid drop in the populations of S. Typhimurium biofilms generated on the surfaces of
gallstones and teeth where the structure of the Salmonella bacteria in the biofilm was broken and
holes were created.
Conclusion:
Clearly, this study indicated that phages might be employed to eliminate S. Typhimurium
biofilms on gallstone and tooth surfaces.
Funder
C U Research Projects Unit
Publisher
Bentham Science Publishers Ltd.
Subject
Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Medicine
Cited by
5 articles.
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