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Author Spotlight: Efficiently Eliminating Bacteriophages from Infected Salmonella Cultures Using Lipopolysaccharides
Published on: June 28, 2024
Isolation and Characterization of Three Lytic Bacteriophages to Overcome Multidrug-, Extensive Drug-, and
Marwan Mahmood Saleh1, Majeed Arsheed Sabbah2, Zahraa Kamel Zedan3
1Department of Biophysics, College of Applied Sciences, University of Anbar, Baghdad, Iraq.
Background:
The worrisome spread of multidrug-resistant (MDR) pathogens necessitates research on nonantibiotic therapeutics. Among these therapeutics, phage treatment uses bacteriophages (phages) as alternative antimicrobial agents.
Objectives:
This project evaluates the lytic efficiency of phage cocktails in vitro versus MDR, extensive drug-resistant (XDR), and pandrug-resistant (PDR) P. aeruginosa isolates.
Methods:
We utilized host range and genetic information to generate a three-phage cocktail capable of killing multiple clinical strains of P. aeruginosa and examined the effectiveness of the cocktail in this study. The isolates (114) had variable resistance to 13 antibiotics. A phage-enrichment approach was used to purify the bacteriophage cocktail; a phage lysate with a high titer (5 × 109 PFU/mL) was prepared and tested against 114 P. aeruginosa isolates.
Findings:
The results showed that a cocktail of three phages (MMS1, MMS2, and MMS3) could lyse P. aeruginosa in both planktonic liquid and dish cultures. The MMS cocktail phages were shown to be viable between 4 and 50°C at pH 4-9. A one-step growth curve showed that the MMS phages had a latent period of 15 min and a burst period of approximately 18 min based on the size of approximately 265 offspring phages per host cell. The MMS3 phage was sequenced and shown to lack genes associated with bacterial pathogenicity or antibiotic resistance.
Conclusions:
Notably, XDR and PDR isolates were sensitive to the phage cocktail, a prospective substitute for antibiotics that does not contribute to the growth of antibiotic resistance, suggesting that the phage cocktail might be useful for generating personalized phage therapeutics.
Insights
A novel phage cocktail effectively lyses multidrug-resistant (MDR) and extensively drug-resistant (XDR) Pseudomonas aeruginosa. This bacteriophage therapy shows promise as a safe, nonantibiotic alternative for treating resistant bacterial infections.
Area of Science:
- Microbiology
- Bacteriophage Therapy
- Antimicrobial Resistance
Background:
- The rise of multidrug-resistant (MDR) pathogens demands novel nonantibiotic therapeutics.
- Bacteriophage (phage) therapy presents a promising alternative antimicrobial strategy.
Purpose of the Study:
- To evaluate the in vitro lytic efficacy of a three-phage cocktail against multidrug-resistant (MDR), extensive drug-resistant (XDR), and pandrug-resistant (PDR) Pseudomonas aeruginosa isolates.
Main Methods:
- A three-phage cocktail (MMS1, MMS2, MMS3) was generated using host range and genetic data.
- The cocktail was purified via phage enrichment and tested against 114 P. aeruginosa isolates with variable antibiotic resistance.
Main Results:
- The MMS phage cocktail demonstrated lytic activity against P. aeruginosa in both planktonic and dish cultures.
- Phages remained viable across a temperature range of 4-50°C and pH 4-9.
- Sequencing of MMS3 confirmed the absence of bacterial pathogenicity or antibiotic resistance genes.
Conclusions:
- The phage cocktail effectively lysed XDR and PDR P. aeruginosa isolates, indicating its potential as an antibiotic substitute.
- This bacteriophage approach does not promote antibiotic resistance and may be valuable for personalized phage therapeutics.
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