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Targeting Biofilm of MDR Providencia stuartii by Phages Using a Catheter Model.

Authors :
Rakov C
Ben Porat S
Alkalay-Oren S
Yerushalmy O
Abdalrhman M
Gronovich N
Huang L
Pride D
Coppenhagen-Glazer S
Nir-Paz R
Hazan R
Source :
Antibiotics (Basel, Switzerland) [Antibiotics (Basel)] 2021 Apr 02; Vol. 10 (4). Date of Electronic Publication: 2021 Apr 02.
Publication Year :
2021

Abstract

Providencia spp. are emerging pathogens mainly in nosocomial infections. Providencia stuartii in particular is involved in urinary tract infections and contributes significantly to the high incidence of biofilm-formation in catheterized patients. Furthermore, recent reports suggested a role for multiple drug resistant (MDR) P. stuartii in hospital-associated outbreaks which leads to excessive complications resulting in challenging treatments. Phage therapy is currently one of the most promising solutions to combat antibiotic-resistant infections. However, the number of available phages targeting Providencia spp. is extremely limited, restricting the use of phage therapy in such cases. In the present study, we describe the isolation and characterization of 17 lytic and temperate bacteriophages targeting clinical isolates of Providencia spp. as part of the Israeli Phage Bank (IPB). These phages, isolated from sewage samples, were evaluated for host range activity and effectively eradicated 95% of the tested bacterial strains isolated from different geographic locations and displaying a wide range of antibiotic resistance. Their lytic activity is demonstrated on agar plates, planktonic cultures, and biofilm formed in a catheter model. The results suggest that these bacteriophages can potentially be used for treatment of antibiotic-resistant Providencia spp. infections in general and of urinary tract infections in particular.

Details

Language :
English
ISSN :
2079-6382
Volume :
10
Issue :
4
Database :
MEDLINE
Journal :
Antibiotics (Basel, Switzerland)
Publication Type :
Academic Journal
Accession number :
33918377
Full Text :
https://doi.org/10.3390/antibiotics10040375