Genomic variation in <i>Pseudomonas aeruginosa</i> clinical respiratory isolates with <i>de</i> <i>novo</i> resistance to a bacteriophage cocktail

<i>Pseudomonas aeruginosa</i> is an opportunistic pathogen that can cause sinus infections and pneumonia in cystic fibrosis (CF) patients. Bacteriophage therapy is being investigated as a treatment for antibiotic-resistant <i>P. aeruginosa</i> infections. Although virulent bacteriophages have shown promise in treating <i>P. aeruginosa</i> infections, the development of bacteriophage-insensitive mutants (BIMs) in the presence of bacteriophages has been described. The aim of this study was to examine the genetic changes associated with the BIM phenotype. Biofilms of three genetically distinct <i>P. aeruginosa</i> strains, including PAO1 (ATCC 15692), and two clinical respiratory isolates (one CF and one non-CF) were grown for 7 days and treated with either a cocktail of four bacteriophages or a vehicle control for 7 consecutive days. BIMs isolated from the biofilms were detected by streak assays, and resistance to the phage cocktail was confirmed using spot test assays. Comparison of whole genome sequencing between the recovered BIMs and their respective vehicle control-treated phage-sensitive isolates revealed structural variants in two strains, and several small variants in all three strains. These variations involved a TonB-dependent outer membrane receptor in one strain, and mutations in lipopolysaccharide synthesis genes in two strains. Prophage deletion and induction were also noted in two strains, as well as mutations in several genes associated with virulence factors. Mutations in genes involved in susceptibility to conventional antibiotics were also identified in BIMs, with both decreased and increased antibiotic sensitivity to various antibiotics being observed. These findings may have implications for future applications of lytic phage therapy.IMPORTANCELytic bacteriophages are viruses that infect and kill bacteria and can be used to treat difficult-to-treat bacterial infections, including biofilm-associated infections and multidrug-resistant bacteria. <i>Pseudomonas aeruginosa</i> is a bacterium that can cause life-threatening infections. Lytic bacteriophage therapy has been trialed in the treatment of <i>P. aeruginosa</i> infections; however, sometimes bacteria develop resistance to the bacteriophages. This study sheds light on the genetic mechanisms of such resistance, and how this might be harnessed to restore the sensitivity of multidrug-resistant <i>P. aeruginosa</i> to conventional antibiotics.

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Publication Details

Journal
Microbiology Spectrum
Published
2025-03-31
DOI
https://doi.org/10.1128/spectrum.02149-24
Primary Topic
Bacteriophages and microbial interactions
Type
article
Field-Weighted Citation Impact
0.00
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article

Genomic variation in Pseudomonas aeruginosa clinical respiratory isolates with de novo resistance to a bacteriophage cocktail

Alkis J. Psaltis, Stephanie Fong, Sarah Vreugde, George Bouras et al.
Microbiology Spectrum
Bacteriophages and microbial interactions
article

Genomic variation in Pseudomonas aeruginosa clinical respiratory isolates with de novo resistance to a bacteriophage cocktail

Alkis J. Psaltis, Stephanie Fong, Sarah Vreugde, George Bouras, Sholeh Feizi, Sandra Morales, Peter‐John Wormald, Ghais Houtak, Roshan Nepal
article en

Abstract

<i>Pseudomonas aeruginosa</i> is an opportunistic pathogen that can cause sinus infections and pneumonia in cystic fibrosis (CF) patients. Bacteriophage therapy is being investigated as a treatment for antibiotic-resistant <i>P. aeruginosa</i> infections. Although virulent bacteriophages have shown promise in treating <i>P. aeruginosa</i> infections, the development of bacteriophage-insensitive mutants (BIMs) in the presence of bacteriophages has been described. The aim of this study was to examine the genetic changes associated with the BIM phenotype. Biofilms of three genetically distinct <i>P. aeruginosa</i> strains, including PAO1 (ATCC 15692), and two clinical respiratory isolates (one CF and one non-CF) were grown for 7 days and treated with either a cocktail of four bacteriophages or a vehicle control for 7 consecutive days. BIMs isolated from the biofilms were detected by streak assays, and resistance to the phage cocktail was confirmed using spot test assays. Comparison of whole genome sequencing between the recovered BIMs and their respective vehicle control-treated phage-sensitive isolates revealed structural variants in two strains, and several small variants in all three strains. These variations involved a TonB-dependent outer membrane receptor in one strain, and mutations in lipopolysaccharide synthesis genes in two strains. Prophage deletion and induction were also noted in two strains, as well as mutations in several genes associated with virulence factors. Mutations in genes involved in susceptibility to conventional antibiotics were also identified in BIMs, with both decreased and increased antibiotic sensitivity to various antibiotics being observed. These findings may have implications for future applications of lytic phage therapy.IMPORTANCELytic bacteriophages are viruses that infect and kill bacteria and can be used to treat difficult-to-treat bacterial infections, including biofilm-associated infections and multidrug-resistant bacteria. <i>Pseudomonas aeruginosa</i> is a bacterium that can cause life-threatening infections. Lytic bacteriophage therapy has been trialed in the treatment of <i>P. aeruginosa</i> infections; however, sometimes bacteria develop resistance to the bacteriophages. This study sheds light on the genetic mechanisms of such resistance, and how this might be harnessed to restore the sensitivity of multidrug-resistant <i>P. aeruginosa</i> to conventional antibiotics.

Microbiology SpectrumVol. 13(5)
AmpliPhi Biosciences (United States) (US), The University of Adelaide (AU)
Good health and well-being
Openalex Percentile: Top 94%
Bacteriophages and microbial interactions
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