Cargando…
Novel Bacteriophages Show Activity against Selected Australian Clinical Strains of Pseudomonas aeruginosa
Multi-drug resistant (MDR) clinical strains of Pseudomonas aeruginosa are the most prevalent bacteria in the lungs of patients with cystic fibrosis (CF) and burn wounds and among the most common in immunocompromised hospital patients in Australia. There are currently no promising antibiotics in the...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8875357/ https://www.ncbi.nlm.nih.gov/pubmed/35208664 http://dx.doi.org/10.3390/microorganisms10020210 |
_version_ | 1784657893446909952 |
---|---|
author | Namonyo, Samuel Carvalho, Gilda Guo, Jianhua Weynberg, Karen D. |
author_facet | Namonyo, Samuel Carvalho, Gilda Guo, Jianhua Weynberg, Karen D. |
author_sort | Namonyo, Samuel |
collection | PubMed |
description | Multi-drug resistant (MDR) clinical strains of Pseudomonas aeruginosa are the most prevalent bacteria in the lungs of patients with cystic fibrosis (CF) and burn wounds and among the most common in immunocompromised hospital patients in Australia. There are currently no promising antibiotics in the pipeline being developed against these strains. Phage therapy, which uses viruses known as bacteriophages to infect and kill pathogenic bacteria, could be a possible alternative treatment. To this end, we isolated and characterised four novel phages against Australian clinical strains of P. aeruginosa isolated from patients with cystic fibrosis, from infected blood and joint aspirate in Southeast Queensland, Australia. Activated sludge was enriched for phages using the clinical strains, and four bacteriophages were isolated. The phages were able to cause lysis in a further three identified clinical isolates. Morphology showed that they were all tailed phages (of the order Caudovirales), two belonging to the family Myoviridae and the others assigned to the Podoviridae and Siphoviridae. Their genomes were sequenced to reveal a doubled stranded DNA topology with genome sizes ranging from 42 kb to 65 kb. In isolating and characterising these novel phages, we directed our efforts toward the development and use of these phages as candidates for phage therapy as an alternative strategy for the management or elimination of these pathogenic strains. Here we describe novel phage candidates for potential therapeutic treatment of MDR Australian clinical isolates of P. aeruginosa. |
format | Online Article Text |
id | pubmed-8875357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88753572022-02-26 Novel Bacteriophages Show Activity against Selected Australian Clinical Strains of Pseudomonas aeruginosa Namonyo, Samuel Carvalho, Gilda Guo, Jianhua Weynberg, Karen D. Microorganisms Article Multi-drug resistant (MDR) clinical strains of Pseudomonas aeruginosa are the most prevalent bacteria in the lungs of patients with cystic fibrosis (CF) and burn wounds and among the most common in immunocompromised hospital patients in Australia. There are currently no promising antibiotics in the pipeline being developed against these strains. Phage therapy, which uses viruses known as bacteriophages to infect and kill pathogenic bacteria, could be a possible alternative treatment. To this end, we isolated and characterised four novel phages against Australian clinical strains of P. aeruginosa isolated from patients with cystic fibrosis, from infected blood and joint aspirate in Southeast Queensland, Australia. Activated sludge was enriched for phages using the clinical strains, and four bacteriophages were isolated. The phages were able to cause lysis in a further three identified clinical isolates. Morphology showed that they were all tailed phages (of the order Caudovirales), two belonging to the family Myoviridae and the others assigned to the Podoviridae and Siphoviridae. Their genomes were sequenced to reveal a doubled stranded DNA topology with genome sizes ranging from 42 kb to 65 kb. In isolating and characterising these novel phages, we directed our efforts toward the development and use of these phages as candidates for phage therapy as an alternative strategy for the management or elimination of these pathogenic strains. Here we describe novel phage candidates for potential therapeutic treatment of MDR Australian clinical isolates of P. aeruginosa. MDPI 2022-01-19 /pmc/articles/PMC8875357/ /pubmed/35208664 http://dx.doi.org/10.3390/microorganisms10020210 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Namonyo, Samuel Carvalho, Gilda Guo, Jianhua Weynberg, Karen D. Novel Bacteriophages Show Activity against Selected Australian Clinical Strains of Pseudomonas aeruginosa |
title | Novel Bacteriophages Show Activity against Selected Australian Clinical Strains of Pseudomonas aeruginosa |
title_full | Novel Bacteriophages Show Activity against Selected Australian Clinical Strains of Pseudomonas aeruginosa |
title_fullStr | Novel Bacteriophages Show Activity against Selected Australian Clinical Strains of Pseudomonas aeruginosa |
title_full_unstemmed | Novel Bacteriophages Show Activity against Selected Australian Clinical Strains of Pseudomonas aeruginosa |
title_short | Novel Bacteriophages Show Activity against Selected Australian Clinical Strains of Pseudomonas aeruginosa |
title_sort | novel bacteriophages show activity against selected australian clinical strains of pseudomonas aeruginosa |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8875357/ https://www.ncbi.nlm.nih.gov/pubmed/35208664 http://dx.doi.org/10.3390/microorganisms10020210 |
work_keys_str_mv | AT namonyosamuel novelbacteriophagesshowactivityagainstselectedaustralianclinicalstrainsofpseudomonasaeruginosa AT carvalhogilda novelbacteriophagesshowactivityagainstselectedaustralianclinicalstrainsofpseudomonasaeruginosa AT guojianhua novelbacteriophagesshowactivityagainstselectedaustralianclinicalstrainsofpseudomonasaeruginosa AT weynbergkarend novelbacteriophagesshowactivityagainstselectedaustralianclinicalstrainsofpseudomonasaeruginosa |