JD419, a Staphylococcus aureus Phage With a Unique Morphology and Broad Host Range

T Feng, S Leptihn, K Dong, B Loh, Y Zhang… - Frontiers in …, 2021 - frontiersin.org
T Feng, S Leptihn, K Dong, B Loh, Y Zhang, MI Stefan, M Li, X Guo, Z Cui
Frontiers in microbiology, 2021frontiersin.org
Phage therapy represents a possible treatment option to cure infections caused by multidrug-
resistant bacteria, including methicillin and vancomycin-resistant Staphylococcus aureus, to
which most antibiotics have become ineffective. In the present study, we report the isolation
and complete characterization of a novel phage named JD219 exhibiting a broad host range
able to infect 61 of 138 clinical strains of S. aureus tested, which included MRSA strains as
well. The phage JD419 exhibits a unique morphology with an elongated capsid and a …
Phage therapy represents a possible treatment option to cure infections caused by multidrug-resistant bacteria, including methicillin and vancomycin-resistant Staphylococcus aureus, to which most antibiotics have become ineffective. In the present study, we report the isolation and complete characterization of a novel phage named JD219 exhibiting a broad host range able to infect 61 of 138 clinical strains of S. aureus tested, which included MRSA strains as well. The phage JD419 exhibits a unique morphology with an elongated capsid and a flexible tail. To evaluate the potential of JD419 to be used as a therapeutic phage, we tested the ability of the phage particles to remain infectious after treatment exceeding physiological pH or temperature. The activity was retained at pH values of 6.0–8.0 and below 50°C. As phages can contain virulence genes, JD419’s complete genome was sequenced. The 45509 bp genome is predicted to contain 65 ORFs, none of which show homology to any known virulence or antibiotic resistance genes. Genome analysis indicates that JD419 is a temperate phage, despite observing rapid replication and lysis of host strains. Following the recent advances in synthetic biology, JD419 can be modified by gene engineering to remove prophage-related genes, preventing potential lysogeny, in order to be deployed as a therapeutic phage.
Frontiers
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