The untapped potential of phage model systems as therapeutic agents.
作者信息
Romeyer Dherbey Jordan, Bertels Frederic
机构信息
Microbial Population Biology, Max Planck Institute for Evolutionary Biology, August-Thienemann-Straße 2, Plön, Schleswig-Holstein 24306, Germany.
出版信息
Virus Evol. 2024 Jan 13;10(1):veae007. doi: 10.1093/ve/veae007. eCollection 2024.
With the emergence of widespread antibiotic resistance, phages are an appealing alternative to antibiotics in the fight against multidrug-resistant bacteria. Over the past few years, many phages have been isolated from various environments to treat bacterial pathogens. While isolating novel phages for treatment has had some success for compassionate use, developing novel phages into a general therapeutic will require considerable time and financial resource investments. These investments may be less significant for well-established phage model systems. The knowledge acquired from decades of research on their structure, life cycle, and evolution ensures safe application and efficient handling. However, one major downside of the established phage model systems is their inability to infect pathogenic bacteria. This problem is not insurmountable; phage host range can be extended through genetic engineering or evolution experiments. In the future, breeding model phages to infect pathogens could provide a new avenue to develop phage therapeutic agents.
相似文献
Virus Evol. 2024-1-13
Antibiotics (Basel). 2021-2-19
Bacteriophage. 2013-1-1
Microbiol Spectr. 2022-2-23
Prog Mol Biol Transl Sci. 2023
Front Cell Infect Microbiol. 2019-2-18
mSystems. 2022-8-30
引用本文的文献
PLoS Comput Biol. 2025-2-4
bioRxiv. 2024-9-7
本文引用的文献
Annu Rev Virol. 2023-9-29
Science. 2023-7-14
Phage (New Rochelle). 2023-6-1
ACS Synth Biol. 2023-3-17
Arch Microbiol Immunol. 2022