Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2018 Mar 30;10(4):163.
doi: 10.3390/v10040163.

In Vitro Characteristics of Phages to Guide 'Real Life' Phage Therapy Suitability

Affiliations
Review

In Vitro Characteristics of Phages to Guide 'Real Life' Phage Therapy Suitability

Eoghan Casey et al. Viruses. .

Abstract

The increasing problem of antibiotic-resistant pathogens has put enormous pressure on healthcare providers to reduce the application of antibiotics and to identify alternative therapies. Phages represent such an alternative with significant application potential, either on their own or in combination with antibiotics to enhance the effectiveness of traditional therapies. However, while phage therapy may offer exciting therapeutic opportunities, its evaluation for safe and appropriate use in humans needs to be guided initially by reliable and appropriate assessment techniques at the laboratory level. Here, we review the process of phage isolation and the application of individual pathogens or reference collections for the development of specific or "off-the-shelf" preparations. Furthermore, we evaluate current characterization approaches to assess the in vitro therapeutic potential of a phage including its spectrum of activity, genome characteristics, storage and administration requirements and effectiveness against biofilms. Lytic characteristics and the ability to overcome anti-phage systems are also covered. These attributes direct phage selection for their ultimate application as antimicrobial agents. We also discuss current pitfalls in this research area and propose that priority should be given to unify current phage characterization approaches.

Keywords: antibiotic-resistance; biofilms; genomics; lysins; pH stability; phage preparation; phage-host interactions.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Suggested workflow for selection of phage therapy candidates, from isolation to implementation including desirable in vitro phenotypes.

References

    1. D’Hérelle F. Sur un microbe invisible antagoniste des bacilles dysentérique. Acad. Sci. Paris. 1917;165:373–375.
    1. Twort F. An investigation on the nature of ultra-microscopic viruses. Lancet. 1915;186:1241–1243. doi: 10.1016/S0140-6736(01)20383-3. - DOI - PMC - PubMed
    1. Duckworth D.H. Who discovered bacteriophage? Bacteriol. Rev. 1976;40:793. - PMC - PubMed
    1. Sabouri S., Sepehrizadeh Z., Amirpour-Rostami S., Skurnik M. A minireview on the in vitro and in vivo experiments with anti-Escherichia coli O157:H7 phages as potential biocontrol and phage therapy agents. Int. J. Food Microbiol. 2017;243:52–57. doi: 10.1016/j.ijfoodmicro.2016.12.004. - DOI - PubMed
    1. Rose T., Verbeken G., De Vos D., Merabishvili M., Vaneechoutte M., Lavigne R., Jennes S., Zizi M., Pirnay J.-P. Experimental phage therapy of burn wound infection: Difficult first steps. Int. J. Burns Trauma. 2014;4:66. - PMC - PubMed

Publication types

MeSH terms