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Published on: October 14, 2011
Completing the BASEL phage collection to unlock hidden diversity for systematic exploration of phage-host
Dorentina Humolli1, Damien Piel1, Enea Maffei1,2
1Institute of Food, Nutrition, and Health (IFNH), ETH Zürich, Zürich, Switzerland.
Abstract:
Research on bacteriophages, the viruses infecting bacteria, has fueled the development of modern molecular biology and inspired their therapeutic application to combat bacterial multidrug resistance. However, most work has so far focused on a few model phages which impedes direct applications of these findings in clinics and suggests that a vast potential of powerful molecular biology has remained untapped. We have therefore recently composed the BASEL collection of Escherichia coli phages (BActeriophage SElection for your Laboratory), which made a relevant diversity of phages infecting the E. coli K-12 laboratory strain accessible to the community. These phages are widely used, but their assorted diversity has remained limited by the E. coli K-12 host. We have therefore now genetically overcome the two major limitations of E. coli K-12, its lack of O-antigen glycans and the presence of resident bacterial immunity. Restoring O-antigen expression resulted in the isolation of diverse additional viral groups like Kagunavirus, Nonanavirus, Gordonclarkvirinae, and Gamaleyavirus, while eliminating all known antiviral defenses of E. coli K-12 additionally enabled us to isolate phages of Wifcevirus genus. Even though some of these viral groups appear to be common in nature, no phages from any of them had previously been isolated using E. coli laboratory strains, and they had thus remained largely understudied. Overall, 37 new phage isolates have been added to complete the BASEL collection. These phages were deeply characterized genomically and phenotypically with regard to host receptors, sensitivity to antiviral defense systems, and host range. Our results highlighted dominant roles of the O-antigen barrier for viral host recognition and of restriction-modification systems in bacterial immunity. We anticipate that the completed BASEL collection will propel research on phage-host interactions and their molecular mechanisms, deepening our understanding of viral ecology and fostering innovations in biotechnology and antimicrobial therapy.
Insights
Researchers expanded the BASEL collection of Escherichia coli phages by overcoming host limitations. This work isolated new viral groups, enhancing phage research for biotechnology and antimicrobial therapy.
Area of Science:
- Virology
- Microbiology
- Molecular Biology
Background:
- Bacteriophage research is crucial for molecular biology and combating antibiotic resistance.
- Limited diversity of commonly studied phages hinders clinical applications.
- The BASEL collection initially focused on Escherichia coli K-12 phages.
Purpose of the Study:
- To overcome limitations of the E. coli K-12 host strain.
- To expand the diversity of isolated phages for research.
- To deepen understanding of phage-host interactions and their mechanisms.
Main Methods:
- Genetically modified E. coli K-12 to restore O-antigen expression.
- Eliminated bacterial antiviral defenses (e.g., restriction-modification systems).
- Isolated and characterized new phage isolates genomically and phenotypically.
Main Results:
- Isolated novel phage groups including Kagunavirus, Nonanavirus, Gordonclarkvirinae, Gamaleyavirus, and Wifcevirus.
- Added 37 new phage isolates to the BASEL collection.
- Demonstrated the importance of O-antigen and restriction-modification systems in phage-host interactions.
Conclusions:
- The expanded BASEL collection provides access to understudied phages.
- This resource will advance research in viral ecology, biotechnology, and phage therapy.
- Understanding phage-host interactions is key for developing novel antimicrobial strategies.
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