As antibiotic-resistant infections increasingly threaten public health, interest in bacteriophages as therapeutics has seen a resurgence. However, laborious strain engineering techniques have limited the pace of discovery and the creation of tailored therapeutic strains.
In a PNAS study scheduled for publication on January 23rd, researchers from New England Biolabs and Yale University describe the first fully synthetic bacteriophage engineering system for Pseudomonas aeruginosa, an antibiotic-resistant bacterium of global concern.
By leveraging golden gate assembly, the method:
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Uses digital sequence data rather than bacteriophage isolates
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Removes the need to propagate physical phage isolates or specialized host bacteria
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Allows for many simultaneous edits instead of iterative editing
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Works with therapeutically relevant bacteriophages that have previously required extremely specialized expertise to study
A related study, which described engineering high-GC content Mycobacterium (tuberculosis) phages, was published in November, and a December study applied the method to engineer biosensing bacteriophages for detecting E. coli in drinking water.
Posted by Dr. Tim Sandle, Pharmaceutical Microbiology Resources (http://www.pharmamicroresources.com/)

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