Table 1.
Key biological aspects in phage–bacterium interaction that may affect clinical outcomes.
Biological mechanism | Biological role | Desired properties for therapy | Implications for therapy | Focus for improvement of clinical outcomes |
---|---|---|---|---|
Phage attachment | Infectivity (lytic activity) | High lytic activity: large burst size | Dosing and timing of administration | Diverse banks of characterized phages; genome engineering |
Receptor specificity | Infectivity (lytic activity; host range) | Defined host range | Targeting; clinical spectrum of activity (target bacteria); resistance | Personalized therapy; curated phage/bacteria banks; AI/machine learning approaches; phage cocktails; phage “training”; genome engineering |
Phage life cycle | Infectivity (lytic activity); transduction | High lytic activity; low transduction rates | Bacterial killing efficiency; transmission of virulence/resistance | Phage genomics; curated phage banks; genome engineering |
Bacterial cell physiological state/ density | Niche colonization and invasion | High lytic activity; high penetration | Dosing and timing of administration; phage/antibiotic synergy; target diseases | Smart delivery |
Bacterial lifestyle | Communal (biofilms); intracellular | High penetration | Penetration (target availability); clinical spectrum of activity (type of disease) | Smart delivery |
Co‐adaptation | Microbial evolution | Poor ability to elicit resistance; stable high infectivity | Resistance development | Phage–phage and phage–antibiotic synergy |