Abstract

Background: The worldwide antibiotic crisis has led to a renewed interest in phage therapy. Lytic phages against bacterial pathogens can be isolated from the environment or selected from a collection in a matter of days. Product discovery costs are very low, but conventional biopharmaceutical production of phages is lengthy, complex and costly. In addition, phage treatment in low-income countries with poor infrastructure, battlefields, healthcare emergency situations (e.g. the 2012 foodborne E. coli 0104:H4 outbreak in Germany) demands a fast, global and decentralized access to phages. To address this demand, we developed a single-use, pre-sterilised, portable and closed biomanufacturing platform for therapeutic phage preparations. Methods & Materials: The basic components of this platform are as follows: a stacked bioreactor vessel with an adaptable number of chambers, in which the host bacterial strain, phage seed, culture medium (soft agar overlay technique) and extraction buffer are injected, is connected to (a) a cascade of clarification, purification and sterilisation filters, (b) phage vent filters, (c) tubings and connectors and (d) a filling system to dispense the final phage suspension into recipients. The following devices are necessary: a peristaltic pump, a fridge, a shaker and an incubator. Twenty-four different prototype assemblies for the production of Pseudomonas aeruginosa phages were tested. The following parameters were measured: pressure in function of volumetric throughput, phage yield and titre, endotoxin level, pH and assembly integrity (leaks). Results: The most suitable of the 24 tested prototype assemblies (presented at the conference) allowed for the production of 1-200 L (per bioreactor chamber) of phage suspension at a concentration of 107 pfu/ml with endotoxin levels and pH compatible with intravenous (IV) application, and this in 24 to 36 h. Conclusion: We developed a small-scale, portable and disposable biomanufacturing platform that allows for bacterial infection treatment at point-of-care, in short time frames, and at low cost, especially useful in remote locations with limited infrastructure since it does not necessarily require a cleanroom environment. MM and HVR contributed equally to this work. Funding: Grant HFM 15-5 of the Royal Higher Institute for Defense.

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