Optimization of bacteriophage propagation in high-yield continuous culture (cellstat) meeting the constraints of industrial manufacturing processes.

J Biosci Bioeng

IUT du Littoral Côte d'Opale, Département Génie Biologique, Université du Littoral Côte d'Opale, Bassin Napoléon B.P. 120, 63327 Boulogne-sur-Mer Cedex, France; Univ. Littoral Côte d'Opale, UMRt 1158 BioEcoAgro, USC ANSES, INRAe, Univ. Artois, Univ. Lille, Univ. Picardie Jules Verne, Univ. Liège, Junia, 62200 Boulogne-sur-Mer, France. Electronic address:

Published: December 2024

AI Article Synopsis

  • Scientists are finding new ways to use bacteriophages, which are viruses that can kill bacteria, in farming and medicine.
  • They created a simple method to produce these bacteriophages that factories can easily use.
  • By using special conditions, they were able to make a lot of a type of bacteriophage called T7, and they made it easier and cheaper for companies to do this.

Article Abstract

The growing use of bacteriophages in the fields of agriculture, agri-food, veterinary treatments, and medicine involves the quantitative production of these bacteriophages. In this study, we propose a bacteriophage production protocol that can easily be transposed to industry. We used a cellstat production system because the latest studies have shown that it is the most suitable process for the production of phages due to volumetric productivity, safety (limitation of co-evolution), and flexibility (choice of growth rate criteria). Sizing of the assembly used makes it possible to extrapolate the results to industrial production. The production conditions are indicated precisely, which would allow manufacturers to adapt the protocol to their own equipment. We propose experimental conditions in order to obtain a stable Escherichia coli population, qualitatively and over time, and production of high-titer T7 bacteriophages. The optimized production conditions (yield, cost and simplicity of the process) are: a buffered peptone water medium concentration of 11 g L and a dilution rate of 1.6 h. Under these conditions, we obtained a production of 7.35×10 plaque-forming units (PFU) L day with a concentration of 9.8×10 PFU mL. The strength of this work lies in its focus on industrial applicability.

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Source
http://dx.doi.org/10.1016/j.jbiosc.2024.09.001DOI Listing

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