A Flexible and Efficient Microfluidics Platform for the Characterization and Isolation of Novel Bacteriophages.

Adam Sidi Mabrouk, Véronique Ongenae, Dennis Claessen, Susanne Brenzinger, Ariane Briegel
Author Information
  1. Adam Sidi Mabrouk: Department of Microbial Sciences, Institute of Biology, Leiden University, Leiden, The Netherlands. ORCID
  2. Véronique Ongenae: Department of Microbial Sciences, Institute of Biology, Leiden University, Leiden, The Netherlands. ORCID
  3. Dennis Claessen: Department of Microbial Sciences, Institute of Biology, Leiden University, Leiden, The Netherlands. ORCID
  4. Susanne Brenzinger: Department of Microbiology, University of Würzburg, Biocenter, Würzburg, Germany. ORCID
  5. Ariane Briegel: Department of Microbial Sciences, Institute of Biology, Leiden University, Leiden, The Netherlands. ORCID

Abstract

Bacteriophages are viruses that infect bacteria. This property makes them highly suitable for varied uses in industry or in the development of the treatment of bacterial infections. However, the conventional methods that are used to isolate and analyze these bacteriophages from the environment are generally cumbersome and time consuming. Here, we adapted a high-throughput microfluidic setup for long-term analysis of bacteriophage-bacteria interaction and demonstrate isolation of phages from environmental samples. Bacteriophages are gaining increased attention for their potential application as agents to combat antibiotic-resistant infections. However, isolation and characterization of new phages are time consuming and limited by currently used methods. The microfluidics platform presented here allows the isolation and long-term analysis of phages and their effect on host cells with fluorescent light microscopy imaging. Furthermore, this new workflow allows high-throughput characterization of environmental samples for the identification of phages alongside gaining detailed insight into the host response. Taken together, this microfluidics platform will be a valuable tool for phage research, enabling faster and more efficient screening and characterization of host-phage interactions.

Keywords

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MeSH Term

Humans
Bacteriophages
Microfluidics
Bacterial Infections
Bacteria

Word Cloud

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