DOE OSTI · 3376524
HtPIP: High-throughput phage isolation platform increases diversity and reduces isolation time using multiple bacteria
Abstract
Bacteriophages are ubiquitous in nature, but relatively few have been isolated and characterized compared to the number of bacterial strains. Phage biotechnology applications benefit from a diverse library of isolated phages to kill or transfer genetic material to a bacterium of interest. However, scaling up phage discovery for diverse bacterial hosts can be time-consuming and costly. Here, we developed an approach to capture novel phages for multiple bacterial strains in parallel from an environmental sample using commercially available 0.2-μM filter plates. Using this High-throughput Phage Isolation Platform (HtPIP), 12 novel phages were isolated spanning 9 diverse bacterial host genera. Eleven of the isolated phages define new phage species, with nine also defining new genera. The HtPIP was used to discover both DNA and RNA phages, including a Tectiviridae infecting Pseudomonas putida mt-2 and a Leviviricetes infecting a Microbacterium isolate, which represents the first cultured RNA phage infecting a host outside of Proteobacteria. Using a metagenomic approach, we demonstrate that the HtPIP captures a higher proportion of novel phages compared to traditional low-throughput methods.
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Diaz, Benjamin Peter [Sandia National Laboratories (SNL-CA), Livermore, CA (United States)] (ORCID:0000000286746414), House, Tessa Olivia [Sandia National Laboratories (SNL-CA), Livermore, CA (United States)], Padala, Meghana Bhuvi [Sandia National Laboratories (SNL-CA), Livermore, CA (United States)], Schoeniger, Joseph Stephen [Sandia National Laboratories (SNL-CA), Livermore, CA (United States)] (ORCID:0000000227197435), Mageeney, Catherine Margaret [Sandia National Laboratories (SNL-CA), Livermore, CA (United States)] (ORCID:0000000179691622). 2026-06-18. HtPIP: High-throughput phage isolation platform increases diversity and reduces isolation time using multiple bacteria. https://doi.org/10.3389/fmicb.2026.1845440
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