Abstract
<jats:title>Abstract</jats:title> <jats:p> Bacteriophage therapeutics are alternatives to antibiotics for treating multi-drug-resistant (MDR) bacterial infections. Bacteriophages kill host bacteria species with targeted precision, unlike the broad-spectrum nature of antibiotics. While the precision and the natural occurrence of phages in the environment have drawn attention to phages as new “drugs” in the time of accelerated antibiotic resistance, it remains poorly understood how phage treatment impacts the community of organisms composing the microbiome. Before phage therapies can be more widespread in practice, this understanding is required. <jats:italic>Caenorhabditis elegans</jats:italic> lends itself as an excellent model organism to address this question, as worm populations are raised under sterile conditions and the gut microbiome can be populated experimentally by the worms’ natural bacterivore diet. Here we have established a <jats:italic>C. elegans</jats:italic> infection and phage treatment model using fluorescent <jats:italic>Pseudomonas aeruginosa</jats:italic> PA14 to quantify infection. We isolated and whole genome sequenced PA14-specific lytic phage from wastewater samples near West Point, New York. To characterize the impact of treatment on the microbiome, we populated the <jats:italic>C. elegans</jats:italic> gut microbiome with 11 strains of the native <jats:italic>C. elegans</jats:italic> microbiome (CeMbio) and used PacBio sequencing of the full length 16S rRNA gene to characterize the microbiome during PA14 infection in the presence and absence of phage treatment ( <jats:italic>n</jats:italic> = 100 worms per sample, 4 replicates per condition). Taxonomic classification, phylogenetic analysis, and diversity analysis performed using a HiFi 16S bioinformatics pipeline revealed that phage treatment and infection level did not change the overall composition of the <jats:italic>C. elegans</jats:italic> gut microbiome. </jats:p> <jats:sec> <jats:title>Importance</jats:title> <jats:p> Multidrug resistant infections are emerging faster than new antibiotic compounds can be synthesized. Bacteriophages are natural viruses of bacteria that seek out and kill only their host bacteria species. Bacteriophage therapeutics are a promising solution for drug resistant infections in patients where no other treatment exists. However, while phage treatment is effective, there is little understanding about what happens within the complex community of the microbiome when a phage treatment is employed. Here we establish a new model utilizing <jats:italic>C. elegans</jats:italic> to integrate a multidrug resistant infection, phage treatment, and the native microbiome of the <jats:italic>C. elegans</jats:italic> worm to address how the microbiome changes in response to phage treatment. We find that the microbiome remains unchanged after bacteriophage treatment, highlighting the targeted specificity of phage therapy and suggests fewer side effects for phage therapy than antibiotic treatment for the same infection. </jats:p> </jats:sec>