Abstract

Antibiotic resistant bacterial pathogens are increasingly prevalent, driving the need for alternative approaches to chemical antibiotics when treating infections. One such approach is bacteriophage therapy: the use of bacteria-specific viruses that lyse (kill) their host cells. Just as the effect of environmental conditions (e.g. elevated temperature) on antibiotic efficacy is well-studied, the effect of environmental stressors on the potency of phage therapy candidates demands examination. Therapeutic phage OMKO1 infects and kills the opportunistic human pathogen Pseudomonas aeruginosa. Here, we used phage OMKO1 as a model to test how environmental stressors can lead to damage and decay of virus particles. We assessed the effects of elevated temperatures, saline concentrations, and urea concentrations. We observed that OMKO1 particles were highly tolerant to different saline concentrations, but decayed more rapidly at elevated temperatures and under high concentrations of urea. Additionally, we found that exposure to elevated temperature reduced the ability of surviving phage particles to suppress the growth of P. aeruginosa, suggesting a temperature-induced damage. Our findings demonstrate that OMKO1 is highly tolerant to a range of conditions that could be experienced inside and outside the human body, while also showing the need for careful characterization of therapeutic phages to ensure that environmental exposure does not compromise their expected potency, dosing, and pharmacokinetics.

Highlights

  • Widespread use of antibiotics– in human therapy and animal agriculture–has selected for the evolution of multi-drug resistant bacterial pathogens, commonly associated with poorer prognosis and higher morbidity in human infections [1, 2]

  • We found that phage particles which survived elevated temperatures had reduced fitness, as measured by their ability to suppress the growth of susceptible bacterial cells (Fig 1C)

  • Along with the observed abnormal plaque morphology after heat shock, these results indicate a strong plastic response of phage fitness to high temperature exposure

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Summary

Introduction

Widespread use of antibiotics– in human therapy and animal agriculture–has selected for the evolution of multi-drug resistant bacterial pathogens, commonly associated with poorer prognosis and higher morbidity in human infections [1, 2]. One alternative or complementary approach to treating bacterial infections with chemical antibiotics is bacteriophage therapy [3], where bacteria-specific viruses with lytic replication cycles are used to kill (lyse) target bacterial cells. Like antibiotic molecules, can be sensitive to environmental conditions. Just as past work has assessed the sensitivity of chemical antibiotics to conditions like high temperature [4,5,6,7], it is important to observe how phage particle.

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