Optimizing concentration and timing of a phage spray application to reduce Listeria monocytogenes on honeydew melon

Britta Leverentz1, William S Conway, Wojciech Janisiewicz

  • 1Produce Quality and Safety, Henry A. Wallace Beltsville Agricultural Research Center, Agricultural Research Service, US Department of Agriculture, Beltsville, Maryland 20705, USA.

Insights

Applying bacteriophages (phages) before or immediately after contamination effectively controls Listeria monocytogenes on honeydew melon. Optimal control requires high phage concentrations and prompt application post-processing.

Area of Science:

  • Food microbiology
  • Bacteriophage applications
  • Food safety

Background:

  • Listeria monocytogenes is a significant foodborne pathogen, frequently contaminating fresh produce.
  • Bacteriophages offer a biological control method against bacterial contamination in food systems.
  • Timely application and concentration are critical factors for phage efficacy.

Purpose of the Study:

  • To determine the optimal timing and concentration of a phage cocktail for controlling Listeria monocytogenes on honeydew melon.
  • To evaluate the efficacy of phage application at various time points relative to contamination.
  • To assess the impact of phage concentration on pathogen reduction and growth suppression.

Main Methods:

  • Honeydew melon pieces were treated with a phage cocktail at different intervals before and after inoculation with Listeria monocytogenes.
  • Bacterial populations were enumerated after 7 days of storage at 10°C.
  • Phage efficacy was tested at concentrations ranging from 10^4 to 10^8 PFU/ml.
  • An attempt was made to enhance phage effectiveness on apple tissue using MnCl2.

Main Results:

  • Phage application was most effective when applied 0-1 hour before or at the time of contamination, reducing Listeria by up to 6.8 log units.
  • All tested phage concentrations (10^4–10^8 PFU/ml) reduced bacterial populations, with higher concentrations being more effective.
  • A concentration of approximately 10^8 PFU/ml was needed for immediate non-detectable levels, and suppressed growth throughout storage.
  • The combination of phage and MnCl2 did not enhance efficacy on apple tissue.

Conclusions:

  • Prompt application of bacteriophages, ideally before or immediately after contamination, is crucial for controlling Listeria monocytogenes on honeydew melon.
  • Optimizing phage efficacy requires a concentration of at least 10^8 PFU/ml and application within 1 hour post-processing.
  • Bacteriophages show significant potential as a food safety intervention for fresh produce.

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