Efficacy and mechanisms of murine norovirus inhibition by pulsed-light technology

Allison Vimont1, Ismaïl Fliss1, Julie Jean2

  • 1Institute of Nutrition and Functional Foods, Université Laval, Québec, Québec, Canada.

Insights

Pulsed light effectively inactivates murine norovirus 1 (MNV-1), a human norovirus surrogate, across various conditions. This nonthermal technology shows promise for disinfecting water and food contact surfaces, even with biofilms.

Area of Science:

  • Food Science and Technology
  • Microbiology
  • Water Treatment

Background:

  • Pulsed light (PL) is an FDA-approved nonthermal technology for microbial inactivation on food.
  • Human noroviruses are significant foodborne pathogens, necessitating effective inactivation methods.
  • Murine norovirus 1 (MNV-1) serves as a reliable surrogate for studying human norovirus inactivation.

Purpose of the Study:

  • To evaluate the efficacy of pulsed light for inactivating MNV-1.
  • To assess inactivation in diverse aqueous matrices and on food contact surfaces.
  • To elucidate the mechanisms underlying pulsed light's antiviral activity.

Main Methods:

  • MNV-1 suspensions and surface treatments were exposed to pulsed light (broad spectrum, 200-1000 nm).
  • Inactivation was tested in various water types (PBS, hard, mineral, turbid, effluent) and on surfaces (HDPE, PVC, stainless steel).
  • Viral structure, protein, and RNA integrity were analyzed post-treatment.

Main Results:

  • Over 3 log10 reduction in viral infectivity achieved in <3s on clean surfaces and in clear suspensions.
  • Effective inactivation (over 3 log10) observed within 6s on fouled surfaces, except stainless steel.
  • Pulsed light disrupted MNV-1 morphology, degraded viral proteins, and damaged RNA.

Conclusions:

  • Pulsed light is a highly effective nonthermal technology for inactivating MNV-1.
  • It offers a viable alternative for disinfecting wastewaters, beverages, drinking water, and food-handling surfaces.
  • Mechanisms involve structural disruption and biomolecular degradation of the virus.