Comparative study on the inactivation of MS2 and M13 bacteriophages using energetic femtosecond lasers

Aziz Berchtikou1, Esen Sokullu1, Sharifun Nahar1

  • 1INRS - Centre Énergie Matériaux Télécommunications, Varennes, Québec, Canada.

Insights

Femtosecond laser inactivation of viruses shows shape-dependent efficiency. Near-spherical MS2 is inactivated by 400nm lasers, while filamentous M13 is more affected by 800nm lasers, revealing distinct viral inactivation mechanisms.

Area of Science:

  • Biophysics
  • Laser Physics
  • Virology

Background:

  • Femtosecond (fs) laser irradiation offers a non-ionizing method for virus inactivation.
  • Understanding virus inactivation mechanisms is crucial for developing novel antiviral strategies.

Purpose of the Study:

  • To compare the inactivation efficiency of fs laser pulses on two bacteriophages, MS2 (near-spherical) and M13 (filamentous), with different capsid structures.
  • To investigate the influence of laser wavelength (400 nm vs. 800 nm) and parameters on viral inactivation.
  • To elucidate the distinct inactivation mechanisms for viruses with varying geometric constraints.

Main Methods:

  • Inactivation of MS2 and M13 bacteriophages using energetic visible and near-infrared fs laser pulses.
  • Systematic variation of laser pulse energy, duration, and exposure time.
  • Analysis of viral capsid protein aggregation and genome exposure as indicators of inactivation.

Main Results:

  • 400 nm fs laser inactivation was significantly more efficient for MS2 than M13.
  • 800 nm fs laser inactivation showed slightly higher efficiency for M13 compared to MS2.
  • MS2 inactivation was dominated by capsid protein aggregation, while M13 inactivation involved breaking of secondary protein links.

Conclusions:

  • The geometric constraints and capsid properties of viruses influence their inactivation efficiency by fs lasers.
  • Different fs laser wavelengths and parameters can target specific viral structures and mechanisms.
  • Fs laser irradiation presents a versatile tool for virus inactivation, with mechanisms dependent on viral morphology.