Volume 13, Issue 10 e202000109
REVIEW ARTICLE

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

Aziz Berchtikou

Aziz Berchtikou

INRS – Centre Énergie Matériaux Télécommunications, Varennes, Québec, Canada

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Esen Sokullu

Esen Sokullu

INRS – Centre Énergie Matériaux Télécommunications, Varennes, Québec, Canada

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Sharifun Nahar

Sharifun Nahar

INRS – Centre Énergie Matériaux Télécommunications, Varennes, Québec, Canada

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Peter Tijssen

Peter Tijssen

INRS – Centre Armand-Frappier Santé Biotechnologie, Laval, Québec, Canada

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Marc A. Gauthier

Marc A. Gauthier

INRS – Centre Énergie Matériaux Télécommunications, Varennes, Québec, Canada

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Tsuneyuki Ozaki

Corresponding Author

Tsuneyuki Ozaki

INRS – Centre Énergie Matériaux Télécommunications, Varennes, Québec, Canada

Correspondence

Tsuneyuki Ozaki, INRS – Centre Énergie Matériaux Télécommunications, 1650 Boulevard Lionel-Boulet, Varennes, Québec J3X 1S2, Canada.

Email: [email protected]

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First published: 17 June 2020
Citations: 2

Funding information: Natural Sciences and Engineering Research Council (NSERC) of Canada

Abstract

Femtosecond (fs) laser irradiation techniques are emerging tools for inactivating viruses that do not involve ionizing radiation. In this work, the inactivation of two bacteriophages representing protective capsids with different geometric constraints, that is, the near-spherical MS2 (with a diameter of 27 nm) and the filamentous M13 (with a length of 880 nm) is compared using energetic visible and near-infrared fs laser pulses with various energies, pulse durations, and exposure times. Intriguingly, the results show that inactivation using 400 nm lasers is substantially more efficient for MS2 compared to M13. In contrast, using 800 nm lasers, M13 was slightly more efficiently inactivated. For both viruses, the genome was exposed to a harmful environment upon fs-laser irradiation. However, in addition to the protection of the genome, the metastable capsids differ in many properties required for stepwise cell entry that may explain their dissimilar behavior after (partial) disassembly. For MS2, the dominant mechanism of fs-laser inactivation was the aggregation of the viral capsid proteins, whereas aggregation did not affect M13 inactivation, suggesting that the dominant mechanism of M13 inactivation was related to breaking of secondary protein links.image

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