Exploring non-alcohol-based disinfectant: virucidal efficacy of arginine and Zinc chloride against feline calicivirus

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Exploring non-alcohol-based disinfectant: virucidal efficacy of arginine and Zinc chloride against feline calicivirus
Title:
Exploring non-alcohol-based disinfectant: virucidal efficacy of arginine and Zinc chloride against feline calicivirus
Journal Title:
Frontiers in Microbiology
Publication Date:
13 February 2025
Citation:
Kong Li Ying, M., Masirevic, S., Tan, Y. W., Marzinek, J. K., Fox, S. J., Verma, C. S., Bond, P. J., Ishida, Y., Liu, J., Chua, C. S., & Chu, J. J. H. (2025). Exploring non-alcohol-based disinfectant: virucidal efficacy of arginine and Zinc chloride against feline calicivirus. Frontiers in Microbiology, 16. https://doi.org/10.3389/fmicb.2025.1550295
Abstract:
IntroductionNorovirus, a leading cause of acute gastroenteritis worldwide, is notably stable in the environment due to its non-enveloped nature. In the absence of effective vaccines or treatments, disinfection remains the primary prevention strategy, highlighting the importance of virucidal efficacy in household care products. Conventional effective disinfectants are predominantly alcohol-based, but alcohol is known to pose health risks, such as skin irritation. This study investigates a non-alcohol-based alternative, specifically a combination of Arginine and Zinc chloride (ZnCl2).MethodsUtilizing MS2 bacteriophage as a surrogate, we identified a robust combination of arginine and ZnCl2 that is effective against Feline Calicivirus (FCV), a mammalian virus surrogate model for Norovirus.ResultsOur results determined a 5 min contact time at pH 11 as optimal, achieving significant virucidal activity against FCV without pH-induced reversibility. Dynamic Light Scattering (DLS) and transmission electron microscopy (TEM) analyses suggested that the mechanism of action for the Arg-Zn2+-Arg complex does not involve capsid disruption. Further insights from molecular modeling studies revealed that the complex potentially inhibits FCV by occupying a key capsid binding pocket essential for Junctional Adhesion Molecule (JAM) receptor engagement, thereby preventing viral entry.ConclusionThese findings allow us to propose a novel and non-alcohol-based virucidal approach against viruses from the Caliciviridae family, highlighting the potential of Arg-Zn2+-Arg complexes in public health protection.
License type:
Attribution 4.0 International (CC BY 4.0)
Funding Info:
This research / project is supported by the Biomedical Research Council, A*STAR - NA
Grant Reference no. : C232316018

This research / project is supported by the A*STAR-P&G collaborations - NA
Grant Reference no. : APG2013-112 / C22HA16013
Description:
©2025 KongLi Ying, Masirevic, Tan, Marzinek, Fox, Verma, Bond, Ishida, Liu, Chua and Chu. This is an open-access article distributed under the terms of the Creative CommonsAttribution License (CC BY). This paper was first published by Frontiers Media at https://doi.org/10.3389/fmicb.2025.1550295
ISSN:
1664-302X
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