Impact of pH and protein hydrophobicity on norovirus inactivation by heat-denatured lysozyme.
Amino Acid Sequence
Animals
Gene Expression Regulation
Hot Temperature
Hydrogen-Ion Concentration
Hydrophobic and Hydrophilic Interactions
Macrophages
/ virology
Mice
Muramidase
/ chemistry
Norovirus
/ physiology
Peptides
/ chemistry
Protein Denaturation
Protein Domains
RAW 264.7 Cells
Virus Inactivation
Journal
PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081
Informations de publication
Date de publication:
2020
2020
Historique:
received:
18
05
2020
accepted:
04
08
2020
entrez:
20
8
2020
pubmed:
20
8
2020
medline:
21
10
2020
Statut:
epublish
Résumé
Norovirus, the leading cause of non-bacterial food poisoning, is responsible for several outbreaks associated with bivalves and ready-to-eat food products worldwide. As norovirus is resistant to alcohol, which is commonly used in food manufacturing processes, sodium hypochlorite is used for its inactivation. However, sodium hypochlorite has two disadvantages: it cannot be added to foods, and its effect is significantly reduced in the presence of organic compounds. Thus, a novel disinfectant against norovirus is urgently required for food hygiene. Thermally denatured egg white lysozyme inactivates norovirus; however, the optimal inactivating conditions and the underlying mechanism are unclear. In the present study, the inactivating mechanism of heat-denatured lysozyme against norovirus was analyzed using murine norovirus strain 1 (MNV-1). We found that the inactivating effect was enhanced by adjusting the pH of the lysozyme solution before thermal denaturation to 6.5 or higher. The reaction of heat-denatured lysozyme and MNV-1 was irreversible, and norovirus was completely inactivated after exposure to heat-denatured lysozyme. Furthermore, it was found that lysozyme residues 5-39 contributed to the norovirus-inactivating effect. Notably, the hydrophobicity and positive charges in this region contributed to the norovirus-inactivating effect, as evidenced by the norovirus inactivation test using mutated residues 5-39. These findings are novel and highlight the possible application of heat-denatured lysozyme as a disinfectant against norovirus in a wide range of food processes.
Identifiants
pubmed: 32813716
doi: 10.1371/journal.pone.0237888
pii: PONE-D-20-14783
pmc: PMC7437907
doi:
Substances chimiques
Peptides
0
Muramidase
EC 3.2.1.17
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0237888Déclaration de conflit d'intérêts
One of the authors, Masahiro Ichikawa, is an employee of a commercial company (Kewpie Corporation). The funder, Kewpie Corporation, provided support in the form of salary for Masahiro Ichikawa but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. This does not alter the authors’ adherence to all of the PLOS ONE policies on sharing data and materials.
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