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Protein-bound sialic acid in saliva contributes directly to salivary anti-influenza virus activity
The oral cavity is an entrance for respiratory viruses, such as influenza. Recently, saliva has been shown to exert both antimicrobial and antiviral activities. Thus, saliva may be a biological factor that contributes to the prevention of influenza infection. However, the actual salivary anti-influe...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033866/ https://www.ncbi.nlm.nih.gov/pubmed/35459785 http://dx.doi.org/10.1038/s41598-022-10559-4 |
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author | Kobayashi, Kaori Shono, Chika Mori, Takuya Kitazawa, Hidefumi Ota, Noriyasu Kurebayashi, Yuki Suzuki, Takashi |
author_facet | Kobayashi, Kaori Shono, Chika Mori, Takuya Kitazawa, Hidefumi Ota, Noriyasu Kurebayashi, Yuki Suzuki, Takashi |
author_sort | Kobayashi, Kaori |
collection | PubMed |
description | The oral cavity is an entrance for respiratory viruses, such as influenza. Recently, saliva has been shown to exert both antimicrobial and antiviral activities. Thus, saliva may be a biological factor that contributes to the prevention of influenza infection. However, the actual salivary anti-influenza A virus (IAV) activity in individuals and its determinant factors are unknown. By assessing individual variations in salivary anti-IAV activity in 92 people using an established new high-throughput system in this study, we found that the anti-IAV activity varied widely between individuals and showed a significant positive correlation with protein-bound sialic acid (BSA) level (ρ = 0.473; p < 0.001). Furthermore, the anti-IAV activity of saliva with enzymatically reduced BSA content was significantly lower. These results indicate that BSA is a direct regulator of salivary anti-IAV activity and is a determinant of individual differences. Additionally, after comparing the anti-IAV activity across the groups by age, anti-IAV activity in young people (aged 5–19 years) were lower than in adults aged 20–59 years and elderly people aged 60–79 years. Our study suggests that BSA levels in saliva may be important in preventing influenza infection. |
format | Online Article Text |
id | pubmed-9033866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90338662022-04-25 Protein-bound sialic acid in saliva contributes directly to salivary anti-influenza virus activity Kobayashi, Kaori Shono, Chika Mori, Takuya Kitazawa, Hidefumi Ota, Noriyasu Kurebayashi, Yuki Suzuki, Takashi Sci Rep Article The oral cavity is an entrance for respiratory viruses, such as influenza. Recently, saliva has been shown to exert both antimicrobial and antiviral activities. Thus, saliva may be a biological factor that contributes to the prevention of influenza infection. However, the actual salivary anti-influenza A virus (IAV) activity in individuals and its determinant factors are unknown. By assessing individual variations in salivary anti-IAV activity in 92 people using an established new high-throughput system in this study, we found that the anti-IAV activity varied widely between individuals and showed a significant positive correlation with protein-bound sialic acid (BSA) level (ρ = 0.473; p < 0.001). Furthermore, the anti-IAV activity of saliva with enzymatically reduced BSA content was significantly lower. These results indicate that BSA is a direct regulator of salivary anti-IAV activity and is a determinant of individual differences. Additionally, after comparing the anti-IAV activity across the groups by age, anti-IAV activity in young people (aged 5–19 years) were lower than in adults aged 20–59 years and elderly people aged 60–79 years. Our study suggests that BSA levels in saliva may be important in preventing influenza infection. Nature Publishing Group UK 2022-04-22 /pmc/articles/PMC9033866/ /pubmed/35459785 http://dx.doi.org/10.1038/s41598-022-10559-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kobayashi, Kaori Shono, Chika Mori, Takuya Kitazawa, Hidefumi Ota, Noriyasu Kurebayashi, Yuki Suzuki, Takashi Protein-bound sialic acid in saliva contributes directly to salivary anti-influenza virus activity |
title | Protein-bound sialic acid in saliva contributes directly to salivary anti-influenza virus activity |
title_full | Protein-bound sialic acid in saliva contributes directly to salivary anti-influenza virus activity |
title_fullStr | Protein-bound sialic acid in saliva contributes directly to salivary anti-influenza virus activity |
title_full_unstemmed | Protein-bound sialic acid in saliva contributes directly to salivary anti-influenza virus activity |
title_short | Protein-bound sialic acid in saliva contributes directly to salivary anti-influenza virus activity |
title_sort | protein-bound sialic acid in saliva contributes directly to salivary anti-influenza virus activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033866/ https://www.ncbi.nlm.nih.gov/pubmed/35459785 http://dx.doi.org/10.1038/s41598-022-10559-4 |
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