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Enteric viruses replicate in salivary glands and infect through saliva
Enteric viruses like norovirus, rotavirus and astrovirus have long been accepted as spreading in the population through fecal–oral transmission: viruses are shed into feces from one host and enter the oral cavity of another, bypassing salivary glands (SGs) and reaching the intestines to replicate, b...
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/PMC9243862/ https://www.ncbi.nlm.nih.gov/pubmed/35768512 http://dx.doi.org/10.1038/s41586-022-04895-8 |
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author | Ghosh, S. Kumar, M. Santiana, M. Mishra, A. Zhang, M. Labayo, H. Chibly, A. M. Nakamura, H. Tanaka, T. Henderson, W. Lewis, E. Voss, O. Su, Y. Belkaid, Y. Chiorini, J. A. Hoffman, M. P. Altan-Bonnet, N. |
author_facet | Ghosh, S. Kumar, M. Santiana, M. Mishra, A. Zhang, M. Labayo, H. Chibly, A. M. Nakamura, H. Tanaka, T. Henderson, W. Lewis, E. Voss, O. Su, Y. Belkaid, Y. Chiorini, J. A. Hoffman, M. P. Altan-Bonnet, N. |
author_sort | Ghosh, S. |
collection | PubMed |
description | Enteric viruses like norovirus, rotavirus and astrovirus have long been accepted as spreading in the population through fecal–oral transmission: viruses are shed into feces from one host and enter the oral cavity of another, bypassing salivary glands (SGs) and reaching the intestines to replicate, be shed in feces and repeat the transmission cycle(1). Yet there are viruses (for example, rabies) that infect the SGs(2,3), making the oral cavity one site of replication and saliva one conduit of transmission. Here we report that enteric viruses productively and persistently infect SGs, reaching titres comparable to those in the intestines. We demonstrate that enteric viruses get released into the saliva, identifying a second route of viral transmission. This is particularly significant for infected infants, whose saliva directly transmits enteric viruses to their mothers’ mammary glands through backflow during suckling. This sidesteps the conventional gut–mammary axis route(4) and leads to a rapid surge in maternal milk secretory IgA antibodies(5,6). Lastly, we show that SG-derived spheroids(7) and cell lines(8) can replicate and propagate enteric viruses, generating a scalable and manageable system of production. Collectively, our research uncovers a new transmission route for enteric viruses with implications for therapeutics, diagnostics and importantly sanitation measures to prevent spread through saliva. |
format | Online Article Text |
id | pubmed-9243862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-92438622022-06-30 Enteric viruses replicate in salivary glands and infect through saliva Ghosh, S. Kumar, M. Santiana, M. Mishra, A. Zhang, M. Labayo, H. Chibly, A. M. Nakamura, H. Tanaka, T. Henderson, W. Lewis, E. Voss, O. Su, Y. Belkaid, Y. Chiorini, J. A. Hoffman, M. P. Altan-Bonnet, N. Nature Article Enteric viruses like norovirus, rotavirus and astrovirus have long been accepted as spreading in the population through fecal–oral transmission: viruses are shed into feces from one host and enter the oral cavity of another, bypassing salivary glands (SGs) and reaching the intestines to replicate, be shed in feces and repeat the transmission cycle(1). Yet there are viruses (for example, rabies) that infect the SGs(2,3), making the oral cavity one site of replication and saliva one conduit of transmission. Here we report that enteric viruses productively and persistently infect SGs, reaching titres comparable to those in the intestines. We demonstrate that enteric viruses get released into the saliva, identifying a second route of viral transmission. This is particularly significant for infected infants, whose saliva directly transmits enteric viruses to their mothers’ mammary glands through backflow during suckling. This sidesteps the conventional gut–mammary axis route(4) and leads to a rapid surge in maternal milk secretory IgA antibodies(5,6). Lastly, we show that SG-derived spheroids(7) and cell lines(8) can replicate and propagate enteric viruses, generating a scalable and manageable system of production. Collectively, our research uncovers a new transmission route for enteric viruses with implications for therapeutics, diagnostics and importantly sanitation measures to prevent spread through saliva. Nature Publishing Group UK 2022-06-29 2022 /pmc/articles/PMC9243862/ /pubmed/35768512 http://dx.doi.org/10.1038/s41586-022-04895-8 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Ghosh, S. Kumar, M. Santiana, M. Mishra, A. Zhang, M. Labayo, H. Chibly, A. M. Nakamura, H. Tanaka, T. Henderson, W. Lewis, E. Voss, O. Su, Y. Belkaid, Y. Chiorini, J. A. Hoffman, M. P. Altan-Bonnet, N. Enteric viruses replicate in salivary glands and infect through saliva |
title | Enteric viruses replicate in salivary glands and infect through saliva |
title_full | Enteric viruses replicate in salivary glands and infect through saliva |
title_fullStr | Enteric viruses replicate in salivary glands and infect through saliva |
title_full_unstemmed | Enteric viruses replicate in salivary glands and infect through saliva |
title_short | Enteric viruses replicate in salivary glands and infect through saliva |
title_sort | enteric viruses replicate in salivary glands and infect through saliva |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9243862/ https://www.ncbi.nlm.nih.gov/pubmed/35768512 http://dx.doi.org/10.1038/s41586-022-04895-8 |
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