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Virus and host-specific differences in oral human herpesvirus shedding kinetics among Ugandan women and children

Human herpesviruses (HHV) establish lifelong latent infection and are transmitted primarily via shedding at mucosal surfaces. Each HHV causes a unique spectrum of disease depending on the infected individual’s age and immunity. We collected weekly oral swabs from young children and mothers in 32 Uga...

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Autores principales: Matrajt, Laura, Gantt, Soren, Mayer, Bryan T., Krantz, Elizabeth M., Orem, Jackson, Wald, Anna, Corey, Lawrence, Schiffer, Joshua T., Casper, Corey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5638921/
https://www.ncbi.nlm.nih.gov/pubmed/29026166
http://dx.doi.org/10.1038/s41598-017-12994-0
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author Matrajt, Laura
Gantt, Soren
Mayer, Bryan T.
Krantz, Elizabeth M.
Orem, Jackson
Wald, Anna
Corey, Lawrence
Schiffer, Joshua T.
Casper, Corey
author_facet Matrajt, Laura
Gantt, Soren
Mayer, Bryan T.
Krantz, Elizabeth M.
Orem, Jackson
Wald, Anna
Corey, Lawrence
Schiffer, Joshua T.
Casper, Corey
author_sort Matrajt, Laura
collection PubMed
description Human herpesviruses (HHV) establish lifelong latent infection and are transmitted primarily via shedding at mucosal surfaces. Each HHV causes a unique spectrum of disease depending on the infected individual’s age and immunity. We collected weekly oral swabs from young children and mothers in 32 Ugandan households for a median of one year. We characterized kinetics of oral shedding during primary and chronic infection for each virus. Cytomegalovirus (CMV), Epstein-Barr virus (EBV), and HHV-6 were shed at high rates following primary infection. The rate of oral herpes simplex virus (HSV) shedding was lower overall, and children and mothers with chronic HSV infection had lower shedding rates than children with primary infection. CMV shedding rate and viral load were higher in children with primary infection compared to children with chronic infection, and even lower in mothers with chronic infection. HHV-6 shedding rate and viral load were similar between children with primary or chronic infection, but lower in mothers. EBV shedding rate and quantity decreased less dramatically in mothers versus children, with HIV-positive mothers shedding at a higher rate than HIV-negative mothers. Each HHV has a distinct pattern of oral shedding which depends partially on the age and immune status of the host.
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spelling pubmed-56389212017-10-18 Virus and host-specific differences in oral human herpesvirus shedding kinetics among Ugandan women and children Matrajt, Laura Gantt, Soren Mayer, Bryan T. Krantz, Elizabeth M. Orem, Jackson Wald, Anna Corey, Lawrence Schiffer, Joshua T. Casper, Corey Sci Rep Article Human herpesviruses (HHV) establish lifelong latent infection and are transmitted primarily via shedding at mucosal surfaces. Each HHV causes a unique spectrum of disease depending on the infected individual’s age and immunity. We collected weekly oral swabs from young children and mothers in 32 Ugandan households for a median of one year. We characterized kinetics of oral shedding during primary and chronic infection for each virus. Cytomegalovirus (CMV), Epstein-Barr virus (EBV), and HHV-6 were shed at high rates following primary infection. The rate of oral herpes simplex virus (HSV) shedding was lower overall, and children and mothers with chronic HSV infection had lower shedding rates than children with primary infection. CMV shedding rate and viral load were higher in children with primary infection compared to children with chronic infection, and even lower in mothers with chronic infection. HHV-6 shedding rate and viral load were similar between children with primary or chronic infection, but lower in mothers. EBV shedding rate and quantity decreased less dramatically in mothers versus children, with HIV-positive mothers shedding at a higher rate than HIV-negative mothers. Each HHV has a distinct pattern of oral shedding which depends partially on the age and immune status of the host. Nature Publishing Group UK 2017-10-12 /pmc/articles/PMC5638921/ /pubmed/29026166 http://dx.doi.org/10.1038/s41598-017-12994-0 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Matrajt, Laura
Gantt, Soren
Mayer, Bryan T.
Krantz, Elizabeth M.
Orem, Jackson
Wald, Anna
Corey, Lawrence
Schiffer, Joshua T.
Casper, Corey
Virus and host-specific differences in oral human herpesvirus shedding kinetics among Ugandan women and children
title Virus and host-specific differences in oral human herpesvirus shedding kinetics among Ugandan women and children
title_full Virus and host-specific differences in oral human herpesvirus shedding kinetics among Ugandan women and children
title_fullStr Virus and host-specific differences in oral human herpesvirus shedding kinetics among Ugandan women and children
title_full_unstemmed Virus and host-specific differences in oral human herpesvirus shedding kinetics among Ugandan women and children
title_short Virus and host-specific differences in oral human herpesvirus shedding kinetics among Ugandan women and children
title_sort virus and host-specific differences in oral human herpesvirus shedding kinetics among ugandan women and children
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5638921/
https://www.ncbi.nlm.nih.gov/pubmed/29026166
http://dx.doi.org/10.1038/s41598-017-12994-0
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