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Respiratory and intestinal epithelial cells exhibit differential susceptibility and innate immune responses to contemporary EV-D68 isolates

Enterovirus D68 (EV-D68) has been implicated in outbreaks of severe respiratory illness and is associated with acute flaccid myelitis (AFM). EV-D68 is often detected in patient respiratory samples but has also been detected in stool and wastewater, suggesting the potential for both respiratory and e...

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Autores principales: Freeman, Megan Culler, Wells, Alexandra I, Ciomperlik-Patton, Jessica, Myerburg, Michael M, Yang, Liheng, Konopka-Anstadt, Jennifer, Coyne, Carolyn B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285104/
https://www.ncbi.nlm.nih.gov/pubmed/34196272
http://dx.doi.org/10.7554/eLife.66687
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author Freeman, Megan Culler
Wells, Alexandra I
Ciomperlik-Patton, Jessica
Myerburg, Michael M
Yang, Liheng
Konopka-Anstadt, Jennifer
Coyne, Carolyn B
author_facet Freeman, Megan Culler
Wells, Alexandra I
Ciomperlik-Patton, Jessica
Myerburg, Michael M
Yang, Liheng
Konopka-Anstadt, Jennifer
Coyne, Carolyn B
author_sort Freeman, Megan Culler
collection PubMed
description Enterovirus D68 (EV-D68) has been implicated in outbreaks of severe respiratory illness and is associated with acute flaccid myelitis (AFM). EV-D68 is often detected in patient respiratory samples but has also been detected in stool and wastewater, suggesting the potential for both respiratory and enteric routes of transmission. Here, we used a panel of EV-D68 isolates, including a historical pre-2014 isolate and multiple contemporary isolates from AFM outbreak years, to define the dynamics of viral replication and the host response to infection in primary human airway cells and stem cell-derived enteroids. We show that some recent EV-D68 isolates have decreased sensitivity to acid and temperature compared with earlier isolates and that the respiratory, but not intestinal, epithelium induces a robust type III interferon response that restricts infection. Our findings define the differential responses of the respiratory and intestinal epithelium to contemporary EV-D68 isolates and suggest that a subset of isolates have the potential to target both the human airway and gastrointestinal tracts.
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spelling pubmed-82851042021-07-19 Respiratory and intestinal epithelial cells exhibit differential susceptibility and innate immune responses to contemporary EV-D68 isolates Freeman, Megan Culler Wells, Alexandra I Ciomperlik-Patton, Jessica Myerburg, Michael M Yang, Liheng Konopka-Anstadt, Jennifer Coyne, Carolyn B eLife Microbiology and Infectious Disease Enterovirus D68 (EV-D68) has been implicated in outbreaks of severe respiratory illness and is associated with acute flaccid myelitis (AFM). EV-D68 is often detected in patient respiratory samples but has also been detected in stool and wastewater, suggesting the potential for both respiratory and enteric routes of transmission. Here, we used a panel of EV-D68 isolates, including a historical pre-2014 isolate and multiple contemporary isolates from AFM outbreak years, to define the dynamics of viral replication and the host response to infection in primary human airway cells and stem cell-derived enteroids. We show that some recent EV-D68 isolates have decreased sensitivity to acid and temperature compared with earlier isolates and that the respiratory, but not intestinal, epithelium induces a robust type III interferon response that restricts infection. Our findings define the differential responses of the respiratory and intestinal epithelium to contemporary EV-D68 isolates and suggest that a subset of isolates have the potential to target both the human airway and gastrointestinal tracts. eLife Sciences Publications, Ltd 2021-07-01 /pmc/articles/PMC8285104/ /pubmed/34196272 http://dx.doi.org/10.7554/eLife.66687 Text en https://creativecommons.org/publicdomain/zero/1.0/This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (https://creativecommons.org/publicdomain/zero/1.0/) .
spellingShingle Microbiology and Infectious Disease
Freeman, Megan Culler
Wells, Alexandra I
Ciomperlik-Patton, Jessica
Myerburg, Michael M
Yang, Liheng
Konopka-Anstadt, Jennifer
Coyne, Carolyn B
Respiratory and intestinal epithelial cells exhibit differential susceptibility and innate immune responses to contemporary EV-D68 isolates
title Respiratory and intestinal epithelial cells exhibit differential susceptibility and innate immune responses to contemporary EV-D68 isolates
title_full Respiratory and intestinal epithelial cells exhibit differential susceptibility and innate immune responses to contemporary EV-D68 isolates
title_fullStr Respiratory and intestinal epithelial cells exhibit differential susceptibility and innate immune responses to contemporary EV-D68 isolates
title_full_unstemmed Respiratory and intestinal epithelial cells exhibit differential susceptibility and innate immune responses to contemporary EV-D68 isolates
title_short Respiratory and intestinal epithelial cells exhibit differential susceptibility and innate immune responses to contemporary EV-D68 isolates
title_sort respiratory and intestinal epithelial cells exhibit differential susceptibility and innate immune responses to contemporary ev-d68 isolates
topic Microbiology and Infectious Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285104/
https://www.ncbi.nlm.nih.gov/pubmed/34196272
http://dx.doi.org/10.7554/eLife.66687
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