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Cryptosporidium infection of human small intestinal epithelial cells induces type III interferon and impairs infectivity of Rotavirus
Cryptosporidiosis is a major cause of severe diarrheal disease in infants from resource poor settings. The majority of infections are caused by the human-specific pathogen C. hominis and absence of in vitro growth platforms has limited our understanding of host-pathogen interactions and development...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10491271/ https://www.ncbi.nlm.nih.gov/pubmed/37693422 http://dx.doi.org/10.1101/2023.08.30.555581 |
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author | Greigert, Valentin Saraav, Iti Son, Juhee Dayao, Denise Antia, Avan Tzipori, Saul Witola, William H. Stappenbeck, Thaddeus S. Ding, Siyuan Sibley, L. David |
author_facet | Greigert, Valentin Saraav, Iti Son, Juhee Dayao, Denise Antia, Avan Tzipori, Saul Witola, William H. Stappenbeck, Thaddeus S. Ding, Siyuan Sibley, L. David |
author_sort | Greigert, Valentin |
collection | PubMed |
description | Cryptosporidiosis is a major cause of severe diarrheal disease in infants from resource poor settings. The majority of infections are caused by the human-specific pathogen C. hominis and absence of in vitro growth platforms has limited our understanding of host-pathogen interactions and development of effective treatments. To address this problem, we developed a stem cell-derived culture system for C. hominis using human enterocytes differentiated under air-liquid interface (ALI) conditions. Human ALI cultures supported robust growth and complete development of C. hominis in vitro including all life cycle stages. C. hominis infection induced a strong interferon response from enterocytes, likely driven by an endogenous dsRNA virus in the parasite. Prior infection with Cryptosporidium induced type III IFN secretion and consequently blunted infection with Rotavirus, including live attenuated vaccine strains. The development of hALI provides a platform for further studies on human-specific pathogens, including clinically important coinfections that may alter vaccine efficacy. |
format | Online Article Text |
id | pubmed-10491271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-104912712023-09-09 Cryptosporidium infection of human small intestinal epithelial cells induces type III interferon and impairs infectivity of Rotavirus Greigert, Valentin Saraav, Iti Son, Juhee Dayao, Denise Antia, Avan Tzipori, Saul Witola, William H. Stappenbeck, Thaddeus S. Ding, Siyuan Sibley, L. David bioRxiv Article Cryptosporidiosis is a major cause of severe diarrheal disease in infants from resource poor settings. The majority of infections are caused by the human-specific pathogen C. hominis and absence of in vitro growth platforms has limited our understanding of host-pathogen interactions and development of effective treatments. To address this problem, we developed a stem cell-derived culture system for C. hominis using human enterocytes differentiated under air-liquid interface (ALI) conditions. Human ALI cultures supported robust growth and complete development of C. hominis in vitro including all life cycle stages. C. hominis infection induced a strong interferon response from enterocytes, likely driven by an endogenous dsRNA virus in the parasite. Prior infection with Cryptosporidium induced type III IFN secretion and consequently blunted infection with Rotavirus, including live attenuated vaccine strains. The development of hALI provides a platform for further studies on human-specific pathogens, including clinically important coinfections that may alter vaccine efficacy. Cold Spring Harbor Laboratory 2023-09-06 /pmc/articles/PMC10491271/ /pubmed/37693422 http://dx.doi.org/10.1101/2023.08.30.555581 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Greigert, Valentin Saraav, Iti Son, Juhee Dayao, Denise Antia, Avan Tzipori, Saul Witola, William H. Stappenbeck, Thaddeus S. Ding, Siyuan Sibley, L. David Cryptosporidium infection of human small intestinal epithelial cells induces type III interferon and impairs infectivity of Rotavirus |
title | Cryptosporidium infection of human small intestinal epithelial cells induces type III interferon and impairs infectivity of Rotavirus |
title_full | Cryptosporidium infection of human small intestinal epithelial cells induces type III interferon and impairs infectivity of Rotavirus |
title_fullStr | Cryptosporidium infection of human small intestinal epithelial cells induces type III interferon and impairs infectivity of Rotavirus |
title_full_unstemmed | Cryptosporidium infection of human small intestinal epithelial cells induces type III interferon and impairs infectivity of Rotavirus |
title_short | Cryptosporidium infection of human small intestinal epithelial cells induces type III interferon and impairs infectivity of Rotavirus |
title_sort | cryptosporidium infection of human small intestinal epithelial cells induces type iii interferon and impairs infectivity of rotavirus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10491271/ https://www.ncbi.nlm.nih.gov/pubmed/37693422 http://dx.doi.org/10.1101/2023.08.30.555581 |
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