About: SARS-CoV-2 infection and replication in human fetal and pediatric gastric organoids

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About: SARS-CoV-2 infection and replication in human fetal and pediatric gastric organoids Goto Sponge NotDistinct Permalink

An Entity of Type : schema:ScholarlyArticle, within Data Space : wasabi.inria.fr associated with source document(s)

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type	Academic Article research paper schema:ScholarlyArticle
isDefinedBy	Covid-on-the-Web dataset
title	SARS-CoV-2 infection and replication in human fetal and pediatric gastric organoids
Creator	Bonfante, Francesco Mazzetto, Eva De Coppi, Paolo Eaton, Simon Bortolami, Alessio Pagliari, Matteo Cacchiarelli, Davide Colantuono, Chiara Elvassore, Nicola Filippo, Lucio Gagliano, Onelia Giobbe, Giovanni Jones, Brendan Laterza, Cecilia Li, Wing Luni, Camilla Manfredi, Anna Pellegata, Alessandro Perin, Silvia Stuart, Hannah Sze, Vivian Thapar, Nikhil Zambaiti, Elisa
source	BioRxiv
abstract	Coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is a global public health emergency. COVID-19 typically manifests as a respiratory illness but an increasing number of clinical reports describe gastrointestinal (GI) symptoms. This is particularly true in children in whom GI symptoms are frequent and viral shedding outlasts viral clearance from the respiratory system. By contrast, fetuses seem to be rarely affected by COVID-19, although the virus has been detected in placentas of affected women. These observations raise the question of whether the virus can infect and replicate within the stomach once ingested. Moreover, it is not yet clear whether active replication of SARS-CoV-2 is possible in the stomach of children or in fetuses at different developmental stages. Here we show the novel derivation of fetal gastric organoids from 8-21 post-conception week (PCW) fetuses, and from pediatric biopsies, to be used as an in vitro model for SARS-CoV-2 gastric infection. Gastric organoids recapitulate human stomach with linear increase of gastric mucin 5AC along developmental stages, and expression of gastric markers pepsinogen, somatostatin, gastrin and chromogranin A. In order to investigate SARS-CoV-2 infection with minimal perturbation and under steady-state conditions, we induced a reversed polarity in the gastric organoids (RP-GOs) in suspension. In this condition of exposed apical polarity, the virus can easily access viral receptor angiotensin-converting enzyme 2 (ACE2). The pediatric RP-GOs are fully susceptible to infection with SARS-CoV-2, where viral nucleoprotein is expressed in cells undergoing programmed cell death, while the efficiency of infection is significantly lower in fetal organoids. The RP-GOs derived from pediatric patients show sustained robust viral replication of SARS-CoV-2, compared with organoids derived from fetal stomachs. Transcriptomic analysis shows a moderate innate antiviral response and the lack of differentially expressed genes belonging to the interferon family. Collectively, we established the first expandable human gastric organoid culture across fetal developmental stages, and we support the hypothesis that fetal tissue seems to be less susceptible to SARS-CoV-2 infection, especially in early stages of development. However, the virus can efficiently infect gastric epithelium in pediatric patients, suggesting that the stomach might have an active role in fecal-oral transmission of SARS-CoV-2.
has issue date	2020-06-24(xsd:dateTime)
bibo:doi	10.1101/2020.06.24.167049
has license	biorxiv
sha1sum (hex)	4290addb55b6185c446e20306079938f0caa14a3
schema:url	https://doi.org/10.1101/2020.06.24.167049
resource representing a document's title	SARS-CoV-2 infection and replication in human fetal and pediatric gastric organoids
schema:publication	bioRxiv
resource representing a document's body	covid:4290addb55b6185c446e20306079938f0caa14a3#body_text
is schema:about of	named entity 'SARS-CoV-2' named entity 'pediatric' named entity 'tissue' named entity 'raise' named entity 'organoids' named entity 'infection' named entity 'infection' named entity 'viral' named entity 'ACE2' named entity 'replicate' named entity 'replication' named entity 'hypothesis' named entity 'perturbation' named entity 'steady-state conditions' named entity 'fetuses' named entity 'FREQUENT' named entity 'NUCLEOPROTEIN' named entity 'IS A' named entity 'MARKERS' named entity 'INFECTION' named entity 'NUMBER OF' named entity 'PEDIATRIC' named entity 'SOMATOSTATIN' named entity 'CELLS' named entity 'CLINICAL REPORTS' named entity 'POLARITY' named entity 'BELONGING' named entity 'FETAL TISSUE' named entity 'MANIFESTS' named entity 'MODERATE' named entity 'CULTURE' named entity 'GENES' named entity 'TRUE' named entity 'RARELY' named entity 'COVID-19' named entity 'APICAL' named entity 'FULLY' named entity 'ANTIVIRAL RESPONSE' named entity 'DERIVATION' named entity 'MINIMAL' named entity 'ANALYSIS' named entity 'HUMAN' named entity 'INCREASE' named entity 'USED' named entity 'POSSIBLE' named entity 'CONDITIONS' named entity 'QUESTION' named entity 'GASTRIC MUCIN' named entity 'CONCEPTION' named entity 'NOVEL' named entity 'COMPARED' named entity 'efficiently' named entity 'derived' named entity 'belonging' named entity 'stomach' named entity 'pediatric' named entity 'manifests' named entity 'human' named entity 'viral' named entity 'order' named entity 'robust' named entity 'organoids'

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