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Evidence of Infection of Human Embryonic Stem Cells by SARS-CoV-2
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was initially described to target the respiratory system and now has been reported to infect a variety of cell types, including cardiomyocytes, neurons, hepatocytes, and gut enterocytes. However, it remains unclear whether the virus ca...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9226488/ https://www.ncbi.nlm.nih.gov/pubmed/35755832 http://dx.doi.org/10.3389/fcimb.2022.911313 |
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author | Zeng, Weijie Xing, Fan Ji, Yanxi Yang, Sidi Xu, Tiefeng Huang, Siyao Li, Chunmei Wu, Junyu Cao, Liu Guo, Deyin |
author_facet | Zeng, Weijie Xing, Fan Ji, Yanxi Yang, Sidi Xu, Tiefeng Huang, Siyao Li, Chunmei Wu, Junyu Cao, Liu Guo, Deyin |
author_sort | Zeng, Weijie |
collection | PubMed |
description | The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was initially described to target the respiratory system and now has been reported to infect a variety of cell types, including cardiomyocytes, neurons, hepatocytes, and gut enterocytes. However, it remains unclear whether the virus can directly infect human embryonic stem cells (hESCs) or early embryos. Herein, we sought to investigate this question in a cell-culture system of hESCs. Both the RNA and S protein of SARS-CoV-2 were detected in the infected hESCs and the formation of syncytium was observed. The increased level of subgenomic viral RNA and the presence of dsRNA indicate active replication of SARS-CoV-2 in hESCs. The increase of viral titers in the supernatants revealed virion release, further indicating the successful life cycle of SARS-CoV-2 in hESCs. Remarkably, immunofluorescence microscopy showed that only a small portion of hESCs were infected, which may reflect low expression of SARS-CoV-2 receptors. By setting |log2 (fold change)| > 0.5 as the threshold, a total of 1,566 genes were differentially expressed in SARS-CoV-2-infected hESCs, among which 17 interferon-stimulated genes (ISGs) were significantly upregulated. Altogether, our results provide novel evidence to support the ability of SARS-CoV-2 to infect and replicate in hESCs. |
format | Online Article Text |
id | pubmed-9226488 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92264882022-06-25 Evidence of Infection of Human Embryonic Stem Cells by SARS-CoV-2 Zeng, Weijie Xing, Fan Ji, Yanxi Yang, Sidi Xu, Tiefeng Huang, Siyao Li, Chunmei Wu, Junyu Cao, Liu Guo, Deyin Front Cell Infect Microbiol Cellular and Infection Microbiology The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was initially described to target the respiratory system and now has been reported to infect a variety of cell types, including cardiomyocytes, neurons, hepatocytes, and gut enterocytes. However, it remains unclear whether the virus can directly infect human embryonic stem cells (hESCs) or early embryos. Herein, we sought to investigate this question in a cell-culture system of hESCs. Both the RNA and S protein of SARS-CoV-2 were detected in the infected hESCs and the formation of syncytium was observed. The increased level of subgenomic viral RNA and the presence of dsRNA indicate active replication of SARS-CoV-2 in hESCs. The increase of viral titers in the supernatants revealed virion release, further indicating the successful life cycle of SARS-CoV-2 in hESCs. Remarkably, immunofluorescence microscopy showed that only a small portion of hESCs were infected, which may reflect low expression of SARS-CoV-2 receptors. By setting |log2 (fold change)| > 0.5 as the threshold, a total of 1,566 genes were differentially expressed in SARS-CoV-2-infected hESCs, among which 17 interferon-stimulated genes (ISGs) were significantly upregulated. Altogether, our results provide novel evidence to support the ability of SARS-CoV-2 to infect and replicate in hESCs. Frontiers Media S.A. 2022-06-10 /pmc/articles/PMC9226488/ /pubmed/35755832 http://dx.doi.org/10.3389/fcimb.2022.911313 Text en Copyright © 2022 Zeng, Xing, Ji, Yang, Xu, Huang, Li, Wu, Cao and Guo https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Zeng, Weijie Xing, Fan Ji, Yanxi Yang, Sidi Xu, Tiefeng Huang, Siyao Li, Chunmei Wu, Junyu Cao, Liu Guo, Deyin Evidence of Infection of Human Embryonic Stem Cells by SARS-CoV-2 |
title | Evidence of Infection of Human Embryonic Stem Cells by SARS-CoV-2 |
title_full | Evidence of Infection of Human Embryonic Stem Cells by SARS-CoV-2 |
title_fullStr | Evidence of Infection of Human Embryonic Stem Cells by SARS-CoV-2 |
title_full_unstemmed | Evidence of Infection of Human Embryonic Stem Cells by SARS-CoV-2 |
title_short | Evidence of Infection of Human Embryonic Stem Cells by SARS-CoV-2 |
title_sort | evidence of infection of human embryonic stem cells by sars-cov-2 |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9226488/ https://www.ncbi.nlm.nih.gov/pubmed/35755832 http://dx.doi.org/10.3389/fcimb.2022.911313 |
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