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Clinical and Gene Features of SARS-CoV-2-Positive Recurrence in Patients Recovered From COVID-19
There are still frequent reports that a number of recovered coronavirus disease 2019 (COVID-19) patients following discharge have re-detectable positive (RP) results by RT-PCR. Understanding the clinical and molecular characteristics of RP patients may have implications for curbing the COVID-19 pand...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9217101/ https://www.ncbi.nlm.nih.gov/pubmed/35755819 http://dx.doi.org/10.3389/fmolb.2022.875418 |
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author | Peng, Yuying Wang, Shaoqi Chai, Ruihuan Chen, Yong Li, Nan Zeng, Boning Tang, Qian Zheng, Kai Liang, Youfang Xie, Shouxia Huang, Wei Wang, Shaoxiang Wang, Xiao |
author_facet | Peng, Yuying Wang, Shaoqi Chai, Ruihuan Chen, Yong Li, Nan Zeng, Boning Tang, Qian Zheng, Kai Liang, Youfang Xie, Shouxia Huang, Wei Wang, Shaoxiang Wang, Xiao |
author_sort | Peng, Yuying |
collection | PubMed |
description | There are still frequent reports that a number of recovered coronavirus disease 2019 (COVID-19) patients following discharge have re-detectable positive (RP) results by RT-PCR. Understanding the clinical and molecular characteristics of RP patients may have implications for curbing the COVID-19 pandemic. In this study, 318 COVID-19 convalescent patients, including 59 RP patients and 259 non-RP (NRP) patients, were enrolled. Among RP patients, women accounted for a significantly high proportion (67.8%), and the titers of IgG and IgM antibodies in this group were also significantly high. Differentially expressed genes (DEGs), including 692 upregulated and 383 downregulated genes, overlapped in two public GEO datasets containing RP and NRP blood cell samples. Enrichment analysis indicated that these DEGs were related to several key signaling pathways, such as viral infection, immune activation, and inflammatory responses. Importantly, 59 indicator genes constituting the core network exhibited high diagnostic values and were correlated with markers of different immune cells. Among these, 12 drug-related genes were associated with the RP results. Our work suggests that, in addition to clinically available features, blood cell transcriptome sequencing can be performed to obtain gene signatures for diagnosis of RP patients. |
format | Online Article Text |
id | pubmed-9217101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92171012022-06-23 Clinical and Gene Features of SARS-CoV-2-Positive Recurrence in Patients Recovered From COVID-19 Peng, Yuying Wang, Shaoqi Chai, Ruihuan Chen, Yong Li, Nan Zeng, Boning Tang, Qian Zheng, Kai Liang, Youfang Xie, Shouxia Huang, Wei Wang, Shaoxiang Wang, Xiao Front Mol Biosci Molecular Biosciences There are still frequent reports that a number of recovered coronavirus disease 2019 (COVID-19) patients following discharge have re-detectable positive (RP) results by RT-PCR. Understanding the clinical and molecular characteristics of RP patients may have implications for curbing the COVID-19 pandemic. In this study, 318 COVID-19 convalescent patients, including 59 RP patients and 259 non-RP (NRP) patients, were enrolled. Among RP patients, women accounted for a significantly high proportion (67.8%), and the titers of IgG and IgM antibodies in this group were also significantly high. Differentially expressed genes (DEGs), including 692 upregulated and 383 downregulated genes, overlapped in two public GEO datasets containing RP and NRP blood cell samples. Enrichment analysis indicated that these DEGs were related to several key signaling pathways, such as viral infection, immune activation, and inflammatory responses. Importantly, 59 indicator genes constituting the core network exhibited high diagnostic values and were correlated with markers of different immune cells. Among these, 12 drug-related genes were associated with the RP results. Our work suggests that, in addition to clinically available features, blood cell transcriptome sequencing can be performed to obtain gene signatures for diagnosis of RP patients. Frontiers Media S.A. 2022-06-08 /pmc/articles/PMC9217101/ /pubmed/35755819 http://dx.doi.org/10.3389/fmolb.2022.875418 Text en Copyright © 2022 Peng, Wang, Chai, Chen, Li, Zeng, Tang, Zheng, Liang, Xie, Huang, Wang and Wang. 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 | Molecular Biosciences Peng, Yuying Wang, Shaoqi Chai, Ruihuan Chen, Yong Li, Nan Zeng, Boning Tang, Qian Zheng, Kai Liang, Youfang Xie, Shouxia Huang, Wei Wang, Shaoxiang Wang, Xiao Clinical and Gene Features of SARS-CoV-2-Positive Recurrence in Patients Recovered From COVID-19 |
title | Clinical and Gene Features of SARS-CoV-2-Positive Recurrence in Patients Recovered From COVID-19 |
title_full | Clinical and Gene Features of SARS-CoV-2-Positive Recurrence in Patients Recovered From COVID-19 |
title_fullStr | Clinical and Gene Features of SARS-CoV-2-Positive Recurrence in Patients Recovered From COVID-19 |
title_full_unstemmed | Clinical and Gene Features of SARS-CoV-2-Positive Recurrence in Patients Recovered From COVID-19 |
title_short | Clinical and Gene Features of SARS-CoV-2-Positive Recurrence in Patients Recovered From COVID-19 |
title_sort | clinical and gene features of sars-cov-2-positive recurrence in patients recovered from covid-19 |
topic | Molecular Biosciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9217101/ https://www.ncbi.nlm.nih.gov/pubmed/35755819 http://dx.doi.org/10.3389/fmolb.2022.875418 |
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