Cargando…

Respiratory immune status and microbiome in recovered COVID-19 patients revealed by metatranscriptomic analyses

Coronavirus disease 2019 (COVID-19) is currently a severe threat to global public health, and the immune response to COVID-19 infection has been widely investigated. However, the immune status and microecological changes in the respiratory systems of patients with COVID-19 after recovery have rarely...

Descripción completa

Detalles Bibliográficos
Autores principales: Meng, Huan, Wang, Shuang, Tang, Xiaomeng, Guo, Jingjing, Xu, Xinming, Wang, Dagang, Jin, Fangfang, Zheng, Mei, Yin, Shangqi, He, Chaonan, Han, Ying, Chen, Jin, Han, Jinyu, Ren, Chaobo, Gao, Yantao, Liu, Huifang, Wang, Yajie, Jin, Ronghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9724627/
https://www.ncbi.nlm.nih.gov/pubmed/36483456
http://dx.doi.org/10.3389/fcimb.2022.1011672
_version_ 1784844459584782336
author Meng, Huan
Wang, Shuang
Tang, Xiaomeng
Guo, Jingjing
Xu, Xinming
Wang, Dagang
Jin, Fangfang
Zheng, Mei
Yin, Shangqi
He, Chaonan
Han, Ying
Chen, Jin
Han, Jinyu
Ren, Chaobo
Gao, Yantao
Liu, Huifang
Wang, Yajie
Jin, Ronghua
author_facet Meng, Huan
Wang, Shuang
Tang, Xiaomeng
Guo, Jingjing
Xu, Xinming
Wang, Dagang
Jin, Fangfang
Zheng, Mei
Yin, Shangqi
He, Chaonan
Han, Ying
Chen, Jin
Han, Jinyu
Ren, Chaobo
Gao, Yantao
Liu, Huifang
Wang, Yajie
Jin, Ronghua
author_sort Meng, Huan
collection PubMed
description Coronavirus disease 2019 (COVID-19) is currently a severe threat to global public health, and the immune response to COVID-19 infection has been widely investigated. However, the immune status and microecological changes in the respiratory systems of patients with COVID-19 after recovery have rarely been considered. We selected 72 patients with severe COVID-19 infection, 57 recovered from COVID-19 infection, and 65 with non-COVID-19 pneumonia, for metatranscriptomic sequencing and bioinformatics analysis. Accordingly, the differentially expressed genes between the infected and other groups were enriched in the chemokine signaling pathway, NOD-like receptor signaling pathway, phagosome, TNF signaling pathway, NF-kappa B signaling pathway, Toll-like receptor signaling pathway, and C-type lectin receptor signaling pathway. We speculate that IL17RD, CD74, and TNFSF15 may serve as disease biomarkers in COVID-19. Additionally, principal coordinate analysis revealed significant differences between groups. In particular, frequent co-infections with the genera Streptococcus, Veillonella, Gemella, and Neisseria, among others, were found in COVID-19 patients. Moreover, the random forest prediction model with differential genes showed a mean area under the curve (AUC) of 0.77, and KCNK12, IL17RD, LOC100507412, PTPRT, MYO15A, MPDZ, FLRT2, SPEG, SERPINB3, and KNDC1 were identified as the most important genes distinguishing the infected group from the recovered group. Agrobacterium tumefaciens, Klebsiella michiganensis, Acinetobacter pittii, Bacillus sp. FJAT.14266, Brevundimonas naejangsanensis, Pseudopropionibacterium propionicum, Priestia megaterium, Dialister pneumosintes, Veillonella rodentium, and Pseudomonas protegens were selected as candidate microbial markers for monitoring the recovery of COVID patients. These results will facilitate the diagnosis, treatment, and prognosis of COVID patients recovering from severe illness.
format Online
Article
Text
id pubmed-9724627
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-97246272022-12-07 Respiratory immune status and microbiome in recovered COVID-19 patients revealed by metatranscriptomic analyses Meng, Huan Wang, Shuang Tang, Xiaomeng Guo, Jingjing Xu, Xinming Wang, Dagang Jin, Fangfang Zheng, Mei Yin, Shangqi He, Chaonan Han, Ying Chen, Jin Han, Jinyu Ren, Chaobo Gao, Yantao Liu, Huifang Wang, Yajie Jin, Ronghua Front Cell Infect Microbiol Cellular and Infection Microbiology Coronavirus disease 2019 (COVID-19) is currently a severe threat to global public health, and the immune response to COVID-19 infection has been widely investigated. However, the immune status and microecological changes in the respiratory systems of patients with COVID-19 after recovery have rarely been considered. We selected 72 patients with severe COVID-19 infection, 57 recovered from COVID-19 infection, and 65 with non-COVID-19 pneumonia, for metatranscriptomic sequencing and bioinformatics analysis. Accordingly, the differentially expressed genes between the infected and other groups were enriched in the chemokine signaling pathway, NOD-like receptor signaling pathway, phagosome, TNF signaling pathway, NF-kappa B signaling pathway, Toll-like receptor signaling pathway, and C-type lectin receptor signaling pathway. We speculate that IL17RD, CD74, and TNFSF15 may serve as disease biomarkers in COVID-19. Additionally, principal coordinate analysis revealed significant differences between groups. In particular, frequent co-infections with the genera Streptococcus, Veillonella, Gemella, and Neisseria, among others, were found in COVID-19 patients. Moreover, the random forest prediction model with differential genes showed a mean area under the curve (AUC) of 0.77, and KCNK12, IL17RD, LOC100507412, PTPRT, MYO15A, MPDZ, FLRT2, SPEG, SERPINB3, and KNDC1 were identified as the most important genes distinguishing the infected group from the recovered group. Agrobacterium tumefaciens, Klebsiella michiganensis, Acinetobacter pittii, Bacillus sp. FJAT.14266, Brevundimonas naejangsanensis, Pseudopropionibacterium propionicum, Priestia megaterium, Dialister pneumosintes, Veillonella rodentium, and Pseudomonas protegens were selected as candidate microbial markers for monitoring the recovery of COVID patients. These results will facilitate the diagnosis, treatment, and prognosis of COVID patients recovering from severe illness. Frontiers Media S.A. 2022-11-22 /pmc/articles/PMC9724627/ /pubmed/36483456 http://dx.doi.org/10.3389/fcimb.2022.1011672 Text en Copyright © 2022 Meng, Wang, Tang, Guo, Xu, Wang, Jin, Zheng, Yin, He, Han, Chen, Han, Ren, Gao, Liu, Wang and Jin 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
Meng, Huan
Wang, Shuang
Tang, Xiaomeng
Guo, Jingjing
Xu, Xinming
Wang, Dagang
Jin, Fangfang
Zheng, Mei
Yin, Shangqi
He, Chaonan
Han, Ying
Chen, Jin
Han, Jinyu
Ren, Chaobo
Gao, Yantao
Liu, Huifang
Wang, Yajie
Jin, Ronghua
Respiratory immune status and microbiome in recovered COVID-19 patients revealed by metatranscriptomic analyses
title Respiratory immune status and microbiome in recovered COVID-19 patients revealed by metatranscriptomic analyses
title_full Respiratory immune status and microbiome in recovered COVID-19 patients revealed by metatranscriptomic analyses
title_fullStr Respiratory immune status and microbiome in recovered COVID-19 patients revealed by metatranscriptomic analyses
title_full_unstemmed Respiratory immune status and microbiome in recovered COVID-19 patients revealed by metatranscriptomic analyses
title_short Respiratory immune status and microbiome in recovered COVID-19 patients revealed by metatranscriptomic analyses
title_sort respiratory immune status and microbiome in recovered covid-19 patients revealed by metatranscriptomic analyses
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9724627/
https://www.ncbi.nlm.nih.gov/pubmed/36483456
http://dx.doi.org/10.3389/fcimb.2022.1011672
work_keys_str_mv AT menghuan respiratoryimmunestatusandmicrobiomeinrecoveredcovid19patientsrevealedbymetatranscriptomicanalyses
AT wangshuang respiratoryimmunestatusandmicrobiomeinrecoveredcovid19patientsrevealedbymetatranscriptomicanalyses
AT tangxiaomeng respiratoryimmunestatusandmicrobiomeinrecoveredcovid19patientsrevealedbymetatranscriptomicanalyses
AT guojingjing respiratoryimmunestatusandmicrobiomeinrecoveredcovid19patientsrevealedbymetatranscriptomicanalyses
AT xuxinming respiratoryimmunestatusandmicrobiomeinrecoveredcovid19patientsrevealedbymetatranscriptomicanalyses
AT wangdagang respiratoryimmunestatusandmicrobiomeinrecoveredcovid19patientsrevealedbymetatranscriptomicanalyses
AT jinfangfang respiratoryimmunestatusandmicrobiomeinrecoveredcovid19patientsrevealedbymetatranscriptomicanalyses
AT zhengmei respiratoryimmunestatusandmicrobiomeinrecoveredcovid19patientsrevealedbymetatranscriptomicanalyses
AT yinshangqi respiratoryimmunestatusandmicrobiomeinrecoveredcovid19patientsrevealedbymetatranscriptomicanalyses
AT hechaonan respiratoryimmunestatusandmicrobiomeinrecoveredcovid19patientsrevealedbymetatranscriptomicanalyses
AT hanying respiratoryimmunestatusandmicrobiomeinrecoveredcovid19patientsrevealedbymetatranscriptomicanalyses
AT chenjin respiratoryimmunestatusandmicrobiomeinrecoveredcovid19patientsrevealedbymetatranscriptomicanalyses
AT hanjinyu respiratoryimmunestatusandmicrobiomeinrecoveredcovid19patientsrevealedbymetatranscriptomicanalyses
AT renchaobo respiratoryimmunestatusandmicrobiomeinrecoveredcovid19patientsrevealedbymetatranscriptomicanalyses
AT gaoyantao respiratoryimmunestatusandmicrobiomeinrecoveredcovid19patientsrevealedbymetatranscriptomicanalyses
AT liuhuifang respiratoryimmunestatusandmicrobiomeinrecoveredcovid19patientsrevealedbymetatranscriptomicanalyses
AT wangyajie respiratoryimmunestatusandmicrobiomeinrecoveredcovid19patientsrevealedbymetatranscriptomicanalyses
AT jinronghua respiratoryimmunestatusandmicrobiomeinrecoveredcovid19patientsrevealedbymetatranscriptomicanalyses