Cargando…
Cilia-related gene signature in the nasal mucosa correlates with disease severity and outcomes in critical respiratory syncytial virus bronchiolitis
BACKGROUND: Respiratory syncytial virus (RSV) can cause life-threatening respiratory failure in infants. We sought to characterize the local host response to RSV infection in the nasal mucosa of infants with critical bronchiolitis and to identify early admission gene signatures associated with clini...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540395/ https://www.ncbi.nlm.nih.gov/pubmed/36211387 http://dx.doi.org/10.3389/fimmu.2022.924792 |
_version_ | 1784803698189271040 |
---|---|
author | Koch, Clarissa M. Prigge, Andrew D. Setar, Leah Anekalla, Kishore R. Do-Umehara, Hahn Chi Abdala-Valencia, Hiam Politanska, Yuliya Shukla, Avani Chavez, Jairo Hahn, Grant R. Coates, Bria M. |
author_facet | Koch, Clarissa M. Prigge, Andrew D. Setar, Leah Anekalla, Kishore R. Do-Umehara, Hahn Chi Abdala-Valencia, Hiam Politanska, Yuliya Shukla, Avani Chavez, Jairo Hahn, Grant R. Coates, Bria M. |
author_sort | Koch, Clarissa M. |
collection | PubMed |
description | BACKGROUND: Respiratory syncytial virus (RSV) can cause life-threatening respiratory failure in infants. We sought to characterize the local host response to RSV infection in the nasal mucosa of infants with critical bronchiolitis and to identify early admission gene signatures associated with clinical outcomes. METHODS: Nasal scrape biopsies were obtained from 33 infants admitted to the pediatric intensive care unit (PICU) with critical RSV bronchiolitis requiring non-invasive respiratory support (NIS) or invasive mechanical ventilation (IMV), and RNA sequencing (RNA-seq) was performed. Gene expression in participants who required shortened NIS (</= 3 days), prolonged NIS (> 3 days), and IMV was compared. FINDINGS: Increased expression of ciliated cell genes and estimated ciliated cell abundance, but not immune cell abundance, positively correlated with duration of hospitalization in infants with critical bronchiolitis. A ciliated cell signature characterized infants who required NIS for > 3 days while a basal cell signature was present in infants who required NIS for </= 3 days, despite both groups requiring an equal degree of respiratory support at the time of sampling. Infants who required invasive mechanical ventilation had increased expression of genes involved in neutrophil activation and cell death. INTERPRETATION: Increased expression of cilia-related genes in clinically indistinguishable infants with critical RSV may differentiate between infants who will require prolonged hospitalization and infants who will recover quickly. Validation of these findings in a larger cohort is needed to determine whether a cilia-related gene signature can predict duration of illness in infants with critical bronchiolitis. The ability to identify which infants with critical RSV bronchiolitis may require prolonged hospitalization using non-invasive nasal samples would provide invaluable prognostic information to parents and medical providers. |
format | Online Article Text |
id | pubmed-9540395 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95403952022-10-08 Cilia-related gene signature in the nasal mucosa correlates with disease severity and outcomes in critical respiratory syncytial virus bronchiolitis Koch, Clarissa M. Prigge, Andrew D. Setar, Leah Anekalla, Kishore R. Do-Umehara, Hahn Chi Abdala-Valencia, Hiam Politanska, Yuliya Shukla, Avani Chavez, Jairo Hahn, Grant R. Coates, Bria M. Front Immunol Immunology BACKGROUND: Respiratory syncytial virus (RSV) can cause life-threatening respiratory failure in infants. We sought to characterize the local host response to RSV infection in the nasal mucosa of infants with critical bronchiolitis and to identify early admission gene signatures associated with clinical outcomes. METHODS: Nasal scrape biopsies were obtained from 33 infants admitted to the pediatric intensive care unit (PICU) with critical RSV bronchiolitis requiring non-invasive respiratory support (NIS) or invasive mechanical ventilation (IMV), and RNA sequencing (RNA-seq) was performed. Gene expression in participants who required shortened NIS (</= 3 days), prolonged NIS (> 3 days), and IMV was compared. FINDINGS: Increased expression of ciliated cell genes and estimated ciliated cell abundance, but not immune cell abundance, positively correlated with duration of hospitalization in infants with critical bronchiolitis. A ciliated cell signature characterized infants who required NIS for > 3 days while a basal cell signature was present in infants who required NIS for </= 3 days, despite both groups requiring an equal degree of respiratory support at the time of sampling. Infants who required invasive mechanical ventilation had increased expression of genes involved in neutrophil activation and cell death. INTERPRETATION: Increased expression of cilia-related genes in clinically indistinguishable infants with critical RSV may differentiate between infants who will require prolonged hospitalization and infants who will recover quickly. Validation of these findings in a larger cohort is needed to determine whether a cilia-related gene signature can predict duration of illness in infants with critical bronchiolitis. The ability to identify which infants with critical RSV bronchiolitis may require prolonged hospitalization using non-invasive nasal samples would provide invaluable prognostic information to parents and medical providers. Frontiers Media S.A. 2022-09-23 /pmc/articles/PMC9540395/ /pubmed/36211387 http://dx.doi.org/10.3389/fimmu.2022.924792 Text en Copyright © 2022 Koch, Prigge, Setar, Anekalla, Do-Umehara, Abdala-Valencia, Politanska, Shukla, Chavez, Hahn and Coates 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 | Immunology Koch, Clarissa M. Prigge, Andrew D. Setar, Leah Anekalla, Kishore R. Do-Umehara, Hahn Chi Abdala-Valencia, Hiam Politanska, Yuliya Shukla, Avani Chavez, Jairo Hahn, Grant R. Coates, Bria M. Cilia-related gene signature in the nasal mucosa correlates with disease severity and outcomes in critical respiratory syncytial virus bronchiolitis |
title | Cilia-related gene signature in the nasal mucosa correlates with disease severity and outcomes in critical respiratory syncytial virus bronchiolitis |
title_full | Cilia-related gene signature in the nasal mucosa correlates with disease severity and outcomes in critical respiratory syncytial virus bronchiolitis |
title_fullStr | Cilia-related gene signature in the nasal mucosa correlates with disease severity and outcomes in critical respiratory syncytial virus bronchiolitis |
title_full_unstemmed | Cilia-related gene signature in the nasal mucosa correlates with disease severity and outcomes in critical respiratory syncytial virus bronchiolitis |
title_short | Cilia-related gene signature in the nasal mucosa correlates with disease severity and outcomes in critical respiratory syncytial virus bronchiolitis |
title_sort | cilia-related gene signature in the nasal mucosa correlates with disease severity and outcomes in critical respiratory syncytial virus bronchiolitis |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540395/ https://www.ncbi.nlm.nih.gov/pubmed/36211387 http://dx.doi.org/10.3389/fimmu.2022.924792 |
work_keys_str_mv | AT kochclarissam ciliarelatedgenesignatureinthenasalmucosacorrelateswithdiseaseseverityandoutcomesincriticalrespiratorysyncytialvirusbronchiolitis AT priggeandrewd ciliarelatedgenesignatureinthenasalmucosacorrelateswithdiseaseseverityandoutcomesincriticalrespiratorysyncytialvirusbronchiolitis AT setarleah ciliarelatedgenesignatureinthenasalmucosacorrelateswithdiseaseseverityandoutcomesincriticalrespiratorysyncytialvirusbronchiolitis AT anekallakishorer ciliarelatedgenesignatureinthenasalmucosacorrelateswithdiseaseseverityandoutcomesincriticalrespiratorysyncytialvirusbronchiolitis AT doumeharahahnchi ciliarelatedgenesignatureinthenasalmucosacorrelateswithdiseaseseverityandoutcomesincriticalrespiratorysyncytialvirusbronchiolitis AT abdalavalenciahiam ciliarelatedgenesignatureinthenasalmucosacorrelateswithdiseaseseverityandoutcomesincriticalrespiratorysyncytialvirusbronchiolitis AT politanskayuliya ciliarelatedgenesignatureinthenasalmucosacorrelateswithdiseaseseverityandoutcomesincriticalrespiratorysyncytialvirusbronchiolitis AT shuklaavani ciliarelatedgenesignatureinthenasalmucosacorrelateswithdiseaseseverityandoutcomesincriticalrespiratorysyncytialvirusbronchiolitis AT chavezjairo ciliarelatedgenesignatureinthenasalmucosacorrelateswithdiseaseseverityandoutcomesincriticalrespiratorysyncytialvirusbronchiolitis AT hahngrantr ciliarelatedgenesignatureinthenasalmucosacorrelateswithdiseaseseverityandoutcomesincriticalrespiratorysyncytialvirusbronchiolitis AT coatesbriam ciliarelatedgenesignatureinthenasalmucosacorrelateswithdiseaseseverityandoutcomesincriticalrespiratorysyncytialvirusbronchiolitis |