Cargando…
Age-Related Changes in the Nasopharyngeal Microbiome Are Associated With Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and Symptoms Among Children, Adolescents, and Young Adults
BACKGROUND: Children are less susceptible to SARS-CoV-2 infection and typically have milder illness courses than adults, but the factors underlying these age-associated differences are not well understood. The upper respiratory microbiome undergoes substantial shifts during childhood and is increasi...
Autores principales: | , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8903463/ https://www.ncbi.nlm.nih.gov/pubmed/35247047 http://dx.doi.org/10.1093/cid/ciac184 |
_version_ | 1784664746054647808 |
---|---|
author | Hurst, Jillian H McCumber, Alexander W Aquino, Jhoanna N Rodriguez, Javier Heston, Sarah M Lugo, Debra J Rotta, Alexandre T Turner, Nicholas A Pfeiffer, Trevor S Gurley, Thaddeus C Moody, M Anthony Denny, Thomas N Rawls, John F Clark, James S Woods, Christopher W Kelly, Matthew S |
author_facet | Hurst, Jillian H McCumber, Alexander W Aquino, Jhoanna N Rodriguez, Javier Heston, Sarah M Lugo, Debra J Rotta, Alexandre T Turner, Nicholas A Pfeiffer, Trevor S Gurley, Thaddeus C Moody, M Anthony Denny, Thomas N Rawls, John F Clark, James S Woods, Christopher W Kelly, Matthew S |
author_sort | Hurst, Jillian H |
collection | PubMed |
description | BACKGROUND: Children are less susceptible to SARS-CoV-2 infection and typically have milder illness courses than adults, but the factors underlying these age-associated differences are not well understood. The upper respiratory microbiome undergoes substantial shifts during childhood and is increasingly recognized to influence host defense against respiratory pathogens. Thus, we sought to identify upper respiratory microbiome features associated with SARS-CoV-2 infection susceptibility and illness severity. METHODS: We collected clinical data and nasopharyngeal swabs from 285 children, adolescents, and young adults (<21 years) with documented SARS-CoV-2 exposure. We used 16S ribosomal RNA gene sequencing to characterize the nasopharyngeal microbiome and evaluated for age-adjusted associations between microbiome characteristics and SARS-CoV-2 infection status and respiratory symptoms. RESULTS: Nasopharyngeal microbiome composition varied with age (PERMANOVA, P < .001; R(2) = 0.06) and between SARS-CoV-2–infected individuals with and without respiratory symptoms (PERMANOVA, P = .002; R(2) = 0.009). SARS-CoV-2–infected participants with Corynebacterium/Dolosigranulum-dominant microbiome profiles were less likely to have respiratory symptoms than infected participants with other nasopharyngeal microbiome profiles (OR: .38; 95% CI: .18–.81). Using generalized joint attributed modeling, we identified 9 bacterial taxa associated with SARS-CoV-2 infection and 6 taxa differentially abundant among SARS-CoV-2–infected participants with respiratory symptoms; the magnitude of these associations was strongly influenced by age. CONCLUSIONS: We identified interactive relationships between age and specific nasopharyngeal microbiome features that are associated with SARS-CoV-2 infection susceptibility and symptoms in children, adolescents, and young adults. Our data suggest that the upper respiratory microbiome may be a mechanism by which age influences SARS-CoV-2 susceptibility and illness severity. |
format | Online Article Text |
id | pubmed-8903463 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-89034632022-03-09 Age-Related Changes in the Nasopharyngeal Microbiome Are Associated With Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and Symptoms Among Children, Adolescents, and Young Adults Hurst, Jillian H McCumber, Alexander W Aquino, Jhoanna N Rodriguez, Javier Heston, Sarah M Lugo, Debra J Rotta, Alexandre T Turner, Nicholas A Pfeiffer, Trevor S Gurley, Thaddeus C Moody, M Anthony Denny, Thomas N Rawls, John F Clark, James S Woods, Christopher W Kelly, Matthew S Clin Infect Dis Major Article BACKGROUND: Children are less susceptible to SARS-CoV-2 infection and typically have milder illness courses than adults, but the factors underlying these age-associated differences are not well understood. The upper respiratory microbiome undergoes substantial shifts during childhood and is increasingly recognized to influence host defense against respiratory pathogens. Thus, we sought to identify upper respiratory microbiome features associated with SARS-CoV-2 infection susceptibility and illness severity. METHODS: We collected clinical data and nasopharyngeal swabs from 285 children, adolescents, and young adults (<21 years) with documented SARS-CoV-2 exposure. We used 16S ribosomal RNA gene sequencing to characterize the nasopharyngeal microbiome and evaluated for age-adjusted associations between microbiome characteristics and SARS-CoV-2 infection status and respiratory symptoms. RESULTS: Nasopharyngeal microbiome composition varied with age (PERMANOVA, P < .001; R(2) = 0.06) and between SARS-CoV-2–infected individuals with and without respiratory symptoms (PERMANOVA, P = .002; R(2) = 0.009). SARS-CoV-2–infected participants with Corynebacterium/Dolosigranulum-dominant microbiome profiles were less likely to have respiratory symptoms than infected participants with other nasopharyngeal microbiome profiles (OR: .38; 95% CI: .18–.81). Using generalized joint attributed modeling, we identified 9 bacterial taxa associated with SARS-CoV-2 infection and 6 taxa differentially abundant among SARS-CoV-2–infected participants with respiratory symptoms; the magnitude of these associations was strongly influenced by age. CONCLUSIONS: We identified interactive relationships between age and specific nasopharyngeal microbiome features that are associated with SARS-CoV-2 infection susceptibility and symptoms in children, adolescents, and young adults. Our data suggest that the upper respiratory microbiome may be a mechanism by which age influences SARS-CoV-2 susceptibility and illness severity. Oxford University Press 2022-03-05 /pmc/articles/PMC8903463/ /pubmed/35247047 http://dx.doi.org/10.1093/cid/ciac184 Text en © The Author(s) 2022. Published by Oxford University Press for the Infectious Diseases Society of America. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Major Article Hurst, Jillian H McCumber, Alexander W Aquino, Jhoanna N Rodriguez, Javier Heston, Sarah M Lugo, Debra J Rotta, Alexandre T Turner, Nicholas A Pfeiffer, Trevor S Gurley, Thaddeus C Moody, M Anthony Denny, Thomas N Rawls, John F Clark, James S Woods, Christopher W Kelly, Matthew S Age-Related Changes in the Nasopharyngeal Microbiome Are Associated With Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and Symptoms Among Children, Adolescents, and Young Adults |
title | Age-Related Changes in the Nasopharyngeal Microbiome Are Associated With Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and Symptoms Among Children, Adolescents, and Young Adults |
title_full | Age-Related Changes in the Nasopharyngeal Microbiome Are Associated With Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and Symptoms Among Children, Adolescents, and Young Adults |
title_fullStr | Age-Related Changes in the Nasopharyngeal Microbiome Are Associated With Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and Symptoms Among Children, Adolescents, and Young Adults |
title_full_unstemmed | Age-Related Changes in the Nasopharyngeal Microbiome Are Associated With Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and Symptoms Among Children, Adolescents, and Young Adults |
title_short | Age-Related Changes in the Nasopharyngeal Microbiome Are Associated With Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and Symptoms Among Children, Adolescents, and Young Adults |
title_sort | age-related changes in the nasopharyngeal microbiome are associated with severe acute respiratory syndrome coronavirus 2 (sars-cov-2) infection and symptoms among children, adolescents, and young adults |
topic | Major Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8903463/ https://www.ncbi.nlm.nih.gov/pubmed/35247047 http://dx.doi.org/10.1093/cid/ciac184 |
work_keys_str_mv | AT hurstjillianh agerelatedchangesinthenasopharyngealmicrobiomeareassociatedwithsevereacuterespiratorysyndromecoronavirus2sarscov2infectionandsymptomsamongchildrenadolescentsandyoungadults AT mccumberalexanderw agerelatedchangesinthenasopharyngealmicrobiomeareassociatedwithsevereacuterespiratorysyndromecoronavirus2sarscov2infectionandsymptomsamongchildrenadolescentsandyoungadults AT aquinojhoannan agerelatedchangesinthenasopharyngealmicrobiomeareassociatedwithsevereacuterespiratorysyndromecoronavirus2sarscov2infectionandsymptomsamongchildrenadolescentsandyoungadults AT rodriguezjavier agerelatedchangesinthenasopharyngealmicrobiomeareassociatedwithsevereacuterespiratorysyndromecoronavirus2sarscov2infectionandsymptomsamongchildrenadolescentsandyoungadults AT hestonsarahm agerelatedchangesinthenasopharyngealmicrobiomeareassociatedwithsevereacuterespiratorysyndromecoronavirus2sarscov2infectionandsymptomsamongchildrenadolescentsandyoungadults AT lugodebraj agerelatedchangesinthenasopharyngealmicrobiomeareassociatedwithsevereacuterespiratorysyndromecoronavirus2sarscov2infectionandsymptomsamongchildrenadolescentsandyoungadults AT rottaalexandret agerelatedchangesinthenasopharyngealmicrobiomeareassociatedwithsevereacuterespiratorysyndromecoronavirus2sarscov2infectionandsymptomsamongchildrenadolescentsandyoungadults AT turnernicholasa agerelatedchangesinthenasopharyngealmicrobiomeareassociatedwithsevereacuterespiratorysyndromecoronavirus2sarscov2infectionandsymptomsamongchildrenadolescentsandyoungadults AT pfeiffertrevors agerelatedchangesinthenasopharyngealmicrobiomeareassociatedwithsevereacuterespiratorysyndromecoronavirus2sarscov2infectionandsymptomsamongchildrenadolescentsandyoungadults AT gurleythaddeusc agerelatedchangesinthenasopharyngealmicrobiomeareassociatedwithsevereacuterespiratorysyndromecoronavirus2sarscov2infectionandsymptomsamongchildrenadolescentsandyoungadults AT moodymanthony agerelatedchangesinthenasopharyngealmicrobiomeareassociatedwithsevereacuterespiratorysyndromecoronavirus2sarscov2infectionandsymptomsamongchildrenadolescentsandyoungadults AT dennythomasn agerelatedchangesinthenasopharyngealmicrobiomeareassociatedwithsevereacuterespiratorysyndromecoronavirus2sarscov2infectionandsymptomsamongchildrenadolescentsandyoungadults AT rawlsjohnf agerelatedchangesinthenasopharyngealmicrobiomeareassociatedwithsevereacuterespiratorysyndromecoronavirus2sarscov2infectionandsymptomsamongchildrenadolescentsandyoungadults AT clarkjamess agerelatedchangesinthenasopharyngealmicrobiomeareassociatedwithsevereacuterespiratorysyndromecoronavirus2sarscov2infectionandsymptomsamongchildrenadolescentsandyoungadults AT woodschristopherw agerelatedchangesinthenasopharyngealmicrobiomeareassociatedwithsevereacuterespiratorysyndromecoronavirus2sarscov2infectionandsymptomsamongchildrenadolescentsandyoungadults AT kellymatthews agerelatedchangesinthenasopharyngealmicrobiomeareassociatedwithsevereacuterespiratorysyndromecoronavirus2sarscov2infectionandsymptomsamongchildrenadolescentsandyoungadults |