Cargando…

Airway Microbiota Dynamics Uncover a Critical Window for Interplay of Pathogenic Bacteria and Allergy in Childhood Respiratory Disease

Repeated cycles of infection-associated lower airway inflammation drive the pathogenesis of persistent wheezing disease in children. In this study, the occurrence of acute respiratory tract illnesses (ARIs) and the nasopharyngeal microbiome (NPM) were characterized in 244 infants through their first...

Descripción completa

Detalles Bibliográficos
Autores principales: Teo, Shu Mei, Tang, Howard H.F., Mok, Danny, Judd, Louise M., Watts, Stephen C., Pham, Kym, Holt, Barbara J., Kusel, Merci, Serralha, Michael, Troy, Niamh, Bochkov, Yury A., Grindle, Kristine, Lemanske, Robert F., Johnston, Sebastian L., Gern, James E., Sly, Peter D., Holt, Patrick G., Holt, Kathryn E., Inouye, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291254/
https://www.ncbi.nlm.nih.gov/pubmed/30212648
http://dx.doi.org/10.1016/j.chom.2018.08.005
_version_ 1783380227756392448
author Teo, Shu Mei
Tang, Howard H.F.
Mok, Danny
Judd, Louise M.
Watts, Stephen C.
Pham, Kym
Holt, Barbara J.
Kusel, Merci
Serralha, Michael
Troy, Niamh
Bochkov, Yury A.
Grindle, Kristine
Lemanske, Robert F.
Johnston, Sebastian L.
Gern, James E.
Sly, Peter D.
Holt, Patrick G.
Holt, Kathryn E.
Inouye, Michael
author_facet Teo, Shu Mei
Tang, Howard H.F.
Mok, Danny
Judd, Louise M.
Watts, Stephen C.
Pham, Kym
Holt, Barbara J.
Kusel, Merci
Serralha, Michael
Troy, Niamh
Bochkov, Yury A.
Grindle, Kristine
Lemanske, Robert F.
Johnston, Sebastian L.
Gern, James E.
Sly, Peter D.
Holt, Patrick G.
Holt, Kathryn E.
Inouye, Michael
author_sort Teo, Shu Mei
collection PubMed
description Repeated cycles of infection-associated lower airway inflammation drive the pathogenesis of persistent wheezing disease in children. In this study, the occurrence of acute respiratory tract illnesses (ARIs) and the nasopharyngeal microbiome (NPM) were characterized in 244 infants through their first five years of life. Through this analysis, we demonstrate that >80% of infectious events involve viral pathogens, but are accompanied by a shift in the NPM toward dominance by a small range of pathogenic bacterial genera. Unexpectedly, this change frequently precedes the detection of viral pathogens and acute symptoms. Colonization of illness-associated bacteria coupled with early allergic sensitization is associated with persistent wheeze in school-aged children, which is the hallmark of the asthma phenotype. In contrast, these bacterial genera are associated with “transient wheeze” that resolves after age 3 years in non-sensitized children. Thus, to complement early allergic sensitization, monitoring NPM composition may enable early detection and intervention in high-risk children.
format Online
Article
Text
id pubmed-6291254
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Elsevier Inc.
record_format MEDLINE/PubMed
spelling pubmed-62912542019-09-12 Airway Microbiota Dynamics Uncover a Critical Window for Interplay of Pathogenic Bacteria and Allergy in Childhood Respiratory Disease Teo, Shu Mei Tang, Howard H.F. Mok, Danny Judd, Louise M. Watts, Stephen C. Pham, Kym Holt, Barbara J. Kusel, Merci Serralha, Michael Troy, Niamh Bochkov, Yury A. Grindle, Kristine Lemanske, Robert F. Johnston, Sebastian L. Gern, James E. Sly, Peter D. Holt, Patrick G. Holt, Kathryn E. Inouye, Michael Cell Host Microbe Article Repeated cycles of infection-associated lower airway inflammation drive the pathogenesis of persistent wheezing disease in children. In this study, the occurrence of acute respiratory tract illnesses (ARIs) and the nasopharyngeal microbiome (NPM) were characterized in 244 infants through their first five years of life. Through this analysis, we demonstrate that >80% of infectious events involve viral pathogens, but are accompanied by a shift in the NPM toward dominance by a small range of pathogenic bacterial genera. Unexpectedly, this change frequently precedes the detection of viral pathogens and acute symptoms. Colonization of illness-associated bacteria coupled with early allergic sensitization is associated with persistent wheeze in school-aged children, which is the hallmark of the asthma phenotype. In contrast, these bacterial genera are associated with “transient wheeze” that resolves after age 3 years in non-sensitized children. Thus, to complement early allergic sensitization, monitoring NPM composition may enable early detection and intervention in high-risk children. Elsevier Inc. 2018-09-12 2018-09-12 /pmc/articles/PMC6291254/ /pubmed/30212648 http://dx.doi.org/10.1016/j.chom.2018.08.005 Text en © 2018 Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Teo, Shu Mei
Tang, Howard H.F.
Mok, Danny
Judd, Louise M.
Watts, Stephen C.
Pham, Kym
Holt, Barbara J.
Kusel, Merci
Serralha, Michael
Troy, Niamh
Bochkov, Yury A.
Grindle, Kristine
Lemanske, Robert F.
Johnston, Sebastian L.
Gern, James E.
Sly, Peter D.
Holt, Patrick G.
Holt, Kathryn E.
Inouye, Michael
Airway Microbiota Dynamics Uncover a Critical Window for Interplay of Pathogenic Bacteria and Allergy in Childhood Respiratory Disease
title Airway Microbiota Dynamics Uncover a Critical Window for Interplay of Pathogenic Bacteria and Allergy in Childhood Respiratory Disease
title_full Airway Microbiota Dynamics Uncover a Critical Window for Interplay of Pathogenic Bacteria and Allergy in Childhood Respiratory Disease
title_fullStr Airway Microbiota Dynamics Uncover a Critical Window for Interplay of Pathogenic Bacteria and Allergy in Childhood Respiratory Disease
title_full_unstemmed Airway Microbiota Dynamics Uncover a Critical Window for Interplay of Pathogenic Bacteria and Allergy in Childhood Respiratory Disease
title_short Airway Microbiota Dynamics Uncover a Critical Window for Interplay of Pathogenic Bacteria and Allergy in Childhood Respiratory Disease
title_sort airway microbiota dynamics uncover a critical window for interplay of pathogenic bacteria and allergy in childhood respiratory disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291254/
https://www.ncbi.nlm.nih.gov/pubmed/30212648
http://dx.doi.org/10.1016/j.chom.2018.08.005
work_keys_str_mv AT teoshumei airwaymicrobiotadynamicsuncoveracriticalwindowforinterplayofpathogenicbacteriaandallergyinchildhoodrespiratorydisease
AT tanghowardhf airwaymicrobiotadynamicsuncoveracriticalwindowforinterplayofpathogenicbacteriaandallergyinchildhoodrespiratorydisease
AT mokdanny airwaymicrobiotadynamicsuncoveracriticalwindowforinterplayofpathogenicbacteriaandallergyinchildhoodrespiratorydisease
AT juddlouisem airwaymicrobiotadynamicsuncoveracriticalwindowforinterplayofpathogenicbacteriaandallergyinchildhoodrespiratorydisease
AT wattsstephenc airwaymicrobiotadynamicsuncoveracriticalwindowforinterplayofpathogenicbacteriaandallergyinchildhoodrespiratorydisease
AT phamkym airwaymicrobiotadynamicsuncoveracriticalwindowforinterplayofpathogenicbacteriaandallergyinchildhoodrespiratorydisease
AT holtbarbaraj airwaymicrobiotadynamicsuncoveracriticalwindowforinterplayofpathogenicbacteriaandallergyinchildhoodrespiratorydisease
AT kuselmerci airwaymicrobiotadynamicsuncoveracriticalwindowforinterplayofpathogenicbacteriaandallergyinchildhoodrespiratorydisease
AT serralhamichael airwaymicrobiotadynamicsuncoveracriticalwindowforinterplayofpathogenicbacteriaandallergyinchildhoodrespiratorydisease
AT troyniamh airwaymicrobiotadynamicsuncoveracriticalwindowforinterplayofpathogenicbacteriaandallergyinchildhoodrespiratorydisease
AT bochkovyurya airwaymicrobiotadynamicsuncoveracriticalwindowforinterplayofpathogenicbacteriaandallergyinchildhoodrespiratorydisease
AT grindlekristine airwaymicrobiotadynamicsuncoveracriticalwindowforinterplayofpathogenicbacteriaandallergyinchildhoodrespiratorydisease
AT lemanskerobertf airwaymicrobiotadynamicsuncoveracriticalwindowforinterplayofpathogenicbacteriaandallergyinchildhoodrespiratorydisease
AT johnstonsebastianl airwaymicrobiotadynamicsuncoveracriticalwindowforinterplayofpathogenicbacteriaandallergyinchildhoodrespiratorydisease
AT gernjamese airwaymicrobiotadynamicsuncoveracriticalwindowforinterplayofpathogenicbacteriaandallergyinchildhoodrespiratorydisease
AT slypeterd airwaymicrobiotadynamicsuncoveracriticalwindowforinterplayofpathogenicbacteriaandallergyinchildhoodrespiratorydisease
AT holtpatrickg airwaymicrobiotadynamicsuncoveracriticalwindowforinterplayofpathogenicbacteriaandallergyinchildhoodrespiratorydisease
AT holtkathryne airwaymicrobiotadynamicsuncoveracriticalwindowforinterplayofpathogenicbacteriaandallergyinchildhoodrespiratorydisease
AT inouyemichael airwaymicrobiotadynamicsuncoveracriticalwindowforinterplayofpathogenicbacteriaandallergyinchildhoodrespiratorydisease