Cargando…

Upper Respiratory Tract Microbiome of Australian Aboriginal and Torres Strait Islander Children in Ear and Nose Health and Disease

The objective of this study was to examine the nasal microbiota in relation to otitis media (OM) status and nose health in Indigenous Australian children. Children 2 to 7 years of age were recruited from two northern Australian (Queensland) communities. Clinical histories were obtained through paren...

Descripción completa

Detalles Bibliográficos
Autores principales: Coleman, Andrea, Zaugg, Julian, Wood, Amanda, Cottrell, Kyra, Håkansson, Eva Grahn, Adams, Jasmyn, Brown, Matthew, Cervin, Anders, Bialasiewicz, Seweryn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8528113/
https://www.ncbi.nlm.nih.gov/pubmed/34668729
http://dx.doi.org/10.1128/Spectrum.00367-21
_version_ 1784586194483412992
author Coleman, Andrea
Zaugg, Julian
Wood, Amanda
Cottrell, Kyra
Håkansson, Eva Grahn
Adams, Jasmyn
Brown, Matthew
Cervin, Anders
Bialasiewicz, Seweryn
author_facet Coleman, Andrea
Zaugg, Julian
Wood, Amanda
Cottrell, Kyra
Håkansson, Eva Grahn
Adams, Jasmyn
Brown, Matthew
Cervin, Anders
Bialasiewicz, Seweryn
author_sort Coleman, Andrea
collection PubMed
description The objective of this study was to examine the nasal microbiota in relation to otitis media (OM) status and nose health in Indigenous Australian children. Children 2 to 7 years of age were recruited from two northern Australian (Queensland) communities. Clinical histories were obtained through parent interviews and reviews of the medical records. Nasal cavity swab samples were obtained, and the children’s ears, nose, and throat were examined. DNA was extracted and analyzed by 16S rRNA amplicon next-generation sequencing of the V3/V4 region, in combination with previously generated culture data. A total of 103 children were recruited (mean age, 4.7 years); 17 (16.8%) were healthy, i.e., normal examination results and no history of OM. The nasal microbiota differed significantly in relation to OM status and nose health. Children with historical OM had greater relative abundance of Moraxella, compared to healthy children, despite both having healthy ears at the time of swabbing. Children with healthy noses had greater relative abundance of Staphylococcus aureus, compared to those with rhinorrhea. Dolosigranulum was correlated with Corynebacterium in healthy children. Haemophilus and Streptococcus were correlated across phenotypes. Ornithobacterium was absent or was present with low relative abundance in healthy children and clustered around otopathogens. It correlated with Helcococcus and Dichelobacter. Dolosigranulum and Corynebacterium form a synergism that promotes upper respiratory tract (URT)/ear health in Indigenous Australian children. Ornithobacterium likely represents “Candidatus Ornithobacterium hominis” and in this population is correlated with a novel bacterium that appears to be related to poor URT/ear health. IMPORTANCE Recurring and chronic infections of the ear (OM) are disproportionately prevalent in disadvantaged communities across the globe and, in particular, within Indigenous communities. Despite numerous intervention strategies, OM persists as a major health issue and is the leading cause of preventable hearing loss. In disadvantaged communities, this hearing loss is associated with negative educational and social development outcomes, and consequently, poorer employment prospects and increased contact with the justice system in adulthood. Thus, a better understanding of the microbial ecology is needed in order to identify new targets to treat, as well as to prevent the infections. This study used a powerful combination of 16S rRNA gene sequencing and extended culturomics to show that Dolosigranulum pigrum, a bacterium previously identified as a candidate protective species, may require cocolonization with Corynebacterium pseudodiphtheriticum in order to prevent OM. Additionally, emerging and potentially novel pathogens and bacteria were identified.
format Online
Article
Text
id pubmed-8528113
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-85281132021-11-08 Upper Respiratory Tract Microbiome of Australian Aboriginal and Torres Strait Islander Children in Ear and Nose Health and Disease Coleman, Andrea Zaugg, Julian Wood, Amanda Cottrell, Kyra Håkansson, Eva Grahn Adams, Jasmyn Brown, Matthew Cervin, Anders Bialasiewicz, Seweryn Microbiol Spectr Research Article The objective of this study was to examine the nasal microbiota in relation to otitis media (OM) status and nose health in Indigenous Australian children. Children 2 to 7 years of age were recruited from two northern Australian (Queensland) communities. Clinical histories were obtained through parent interviews and reviews of the medical records. Nasal cavity swab samples were obtained, and the children’s ears, nose, and throat were examined. DNA was extracted and analyzed by 16S rRNA amplicon next-generation sequencing of the V3/V4 region, in combination with previously generated culture data. A total of 103 children were recruited (mean age, 4.7 years); 17 (16.8%) were healthy, i.e., normal examination results and no history of OM. The nasal microbiota differed significantly in relation to OM status and nose health. Children with historical OM had greater relative abundance of Moraxella, compared to healthy children, despite both having healthy ears at the time of swabbing. Children with healthy noses had greater relative abundance of Staphylococcus aureus, compared to those with rhinorrhea. Dolosigranulum was correlated with Corynebacterium in healthy children. Haemophilus and Streptococcus were correlated across phenotypes. Ornithobacterium was absent or was present with low relative abundance in healthy children and clustered around otopathogens. It correlated with Helcococcus and Dichelobacter. Dolosigranulum and Corynebacterium form a synergism that promotes upper respiratory tract (URT)/ear health in Indigenous Australian children. Ornithobacterium likely represents “Candidatus Ornithobacterium hominis” and in this population is correlated with a novel bacterium that appears to be related to poor URT/ear health. IMPORTANCE Recurring and chronic infections of the ear (OM) are disproportionately prevalent in disadvantaged communities across the globe and, in particular, within Indigenous communities. Despite numerous intervention strategies, OM persists as a major health issue and is the leading cause of preventable hearing loss. In disadvantaged communities, this hearing loss is associated with negative educational and social development outcomes, and consequently, poorer employment prospects and increased contact with the justice system in adulthood. Thus, a better understanding of the microbial ecology is needed in order to identify new targets to treat, as well as to prevent the infections. This study used a powerful combination of 16S rRNA gene sequencing and extended culturomics to show that Dolosigranulum pigrum, a bacterium previously identified as a candidate protective species, may require cocolonization with Corynebacterium pseudodiphtheriticum in order to prevent OM. Additionally, emerging and potentially novel pathogens and bacteria were identified. American Society for Microbiology 2021-10-20 /pmc/articles/PMC8528113/ /pubmed/34668729 http://dx.doi.org/10.1128/Spectrum.00367-21 Text en Copyright © 2021 Coleman et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Coleman, Andrea
Zaugg, Julian
Wood, Amanda
Cottrell, Kyra
Håkansson, Eva Grahn
Adams, Jasmyn
Brown, Matthew
Cervin, Anders
Bialasiewicz, Seweryn
Upper Respiratory Tract Microbiome of Australian Aboriginal and Torres Strait Islander Children in Ear and Nose Health and Disease
title Upper Respiratory Tract Microbiome of Australian Aboriginal and Torres Strait Islander Children in Ear and Nose Health and Disease
title_full Upper Respiratory Tract Microbiome of Australian Aboriginal and Torres Strait Islander Children in Ear and Nose Health and Disease
title_fullStr Upper Respiratory Tract Microbiome of Australian Aboriginal and Torres Strait Islander Children in Ear and Nose Health and Disease
title_full_unstemmed Upper Respiratory Tract Microbiome of Australian Aboriginal and Torres Strait Islander Children in Ear and Nose Health and Disease
title_short Upper Respiratory Tract Microbiome of Australian Aboriginal and Torres Strait Islander Children in Ear and Nose Health and Disease
title_sort upper respiratory tract microbiome of australian aboriginal and torres strait islander children in ear and nose health and disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8528113/
https://www.ncbi.nlm.nih.gov/pubmed/34668729
http://dx.doi.org/10.1128/Spectrum.00367-21
work_keys_str_mv AT colemanandrea upperrespiratorytractmicrobiomeofaustralianaboriginalandtorresstraitislanderchildreninearandnosehealthanddisease
AT zauggjulian upperrespiratorytractmicrobiomeofaustralianaboriginalandtorresstraitislanderchildreninearandnosehealthanddisease
AT woodamanda upperrespiratorytractmicrobiomeofaustralianaboriginalandtorresstraitislanderchildreninearandnosehealthanddisease
AT cottrellkyra upperrespiratorytractmicrobiomeofaustralianaboriginalandtorresstraitislanderchildreninearandnosehealthanddisease
AT hakanssonevagrahn upperrespiratorytractmicrobiomeofaustralianaboriginalandtorresstraitislanderchildreninearandnosehealthanddisease
AT adamsjasmyn upperrespiratorytractmicrobiomeofaustralianaboriginalandtorresstraitislanderchildreninearandnosehealthanddisease
AT brownmatthew upperrespiratorytractmicrobiomeofaustralianaboriginalandtorresstraitislanderchildreninearandnosehealthanddisease
AT cervinanders upperrespiratorytractmicrobiomeofaustralianaboriginalandtorresstraitislanderchildreninearandnosehealthanddisease
AT bialasiewiczseweryn upperrespiratorytractmicrobiomeofaustralianaboriginalandtorresstraitislanderchildreninearandnosehealthanddisease