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Ear microbiota and middle ear disease: a longitudinal pilot study of Aboriginal children in a remote south Australian setting

BACKGROUND: Otitis media (OM) is a major disease burden in Australian Aboriginal children, contributing to serious long-term health outcomes. We report a pilot analysis of OM in children attending an outreach ear and hearing clinic in a remote south Australian community over a two-year period. Our s...

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Autores principales: Taylor, Steven L., Papanicolas, Lito E., Richards, Alyson, Ababor, Furdosa, Kang, Wan Xian, Choo, Jocelyn M., Woods, Charmaine, Wesselingh, Steve L., Ooi, Eng H., MacFarlane, Patricia, Rogers, Geraint B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8756658/
https://www.ncbi.nlm.nih.gov/pubmed/35026986
http://dx.doi.org/10.1186/s12866-022-02436-x
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author Taylor, Steven L.
Papanicolas, Lito E.
Richards, Alyson
Ababor, Furdosa
Kang, Wan Xian
Choo, Jocelyn M.
Woods, Charmaine
Wesselingh, Steve L.
Ooi, Eng H.
MacFarlane, Patricia
Rogers, Geraint B.
author_facet Taylor, Steven L.
Papanicolas, Lito E.
Richards, Alyson
Ababor, Furdosa
Kang, Wan Xian
Choo, Jocelyn M.
Woods, Charmaine
Wesselingh, Steve L.
Ooi, Eng H.
MacFarlane, Patricia
Rogers, Geraint B.
author_sort Taylor, Steven L.
collection PubMed
description BACKGROUND: Otitis media (OM) is a major disease burden in Australian Aboriginal children, contributing to serious long-term health outcomes. We report a pilot analysis of OM in children attending an outreach ear and hearing clinic in a remote south Australian community over a two-year period. Our study focuses on longitudinal relationships between ear canal microbiota characteristics with nasopharyngeal microbiota, and clinical and treatment variables. RESULTS: Middle ear health status were assessed in 19 children (aged 3 months to 8 years) presenting in remote western South Australia and medical interventions were recorded. Over the two-year study period, chronic suppurative OM was diagnosed at least once in 7 children (37%), acute OM with perforation in 4 children (21%), OM with effusion in 11 children (58%), while only 1 child had no ear disease. Microbiota analysis of 19 children (51 sets of left and right ear canal swabs and nasopharyngeal swabs) revealed a core group of bacterial taxa that included Corynebacterium, Alloiococcus, Staphylococcus, Haemophilus, Turicella, Streptococcus, and Pseudomonas. Within-subject microbiota similarity (between ears) was significantly greater than inter-subject similarity, regardless of differences in ear disease (p = 0.0006). Longitudinal analysis revealed changes in diagnosis to be associated with more pronounced changes in microbiota characteristics, irrespective of time interval. Ear microbiota characteristics differed significantly according to diagnosis (P (perm) = 0.0001). Diagnoses featuring inflammation with tympanic membrane perforation clustering separately to those in which the tympanic membrane was intact, and characterised by increased Proteobacteria, particularly Haemophilus influenzae, Moraxella catarrhalis, and Oligella. While nasopharyngeal microbiota differed significantly in composition to ear microbiota (P (perm) = 0.0001), inter-site similarity was significantly greater in subjects with perforated tympanic membranes, a relationship that was associated with the relative abundance of H. influenzae in ear samples (r(s) = − 0.71, p = 0.0003). Longitudinal changes in ear microbiology reflected changes in clinical signs and treatment. CONCLUSIONS: Children attending the ear and hearing clinic in a remote Aboriginal community present with a broad spectrum of OM conditions and severities, consistent with other remote Aboriginal communities. Ear microbiota characteristics align with OM diagnosis and change with disease course. Nasopharyngeal microbiota characteristics are consistent with the contribution of acute upper respiratory infection to OM aetiology. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-022-02436-x.
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spelling pubmed-87566582022-01-18 Ear microbiota and middle ear disease: a longitudinal pilot study of Aboriginal children in a remote south Australian setting Taylor, Steven L. Papanicolas, Lito E. Richards, Alyson Ababor, Furdosa Kang, Wan Xian Choo, Jocelyn M. Woods, Charmaine Wesselingh, Steve L. Ooi, Eng H. MacFarlane, Patricia Rogers, Geraint B. BMC Microbiol Research BACKGROUND: Otitis media (OM) is a major disease burden in Australian Aboriginal children, contributing to serious long-term health outcomes. We report a pilot analysis of OM in children attending an outreach ear and hearing clinic in a remote south Australian community over a two-year period. Our study focuses on longitudinal relationships between ear canal microbiota characteristics with nasopharyngeal microbiota, and clinical and treatment variables. RESULTS: Middle ear health status were assessed in 19 children (aged 3 months to 8 years) presenting in remote western South Australia and medical interventions were recorded. Over the two-year study period, chronic suppurative OM was diagnosed at least once in 7 children (37%), acute OM with perforation in 4 children (21%), OM with effusion in 11 children (58%), while only 1 child had no ear disease. Microbiota analysis of 19 children (51 sets of left and right ear canal swabs and nasopharyngeal swabs) revealed a core group of bacterial taxa that included Corynebacterium, Alloiococcus, Staphylococcus, Haemophilus, Turicella, Streptococcus, and Pseudomonas. Within-subject microbiota similarity (between ears) was significantly greater than inter-subject similarity, regardless of differences in ear disease (p = 0.0006). Longitudinal analysis revealed changes in diagnosis to be associated with more pronounced changes in microbiota characteristics, irrespective of time interval. Ear microbiota characteristics differed significantly according to diagnosis (P (perm) = 0.0001). Diagnoses featuring inflammation with tympanic membrane perforation clustering separately to those in which the tympanic membrane was intact, and characterised by increased Proteobacteria, particularly Haemophilus influenzae, Moraxella catarrhalis, and Oligella. While nasopharyngeal microbiota differed significantly in composition to ear microbiota (P (perm) = 0.0001), inter-site similarity was significantly greater in subjects with perforated tympanic membranes, a relationship that was associated with the relative abundance of H. influenzae in ear samples (r(s) = − 0.71, p = 0.0003). Longitudinal changes in ear microbiology reflected changes in clinical signs and treatment. CONCLUSIONS: Children attending the ear and hearing clinic in a remote Aboriginal community present with a broad spectrum of OM conditions and severities, consistent with other remote Aboriginal communities. Ear microbiota characteristics align with OM diagnosis and change with disease course. Nasopharyngeal microbiota characteristics are consistent with the contribution of acute upper respiratory infection to OM aetiology. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-022-02436-x. BioMed Central 2022-01-13 /pmc/articles/PMC8756658/ /pubmed/35026986 http://dx.doi.org/10.1186/s12866-022-02436-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Taylor, Steven L.
Papanicolas, Lito E.
Richards, Alyson
Ababor, Furdosa
Kang, Wan Xian
Choo, Jocelyn M.
Woods, Charmaine
Wesselingh, Steve L.
Ooi, Eng H.
MacFarlane, Patricia
Rogers, Geraint B.
Ear microbiota and middle ear disease: a longitudinal pilot study of Aboriginal children in a remote south Australian setting
title Ear microbiota and middle ear disease: a longitudinal pilot study of Aboriginal children in a remote south Australian setting
title_full Ear microbiota and middle ear disease: a longitudinal pilot study of Aboriginal children in a remote south Australian setting
title_fullStr Ear microbiota and middle ear disease: a longitudinal pilot study of Aboriginal children in a remote south Australian setting
title_full_unstemmed Ear microbiota and middle ear disease: a longitudinal pilot study of Aboriginal children in a remote south Australian setting
title_short Ear microbiota and middle ear disease: a longitudinal pilot study of Aboriginal children in a remote south Australian setting
title_sort ear microbiota and middle ear disease: a longitudinal pilot study of aboriginal children in a remote south australian setting
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8756658/
https://www.ncbi.nlm.nih.gov/pubmed/35026986
http://dx.doi.org/10.1186/s12866-022-02436-x
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