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Comparative analysis of the tonsillar microbiota in IgA nephropathy and other glomerular diseases

Immunoglobulin A nephropathy (IgAN) involves repeated events of gross haematuria with concurrent upper airway infections. The mucosal immune system, especially the tonsil, is considered the initial site of inflammation, although the role of the tonsillar microbiota has not been established in IgAN....

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Autores principales: Park, Ji In, Kim, Tae-Yoon, Oh, Bumjo, Cho, Hyunjeong, Kim, Ji Eun, Yoo, Seong Ho, Lee, Jung Pyo, Kim, Yon Su, Chun, Jongsik, Kim, Bong-Soo, Lee, Hajeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7530979/
https://www.ncbi.nlm.nih.gov/pubmed/33004860
http://dx.doi.org/10.1038/s41598-020-73035-x
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author Park, Ji In
Kim, Tae-Yoon
Oh, Bumjo
Cho, Hyunjeong
Kim, Ji Eun
Yoo, Seong Ho
Lee, Jung Pyo
Kim, Yon Su
Chun, Jongsik
Kim, Bong-Soo
Lee, Hajeong
author_facet Park, Ji In
Kim, Tae-Yoon
Oh, Bumjo
Cho, Hyunjeong
Kim, Ji Eun
Yoo, Seong Ho
Lee, Jung Pyo
Kim, Yon Su
Chun, Jongsik
Kim, Bong-Soo
Lee, Hajeong
author_sort Park, Ji In
collection PubMed
description Immunoglobulin A nephropathy (IgAN) involves repeated events of gross haematuria with concurrent upper airway infections. The mucosal immune system, especially the tonsil, is considered the initial site of inflammation, although the role of the tonsillar microbiota has not been established in IgAN. In this study, we compared the tonsillar microbiota of patients with IgAN (n = 21) and other glomerular diseases (n = 36) as well as, healthy controls (n = 23) from three medical centres in Korea. The microbiota was analysed from tonsil swabs using the Illumina MiSeq system based on 16S rRNA gene. Tonsillar bacterial diversity was higher in IgAN than in other glomerular diseases, although it did not differ from that of healthy controls. Principal coordinates analysis revealed differences between the tonsillar microbiota of IgAN and both healthy and disease controls. The proportions of Rahnella, Ruminococcus_g2, and Clostridium_g21 were significantly higher in patients with IgAN than in healthy controls (corrected p < 0.05). The relative abundances of several taxa were correlated with the estimated glomerular filtration rate, blood urea nitrogen, haemoglobin, and serum albumin levels. Based on our findings, tonsillar microbiota may be associated with clinical features and possible immunologic pathogenesis of IgAN.
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spelling pubmed-75309792020-10-06 Comparative analysis of the tonsillar microbiota in IgA nephropathy and other glomerular diseases Park, Ji In Kim, Tae-Yoon Oh, Bumjo Cho, Hyunjeong Kim, Ji Eun Yoo, Seong Ho Lee, Jung Pyo Kim, Yon Su Chun, Jongsik Kim, Bong-Soo Lee, Hajeong Sci Rep Article Immunoglobulin A nephropathy (IgAN) involves repeated events of gross haematuria with concurrent upper airway infections. The mucosal immune system, especially the tonsil, is considered the initial site of inflammation, although the role of the tonsillar microbiota has not been established in IgAN. In this study, we compared the tonsillar microbiota of patients with IgAN (n = 21) and other glomerular diseases (n = 36) as well as, healthy controls (n = 23) from three medical centres in Korea. The microbiota was analysed from tonsil swabs using the Illumina MiSeq system based on 16S rRNA gene. Tonsillar bacterial diversity was higher in IgAN than in other glomerular diseases, although it did not differ from that of healthy controls. Principal coordinates analysis revealed differences between the tonsillar microbiota of IgAN and both healthy and disease controls. The proportions of Rahnella, Ruminococcus_g2, and Clostridium_g21 were significantly higher in patients with IgAN than in healthy controls (corrected p < 0.05). The relative abundances of several taxa were correlated with the estimated glomerular filtration rate, blood urea nitrogen, haemoglobin, and serum albumin levels. Based on our findings, tonsillar microbiota may be associated with clinical features and possible immunologic pathogenesis of IgAN. Nature Publishing Group UK 2020-10-01 /pmc/articles/PMC7530979/ /pubmed/33004860 http://dx.doi.org/10.1038/s41598-020-73035-x Text en © The Author(s) 2020 Open Access This 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/.
spellingShingle Article
Park, Ji In
Kim, Tae-Yoon
Oh, Bumjo
Cho, Hyunjeong
Kim, Ji Eun
Yoo, Seong Ho
Lee, Jung Pyo
Kim, Yon Su
Chun, Jongsik
Kim, Bong-Soo
Lee, Hajeong
Comparative analysis of the tonsillar microbiota in IgA nephropathy and other glomerular diseases
title Comparative analysis of the tonsillar microbiota in IgA nephropathy and other glomerular diseases
title_full Comparative analysis of the tonsillar microbiota in IgA nephropathy and other glomerular diseases
title_fullStr Comparative analysis of the tonsillar microbiota in IgA nephropathy and other glomerular diseases
title_full_unstemmed Comparative analysis of the tonsillar microbiota in IgA nephropathy and other glomerular diseases
title_short Comparative analysis of the tonsillar microbiota in IgA nephropathy and other glomerular diseases
title_sort comparative analysis of the tonsillar microbiota in iga nephropathy and other glomerular diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7530979/
https://www.ncbi.nlm.nih.gov/pubmed/33004860
http://dx.doi.org/10.1038/s41598-020-73035-x
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