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Fungal Gut Microbiome in Myasthenia Gravis: A Sub-Analysis of the MYBIOM Study
An altered gut microbiota is a possible contributing pathogenic factor in myasthenia gravis (MG), an autoimmune neuromuscular disease. However, the significance of the fungal microbiome is an understudied and neglected part of the intestinal microbiome in MG. We performed a sub-analysis of the MYBIO...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10218993/ https://www.ncbi.nlm.nih.gov/pubmed/37233280 http://dx.doi.org/10.3390/jof9050569 |
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author | Verhasselt, Hedda Luise Ramakrishnan, Elakiya Schlag, Melina Marchesi, Julian R Buer, Jan Kleinschnitz, Christoph Hagenacker, Tim Totzeck, Andreas |
author_facet | Verhasselt, Hedda Luise Ramakrishnan, Elakiya Schlag, Melina Marchesi, Julian R Buer, Jan Kleinschnitz, Christoph Hagenacker, Tim Totzeck, Andreas |
author_sort | Verhasselt, Hedda Luise |
collection | PubMed |
description | An altered gut microbiota is a possible contributing pathogenic factor in myasthenia gravis (MG), an autoimmune neuromuscular disease. However, the significance of the fungal microbiome is an understudied and neglected part of the intestinal microbiome in MG. We performed a sub-analysis of the MYBIOM study including faecal samples from patients with MG (n = 41), non-inflammatory neurological disorder (NIND, n = 18), chronic inflammatory demyelinating polyradiculoneuropathy (CIDP, n = 6) and healthy volunteers (n = 12) by sequencing the internal transcribed spacer 2 (ITS2). Fungal reads were obtained in 51 out of 77 samples. No differences were found in alpha-diversity indices computed between the MG, NIND, CIDP and HV groups, indicating an unaltered fungal diversity and structure. Overall, four mould species (Penicillium aurantiogriseum, Mycosphaerella tassiana, Cladosporium ramonetellum and Alternaria betae-kenyensis) and five yeast species (Candida. albicans, Candida. sake, Candida. dubliniensis, Pichia deserticola and Kregervanrija delftensis) were identified. Besides one MG patient with abundant Ca. albicans, no prominent dysbiosis in the MG group of the mycobiome was found. Not all fungal sequences within all groups were successfully assigned, so further sub-analysis was withdrawn, limiting robust conclusions. |
format | Online Article Text |
id | pubmed-10218993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102189932023-05-27 Fungal Gut Microbiome in Myasthenia Gravis: A Sub-Analysis of the MYBIOM Study Verhasselt, Hedda Luise Ramakrishnan, Elakiya Schlag, Melina Marchesi, Julian R Buer, Jan Kleinschnitz, Christoph Hagenacker, Tim Totzeck, Andreas J Fungi (Basel) Communication An altered gut microbiota is a possible contributing pathogenic factor in myasthenia gravis (MG), an autoimmune neuromuscular disease. However, the significance of the fungal microbiome is an understudied and neglected part of the intestinal microbiome in MG. We performed a sub-analysis of the MYBIOM study including faecal samples from patients with MG (n = 41), non-inflammatory neurological disorder (NIND, n = 18), chronic inflammatory demyelinating polyradiculoneuropathy (CIDP, n = 6) and healthy volunteers (n = 12) by sequencing the internal transcribed spacer 2 (ITS2). Fungal reads were obtained in 51 out of 77 samples. No differences were found in alpha-diversity indices computed between the MG, NIND, CIDP and HV groups, indicating an unaltered fungal diversity and structure. Overall, four mould species (Penicillium aurantiogriseum, Mycosphaerella tassiana, Cladosporium ramonetellum and Alternaria betae-kenyensis) and five yeast species (Candida. albicans, Candida. sake, Candida. dubliniensis, Pichia deserticola and Kregervanrija delftensis) were identified. Besides one MG patient with abundant Ca. albicans, no prominent dysbiosis in the MG group of the mycobiome was found. Not all fungal sequences within all groups were successfully assigned, so further sub-analysis was withdrawn, limiting robust conclusions. MDPI 2023-05-13 /pmc/articles/PMC10218993/ /pubmed/37233280 http://dx.doi.org/10.3390/jof9050569 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Verhasselt, Hedda Luise Ramakrishnan, Elakiya Schlag, Melina Marchesi, Julian R Buer, Jan Kleinschnitz, Christoph Hagenacker, Tim Totzeck, Andreas Fungal Gut Microbiome in Myasthenia Gravis: A Sub-Analysis of the MYBIOM Study |
title | Fungal Gut Microbiome in Myasthenia Gravis: A Sub-Analysis of the MYBIOM Study |
title_full | Fungal Gut Microbiome in Myasthenia Gravis: A Sub-Analysis of the MYBIOM Study |
title_fullStr | Fungal Gut Microbiome in Myasthenia Gravis: A Sub-Analysis of the MYBIOM Study |
title_full_unstemmed | Fungal Gut Microbiome in Myasthenia Gravis: A Sub-Analysis of the MYBIOM Study |
title_short | Fungal Gut Microbiome in Myasthenia Gravis: A Sub-Analysis of the MYBIOM Study |
title_sort | fungal gut microbiome in myasthenia gravis: a sub-analysis of the mybiom study |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10218993/ https://www.ncbi.nlm.nih.gov/pubmed/37233280 http://dx.doi.org/10.3390/jof9050569 |
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