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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...

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Autores principales: Verhasselt, Hedda Luise, Ramakrishnan, Elakiya, Schlag, Melina, Marchesi, Julian R, Buer, Jan, Kleinschnitz, Christoph, Hagenacker, Tim, Totzeck, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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.
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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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