Association between Parkinson’s disease and the faecal eukaryotic microbiota

Abstract Parkinson’s disease (PD) is one of the most common neurodegenerative disease, and is so far not considered curable. PD patients suffer from several motor and non-motor symptoms, including gastrointestinal dysfunctions and alterations of the enteric nervous system. Constipation and additiona...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Severin Weis, Alexandra Meisner, Andreas Schwiertz, Marcus M. Unger, Anouck Becker, Klaus Faßbender, Sylvia Schnell, Karl-Herbert Schäfer, Markus Egert
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
Materias:
Acceso en línea:https://doaj.org/article/b43a5de64b4c404a96985bf3fa5b0f2a
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:b43a5de64b4c404a96985bf3fa5b0f2a
record_format dspace
spelling oai:doaj.org-article:b43a5de64b4c404a96985bf3fa5b0f2a2021-11-21T12:26:42ZAssociation between Parkinson’s disease and the faecal eukaryotic microbiota10.1038/s41531-021-00244-02373-8057https://doaj.org/article/b43a5de64b4c404a96985bf3fa5b0f2a2021-11-01T00:00:00Zhttps://doi.org/10.1038/s41531-021-00244-0https://doaj.org/toc/2373-8057Abstract Parkinson’s disease (PD) is one of the most common neurodegenerative disease, and is so far not considered curable. PD patients suffer from several motor and non-motor symptoms, including gastrointestinal dysfunctions and alterations of the enteric nervous system. Constipation and additional intestinal affections can precede the classical motor symptoms by several years. Recently, we reported effects of PD and related medications on the faecal bacterial community of 34 German PD patients and 25 age-matched controls. Here, we used the same collective and analysed the V6 and V7 hypervariable region of PCR-amplified, eukaryotic 18S rRNA genes using an Illumina MiSeq platform. In all, 53% (18) of the PD samples and 72% (18) of the control samples yielded sufficient amplicons for downstream community analyses. The PD samples showed a significantly lower alpha and a different beta eukaryotic diversity than the controls. Most strikingly, we observed a significantly higher relative abundance of sequence affiliated with the Geotrichum genus in the PD samples (39.7%), when compared to the control samples (0.05%). In addition, we observed lower relative abundances of sequences affiliated with Aspergillus/Penicillium, Charophyta/Linum, unidentified Opisthokonta and three genera of minor abundant zooflagellates in the PD samples. Our data add knowledge to the small body of data about the eukaryotic microbiota of PD patients and suggest a potential association of certain gut eukaryotes and PD.Severin WeisAlexandra MeisnerAndreas SchwiertzMarcus M. UngerAnouck BeckerKlaus FaßbenderSylvia SchnellKarl-Herbert SchäferMarkus EgertNature PortfolioarticleNeurology. Diseases of the nervous systemRC346-429ENnpj Parkinson's Disease, Vol 7, Iss 1, Pp 1-7 (2021)
institution DOAJ
collection DOAJ
language EN
topic Neurology. Diseases of the nervous system
RC346-429
spellingShingle Neurology. Diseases of the nervous system
RC346-429
Severin Weis
Alexandra Meisner
Andreas Schwiertz
Marcus M. Unger
Anouck Becker
Klaus Faßbender
Sylvia Schnell
Karl-Herbert Schäfer
Markus Egert
Association between Parkinson’s disease and the faecal eukaryotic microbiota
description Abstract Parkinson’s disease (PD) is one of the most common neurodegenerative disease, and is so far not considered curable. PD patients suffer from several motor and non-motor symptoms, including gastrointestinal dysfunctions and alterations of the enteric nervous system. Constipation and additional intestinal affections can precede the classical motor symptoms by several years. Recently, we reported effects of PD and related medications on the faecal bacterial community of 34 German PD patients and 25 age-matched controls. Here, we used the same collective and analysed the V6 and V7 hypervariable region of PCR-amplified, eukaryotic 18S rRNA genes using an Illumina MiSeq platform. In all, 53% (18) of the PD samples and 72% (18) of the control samples yielded sufficient amplicons for downstream community analyses. The PD samples showed a significantly lower alpha and a different beta eukaryotic diversity than the controls. Most strikingly, we observed a significantly higher relative abundance of sequence affiliated with the Geotrichum genus in the PD samples (39.7%), when compared to the control samples (0.05%). In addition, we observed lower relative abundances of sequences affiliated with Aspergillus/Penicillium, Charophyta/Linum, unidentified Opisthokonta and three genera of minor abundant zooflagellates in the PD samples. Our data add knowledge to the small body of data about the eukaryotic microbiota of PD patients and suggest a potential association of certain gut eukaryotes and PD.
format article
author Severin Weis
Alexandra Meisner
Andreas Schwiertz
Marcus M. Unger
Anouck Becker
Klaus Faßbender
Sylvia Schnell
Karl-Herbert Schäfer
Markus Egert
author_facet Severin Weis
Alexandra Meisner
Andreas Schwiertz
Marcus M. Unger
Anouck Becker
Klaus Faßbender
Sylvia Schnell
Karl-Herbert Schäfer
Markus Egert
author_sort Severin Weis
title Association between Parkinson’s disease and the faecal eukaryotic microbiota
title_short Association between Parkinson’s disease and the faecal eukaryotic microbiota
title_full Association between Parkinson’s disease and the faecal eukaryotic microbiota
title_fullStr Association between Parkinson’s disease and the faecal eukaryotic microbiota
title_full_unstemmed Association between Parkinson’s disease and the faecal eukaryotic microbiota
title_sort association between parkinson’s disease and the faecal eukaryotic microbiota
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/b43a5de64b4c404a96985bf3fa5b0f2a
work_keys_str_mv AT severinweis associationbetweenparkinsonsdiseaseandthefaecaleukaryoticmicrobiota
AT alexandrameisner associationbetweenparkinsonsdiseaseandthefaecaleukaryoticmicrobiota
AT andreasschwiertz associationbetweenparkinsonsdiseaseandthefaecaleukaryoticmicrobiota
AT marcusmunger associationbetweenparkinsonsdiseaseandthefaecaleukaryoticmicrobiota
AT anouckbecker associationbetweenparkinsonsdiseaseandthefaecaleukaryoticmicrobiota
AT klausfaßbender associationbetweenparkinsonsdiseaseandthefaecaleukaryoticmicrobiota
AT sylviaschnell associationbetweenparkinsonsdiseaseandthefaecaleukaryoticmicrobiota
AT karlherbertschafer associationbetweenparkinsonsdiseaseandthefaecaleukaryoticmicrobiota
AT markusegert associationbetweenparkinsonsdiseaseandthefaecaleukaryoticmicrobiota
_version_ 1718419026413092864