Cargando…

Patients with Infections of The Central Nervous System Have Lowered Gut Microbiota Alpha Diversity

There are multiple lines of evidence for the existence of communication between the central nervous system (CNS), gut, and intestinal microbiome. Despite extensive analysis conducted on various neurological disorders, the gut microbiome was not yet analyzed in neuroinfections. In the current study,...

Descripción completa

Detalles Bibliográficos
Autores principales: Grochowska, Marta, Laskus, Tomasz, Paciorek, Marcin, Pollak, Agnieszka, Lechowicz, Urszula, Makowiecki, Michał, Horban, Andrzej, Radkowski, Marek, Perlejewski, Karol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9318043/
https://www.ncbi.nlm.nih.gov/pubmed/35877424
http://dx.doi.org/10.3390/cimb44070200
_version_ 1784755201908932608
author Grochowska, Marta
Laskus, Tomasz
Paciorek, Marcin
Pollak, Agnieszka
Lechowicz, Urszula
Makowiecki, Michał
Horban, Andrzej
Radkowski, Marek
Perlejewski, Karol
author_facet Grochowska, Marta
Laskus, Tomasz
Paciorek, Marcin
Pollak, Agnieszka
Lechowicz, Urszula
Makowiecki, Michał
Horban, Andrzej
Radkowski, Marek
Perlejewski, Karol
author_sort Grochowska, Marta
collection PubMed
description There are multiple lines of evidence for the existence of communication between the central nervous system (CNS), gut, and intestinal microbiome. Despite extensive analysis conducted on various neurological disorders, the gut microbiome was not yet analyzed in neuroinfections. In the current study, we analyzed the gut microbiome in 47 consecutive patients hospitalized with neuroinfection (26 patients had viral encephalitis/meningitis; 8 patients had bacterial meningitis) and in 20 matched for age and gender health controls. Using the QIIME pipeline, 16S rRNA sequencing and classification into operational taxonomic units (OTUs) were performed on the earliest stool sample available. Bacterial taxa such as Clostridium, Anaerostipes, Lachnobacterium, Lachnospira, and Roseburia were decreased in patients with neuroinfection when compared to controls. Alpha diversity metrics showed lower within-sample diversity in patients with neuroinfections, though there were no differences in beta diversity. Furthermore, there was no significant change by short-term (1–3 days) antibiotic treatment on the gut microbiota, although alpha diversity metrics, such as Chao1 and Shannon’s index, were close to being statistically significant. The cause of differences between patients with neuroinfections and controls is unclear and could be due to inflammation accompanying the disease; however, the effect of diet modification and/or hospitalization cannot be excluded.
format Online
Article
Text
id pubmed-9318043
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-93180432022-07-27 Patients with Infections of The Central Nervous System Have Lowered Gut Microbiota Alpha Diversity Grochowska, Marta Laskus, Tomasz Paciorek, Marcin Pollak, Agnieszka Lechowicz, Urszula Makowiecki, Michał Horban, Andrzej Radkowski, Marek Perlejewski, Karol Curr Issues Mol Biol Article There are multiple lines of evidence for the existence of communication between the central nervous system (CNS), gut, and intestinal microbiome. Despite extensive analysis conducted on various neurological disorders, the gut microbiome was not yet analyzed in neuroinfections. In the current study, we analyzed the gut microbiome in 47 consecutive patients hospitalized with neuroinfection (26 patients had viral encephalitis/meningitis; 8 patients had bacterial meningitis) and in 20 matched for age and gender health controls. Using the QIIME pipeline, 16S rRNA sequencing and classification into operational taxonomic units (OTUs) were performed on the earliest stool sample available. Bacterial taxa such as Clostridium, Anaerostipes, Lachnobacterium, Lachnospira, and Roseburia were decreased in patients with neuroinfection when compared to controls. Alpha diversity metrics showed lower within-sample diversity in patients with neuroinfections, though there were no differences in beta diversity. Furthermore, there was no significant change by short-term (1–3 days) antibiotic treatment on the gut microbiota, although alpha diversity metrics, such as Chao1 and Shannon’s index, were close to being statistically significant. The cause of differences between patients with neuroinfections and controls is unclear and could be due to inflammation accompanying the disease; however, the effect of diet modification and/or hospitalization cannot be excluded. MDPI 2022-06-29 /pmc/articles/PMC9318043/ /pubmed/35877424 http://dx.doi.org/10.3390/cimb44070200 Text en © 2022 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 Article
Grochowska, Marta
Laskus, Tomasz
Paciorek, Marcin
Pollak, Agnieszka
Lechowicz, Urszula
Makowiecki, Michał
Horban, Andrzej
Radkowski, Marek
Perlejewski, Karol
Patients with Infections of The Central Nervous System Have Lowered Gut Microbiota Alpha Diversity
title Patients with Infections of The Central Nervous System Have Lowered Gut Microbiota Alpha Diversity
title_full Patients with Infections of The Central Nervous System Have Lowered Gut Microbiota Alpha Diversity
title_fullStr Patients with Infections of The Central Nervous System Have Lowered Gut Microbiota Alpha Diversity
title_full_unstemmed Patients with Infections of The Central Nervous System Have Lowered Gut Microbiota Alpha Diversity
title_short Patients with Infections of The Central Nervous System Have Lowered Gut Microbiota Alpha Diversity
title_sort patients with infections of the central nervous system have lowered gut microbiota alpha diversity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9318043/
https://www.ncbi.nlm.nih.gov/pubmed/35877424
http://dx.doi.org/10.3390/cimb44070200
work_keys_str_mv AT grochowskamarta patientswithinfectionsofthecentralnervoussystemhaveloweredgutmicrobiotaalphadiversity
AT laskustomasz patientswithinfectionsofthecentralnervoussystemhaveloweredgutmicrobiotaalphadiversity
AT paciorekmarcin patientswithinfectionsofthecentralnervoussystemhaveloweredgutmicrobiotaalphadiversity
AT pollakagnieszka patientswithinfectionsofthecentralnervoussystemhaveloweredgutmicrobiotaalphadiversity
AT lechowiczurszula patientswithinfectionsofthecentralnervoussystemhaveloweredgutmicrobiotaalphadiversity
AT makowieckimichał patientswithinfectionsofthecentralnervoussystemhaveloweredgutmicrobiotaalphadiversity
AT horbanandrzej patientswithinfectionsofthecentralnervoussystemhaveloweredgutmicrobiotaalphadiversity
AT radkowskimarek patientswithinfectionsofthecentralnervoussystemhaveloweredgutmicrobiotaalphadiversity
AT perlejewskikarol patientswithinfectionsofthecentralnervoussystemhaveloweredgutmicrobiotaalphadiversity