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Tytuł pozycji:

A Comparative Pilot Study of Bacterial and Fungal Dysbiosis in Neurodevelopmental Disorders and Gastrointestinal Disorders: Commonalities, Specificities and Correlations with Lifestyle

Tytuł:
A Comparative Pilot Study of Bacterial and Fungal Dysbiosis in Neurodevelopmental Disorders and Gastrointestinal Disorders: Commonalities, Specificities and Correlations with Lifestyle
Autorzy:
Ibrahim Laswi
Ameena Shafiq
Dana Al-Ali
Zain Burney
Krishnadev Pillai
Mohammad Salameh
Nada Mhaimeed
Dalia Zakaria
Ali Chaari
Noha A. Yousri
Ghizlane Bendriss
Temat:
dysbiosis
microbiome
bacteriome
mycobiome
neurodevelopmental disorders
gastrointestinal disorders
Biology (General)
QH301-705.5
Źródło:
Microorganisms, Vol 9, Iss 4, p 741 (2021)
Wydawca:
MDPI AG, 2021.
Rok publikacji:
2021
Kolekcja:
LCC:Biology (General)
Typ dokumentu:
article
Opis pliku:
electronic resource
Język:
English
ISSN:
2076-2607
Relacje:
https://www.mdpi.com/2076-2607/9/4/741; https://doaj.org/toc/2076-2607
DOI:
10.3390/microorganisms9040741
Dostęp URL:
https://doaj.org/article/bce2185ce69142c199efdf02bbcc0423  Link otwiera się w nowym oknie
Numer akcesji:
edsdoj.bce2185ce69142c199efdf02bbcc0423
Czasopismo naukowe
Gastrointestinal disorders (GIDs) are a common comorbidity in patients with neurodevelopmental disorders (NDDs), while anxiety-like behaviors are common among patients with gastrointestinal diseases. It is still unclear as to which microbes differentiate these two groups. This pilot study aims at proposing an answer by exploring both the bacteriome and the mycobiome in a cohort of 55 volunteers with NDD, GID or controls, while accounting for additional variables that are not commonly included such as probiotic intake and diet. Recruited participants answered a questionnaire and provided a stool sample using the Fisherbrand collection kit. Bacterial and fungal DNA was extracted using the Qiagen Stool minikit. Sequencing (16sRNA and ITS) and phylogenetic analyses were performed using the PE300 Illumina Miseq v3 sequencing. Statistical analysis was performed using the R package. Results showed a significant decrease in bacterial alpha diversity in both NDD and GID, but an increased fungal alpha diversity in NDD. Data pointed at a significant bacterial dysbiosis between the three groups, but the mycobiome dysbiosis is more pronounced in NDD than in GID. Fungi seem to be more affected by probiotics, diet and antibiotic exposure and are proposed to be the main key player in differentiation between NDD and GID dybiosis.

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