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Viral dysbiosis in children with new-onset celiac disease
by
Al Sarkhy, Ahmed
, Alasmi, Mona
, AlSaleem, Badr
, Al-Hussaini, Abdulrahman
, Assiri, Asaad
, El Mouzan, Mohammad
, Al Mofarreh, Mohammad
, Saeed, Anjum
in
Adolescent
/ Age of Onset
/ Autoimmune diseases
/ Bacteria
/ Biology and Life Sciences
/ Case-Control Studies
/ Celiac disease
/ Celiac Disease - virology
/ Child
/ Children
/ Complications and side effects
/ Deoxyribonucleic acid
/ Diagnosis
/ Discriminant analysis
/ Diseases
/ DNA
/ DNA, Viral - genetics
/ Dysbacteriosis
/ Dysbiosis - diagnosis
/ Dysbiosis - virology
/ Feces
/ Feces - virology
/ Female
/ Gastroenterology
/ Gluten
/ High-Throughput Nucleotide Sequencing
/ Hospitals
/ Humans
/ Immune system
/ Immunoglobulins
/ Inflammatory bowel disease
/ Laboratories
/ Male
/ Medicine and Health Sciences
/ Metabolism
/ Metagenomics
/ Metagenomics - methods
/ Microbiomes
/ Mucosa
/ Mucous Membrane - virology
/ Pathogenesis
/ Pediatrics
/ People and Places
/ Phages
/ Phylogeny
/ Physical Sciences
/ Research and Analysis Methods
/ Separation
/ Sequence Analysis, DNA - methods
/ Species
/ Taxonomy
/ Viruses
/ Viruses - classification
/ Viruses - genetics
/ Viruses - isolation & purification
2022
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Viral dysbiosis in children with new-onset celiac disease
by
Al Sarkhy, Ahmed
, Alasmi, Mona
, AlSaleem, Badr
, Al-Hussaini, Abdulrahman
, Assiri, Asaad
, El Mouzan, Mohammad
, Al Mofarreh, Mohammad
, Saeed, Anjum
in
Adolescent
/ Age of Onset
/ Autoimmune diseases
/ Bacteria
/ Biology and Life Sciences
/ Case-Control Studies
/ Celiac disease
/ Celiac Disease - virology
/ Child
/ Children
/ Complications and side effects
/ Deoxyribonucleic acid
/ Diagnosis
/ Discriminant analysis
/ Diseases
/ DNA
/ DNA, Viral - genetics
/ Dysbacteriosis
/ Dysbiosis - diagnosis
/ Dysbiosis - virology
/ Feces
/ Feces - virology
/ Female
/ Gastroenterology
/ Gluten
/ High-Throughput Nucleotide Sequencing
/ Hospitals
/ Humans
/ Immune system
/ Immunoglobulins
/ Inflammatory bowel disease
/ Laboratories
/ Male
/ Medicine and Health Sciences
/ Metabolism
/ Metagenomics
/ Metagenomics - methods
/ Microbiomes
/ Mucosa
/ Mucous Membrane - virology
/ Pathogenesis
/ Pediatrics
/ People and Places
/ Phages
/ Phylogeny
/ Physical Sciences
/ Research and Analysis Methods
/ Separation
/ Sequence Analysis, DNA - methods
/ Species
/ Taxonomy
/ Viruses
/ Viruses - classification
/ Viruses - genetics
/ Viruses - isolation & purification
2022
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Viral dysbiosis in children with new-onset celiac disease
by
Al Sarkhy, Ahmed
, Alasmi, Mona
, AlSaleem, Badr
, Al-Hussaini, Abdulrahman
, Assiri, Asaad
, El Mouzan, Mohammad
, Al Mofarreh, Mohammad
, Saeed, Anjum
in
Adolescent
/ Age of Onset
/ Autoimmune diseases
/ Bacteria
/ Biology and Life Sciences
/ Case-Control Studies
/ Celiac disease
/ Celiac Disease - virology
/ Child
/ Children
/ Complications and side effects
/ Deoxyribonucleic acid
/ Diagnosis
/ Discriminant analysis
/ Diseases
/ DNA
/ DNA, Viral - genetics
/ Dysbacteriosis
/ Dysbiosis - diagnosis
/ Dysbiosis - virology
/ Feces
/ Feces - virology
/ Female
/ Gastroenterology
/ Gluten
/ High-Throughput Nucleotide Sequencing
/ Hospitals
/ Humans
/ Immune system
/ Immunoglobulins
/ Inflammatory bowel disease
/ Laboratories
/ Male
/ Medicine and Health Sciences
/ Metabolism
/ Metagenomics
/ Metagenomics - methods
/ Microbiomes
/ Mucosa
/ Mucous Membrane - virology
/ Pathogenesis
/ Pediatrics
/ People and Places
/ Phages
/ Phylogeny
/ Physical Sciences
/ Research and Analysis Methods
/ Separation
/ Sequence Analysis, DNA - methods
/ Species
/ Taxonomy
/ Viruses
/ Viruses - classification
/ Viruses - genetics
/ Viruses - isolation & purification
2022
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Journal Article
Viral dysbiosis in children with new-onset celiac disease
2022
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Overview
Viruses are common components of the intestinal microbiome, modulating host bacterial metabolism and interacting with the immune system, with a possible role in the pathogenesis of immune-mediated diseases such as celiac disease (CeD). The objective of this study was to characterize the virome profile in children with new-onset CeD. We used metagenomic analysis of viral DNA in mucosal and fecal samples from children with CeD and controls and performed sequencing using the Nextera XT library preparation kit. Abundance log2 fold changes were calculated using differential expression and linear discriminant effect size. Shannon alpha and Bray–Curtis beta diversity were determined. A total of 40 children with CeD and 39 controls were included. We found viral dysbiosis in both fecal and mucosal samples. Examples of significantly more abundant species in fecal samples of children with CeD included
Human polyomavirus 2
,
Enterobacteria phage mEpX1
, and
Enterobacteria phage mEpX2
; whereas less abundant species included
Lactococcus phages ul36 and Streptococcus phage Abc2
. In mucosal samples however, no species were significantly associated with CeD. Shannon alpha diversity was not significantly different between CeD and non-CeD groups and Bray–Curtis beta diversity showed no significant separation between CeD and non-CeD samples in either mucosal or stool samples, whereas separation was clear in all samples. We identified significant viral dysbiosis in children with CeD, suggesting a potential role in the pathogenesis of CeD indicating the need for further studies.
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject
/ Bacteria
/ Child
/ Children
/ Complications and side effects
/ Diseases
/ DNA
/ Feces
/ Female
/ Gluten
/ High-Throughput Nucleotide Sequencing
/ Humans
/ Male
/ Medicine and Health Sciences
/ Mucosa
/ Phages
/ Research and Analysis Methods
/ Sequence Analysis, DNA - methods
/ Species
/ Taxonomy
/ Viruses
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