Metagenomic analysis of microbiological changes on the ocular surface of diabetic children and adolescents with a dry eye

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Reviewed Marked as Reviewed by ChiomaBlessing on 2023-12-22
study design
Citation
PMID PubMed identifier for scientific articles.
DOI Digital object identifier for electronic documents.
URI
Authors
Chen Z, Xiao Y, Jia Y, Lin Q, Qian Y, Cui L, Xiang Z, Li M, Yang C, Zou H
Journal
BMC microbiology
Year
2023
Keywords:
Children and adolescents, Diabetes mellitus, Dry eye, Metagenome, Microecology, Ocular surface
BACKGROUND: Microbiome changes on the ocular surface may cause dry eyes. A metagenome assay was used to compare the microbiome composition and function of the ocular surface between diabetic children and adolescents with dry eye, diabetic children and adolescents without dry eye, and normal children. MATERIALS AND METHODS: Twenty children and adolescents aged 8 to 16 with diabetes were selected from the Shanghai Children and Adolescent Diabetes Eye Study. Ten healthy children and adolescents belonging to the same age group were selected from the outpatient clinic during the same period. The participants were classified into the dry eye group (DM-DE group, n = 10), the non-dry eye group (DM-NDE group, n = 10) and the normal group (NDM group, n = 10). A conjunctival sac swab was collected for metagenomic sequencing, and the relationship between the microbiome composition and functional gene differences on the ocular surface with dry eye was studied. RESULTS: The classification composition and metabolic function of the microorganisms on the ocular surface of children in the 3 groups were analyzed. It was found that children's ocular microbiota was composed of bacteria, viruses and fungi. There were significant differences in α diversity and β diversity of microbial composition of ocular surface between DM-DE group and NDM group(P<0.05). There were significant differences in α and β diversity of metabolic pathways between the two groups(P<0.05). The functional pathways of ocular surface microorganisms in diabetic children with dry eyes were mainly derived from human disease, antibiotic resistance genes, carbohydrate, coenzyme and lipid transport and metabolism-related functional genes; In normal children, the functional pathways were mainly derived from replication, recombination, repair, signal transduction and defense-related functional genes. CONCLUSION: The DM-DE group have unique microbial composition and functional metabolic pathways. The dominant species and unique metabolic pathways of the ocular surface in the DM-DE group may be involved in the pathogenesis of dry eye in diabetic children.

Experiment 1


Reviewed Marked as Reviewed by ChiomaBlessing on 2023-12-22

Curated date: 2023/11/11

Curator: Mary Bearkland

Revision editor(s): Mary Bearkland, ChiomaBlessing

Subjects

Location of subjects
China
Host species Species from which microbiome was sampled. Contact us to have more species added.
Homo sapiens
Body site Anatomical site where microbial samples were extracted from according to the Uber Anatomy Ontology
Conjunctival sac Conjunctiva serous sac,Subbrillar sac,Conjunctival sac,conjunctival sac
Condition The experimental condition / phenotype studied according to the Experimental Factor Ontology
Dry eye syndrome dry eye,Dry Eye Syndrome,dry eye syndrome,Dry Eye Syndromes,dry eye(s),eye(s), dry,KCS,Keraconjunctivitis sicca,Keratoconjunctivitis Sicca,Keratoconjunctivitis sicca,keratoconjunctivitis sicca,Keratoconjunctivitis sicca (disorder),sicca, keratoconjunctivitis,Tear film insufficiency,tear film insufficiency,Dry eye syndrome
Group 0 name Corresponds to the control (unexposed) group for case-control studies
Normal healthy (NDM) children
Group 1 name Corresponds to the case (exposed) group for case-control studies
Diabetic children with Dry Eye Disease (DM-DE)
Group 1 definition Diagnostic criteria applied to define the specific condition / phenotype represented in the case (exposed) group
Children aged 8-16 with Diabetes and Dry Eye Disease
Group 0 sample size Number of subjects in the control (unexposed) group
10
Group 1 sample size Number of subjects in the case (exposed) group
10

Lab analysis

Sequencing type
WMS
16S variable region One or more hypervariable region(s) of the bacterial 16S gene
Not specified
Sequencing platform Manufacturer and experimental platform used for quantifying microbial abundance
Illumina

Statistical Analysis

Data transformation Data transformation applied to microbial abundance measurements prior to differential abundance testing (if any).
relative abundances
Statistical test
LEfSe
Significance threshold p-value or FDR threshold used for differential abundance testing (if any)
0.05
Matched on Factors on which subjects have been matched on in a case-control study
age, body mass index, sex

Alpha Diversity

Chao1 Abundance-based estimator of species richness
decreased
Richness Number of species
decreased

Signature 1

Reviewed Marked as Reviewed by ChiomaBlessing on 2023-12-22

Curated date: 2023/11/11

Curator: Mary Bearkland

Revision editor(s): Mary Bearkland, ChiomaBlessing

Source: Figure 3g and Results within text (Page 7, Last 6 lines, Under subheading: Composition and difference analysis of the ocular microbiome)

Description: Fig 3g: Species composition with significant difference at the species level between the NDM and DM-DE groups (top 20)

Abundance in Group 1: decreased abundance in Diabetic children with Dry Eye Disease (DM-DE)

NCBI Quality ControlLinks
Mycobacteroides abscessus
Novosphingobium nitrogenifigens
Novosphingobium sp. Fuku2-ISO-50
Paenibacillus odorifer
Staphylococcus aureus
Streptococcus gordonii
Vibrio agarivorans

Revision editor(s): Mary Bearkland, ChiomaBlessing

Signature 2

Reviewed Marked as Reviewed by ChiomaBlessing on 2023-12-22

Curated date: 2023/11/11

Curator: Mary Bearkland

Revision editor(s): Mary Bearkland, ChiomaBlessing

Source: Figure 3g and Results within text (Page 7, Last 6 lines, Under subheading: Composition and difference analysis of the ocular microbiome)

Description: Figure 3g Species composition with significant difference at the species level between the NDM and DM-DE groups (top 20)

Abundance in Group 1: increased abundance in Diabetic children with Dry Eye Disease (DM-DE)

NCBI Quality ControlLinks
Cordyceps militaris
Enterobacter mori
Leuconostoc sp. DORA_2
Salmonella enterica
Vibrio vulnificus

Revision editor(s): Mary Bearkland, ChiomaBlessing

Experiment 2


Reviewed Marked as Reviewed by ChiomaBlessing on 2023-12-26

Curated date: 2023/11/18

Curator: Mary Bearkland

Revision editor(s): Mary Bearkland, ChiomaBlessing

Differences from previous experiment shown

Subjects

Lab analysis

Statistical Analysis

Statistical test
ANOSIM

Alpha Diversity

Chao1 Abundance-based estimator of species richness
decreased
Richness Number of species
decreased

Signature 1

Reviewed Marked as Reviewed by ChiomaBlessing on 2023-12-26

Curated date: 2023/11/18

Curator: Mary Bearkland

Revision editor(s): Mary Bearkland, ChiomaBlessing

Source: Text on page 5; Under subheading "Composition and difference analysis of the ocular microbiome"

Description: Composition and Differential analysis of the ocular microbiome between NDM and DM-DE groups

Abundance in Group 1: increased abundance in Diabetic children with Dry Eye Disease (DM-DE)

NCBI Quality ControlLinks
Actinomycetota
Apicomplexa
Ascomycota
Chlamydia trachomatis
Enterobacter
Escherichia coli
Leuconostoc sp. DORA_2
Mycobacterium leprae
Plasmodium ovale
Salmonella enterica
Vibrio

Revision editor(s): Mary Bearkland, ChiomaBlessing

Signature 2

Reviewed Marked as Reviewed by ChiomaBlessing on 2023-12-26

Curated date: 2023/11/18

Curator: Mary Bearkland

Revision editor(s): Mary Bearkland, ChiomaBlessing

Source: Text on page 5; Under subheading "Composition and difference analysis of the ocular microbiome"

Description: Composition and Differential analysis of the ocular microbiome between NDM and DM-DE groups

Abundance in Group 1: decreased abundance in Diabetic children with Dry Eye Disease (DM-DE)

NCBI Quality ControlLinks
Acinetobacter johnsonii
Bacillota
Enterococcus faecalis
Pseudomonadota
Staphylococcus aureus
Streptococcus pneumoniae

Revision editor(s): Mary Bearkland, ChiomaBlessing