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

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...

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Autores principales: Chen, Zhangling, Xiao, Ying, Jia, Yan, Lin, Qiurong, Qian, Yu, Cui, Lipu, Xiang, Zhaoyu, Li, Mingfang, Yang, Chenhao, Zou, Haidong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10557306/
https://www.ncbi.nlm.nih.gov/pubmed/37803284
http://dx.doi.org/10.1186/s12866-023-03013-6
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author Chen, Zhangling
Xiao, Ying
Jia, Yan
Lin, Qiurong
Qian, Yu
Cui, Lipu
Xiang, Zhaoyu
Li, Mingfang
Yang, Chenhao
Zou, Haidong
author_facet Chen, Zhangling
Xiao, Ying
Jia, Yan
Lin, Qiurong
Qian, Yu
Cui, Lipu
Xiang, Zhaoyu
Li, Mingfang
Yang, Chenhao
Zou, Haidong
author_sort Chen, Zhangling
collection PubMed
description 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.
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spelling pubmed-105573062023-10-07 Metagenomic analysis of microbiological changes on the ocular surface of diabetic children and adolescents with a dry eye Chen, Zhangling Xiao, Ying Jia, Yan Lin, Qiurong Qian, Yu Cui, Lipu Xiang, Zhaoyu Li, Mingfang Yang, Chenhao Zou, Haidong BMC Microbiol Research 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. BioMed Central 2023-10-06 /pmc/articles/PMC10557306/ /pubmed/37803284 http://dx.doi.org/10.1186/s12866-023-03013-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Chen, Zhangling
Xiao, Ying
Jia, Yan
Lin, Qiurong
Qian, Yu
Cui, Lipu
Xiang, Zhaoyu
Li, Mingfang
Yang, Chenhao
Zou, Haidong
Metagenomic analysis of microbiological changes on the ocular surface of diabetic children and adolescents with a dry eye
title Metagenomic analysis of microbiological changes on the ocular surface of diabetic children and adolescents with a dry eye
title_full Metagenomic analysis of microbiological changes on the ocular surface of diabetic children and adolescents with a dry eye
title_fullStr Metagenomic analysis of microbiological changes on the ocular surface of diabetic children and adolescents with a dry eye
title_full_unstemmed Metagenomic analysis of microbiological changes on the ocular surface of diabetic children and adolescents with a dry eye
title_short Metagenomic analysis of microbiological changes on the ocular surface of diabetic children and adolescents with a dry eye
title_sort metagenomic analysis of microbiological changes on the ocular surface of diabetic children and adolescents with a dry eye
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10557306/
https://www.ncbi.nlm.nih.gov/pubmed/37803284
http://dx.doi.org/10.1186/s12866-023-03013-6
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