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Comparative analysis of the gut microbiota composition between knee osteoarthritis and Kashin-Beck disease in Northwest China
BACKGROUND: Osteoarthritis (OA) and Kashin-Beck disease (KBD) both are two severe osteochondral disorders. In this study, we aimed to compare the gut microbiota structure between OA and KBD patients. METHODS: Fecal samples collected from OA and KBD patients were used to characterize the gut microbio...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9150333/ https://www.ncbi.nlm.nih.gov/pubmed/35637503 http://dx.doi.org/10.1186/s13075-022-02819-5 |
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author | Ning, Yujie Hu, Minhan Gong, Yi Huang, Ruitian Xu, Ke Chen, Sijie Zhang, Feiyu Liu, Yanli Chen, Feihong Chang, Yanhai Zhao, Guanghui Li, Cheng Zhou, Rong Lammi, Mikko J. Guo, Xiong Wang, Xi |
author_facet | Ning, Yujie Hu, Minhan Gong, Yi Huang, Ruitian Xu, Ke Chen, Sijie Zhang, Feiyu Liu, Yanli Chen, Feihong Chang, Yanhai Zhao, Guanghui Li, Cheng Zhou, Rong Lammi, Mikko J. Guo, Xiong Wang, Xi |
author_sort | Ning, Yujie |
collection | PubMed |
description | BACKGROUND: Osteoarthritis (OA) and Kashin-Beck disease (KBD) both are two severe osteochondral disorders. In this study, we aimed to compare the gut microbiota structure between OA and KBD patients. METHODS: Fecal samples collected from OA and KBD patients were used to characterize the gut microbiota using 16S rDNA gene sequencing. To identify whether gut microbial changes at the species level are associated with the genes or functions of the gut bacteria between OA and KBD groups, metagenomic sequencing of fecal samples from OA and KBD subjects was performed. RESULTS: The OA group was characterized by elevated Epsilonbacteraeota and Firmicutes levels. A total of 52 genera were identified to be significantly differentially abundant between the two groups. The genera Raoultella, Citrobacter, Flavonifractor, g__Lachnospiraceae_UCG-004, and Burkholderia-Caballeronia-Paraburkholderia were more abundant in the OA group. The KBD group was characterized by higher Prevotella_9, Lactobacillus, Coprococcus_2, Senegalimassilia, and Holdemanella. The metagenomic sequencing showed that the Subdoligranulum_sp._APC924/74, Streptococcus_parasanguinis, and Streptococcus_salivarius were significantly increased in abundance in the OA group compared to those in the KBD group, and the species Prevotella_copri, Prevotella_sp._CAG:386, and Prevotella_stercorea were significantly decreased in abundance in the OA group compared to those in the KBD group by using metagenomic sequencing. CONCLUSION: Our study provides a comprehensive landscape of the gut microbiota between OA and KBD patients and provides clues for better understanding the mechanisms underlying the pathogenesis of OA and KBD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-022-02819-5. |
format | Online Article Text |
id | pubmed-9150333 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91503332022-05-31 Comparative analysis of the gut microbiota composition between knee osteoarthritis and Kashin-Beck disease in Northwest China Ning, Yujie Hu, Minhan Gong, Yi Huang, Ruitian Xu, Ke Chen, Sijie Zhang, Feiyu Liu, Yanli Chen, Feihong Chang, Yanhai Zhao, Guanghui Li, Cheng Zhou, Rong Lammi, Mikko J. Guo, Xiong Wang, Xi Arthritis Res Ther Research Article BACKGROUND: Osteoarthritis (OA) and Kashin-Beck disease (KBD) both are two severe osteochondral disorders. In this study, we aimed to compare the gut microbiota structure between OA and KBD patients. METHODS: Fecal samples collected from OA and KBD patients were used to characterize the gut microbiota using 16S rDNA gene sequencing. To identify whether gut microbial changes at the species level are associated with the genes or functions of the gut bacteria between OA and KBD groups, metagenomic sequencing of fecal samples from OA and KBD subjects was performed. RESULTS: The OA group was characterized by elevated Epsilonbacteraeota and Firmicutes levels. A total of 52 genera were identified to be significantly differentially abundant between the two groups. The genera Raoultella, Citrobacter, Flavonifractor, g__Lachnospiraceae_UCG-004, and Burkholderia-Caballeronia-Paraburkholderia were more abundant in the OA group. The KBD group was characterized by higher Prevotella_9, Lactobacillus, Coprococcus_2, Senegalimassilia, and Holdemanella. The metagenomic sequencing showed that the Subdoligranulum_sp._APC924/74, Streptococcus_parasanguinis, and Streptococcus_salivarius were significantly increased in abundance in the OA group compared to those in the KBD group, and the species Prevotella_copri, Prevotella_sp._CAG:386, and Prevotella_stercorea were significantly decreased in abundance in the OA group compared to those in the KBD group by using metagenomic sequencing. CONCLUSION: Our study provides a comprehensive landscape of the gut microbiota between OA and KBD patients and provides clues for better understanding the mechanisms underlying the pathogenesis of OA and KBD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-022-02819-5. BioMed Central 2022-05-30 2022 /pmc/articles/PMC9150333/ /pubmed/35637503 http://dx.doi.org/10.1186/s13075-022-02819-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Article Ning, Yujie Hu, Minhan Gong, Yi Huang, Ruitian Xu, Ke Chen, Sijie Zhang, Feiyu Liu, Yanli Chen, Feihong Chang, Yanhai Zhao, Guanghui Li, Cheng Zhou, Rong Lammi, Mikko J. Guo, Xiong Wang, Xi Comparative analysis of the gut microbiota composition between knee osteoarthritis and Kashin-Beck disease in Northwest China |
title | Comparative analysis of the gut microbiota composition between knee osteoarthritis and Kashin-Beck disease in Northwest China |
title_full | Comparative analysis of the gut microbiota composition between knee osteoarthritis and Kashin-Beck disease in Northwest China |
title_fullStr | Comparative analysis of the gut microbiota composition between knee osteoarthritis and Kashin-Beck disease in Northwest China |
title_full_unstemmed | Comparative analysis of the gut microbiota composition between knee osteoarthritis and Kashin-Beck disease in Northwest China |
title_short | Comparative analysis of the gut microbiota composition between knee osteoarthritis and Kashin-Beck disease in Northwest China |
title_sort | comparative analysis of the gut microbiota composition between knee osteoarthritis and kashin-beck disease in northwest china |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9150333/ https://www.ncbi.nlm.nih.gov/pubmed/35637503 http://dx.doi.org/10.1186/s13075-022-02819-5 |
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