Sex Variations in the Oral Microbiomes of Youths with Severe Periodontitis

Objective. Periodontitis is an inflammatory disease of microbial etiology caused primarily by dysbiosis of the oral microbiota. Our aim was to compare variations in the composition of the oral microbiomes of youths with severe periodontitis according to gender. Methods. Subgingival plaque samples co...

Full description

Saved in:
Bibliographic Details
Main Authors: Ya-Qiong Zhao, Ying-Hui Zhou, Jie Zhao, Yao Feng, Zheng-Rong Gao, Qin Ye, Qiong Liu, Yun Chen, Shao-Hui Zhang, Li Tan, Marie Aimee Dusenge, Jing Hu, Yun-Zhi Feng, Fei Yan, Yue Guo
Format: Article
Language:English
Published: Wiley 2021-01-01
Series:Journal of Immunology Research
Online Access:http://dx.doi.org/10.1155/2021/8124593
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832561161243983872
author Ya-Qiong Zhao
Ying-Hui Zhou
Jie Zhao
Yao Feng
Zheng-Rong Gao
Qin Ye
Qiong Liu
Yun Chen
Shao-Hui Zhang
Li Tan
Marie Aimee Dusenge
Jing Hu
Yun-Zhi Feng
Fei Yan
Yue Guo
author_facet Ya-Qiong Zhao
Ying-Hui Zhou
Jie Zhao
Yao Feng
Zheng-Rong Gao
Qin Ye
Qiong Liu
Yun Chen
Shao-Hui Zhang
Li Tan
Marie Aimee Dusenge
Jing Hu
Yun-Zhi Feng
Fei Yan
Yue Guo
author_sort Ya-Qiong Zhao
collection DOAJ
description Objective. Periodontitis is an inflammatory disease of microbial etiology caused primarily by dysbiosis of the oral microbiota. Our aim was to compare variations in the composition of the oral microbiomes of youths with severe periodontitis according to gender. Methods. Subgingival plaque samples collected from 17 patients with severe periodontitis (11 males and 6 females) were split for 16S rRNA gene sequencing. The composition, α-diversity, and β-diversity of the patients’ oral microbiomes were compared between the males and the females. Linear discriminant analysis effect size (LEfSe) was used to analyze the specific taxa enriched in the two groups. Functional profiles (KEGG pathways) were obtained using PICRUSt based on 16S rRNA gene sequencing data. Results. The Chao1 index and phylogenetic diversity whole tree were significantly higher in males than in females. The Simpson and Shannon indices were not significantly different between the two groups. β-Diversity suggested that the samples were reasonably divided into groups. The Kruskal-Wallis test based on the relative abundance of species, combined with the LEfSe analysis showed that the dominant bacteria in males were Pseudomonas and Papillibacter, whereas the dominant bacteria in women were Fusobacteriales and Tannerella. KEGG analysis predicted that the variation in the oral microbiome may be related to the immune system in women, whereas immune system diseases were the dominant pathway in men. Conclusion. We found sex-specific differences in the oral microbiome in a sample of youths with severe periodontitis. The differences may be related to changes in immune homeostasis and lead to a better understanding of periodontitis.
format Article
id doaj-art-9304d4cdcac449ed91077461e4a73280
institution Kabale University
issn 2314-8861
2314-7156
language English
publishDate 2021-01-01
publisher Wiley
record_format Article
series Journal of Immunology Research
spelling doaj-art-9304d4cdcac449ed91077461e4a732802025-02-03T01:25:48ZengWileyJournal of Immunology Research2314-88612314-71562021-01-01202110.1155/2021/81245938124593Sex Variations in the Oral Microbiomes of Youths with Severe PeriodontitisYa-Qiong Zhao0Ying-Hui Zhou1Jie Zhao2Yao Feng3Zheng-Rong Gao4Qin Ye5Qiong Liu6Yun Chen7Shao-Hui Zhang8Li Tan9Marie Aimee Dusenge10Jing Hu11Yun-Zhi Feng12Fei Yan13Yue Guo14Department of Stomatology, The Second Xiangya Hospital of Central South University, Changsha 410011, Hunan, ChinaNational Clinical Research Center for Metabolic Diseases, Hunan Provincial Key Laboratory of Metabolic Bone Diseases, and Department of Metabolism and Endocrinology, The Second Xiangya Hospital of Central South University, Changsha 410011, Hunan, ChinaDepartment of Stomatology, The Second Xiangya Hospital of Central South University, Changsha 410011, Hunan, ChinaDepartment of Stomatology, The Second Xiangya Hospital of Central South University, Changsha 410011, Hunan, ChinaDepartment of Stomatology, The Second Xiangya Hospital of Central South University, Changsha 410011, Hunan, ChinaDepartment of Stomatology, The Second Xiangya Hospital of Central South University, Changsha 410011, Hunan, ChinaDepartment of Stomatology, The Second Xiangya Hospital of Central South University, Changsha 410011, Hunan, ChinaDepartment of Stomatology, The Second Xiangya Hospital of Central South University, Changsha 410011, Hunan, ChinaDepartment of Stomatology, The Second Xiangya Hospital of Central South University, Changsha 410011, Hunan, ChinaDepartment of Stomatology, The Second Xiangya Hospital of Central South University, Changsha 410011, Hunan, ChinaDepartment of Stomatology, The Second Xiangya Hospital of Central South University, Changsha 410011, Hunan, ChinaDepartment of Stomatology, The Second Xiangya Hospital of Central South University, Changsha 410011, Hunan, ChinaDepartment of Stomatology, The Second Xiangya Hospital of Central South University, Changsha 410011, Hunan, ChinaHunan Key Laboratory of Oral Health Research & Hunan 3D Printing Engineering Research Center of Oral Care & Hunan Clinical Research Center of Oral Major Diseases and Oral Health & Xiangya Stomatological Hospital & Xiangya School of Stomatology, Central South University, Changsha 410008, ChinaDepartment of Stomatology, The Second Xiangya Hospital of Central South University, Changsha 410011, Hunan, ChinaObjective. Periodontitis is an inflammatory disease of microbial etiology caused primarily by dysbiosis of the oral microbiota. Our aim was to compare variations in the composition of the oral microbiomes of youths with severe periodontitis according to gender. Methods. Subgingival plaque samples collected from 17 patients with severe periodontitis (11 males and 6 females) were split for 16S rRNA gene sequencing. The composition, α-diversity, and β-diversity of the patients’ oral microbiomes were compared between the males and the females. Linear discriminant analysis effect size (LEfSe) was used to analyze the specific taxa enriched in the two groups. Functional profiles (KEGG pathways) were obtained using PICRUSt based on 16S rRNA gene sequencing data. Results. The Chao1 index and phylogenetic diversity whole tree were significantly higher in males than in females. The Simpson and Shannon indices were not significantly different between the two groups. β-Diversity suggested that the samples were reasonably divided into groups. The Kruskal-Wallis test based on the relative abundance of species, combined with the LEfSe analysis showed that the dominant bacteria in males were Pseudomonas and Papillibacter, whereas the dominant bacteria in women were Fusobacteriales and Tannerella. KEGG analysis predicted that the variation in the oral microbiome may be related to the immune system in women, whereas immune system diseases were the dominant pathway in men. Conclusion. We found sex-specific differences in the oral microbiome in a sample of youths with severe periodontitis. The differences may be related to changes in immune homeostasis and lead to a better understanding of periodontitis.http://dx.doi.org/10.1155/2021/8124593
spellingShingle Ya-Qiong Zhao
Ying-Hui Zhou
Jie Zhao
Yao Feng
Zheng-Rong Gao
Qin Ye
Qiong Liu
Yun Chen
Shao-Hui Zhang
Li Tan
Marie Aimee Dusenge
Jing Hu
Yun-Zhi Feng
Fei Yan
Yue Guo
Sex Variations in the Oral Microbiomes of Youths with Severe Periodontitis
Journal of Immunology Research
title Sex Variations in the Oral Microbiomes of Youths with Severe Periodontitis
title_full Sex Variations in the Oral Microbiomes of Youths with Severe Periodontitis
title_fullStr Sex Variations in the Oral Microbiomes of Youths with Severe Periodontitis
title_full_unstemmed Sex Variations in the Oral Microbiomes of Youths with Severe Periodontitis
title_short Sex Variations in the Oral Microbiomes of Youths with Severe Periodontitis
title_sort sex variations in the oral microbiomes of youths with severe periodontitis
url http://dx.doi.org/10.1155/2021/8124593
work_keys_str_mv AT yaqiongzhao sexvariationsintheoralmicrobiomesofyouthswithsevereperiodontitis
AT yinghuizhou sexvariationsintheoralmicrobiomesofyouthswithsevereperiodontitis
AT jiezhao sexvariationsintheoralmicrobiomesofyouthswithsevereperiodontitis
AT yaofeng sexvariationsintheoralmicrobiomesofyouthswithsevereperiodontitis
AT zhengronggao sexvariationsintheoralmicrobiomesofyouthswithsevereperiodontitis
AT qinye sexvariationsintheoralmicrobiomesofyouthswithsevereperiodontitis
AT qiongliu sexvariationsintheoralmicrobiomesofyouthswithsevereperiodontitis
AT yunchen sexvariationsintheoralmicrobiomesofyouthswithsevereperiodontitis
AT shaohuizhang sexvariationsintheoralmicrobiomesofyouthswithsevereperiodontitis
AT litan sexvariationsintheoralmicrobiomesofyouthswithsevereperiodontitis
AT marieaimeedusenge sexvariationsintheoralmicrobiomesofyouthswithsevereperiodontitis
AT jinghu sexvariationsintheoralmicrobiomesofyouthswithsevereperiodontitis
AT yunzhifeng sexvariationsintheoralmicrobiomesofyouthswithsevereperiodontitis
AT feiyan sexvariationsintheoralmicrobiomesofyouthswithsevereperiodontitis
AT yueguo sexvariationsintheoralmicrobiomesofyouthswithsevereperiodontitis