Variations of tongue coating microbiota in children with Henoch-Schonlein purpura nephritis

被引:1
作者
Pang, Shuang [1 ]
Zhao, Shuan [2 ,3 ,4 ,5 ]
Bai, Xiaohong [6 ]
Song, Nana [2 ,3 ,4 ,5 ]
Wang, Shengzhi [6 ]
Yu, Jiawei [2 ,3 ,4 ,5 ]
Zhang, Jun [6 ]
Ding, Xiaoqiang [2 ,3 ,4 ,5 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Longhua Hosp, Shanghai 200032, Peoples R China
[2] Fudan Univ, Zhongshan Hosp, Dept Nephrol, Shanghai, Peoples R China
[3] Shanghai Inst Kidney & Dialysis, Shanghai, Peoples R China
[4] Shanghai Key Lab Kidney & Blood Purificat, Shanghai, Peoples R China
[5] Shanghai Med Ctr Kidney Dis, Shanghai, Peoples R China
[6] Liaoning Univ Tradit Chinese Med, Affiliated Hosp, Dept Pediat, Shenyang 110032, Peoples R China
关键词
Microbiota; Tongue coating; Traditional Chinese medicine; 16S rRNA; Henoch-Schonlein purpura nephritis; ORAL MICROBIOTA; INSIGHTS; MALODOR;
D O I
10.1016/j.micpath.2021.105192
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Variations in the oral microbiota have been significantly correlated with the progress of autoimmune diseases, such as immunoglobulin A nephropathy and Henoch-Schonlein purpura (HSP). However, there is no report outlining the character of tongue coating microbiota variations in children with Henoch-Schonlein purpura nephritis (HSPN). Method: A total of 20 children with HSPN and 14 healthy controls were recruited for this research. Tongue coating samples of two groups were collected for 16S rRNA gene sequencing. The diversity, principal component analysis (PCA), nonmetric multidimensional scaling (NMDS), partial least squares discriminant analysis (PLS-DA), and linear discriminant analysis (LDA) effect size (LEfSe) were performed. Microbial function was assessed using the PICRUST. Results: The ACE and Chao indices were greatly lower in the HSPN group than in the HG (P = 0.001). The Shannon and Simpson indices were dramatically reduced in children with HSPN compared with those in the healthy controls (P = 0.005). Bacteroidales, Selenomonadales, Lactobacillales, Fusobacteriales, Neisseriales, and Actinomycetales composed more than 80% of all sequences, while Bacteroidales was the most generous order in both groups. PCA, NMDS and PLS-DA showed a marked difference between the control and HSPN groups. LEfSe analysis showed alteration of tongue coating microbiota in the HSPN group. There were 30 metabolic functions significantly differed between the two groups. Conclusions: Children with HSPN have substantially various tongue coating microbiota compared to healthy controls. Even though this research does not indicate causality, it is beneficial to enhance the possibility for coming microbial-based treatments to enhance the clinical effects of HSPN in children.
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页数:9
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