Compositional and functional aberrance of the gut microbiota in treatment-naïve patients with primary Sjögren's syndrome

瘤胃球菌 微生物学 生物 肠道菌群 毒力 维管菌 梭杆菌 基因组 乳酸菌 拟杆菌 免疫学 链球菌 细菌 基因 遗传学
作者
Xinmiao Jia,Bingxuan Wu,Beidi Chen,Ketian Li,Yudong Liu,Yue Xu,Jun Wang,Xuan Zhang
出处
期刊:Journal of Autoimmunity [Elsevier BV]
卷期号:141: 103050-103050 被引量:8
标识
DOI:10.1016/j.jaut.2023.103050
摘要

To investigate the compositional and functional characteristics of the gut microbiota in primary Sjögren's syndrome (pSS) and compare them with those in systemic lupus erythematosus (SLE). Stool samples from 78 treatment-naïve pSS patients and 78 matched healthy controls were detected by shotgun metagenomic sequencing and compared with those from 49 treatment-naïve SLE patients. The virulence loads and mimotopes of the gut microbiota were also assessed by sequence alignment. The gut microbiota of treatment-naïve pSS patients had lower richness and evenness and showed a different community distribution than that of healthy controls. The microbial species enriched in the pSS-associated gut microbiota included Lactobacillus salivarius, Bacteroides fragilis, Ruminococcus gnavus, Clostridium bartlettii, Clostridium bolteae, Veillonella parvula, and Streptococcus parasanguinis. Lactobacillus salivarius was the most discriminating species in the pSS patients, especially in those with interstitial lung disease (ILD). Among the differentiating microbial pathways, the superpathway of l-phenylalanine biosynthesis was also further enriched in pSS complicated with ILD. There were more virulence genes carried by the gut microbiota in pSS patients, most of which encoded peritrichous flagella, fimbriae, or curli fimbriae, three types of bacterial surface organelles involved in bacterial colonization and invasion. Five microbial peptides with the potential to mimic pSS-related autoepitopes were also enriched in the pSS gut. SLE and pSS shared significant gut microbial traits, including community distribution, altered microbial taxonomy and pathways, and enriched virulence genes. However, Ruminococcus torques was depleted in pSS patients but enriched in SLE patients compared to healthy controls. The gut microbiota in treatment-naïve pSS patients was disturbed and shared significant similarity with that in SLE patients.
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