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Alterations in the gut virome in patients with ankylosing spondylitis

人病毒体 肠道菌群 瘤胃球菌 基因组 长尾病毒科 生物 梭杆菌门 微生物群 失调 免疫学 微生物学 遗传学 噬菌体 拟杆菌 细菌 大肠杆菌 基因 16S核糖体RNA
作者
Chen Li,Yan Zhang,Qiulong Yan,Ruochun Guo,Changming Chen,Shenghui Li,Qian Zhang,Jinxin Meng,Jie Ma,Wei You,Zhisong Wu,Wen Sun
出处
期刊:Frontiers in Immunology [Frontiers Media SA]
卷期号:14 被引量:7
标识
DOI:10.3389/fimmu.2023.1154380
摘要

Introduction Ankylosing spondylitis (AS), a chronic autoimmune disease, has been linked to the gut bacteriome. Methods To investigate the characteristics of the gut virome in AS, we profiled the gut viral community of 193 AS patients and 59 healthy subjects based on a metagenome-wide analysis of fecal metagenomes from two publicly available datasets. Results AS patients revealed a significant decrease in gut viral richness and a considerable alteration of the overall viral structure. At the family level, AS patients had an increased abundance of Gratiaviridae and Quimbyviridae and a decreased abundance of Drexlerviridae and Schitoviridae . We identified 1,004 differentially abundant viral operational taxonomic units (vOTUs) between patients and controls, including a higher proportion of AS-enriched Myoviridae viruses and control-enriched Siphoviridae viruses. Moreover, the AS-enriched vOTUs were more likely to infect bacteria such as Flavonifractor , Achromobacter , and Eggerthellaceae , whereas the control-enriched vOTUs were more likely to be Blautia , Ruminococcus , Collinsella , Prevotella , and Faecalibacterium bacteriophages. Additionally, some viral functional orthologs differed significantly in frequency between the AS-enriched and control-enriched vOTUs, suggesting the functional role of these AS-associated viruses. Moreover, we trained classification models based on gut viral signatures to discriminate AS patients from healthy controls, with an optimal area under the receiver operator characteristic curve (AUC) up to 0.936, suggesting the clinical potential of the gut virome for diagnosing AS. Discussion This work provides novel insight into the AS gut virome, and the findings may guide future mechanistic and therapeutic studies for other autoimmune diseases.
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