AUTHOR=Chen Changming , Yan Qiulong , Yao Xueming , Li Shenghui , Lv Qingbo , Wang Guangyang , Zhong Qin , Tang Fang , Liu Zhengqi , Huang Ying , An Yang , Zhou Jing , Zhang Qiongyu , Zhang Aiqin , Ullah Hayan , Zhang Yue , Liu Can , Zhu Dan , Li Hufan , Sun Wen , Ma Wukai 

TITLE=Alterations of the gut virome in patients with systemic lupus erythematosus

JOURNAL=Frontiers in Immunology

VOLUME=13

YEAR=2023

URL=https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2022.1050895

DOI=10.3389/fimmu.2022.1050895

ISSN=1664-3224

ABSTRACT=<sec><title>Background</title><p>Systemic lupus erythematosus (SLE) is a systemic autoimmune disease that has been linked to the dysbiosis of the gut microbiome and virome. However, the potential characterization of the gut virome in SLE patients needs to be explored more extensively.</p></sec><sec><title>Methods</title><p>Herein, we analyzed the gut viral community of 16 SLE patients and 31 healthy controls using both bulk and virus-like particle (VLP)-based metagenomic sequencing of their fecal samples. A total of 15,999 non-redundant viral operational taxonomic units (vOTUs) were identified from the metagenomic assembled contigs and used for gut virome profiling.</p></sec><sec><title>Results</title><p>SLE patients exhibited a significant decrease in gut viral diversity in the bulk metagenome dataset, but this change was not significant in the VLP metagenome dataset. Also, considerable alterations of the overall gut virome composition and remarkable changes in the viral family compositions were observed in SLE patients compared with healthy controls, as observed in both two technologies. We identified 408 vOTUs (177 SLE-enriched and 231 control-enriched) with significantly different relative abundances between patients and controls in the bulk virome, and 18 vOTUs (17 SLE-enriched in 1 control-enriched) in the VLP virome. The SLE-enriched vOTUs included numerous <italic>Siphoviridae</italic>, <italic>Microviridae</italic>, and <italic>crAss-like</italic> viruses and were frequently predicted to infect <italic>Bacteroides</italic>, <italic>Parabacteroides</italic>, and <italic>Ruminococcus_E</italic>, while the control-enriched contained numerous members of <italic>Siphoviridae</italic> and <italic>Myoviridae</italic> and were predicted to infect <italic>Prevotella</italic> and <italic>Lachnospirales_CAG-274</italic>. We explored the correlations between gut viruses and bacteria and found that some <italic>Lachnospirales_CAG-274</italic> and <italic>Hungatella_A</italic> phages may play key roles in the virus-bacterium network. Furthermore, we explored the gut viral signatures for disease discrimination and achieved an area under the receiver operator characteristic curve (AUC) of above 0.95, suggesting the potential of the gut virome in the prediction of SLE.</p></sec><sec><title>Conclusion</title><p>Our findings demonstrated the alterations in viral diversity and taxonomic composition of the gut virome of SLE patients. Further research into the etiology of SLE and the gut viral community will open up new avenues for treating and preventing SLE and other autoimmune diseases.</p></sec>