{"title":"类风湿性关节炎中不同的口腔 DNA 病毒特征:一项试点研究。","authors":"Mahin Ghorbani, Nooshin Khoshdoozmasouleh","doi":"10.1080/20002297.2024.2348260","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Despite evidence linking viruses and oral microbiome to rheumatoid arthritis (RA), limited whole genome sequencing research has been conducted on the oral virome (a viral component of the microbiome) of untreated RA patients. This pilot research seeks to address this knowledge gap by comparing the oral virome of untreated rheumatoid arthritis patients (RAs) and healthy individuals (HCs).</p><p><strong>Method: </strong>Whole genome DNA sequence of saliva samples from 45 participants including 21 RAs and 24 age and gender matched HCs was obtained from the BioProject: PRJEB6997. Metaphlan3 pipeline and LEfSe analysis were used for the viral signature detection. Wilcoxon pairwise test and ROC analysis were used to validate and predict signatures.</p><p><strong>Results: </strong>RA exhibits higher alpha diversity compared to HCs. <i>Callitrichine gammaherpesvirus</i> 3, <i>Human gammaherpesvirus</i> 4 (EBV), <i>Murid betaherpesvirus</i> 8, and <i>Suid alphaherpesvirus</i> 1 were enriched in RAs, while Aotine betaherpesvirus 1 from the Cytomegalovirus genus was enriched in HCs. In addition, <i>Saccharomyces cerevisiae</i> killer virus M1 (ScV-M1) was found to be enriched in RAs, whereas bacteriophage Hk97virus (Siphoviridae) and Cd119virus (Myoviridae) were enriched in HCs.</p><p><strong>Conclusion: </strong>This study identifies significant DNA oral viral signatures at species level as potential biomarkers for the early detection and diagnosis of rheumatoid arthritis.</p>","PeriodicalId":16598,"journal":{"name":"Journal of Oral Microbiology","volume":"16 1","pages":"2348260"},"PeriodicalIF":3.7000,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11064737/pdf/","citationCount":"0","resultStr":"{\"title\":\"Distinct oral DNA viral signatures in rheumatoid arthritis: a Pilot study.\",\"authors\":\"Mahin Ghorbani, Nooshin Khoshdoozmasouleh\",\"doi\":\"10.1080/20002297.2024.2348260\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Despite evidence linking viruses and oral microbiome to rheumatoid arthritis (RA), limited whole genome sequencing research has been conducted on the oral virome (a viral component of the microbiome) of untreated RA patients. This pilot research seeks to address this knowledge gap by comparing the oral virome of untreated rheumatoid arthritis patients (RAs) and healthy individuals (HCs).</p><p><strong>Method: </strong>Whole genome DNA sequence of saliva samples from 45 participants including 21 RAs and 24 age and gender matched HCs was obtained from the BioProject: PRJEB6997. Metaphlan3 pipeline and LEfSe analysis were used for the viral signature detection. Wilcoxon pairwise test and ROC analysis were used to validate and predict signatures.</p><p><strong>Results: </strong>RA exhibits higher alpha diversity compared to HCs. <i>Callitrichine gammaherpesvirus</i> 3, <i>Human gammaherpesvirus</i> 4 (EBV), <i>Murid betaherpesvirus</i> 8, and <i>Suid alphaherpesvirus</i> 1 were enriched in RAs, while Aotine betaherpesvirus 1 from the Cytomegalovirus genus was enriched in HCs. 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引用次数: 0
摘要
背景:尽管有证据表明病毒和口腔微生物组与类风湿性关节炎(RA)有关,但对未经治疗的类风湿性关节炎患者的口腔病毒组(微生物组的病毒成分)进行的全基因组测序研究却很有限。这项试验性研究旨在通过比较未经治疗的类风湿性关节炎患者(RA)和健康人(HC)的口腔病毒组来填补这一知识空白:方法:从生物项目(BioProject)获得了 45 名参与者唾液样本的全基因组 DNA 序列,其中包括 21 名 RA 和 24 名年龄和性别匹配的 HC:PRJEB6997。使用 Metaphlan3 管道和 LEfSe 分析进行病毒特征检测。Wilcoxon 配对检验和 ROC 分析用于验证和预测特征:与 HCs 相比,RA 表现出更高的α多样性。Callitrichine gammaherpesvirus 3、Human gammaherpesvirus 4 (EBV)、Murid betaherpesvirus 8和Suid alphaherpesvirus 1在RA中富集,而巨细胞病毒属的Aotine betaherpesvirus 1在HC中富集。此外,还发现酵母杀手病毒 M1(ScV-M1)在 RA 中富集,而噬菌体 Hk97virus(Siphoviridae)和 Cd119virus(Myoviridae)在 HC 中富集:本研究在物种水平上确定了重要的 DNA 口腔病毒特征,作为早期检测和诊断类风湿性关节炎的潜在生物标志物。
Distinct oral DNA viral signatures in rheumatoid arthritis: a Pilot study.
Background: Despite evidence linking viruses and oral microbiome to rheumatoid arthritis (RA), limited whole genome sequencing research has been conducted on the oral virome (a viral component of the microbiome) of untreated RA patients. This pilot research seeks to address this knowledge gap by comparing the oral virome of untreated rheumatoid arthritis patients (RAs) and healthy individuals (HCs).
Method: Whole genome DNA sequence of saliva samples from 45 participants including 21 RAs and 24 age and gender matched HCs was obtained from the BioProject: PRJEB6997. Metaphlan3 pipeline and LEfSe analysis were used for the viral signature detection. Wilcoxon pairwise test and ROC analysis were used to validate and predict signatures.
Results: RA exhibits higher alpha diversity compared to HCs. Callitrichine gammaherpesvirus 3, Human gammaherpesvirus 4 (EBV), Murid betaherpesvirus 8, and Suid alphaherpesvirus 1 were enriched in RAs, while Aotine betaherpesvirus 1 from the Cytomegalovirus genus was enriched in HCs. In addition, Saccharomyces cerevisiae killer virus M1 (ScV-M1) was found to be enriched in RAs, whereas bacteriophage Hk97virus (Siphoviridae) and Cd119virus (Myoviridae) were enriched in HCs.
Conclusion: This study identifies significant DNA oral viral signatures at species level as potential biomarkers for the early detection and diagnosis of rheumatoid arthritis.
期刊介绍:
As the first Open Access journal in its field, the Journal of Oral Microbiology aims to be an influential source of knowledge on the aetiological agents behind oral infectious diseases. The journal is an international forum for original research on all aspects of ''oral health''. Articles which seek to understand ''oral health'' through exploration of the pathogenesis, virulence, host-parasite interactions, and immunology of oral infections are of particular interest. However, the journal also welcomes work that addresses the global agenda of oral infectious diseases and articles that present new strategies for treatment and prevention or improvements to existing strategies.
Topics: ''oral health'', microbiome, genomics, host-pathogen interactions, oral infections, aetiologic agents, pathogenesis, molecular microbiology systemic diseases, ecology/environmental microbiology, treatment, diagnostics, epidemiology, basic oral microbiology, and taxonomy/systematics.
Article types: original articles, notes, review articles, mini-reviews and commentaries