微生物组测序数据的定量聚合有助于深入了解皮肤微生物组与银屑病之间的关系

Alfred A. Chan , Patrick T. Tran , Delphine J. Lee
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引用次数: 0

摘要

尽管先前的研究报告了与银屑病相关的不同皮肤微生物组特征,但方法和分析的差异限制了可推广的结论。个别研究报告的结果相互矛盾;例如,丙酸杆菌和葡萄球菌与银屑病皮损和健康皮肤都有显著相关性。定性综述试图对这些研究进行总结,但不同研究的结果和方法存在很大差异。为了更好地统一这些数据,我们利用统一的生物信息学管道和参考数据库对所有公开可用的数据集进行了荟萃分析,以研究皮肤微生物组与银屑病的关联。共分析了来自 6 项研究的 977 份皮肤拭子样本(341 份皮损样本、295 份非皮损样本和 341 份健康样本)。汇总分析结果显示,银屑病患者皮肤拭子样本中金黄色葡萄球菌和拟杆菌等微生物的相对丰度高于健康样本;此外,健康样本中痤疮杆菌、未分类的劳森氏菌和华纳菌的相对丰度也明显高于银屑病患者。此外,根据 16S 基因标记预测的功能途径比较显示,银屑病皮损中 L-鸟氨酸的生物合成和 L-组氨酸的生物合成低于健康对照组。总之,这项荟萃分析使皮肤微生物组与银屑病之间的关联更具普遍性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantitative Aggregation of Microbiome Sequencing Data Provides Insights into the Associations between the Skin Microbiome and Psoriasis

Although prior studies have reported distinct skin microbiome profiles associated with psoriasis, differences in methods and analyses limit generalizable conclusions. Individual studies have actually reported conflicting findings; for example, Propionibacterium and Staphylococcus have been significantly associated with both psoriatic lesions and healthy skin. Qualitative reviews have attempted to summarize this body of work, but there is great variability across the studies’ findings and methods. To better unify these data, we created a meta-analysis of all publicly available datasets by utilizing a uniform bioinformatics pipeline and reference database to investigate associations of the skin microbiome in psoriasis. A total of 977 skin swab samples (341 lesional, 295 nonlesional, and 341 healthy) from 6 studies were analyzed. The aggregated analysis revealed a higher relative abundance of microorganisms, including Staphylococcus aureus and Corynebacterium simulans, among others, from patients with psoriasis than those from healthy swab samples; in addition, Cutibacterium acnes, Lawsonella unclassified, and S warneri were significantly higher in healthy samples. Furthermore, comparison of functional pathways predicted from 16S gene markers showed that L-ornithine biosynthesis and L-histidine biosynthesis were lower in psoriatic lesions than in healthy controls. Taken together, this meta-analysis allows for a more generalizable association between the skin microbiome and psoriasis.

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