1] Área de Genómica y Salud, Centro Superior de Investigación en Salud Pública-Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunidad Valenciana (CSISP-FISABIO), Valencia, Spain [2] CIBER Epidemiología y Salud Pública (CIBERESP), Madrid, Spain [3] Departamento de Genética, Cavanilles Institute on Biodiversity and Evolutionary Biology, University of València, Valencia, Spain.
Clin Transl Gastroenterol. 2013 Jun 13;4(6):e36. doi: 10.1038/ctg.2013.9.
This study aimed to analyze and compare the diversity and structure of the viral and microbial communities in fecal samples from a control group of healthy volunteers and from patients affected by Crohn's disease (CD).
Healthy adult controls (n=8) and patients affected by ileocolic CD (n=11) were examined for the viral and microbial communities in their feces and, in one additional case, in the intestinal tissue. Using two different approaches, we compared the viral and microbial communities in several ways: by group (patients vs. controls), entity (viruses vs. bacteria), read assembly (unassembled vs. assembled reads), and methodology (our approach vs. an existing pipeline). Differences in the viral and microbial composition, and abundance between the two groups were analyzed to identify taxa that are under- or over-represented.
A lower diversity but more variability between the CD samples in both virome and microbiome was found, with a clear distinction between groups based on the microbiome. Only ≈5% of the differential viral biomarkers are more represented in the CD group (Synechococcus phage S CBS1 and Retroviridae family viruses), compared with 95% in the control group. Unrelated patterns of bacteria and bacteriophages were observed.
Our use of an extensive database is critical to retrieve more viral hits than in previous approaches. Unrelated patterns of bacteria and bacteriophages may be due to uneven representation of certain viruses in databases, among other factors. Further characterization of Retroviridae viruses in the CD group could be of interest, given their links with immunodeficiency and the immune responses. To conclude, some methodological considerations underlying the analysis of the viral community composition and abundance are discussed.
本研究旨在分析和比较健康志愿者对照组和克罗恩病(CD)患者粪便样本中的病毒和微生物群落的多样性和结构。
对 8 名健康成年对照者和 11 名患有回肠结肠炎 CD 的患者的粪便以及其中 1 例患者的肠道组织中的病毒和微生物群落进行了检测。我们使用两种不同的方法,通过组(患者与对照)、实体(病毒与细菌)、读组装(未组装与组装读)和方法(我们的方法与现有管道)比较了病毒和微生物群落的几个方面。分析两组之间病毒和微生物组成和丰度的差异,以确定哪些分类群存在代表性不足或过表达。
在病毒组和微生物组中,CD 样本的多样性较低,但变异性更大,且基于微生物组可清楚地区分两组。与对照组相比,仅有约 5%的差异病毒生物标志物(Synechococcus phage S CBS1 和逆转录病毒科病毒)在 CD 组中更为代表。观察到细菌和噬菌体的无关模式。
我们使用广泛的数据库对于检索比以前方法更多的病毒命中至关重要。数据库中某些病毒的不均匀表示等其他因素可能导致细菌和噬菌体的无关模式。鉴于它们与免疫缺陷和免疫反应的关联,对 CD 组中的逆转录病毒进行进一步表征可能会很有趣。最后,讨论了分析病毒群落组成和丰度的一些方法学考虑因素。