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通过高分辨率系统发育分析并与荧光原位杂交技术比较,靶向数字化皮肤炎感染的密螺旋体微生物组。

Targeting the treponemal microbiome of digital dermatitis infections by high-resolution phylogenetic analyses and comparison with fluorescent in situ hybridization.

机构信息

National Veterinary Institute, Technical University of Denmark, Frederiksberg, Denmark.

出版信息

J Clin Microbiol. 2013 Jul;51(7):2212-9. doi: 10.1128/JCM.00320-13. Epub 2013 May 8.

Abstract

Modern pyrosequencing technology allows for a more comprehensive approach than traditional Sanger sequencing for elucidating the etiology of bovine digital dermatitis. We sought to describe the composition and diversity of treponemes in digital dermatitis lesions by using deep sequencing of the V3 and V4 hypervariable regions of the 16S rRNA gene coupled with species-level taxonomic identification. Treponema-specific 16S rRNA gene PCRs and pyrosequencing were performed on biopsy specimens originating from 10 different Catalan dairy herds (n = 36) with digital dermatitis, and this analysis yielded 75,297 sequences. We identified 20 different taxa, including a potentially novel phylotype that displayed 95% sequence identity to members of the Treponema denticola/Treponema pedis-like cluster. Species frequencies and abundances that were determined by pyrosequencing analysis were highly correlated with the results of fluorescent in situ hybridization using phylotype-specific oligonucleotide probes. In a limited number of animals from a single geographic region, we detected most of the Treponema phylotypes that were described in previous investigations of digital dermatitis. Additionally, we identified a number of phylotypes that mapped to oral treponemes of humans and dogs that had not been reported for digital dermatitis lesions. The results presented here support previous observations of a polytreponemal etiology of infections, with Treponema phagedenis-like, Treponema medium/Treponema vincentii-like, and T. denticola/T. pedis-like phylotypes being highly associated with disease. Using this new approach, it has become feasible to study large herds and their surrounding environments, which might provide a basis for a better understanding of the pathogenesis of this disease.

摘要

现代焦磷酸测序技术比传统的 Sanger 测序更全面,可用于阐明牛传染性皮肤病的病因。我们通过对 16S rRNA 基因 V3 和 V4 高变区进行深度测序,并结合种属水平的分类鉴定,旨在描述传染性皮肤病病变中密螺旋体的组成和多样性。对来自 10 个不同加泰罗尼亚奶牛场(n = 36)的 10 个不同奶牛场(n = 36)的活检标本进行了针对 Treponema 的 16S rRNA 基因 PCR 和焦磷酸测序,共获得 75297 个序列。我们鉴定了 20 个不同的分类群,包括一种可能的新拟杆菌,其与 Treponema denticola/Treponema pedis-like 聚类的成员具有 95%的序列同一性。通过焦磷酸测序分析确定的物种频率和丰度与使用种特异性寡核苷酸探针的荧光原位杂交结果高度相关。在来自单一地理区域的少数动物中,我们检测到了以前对传染性皮肤病研究中描述的大多数 Treponema 拟杆菌。此外,我们还鉴定出了一些与人类和犬口腔密螺旋体相对应的拟杆菌,这些密螺旋体以前没有报道过与传染性皮肤病病变有关。本研究结果支持了以前关于感染的多密螺旋体病因的观察结果,其中 Treponema phagedenis-like、Treponema medium/Treponema vincentii-like 和 T. denticola/T. pedis-like 拟杆菌与疾病高度相关。使用这种新方法,可以研究大型牛群及其周围环境,这可能为更好地了解这种疾病的发病机制提供基础。

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