基因组鱼:基于基因组的荧光原位杂交菌株水平的微生物群落可视化

J Pamela Engelberts, Jun Ye, Donovan H Parks, Eilish S McMaster, Allison S McInnes, Ben J Woodcroft, James G Volmer, Simon J McIlroy, Gene W Tyson
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引用次数: 0

摘要

荧光原位杂交(FISH)是一种可视化微生物群落空间组织的有力工具。然而,传统的FISH有一些局限性,包括有限的系统发育分辨率,难以可视化某些谱系,新探针的设计和优化是耗时的,并且不能扩展到已知的微生物生命多样性。在这里,我们提出了一种高通量、基于基因组的FISH方法,可以在复杂的群落中区分菌株。荧光探针是通过荧光激活单细胞分选(FACS)从环境或临床样品中获得的单细胞基因组产生的。GenomeFISH可以区分具有高达99%平均核苷酸同一性的菌株,并成功地应用于模拟群落和人类粪便样本中的菌株可视化。鉴于基因组鱼优越的敏感性和特异性,我们设想它将被广泛用于复杂微生物系统的可视化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GenomeFISH: genome-based fluorescence in situ hybridisation for strain-level visualisation of microbial communities
Fluorescence in situ hybridisation (FISH) is a powerful tool for visualising the spatial organisation of microbial communities. However, traditional FISH has several limitations, including limited phylogenetic resolution, difficulty visualising certain lineages, and the​​ design and optimis​ation of​ new probes is time consuming and does not scale​ to the ​known​ diversity of microbial life. Here, we present GenomeFISH, a high-throughput, genome-based FISH approach that can differentiate strains within complex communities. Fluorescent probes are generated from the genomes of single cells, which are ​obtained ​from environmental or clinical samples through fluorescence activated single-cell sorting (FACS). GenomeFISH can ​distinguish between ​strains with up to 99% average nucleotide identity and was successfully applied to visualise strains in mock communities and human faecal samples. Given the superior sensitivity and specificity of GenomeFISH, we envisage it will become widely used for the visualisation of complex microbial systems.
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