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分子探针技术无需培养即可检测细菌。

Molecular probe technology detects bacteria without culture.

机构信息

Departments of Biochemistry, Stanford University, Stanford, CA, USA.

出版信息

BMC Microbiol. 2012 Mar 9;12:29. doi: 10.1186/1471-2180-12-29.

DOI:10.1186/1471-2180-12-29
PMID:22404909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3316761/
Abstract

BACKGROUND

Our ultimate goal is to detect the entire human microbiome, in health and in disease, in a single reaction tube, and employing only commercially available reagents. To that end, we adapted molecular inversion probes to detect bacteria using solely a massively multiplex molecular technology. This molecular probe technology does not require growth of the bacteria in culture. Rather, the molecular probe technology requires only a sequence of forty sequential bases unique to the genome of the bacterium of interest. In this communication, we report the first results of employing our molecular probes to detect bacteria in clinical samples.

RESULTS

While the assay on Affymetrix GenFlex Tag16K arrays allows the multiplexing of the detection of the bacteria in each clinical sample, one Affymetrix GenFlex Tag16K array must be used for each clinical sample. To multiplex the clinical samples, we introduce a second, independent assay for the molecular probes employing Sequencing by Oligonucleotide Ligation and Detection. By adding one unique oligonucleotide barcode for each clinical sample, we combine the samples after processing, but before sequencing, and sequence them together.

CONCLUSIONS

Overall, we have employed 192 molecular probes representing 40 bacteria to detect the bacteria in twenty-one vaginal swabs as assessed by the Affymetrix GenFlex Tag16K assay and fourteen of those by the Sequencing by Oligonucleotide Ligation and Detection assay. The correlations among the assays were excellent.

摘要

背景

我们的最终目标是在单个反应管中,仅使用市售试剂,检测健康和疾病状态下的人类微生物组。为此,我们采用分子反转探针,仅使用大规模多重分子技术来检测细菌。这种分子探针技术不需要对细菌进行培养。相反,分子探针技术仅需要与目标细菌基因组的四十个连续碱基序列相匹配。在本研究中,我们报告了首次使用我们的分子探针检测临床样本中细菌的结果。

结果

虽然 Affymetrix GenFlex Tag16K 阵列上的检测可实现对每个临床样本中细菌的多重检测,但每个临床样本必须使用一个 Affymetrix GenFlex Tag16K 阵列。为了对临床样本进行多重检测,我们引入了一种独立的测序寡核苷酸连接和检测分子探针检测方法。通过为每个临床样本添加一个独特的寡核苷酸条形码,我们在测序前对样本进行处理后进行合并,并将它们一起测序。

结论

总体而言,我们使用了 192 个代表 40 种细菌的分子探针,通过 Affymetrix GenFlex Tag16K 检测评估了 21 个阴道拭子中的细菌,其中 14 个通过测序寡核苷酸连接和检测检测。这两种检测方法的相关性非常好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16b2/3316761/afe5e7873f3c/1471-2180-12-29-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16b2/3316761/058d544e5e70/1471-2180-12-29-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16b2/3316761/afe5e7873f3c/1471-2180-12-29-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16b2/3316761/058d544e5e70/1471-2180-12-29-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16b2/3316761/afe5e7873f3c/1471-2180-12-29-2.jpg

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