Centre for Integrative Biology, University of Trento, Trento, Italy.
PLoS One. 2013;8(2):e55764. doi: 10.1371/journal.pone.0055764. Epub 2013 Feb 11.
Bacteria are ubiquitous throughout the environment, the most abundant inhabitants of the healthy human microbiome, and causal pathogens in a variety of diseases. Their identification in disease is often an essential step in rapid diagnosis and targeted intervention, particularly in clinical settings. At present, clinical bacterial detection and discrimination is primarily culture-based, requiring both time and microbiological expertise, especially for bacteria that are not easily cultivated. Higher-throughput molecular methods based on PCR amplification or, recently, microarrays are reaching the clinic as well. However, these methods are currently restricted to a small set of microbes or based on conserved phylogenetic markers such as the 16S rRNA gene, which are difficult to resolve at the species or strain levels. Here, we designed and experimentally validated the BactoChip, an oligonucleotide microarray for bacterial detection and quantification. The chip allows the culture-independent identification of bacterial species, also determining their relative abundances in complex communities as occur in the commensal microbiota or in clinical settings. The microarray successfully distinguished among bacterial species from 21 different genera using 60-mer probes targeting a novel set of in silico identified high-resolution marker genes. The BactoChip additionally proved accurate in determining species-level relative abundances over a 100-fold dynamic range in complex bacterial communities and with a low limit of detection (0.1%). In combination with the continually increasing number of sequenced bacterial genomes, future iterations of the technology could enable to highly accurate clinically-oriented tools for rapid assessment of bacterial community composition and relative abundances.
细菌在环境中无处不在,是健康人体微生物组中最丰富的居民,也是多种疾病的致病病原体。在疾病中鉴定细菌通常是快速诊断和靶向干预的关键步骤,特别是在临床环境中。目前,临床细菌的检测和鉴别主要基于培养,需要时间和微生物学专业知识,特别是对于那些不易培养的细菌。基于 PCR 扩增或最近的微阵列的高通量分子方法也正在进入临床。然而,这些方法目前仅限于一小部分微生物,或者基于保守的系统发育标记物,如 16S rRNA 基因,这些标记物很难在物种或菌株水平上得到解决。在这里,我们设计并实验验证了 BactoChip,这是一种用于细菌检测和定量的寡核苷酸微阵列。该芯片允许在不依赖培养的情况下识别细菌物种,还可以确定它们在复杂群落中的相对丰度,这些复杂群落存在于共生微生物群或临床环境中。该微阵列使用针对一组新的、在计算机上鉴定的高分辨率标记基因的 60 个碱基长的探针,成功地区分了来自 21 个不同属的细菌物种。BactoChip 还证明了在复杂细菌群落中,在 100 倍动态范围内和低检测限(0.1%)下,准确确定物种水平相对丰度的能力。结合不断增加的细菌基因组测序数量,该技术的未来迭代可以为快速评估细菌群落组成和相对丰度提供高度准确的临床导向工具。