Pathogen & Microbiome Institute, Northern Arizona University, Flagstaff, AZ, USA.
Translational Genomics Research Institute, Flagstaff, AZ, USA.
BMC Microbiol. 2021 Jun 8;21(1):174. doi: 10.1186/s12866-021-02247-6.
Molecular assays are important tools for pathogen detection but need to be periodically re-evaluated with the discovery of additional genetic diversity that may cause assays to exclude target taxa or include non-target taxa. A single well-developed assay can find broad application across research, clinical, and industrial settings. Pathogen prevalence within a population is estimated using such assays and accurate results are critical for formulating effective public health policies and guiding future research. A variety of assays for the detection of Staphylococcus aureus are currently available. The utility of commercial assays for research is limited, given proprietary signatures and lack of transparent validation.
In silico testing of existing peer-reviewed assays show that most suffer from a lack of sensitivity and specificity. We found no assays that were specifically designed and validated for quantitative use. Here we present a qPCR assay, SaQuant, for the detection and quantification of S. aureus as might be collected on sampling swabs. Sensitivity and specificity of the assay was 95.6 and 99.9 %, respectively, with a limit of detection of between 3 and 5 genome equivalents and a limit of quantification of 8.27 genome equivalents. The presence of DNA from non-target species likely to be found in a swab sample, did not impact qualitative or quantitative abilities of the assay.
This assay has the potential to serve as a valuable tool for the accurate detection and quantification of S. aureus collected from human body sites in order to better understand the dynamics of prevalence and transmission in community settings.
分子检测方法是病原体检测的重要工具,但随着新的遗传多样性的发现,需要定期重新评估,因为这些遗传多样性可能导致检测方法排除目标分类单元或包括非目标分类单元。一个经过充分开发的检测方法可以在研究、临床和工业环境中广泛应用。通过这些检测方法可以估计人群中的病原体流行率,准确的结果对于制定有效的公共卫生政策和指导未来的研究至关重要。目前有多种用于检测金黄色葡萄球菌的检测方法。鉴于商业检测方法具有专有的特征且缺乏透明的验证,因此其在研究中的应用受到限制。
对现有同行评审检测方法的计算机测试表明,大多数方法都存在敏感性和特异性不足的问题。我们没有发现专门设计和验证用于定量检测的方法。在这里,我们提出了一种 qPCR 检测方法 SaQuant,用于检测和定量采集自采样拭子的金黄色葡萄球菌。该方法的灵敏度和特异性分别为 95.6%和 99.9%,检测限为 3 至 5 个基因组当量,定量限为 8.27 个基因组当量。拭子样本中可能存在的非目标物种的 DNA 不会影响检测方法的定性或定量能力。
该检测方法具有准确检测和定量人体部位采集的金黄色葡萄球菌的潜力,以便更好地了解社区环境中流行率和传播的动态。