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Comparison of Updated Methods for Legionella Detection in Environmental Water Samples

机译:环境水样中军团检测更新方法的比较

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摘要

The difficulty of cultivation of Legionella spp. from water samples remains a strenuous task even for experienced laboratories. The long incubation periods for Legionellae make isolation difficult. In addition, the water samples themselves are often contaminated with accompanying microbial flora, and therefore require complex cultivation methods from diagnostic laboratories. In addition to the recent update of the standard culture method ISO 11731:2017, new strategies such as quantitative PCR (qPCR) are often discussed as alternatives or additions to conventional Legionella culture approaches. In this study, we compared ISO 11731:2017 with qPCR assays targeting Legionella spp., Legionella pneumophila, and Legionella pneumophila serogroup 1. In samples with a high burden of accompanying microbial flora, qPCR shows an excellent negative predictive value for Legionella pneumophila, thus making qPCR an excellent tool for pre-selection of negative samples prior to work-intensive culture methods. This and its low limit of detection make qPCR a diagnostic asset in Legionellosis outbreak investigations, where quick-risk assessments are essential, and are a useful method for monitoring risk sites.
机译:军团菌培养难度。即使对于经验丰富的实验室,水样仍然是一个艰苦的任务。 Legionellae的长潜水期使分离困难。此外,水样本身通常含有伴随的微生物菌群,因此需要来自诊断实验室的复杂培养方法。除了最近的标准培养方法ISO 11731:2017的更新外,通常讨论常规军团培养方法的替代品或添加量等新的策略,如定量PCR(QPCR)。在这项研究中,我们将ISO 11731:2017与靶向军团菌SPP的QPCR测定进行比较。,军团菌,和军团菌血清群体1.在伴随着微生物菌群负担的样本中,QPCR显示了Legionella Pneumophila的优异的负面预测值,因此使QPCR成为在工作密集型培养方法之前预先选择负样品的优秀工具。其降低的检测限制使QPCR成为军队爆发调查中的诊断资产,其中快速风险评估至关重要,是监测风险现场的有用方法。

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