肠炎沙门氏菌血清型鼠伤寒沙门氏菌的灵敏分子检测

Hasta Handayani Idrus, Sarwo Handayni, Fitriana Fitriana
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引用次数: 0

摘要

简介:沙门氏菌感染是肠胃炎病例的重要原因,国家沙门氏菌参考实验室在2022年报告了500个分离株。然而,传统的基于培养的检测样本沙门氏菌的方法可能需要4至7天才能确认阳性结果,这由于检测延迟而构成健康风险。鉴于这些健康风险,快速和准确的检测方法对于最大限度地减少假阳性和假阴性结果至关重要。沙门氏菌是肠杆菌科的一种革兰氏阴性细菌,它表现出非凡的耐寒性,在干燥环境中存活数周,在水中存活数月。虽然大多数血清型沙门氏菌引起相对轻微的胃肠炎,但有些,特别是那些从动物传播给人类的沙门氏菌,可导致严重的、危及生命的疾病 方法:qRT-PCR程序涉及的引物和探针的设计针对相同的基因的mPCR试验。这些引物组被重新配置以产生适合于qRT-PCR系统的更小的扩增子 结果:qRT-PCR工艺中,针对特定靶基因精心设计了TaqMan探针:STM2745采用FAM染料检测,STM4492采用Cy5染料检测,Rox染料检测。用鼠伤寒杆菌LT2基因组DNA构建标准曲线。每个样本进行重复分析,并使用Rotor-Gene软件为每个通道分配阈值。 结论:我们的qPCR检测方法在多种基质中检测沙门氏菌是有效的。值得注意的是,我们的结果揭示了不同样品中沙门氏菌的明显检测限。具体而言,另一组研究了平行静脉,利用免疫磁分离技术进行DNA提取的PCR测定的部署。虽然通过我们的实验检测到的沙门氏菌的后续分析可能需要完整的ISO SMT方法进行活培养分离,但这一补充步骤可以与qRT-PCR无缝地进行。
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Sensitive Molecular Detection for Salmonella Enterica Serovars Typhimurium
Introduction: Salmonella infections contribute significantly to gastroenteritis cases, with the National Salmonella Reference Laboratory reporting 500 isolates in 2022. However, traditional culture-based methods for detecting Salmonella in samples can take 4 to 7 days to confirm a positive result, which poses health risks due to delayed detection. Given these health risks, swift and accurate detection methods are essential to minimize both false-positive and false-negative outcomes. Salmonella, a gram-negative bacterium within the Enterobacteriaceae family, demonstrates remarkable hardiness, surviving for several weeks in dry environments and months in water. Although most serotypes of Salmonella cause relatively mild gastroenteritis, some, particularly those transmitted from animals to humans, can lead to severe, life-threatening conditions Methods: The qRT-PCR procedure involved the design of primers and probes targeting the same genes as the mPCR assay. These primer sets were reconfigured to generate smaller amplicons suitable for qRT-PCR systems Results: qRT-PCR process, TaqMan probes were meticulously designed for specific target genes: FAM dye was employed to detect STM2745, Cy5 dye was used for STM4492, and Rox dye was utilized to detect. A standard curve was constructed using Typhimurium LT2 genomic DNA. Each sample underwent duplicate analysis, and Rotor-Gene software was employed to assign threshold values for each channel. Conclusion: The effectiveness of our qPCR assay for the detection of Salmonella across a diverse array of matrices. Notably, our results unveiled distinct limits of detection for Salmonella in various samples. Specifically, a parallel vein, the deployment of a PCR assay, leveraging an immunomagnetic separation technique for DNA extraction, was studied by another group. While subsequent analysis of Salmonella detected via our assay may necessitate the full ISO SMT method for live culture isolation, this supplementary step can be seamlessly conducted alongside qRT-PCR.
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