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Replacing Traditional Diagnostics of Fecal Viral Pathogens by a Comprehensive Panel of Real-Time PCRs

机译:全面的实时PCR替代粪便病毒病原体的传统诊断

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摘要

Molecular DNA-based diagnostics are increasingly being used for diagnosis of viral infections. For enteric viruses, PCR assays have also been developed. The aims of this study were to compile and evaluate a comprehensive panel of PCR assays for diagnosis of viruses causing diarrheal disease and to evaluate its use in a largely pediatric population in a 750-bed university medical center. The PCR panel was designed to include assays for detection of adenovirus, astrovirus, enterovirus, norovirus, parechovirus, rotavirus, and sapovirus. The results of the PCR panel were evaluated in relation to conventional viral diagnostics consisting of viral culture and/or rotavirus and adenovirus rapid antigen tests on samples that were taken for routine diagnostics. Comparing conventional with PCR-based testing, the number of viruses detected increased dramatically from 25 to 106 when PCR assays were used. This increase was due mainly to detection of previously undetected viruses, i.e., astrovirus, norovirus, and sapovirus. In 24% of the samples, norovirus was detected. Also, the lower detection limit of PCR-based adenovirus, enterovirus, parechovirus, and rotavirus diagnostics further increased the detection rate. By focusing on samples from patients with complaints of gastroenteritis, detection of a causative agent was increased from 49% by conventional tests to 97% by molecular diagnostics. However, many samples containing low viral loads were found in patients with complaints other than intestinal complaints. In conclusion, the proposed comprehensive PCR panel with appropriate cutoff values can be used for sensitive, rapid, and clinically relevant diagnosis of gastrointestinal viruses.
机译:基于分子DNA的诊断越来越多地用于病毒感染的诊断。对于肠病毒,还开发了PCR测定法。这项研究的目的是编译和评估用于诊断引起腹泻病的病毒的全面PCR分析方法,并评估其在750床大学医学中心的大部分儿科人群中的使用。 PCR面板设计为包括用于检测腺病毒,星状病毒,肠病毒,诺如病毒,副病毒,轮状病毒和沙波病毒的检测方法。 PCR小组的结果与常规病毒诊断方法相关,包括病毒培养和/或轮状病毒和腺病毒快速抗原检测,这些样本均用于常规诊断。与传统的基于PCR的测试相比,使用PCR分析时,检测到的病毒数量从25种急剧增加到106种。该增加主要是由于检测到先前未检测到的病毒,即星状病毒,诺如病毒和沙波病毒。在24%的样本中,检测到诺如病毒。而且,基于PCR的腺病毒,肠病毒,副病毒和轮状病毒诊断的检测下限进一步提高了检测率。通过专注于患有肠胃炎的患者的样本,病原体的检测率从常规检测的49%增加到了分子诊断的97%。但是,在肠主诉以外的主诉患者中发现了许多病毒载量低的样品。总之,所提出的具有适当临界值的综合PCR检测面板可用于灵敏,快速和临床相关的胃肠道病毒诊断。

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