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在细胞培养上对脑脊液样本进行富集以提高多重逆转录聚合酶链反应检测腮腺炎病毒和肠道病毒的灵敏度。

Enrichment of cerebrospinal fluid samples on cell culture for enhancement of sensitivity of mumps and enterovirus detection by multiplex RT-PCR.

作者信息

Kermanian Masoumeh, Soleimanjahi Hoorieh, Arefian Ehsan, Bamdad Taravat

机构信息

Department of Virology, Faculty of Medical Sciences, Tarbiat Modares University, P.O. Box 14155-331, Tehran, Iran.

出版信息

Diagn Microbiol Infect Dis. 2008 Apr;60(4):375-9. doi: 10.1016/j.diagmicrobio.2007.10.023. Epub 2008 Feb 20.

Abstract

It has been demonstrated that the detection of enteroviruses and mumps virus nucleic acid in cerebrospinal fluid (CSF) specimens improves the management of the patients with aseptic meningitis. To determine the effect of overnight enrichment of mumps and enteroviruses in CSF samples on cell culture for increasing the sensitivity of viral detection, we developed a multiplex reverse transcriptase-polymerase chain reaction (RT-PCR). CSFs were collected from 100 patients younger than 7 years. The samples were tested for the presence of enteroviruses and mumps virus by multiplex RT-PCR method. Negative samples in Multiplex RT-PCR were enriched for viral template RNAs by overnight culture of CSF samples on cells and followed by the optimized Multiplex RT-PCR. Overall, 35% of the CSF samples were positive for enteroviruses, whereas only 1% of CSF samples were positive for both viruses. After enriching in cell culture, 34% of the negative samples showed a positive polymerase chain reaction band for enteroviruses, and a 3% increase was observed for both viruses. The results showed that enrichment of viral template RNAs in cell culture can increase the sensitivity of the multiplex RT-PCR assay and provide a rapid and sensitive method for detection of viral infections.

摘要

已证明,检测脑脊液(CSF)标本中的肠道病毒和腮腺炎病毒核酸可改善无菌性脑膜炎患者的管理。为了确定CSF样本中腮腺炎病毒和肠道病毒过夜富集对细胞培养以提高病毒检测敏感性的影响,我们开发了一种多重逆转录聚合酶链反应(RT-PCR)。从100名7岁以下的患者中收集脑脊液。通过多重RT-PCR方法检测样本中是否存在肠道病毒和腮腺炎病毒。多重RT-PCR中的阴性样本通过在细胞上对CSF样本进行过夜培养来富集病毒模板RNA,然后进行优化的多重RT-PCR。总体而言,35%的CSF样本肠道病毒呈阳性,而两种病毒均呈阳性的CSF样本仅为1%。在细胞培养中富集后,34%的阴性样本肠道病毒聚合酶链反应带呈阳性,两种病毒均观察到增加了3%。结果表明,细胞培养中病毒模板RNA的富集可提高多重RT-PCR检测的敏感性,并为病毒感染的检测提供一种快速灵敏的方法。

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