首页> 美国卫生研究院文献>Journal of Pathogens >Comparison of Algorithms for the Detection of Enteroviruses in Stool Specimens from Children Diagnosed with Acute Flaccid Paralysis
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Comparison of Algorithms for the Detection of Enteroviruses in Stool Specimens from Children Diagnosed with Acute Flaccid Paralysis

机译:急性弛缓性麻痹患儿粪便标本中肠道病毒检测算法的比较

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摘要

This study was designed to compare both the cell culture dependent and independent enterovirus detection algorithms recommended by the WHO and assess how either might impact our perception of the diversity of enterovirus types present in a sample. Sixteen paired samples (16 isolates from RD cell culture and their corresponding stool suspension, i.e., 32 samples) from AFP cases in Nigeria were analyzed in this study. All the samples were subjected to RNA extraction, cDNA synthesis, the WHO recommended RT-snPCR, and its modification. Amplicons were sequenced and strains identified. Enterovirus diversity was the same between the isolates and fecal suspension for the control and five of the samples. It was, however, different for the remaining 10 (62.5%) samples. Nine (CV-B4, E6, E7, E13, E14, E19, E29, EV-B75, and EV-B77) and five (CV-A1, CV-A11, CV-A13, EV-C99, and PV2) EV-B and EV-C types, respectively, were detected. Particularly, E19 and EV-B75 were only recovered from the isolates while E14, EV-B77, CV-A11, and CV-A13 were only recovered from fecal suspension. Both the cell culture dependent and independent protocols bias our perception of the diversity of enterovirus types present in a sample. Hence, effort should be directed at harmonizing both for increased sensitivity.
机译:这项研究旨在比较WHO推荐的依赖细胞培养的肠道病毒检测算法和独立的肠道病毒检测算法,并评估这两种方法可能如何影响我们对样品中肠道病毒类型多样性的看法。本研究分析了尼日利亚AFP病例的16对配对样本(来自RD细胞培养的16种分离株及其相应的粪便悬浮液,即32个样本)。所有样品均经过RNA提取,cDNA合成,WHO推荐的RT-snPCR及其修饰。对扩增子进行测序并鉴定菌株。对照和五个样品的分离株和粪便悬浮液之间的肠道病毒多样性相同。但是,其余10个(62.5%)样品则有所不同。九个(CV-B4,E6,E7,E13,E14,E19,E29,EV-B75和EV-B77)和五个(CV-A1,CV-A11,CV-A13,EV-C99和PV2)EV分别检测到-B和EV-C类型。特别地,仅从分离物中回收E19和EV-B75,而仅从粪便悬浮液中回收E14,EV-B77,CV-A11和CV-A13。依赖于细胞培养的方案和独立方案都使我们对样品中存在的肠道病毒类型的多样性产生了偏见。因此,应该努力协调两者以提高灵敏度。

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