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从OneSwab宫颈阴道标本中快速分离出单纯疱疹病毒1型和单纯疱疹病毒2型。

Rapid isolation of HSV-1 and HSV-2 from OneSwab cervicovaginal specimens.

作者信息

Peña Kristen C, Adelson Martin E, Mordechai Eli, Blaho John A

机构信息

Virology Research Division, Medical Diagnostic Laboratories, LLC, 2439 Kuser Road, Hamilton, NJ 08690-33303, United States.

出版信息

J Virol Methods. 2009 Aug;159(2):146-51. doi: 10.1016/j.jviromet.2009.03.014. Epub 2009 Mar 25.

Abstract

Herpes simplex viruses are significant human pathogens which remain latent in their hosts for life and reactivate to cause disease at or near the initial site of infection. Since HSV infections are associated with high morbidity, rapid detection and diagnosis of these viruses is imperative. While PCR technology for the diagnosis of HSV is now almost utilized universally, virus isolation from mucosa and skin in shell cultures is still applied in many clinical settings. Virus growth in cultured cells alone has the disadvantage that it cannot distinguish between HSV-1 and HSV-2. The aim of this study was to combine these two disparate methods. A protocol was developed to isolate clinical strains directly from the medium used for as the standard source of extraction to isolate DNA. Both HSV-1 and HSV-2 strains were isolated successfully from cervicovaginal swabs transported in OneSwab devices. It was found that the titers of these viruses did not correlate with the C(T) scores determined for the samples using real-time PCR. HSV-2 strains generally had lower titers than those of HSV-1, suggesting that the HSV-2 may be more sensitive to the sample handling procedures. These studies represent the first report of the culture and isolation of HSV from clinical samples using OneSwab intended exclusively for molecular diagnostic analyses.

摘要

单纯疱疹病毒是重要的人类病原体,可在宿主体内终生潜伏,并在感染初始部位或其附近重新激活引发疾病。由于单纯疱疹病毒感染与高发病率相关,因此对这些病毒进行快速检测和诊断至关重要。虽然用于诊断单纯疱疹病毒的PCR技术现在几乎已普遍应用,但在许多临床环境中仍采用在壳培养中从黏膜和皮肤分离病毒的方法。仅在培养细胞中进行病毒培养存在一个缺点,即无法区分单纯疱疹病毒1型和单纯疱疹病毒2型。本研究的目的是将这两种不同的方法结合起来。制定了一种方案,可直接从用作标准DNA提取源的培养基中分离临床菌株。成功地从用OneSwab装置运送的宫颈阴道拭子中分离出了单纯疱疹病毒1型和单纯疱疹病毒2型菌株。研究发现,这些病毒的滴度与使用实时PCR测定的样本C(T)值不相关。单纯疱疹病毒2型菌株的滴度通常低于单纯疱疹病毒1型,这表明单纯疱疹病毒2型可能对样本处理程序更敏感。这些研究是首次报告使用专门用于分子诊断分析的OneSwab从临床样本中培养和分离单纯疱疹病毒。

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