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用于检测环境样本中肠道病毒的集成细胞培养/聚合酶链反应法

Integrated cell culture/PCR for detection of enteric viruses in environmental samples.

作者信息

Reynolds Kelly A

机构信息

University of Arizona, Environmental Research Laboratory, Tuscon, AZ, USA.

出版信息

Methods Mol Biol. 2004;268:69-78. doi: 10.1385/1-59259-766-1:069.

Abstract

Recently, an integrated cell culture/polymerase chain reaction (ICC/PCR) technique has been developed for the detection of viruses in environmental samples providing a reliable method for practical analysis and direct monitoring of environmental samples for viral pathogens. CC/PCR allows for detection of infectious viruses in hours to days compared with the days or weeks necessary with cell culture alone. Bacterial indicator organisms are commonly used to evaluate environmental samples with respect to fecal contamination and potential public health impacts. These organisms do not correlate well with the presence of viruses, but a rapid, reliable method was not previously available for direct virus testing. Using ICC/PCR, environmental samples may be directly surveyed for pathogenic viruses, in a timely manner. Direct virus analysis will lead to better assessment of the presence and risk of human enteric viruses in the environment, so that control measures may be developed with true virus occurrence data. The ICC/PCR approach combines two previously applied virus detection methods, conventional cell culture and PCR amplification, utilizing the major advantages and overcoming the major limitations of each methodology when used alone. Cell culture assay is the standard method for the detection of viable human viruses (i.e., poliovirus, coxsackievirus, echovirus, adenovirus, hepatitis A virus, reovirus, and rotavirus) in environmental samples, serving as the method against which all newer technologies are evaluated. Although cell culture is theoretically capable of detecting a single viable virus in relatively large volumes of sample, the time required for confirmed results with conventional cell culture makes it an impractical method for routine monitoring of environmental samples. Furthermore, cell culture does not detect noncytopathogenic viruses (viruses that are viable, infecting cells, and continually spreading to neighboring cells but that do not cause a visible cytopathogenic effect [CPE] on the cell monolayer). Rotavirus and most wild-type hepatitis A viruses (HAV) are infectious to cell cultures but do not produce a clear CPE.

摘要

最近,一种集成细胞培养/聚合酶链反应(ICC/PCR)技术已被开发用于检测环境样本中的病毒,为环境样本中病毒病原体的实际分析和直接监测提供了一种可靠的方法。与单独使用细胞培养需要数天或数周相比,ICC/PCR能在数小时至数天内检测出感染性病毒。细菌指示生物通常用于评估环境样本的粪便污染情况以及对公众健康的潜在影响。这些生物与病毒的存在并没有很好的相关性,但以前没有一种快速、可靠的方法可用于直接病毒检测。使用ICC/PCR,可以及时直接检测环境样本中的致病病毒。直接病毒分析将有助于更好地评估环境中人类肠道病毒的存在和风险,从而能够根据真实的病毒发生数据制定控制措施。ICC/PCR方法结合了两种先前应用的病毒检测方法,即传统细胞培养和PCR扩增,利用了每种方法单独使用时的主要优点并克服了其主要局限性。细胞培养测定是检测环境样本中活的人类病毒(即脊髓灰质炎病毒、柯萨奇病毒、埃可病毒、腺病毒、甲型肝炎病毒、呼肠孤病毒和轮状病毒)的标准方法,是评估所有新技术的对照方法。虽然理论上细胞培养能够在相对大量的样本中检测到单个活病毒,但传统细胞培养获得确认结果所需的时间使其成为环境样本常规监测的不切实际方法。此外,细胞培养无法检测非细胞病变性病毒(即那些存活、感染细胞并不断扩散到邻近细胞但不会对细胞单层产生可见细胞病变效应[CPE]的病毒)。轮状病毒和大多数野生型甲型肝炎病毒(HAV)可感染细胞培养物,但不会产生明显的CPE。

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