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Use of Propidium Monoazide in Reverse Transcriptase PCR To Distinguish between Infectious and Noninfectious Enteric Viruses in Water Samples

机译:单叠氮丙啶在逆转录酶PCR中用于区分水样中感染性和非感染性肠病毒的用途

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Human enteric viruses can be present in untreated and inadequately treated drinking water. Molecular methods, such as the reverse transcriptase PCR (RT-PCR), can detect viral genomes in a few hours, but they cannot distinguish between infectious and noninfectious viruses. Since only infectious viruses are a public health concern, methods that not only are rapid but also provide information on the infectivity of viruses are of interest. The intercalating dye propidium monoazide (PMA) has been used for distinguishing between viable and nonviable bacteria with DNA genomes, but it has not been used to distinguish between infectious and noninfectious enteric viruses with RNA genomes. In this study, PMA in conjunction with RT-PCR (PMA-RT-PCR) was used to determine the infectivity of enteric RNA viruses in water. Coxsackievirus, poliovirus, echovirus, and Norwalk virus were rendered noninfectious or inactivated by treatment with heat (72°C, 37°C, and 19°C) or hypochlorite. Infectious or native and noninfectious or inactivated viruses were treated with PMA. This was followed by RNA extraction and RT-PCR or quantitative RT-PCR (qRT-PCR) analysis. The PMA-RT-PCR results indicated that PMA treatment did not interfere with detection of infectious or native viruses but prevented detection of noninfectious or inactivated viruses that were rendered noninfectious or inactivated by treatment at 72°C and 37°C and by hypochlorite treatment. However, PMA-RT-PCR was unable to prevent detection of enteroviruses that were rendered noninfectious by treatment at 19°C. After PMA treatment poliovirus that was rendered noninfectious by treatment at 37°C was undetectable by qRT-PCR, but PMA treatment did not affect detection of Norwalk virus. PMA-RT-PCR was also shown to be effective for detecting infectious poliovirus in the presence of noninfectious virus and in an environmental matrix. We concluded that PMA can be used to differentiate between potentially infectious and noninfectious viruses under the conditions defined above.
机译:人肠道病毒可存在于未经处理和未充分处理的饮用水中。分子方法,例如逆转录酶PCR(RT-PCR),可以在几个小时内检测出病毒基因组,但无法区分感染性病毒和非感染性病毒。由于只有感染性病毒才是公共卫生问题,因此人们不仅关注快速而且能提供有关病毒感染性信息的方法。插层染料一叠氮化丙锭(PMA)已用于区分具有DNA基因组的存活细菌和非存活细菌,但尚未用于区分具有RNA基因组的感染性和非感染性肠道病毒。在这项研究中,PMA与RT-PCR(PMA-RT-PCR)一起用于确定肠道RNA病毒在水中的感染性。柯萨奇病毒,脊髓灰质炎病毒,回声病毒和诺沃克病毒通过加热(72°C,37°C和19°C)或次氯酸盐处理而变得无感染性或失活。感染性或天然,非感染性或灭活的病毒用PMA处理。随后进行RNA提取和RT-PCR或定量RT-PCR(qRT-PCR)分析。 PMA-RT-PCR结果表明,PMA处理不会干扰感染性或天然病毒的检测,但会阻止检测通过72°C和37°C的处理以及次氯酸盐处理而变得无感染性或灭活的非感染性或灭活病毒。但是,PMA-RT-PCR无法防止检测到在19°C的处理下变得无感染的肠病毒。在PMA处理后,通过qRT-PCR无法检测到在37°C处理后变得无感染的脊髓灰质炎病毒,但PMA处理并未影响Norwalk病毒的检测。还显示了PMA-RT-PCR在非传染性病毒存在和环境基质中可有效检测传染性脊髓灰质炎病毒。我们得出的结论是,在上述条件下,PMA可用于区分潜在感染性病毒和非感染性病毒。

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