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环境及贝类中的病毒污染:通过聚合酶链反应检测人腺病毒作为人类病毒的指标

Viral pollution in the environment and in shellfish: human adenovirus detection by PCR as an index of human viruses.

作者信息

Pina S, Puig M, Lucena F, Jofre J, Girones R

机构信息

Department of Microbiology, University of Barcelona, 08028-Barcelona, Spain.

出版信息

Appl Environ Microbiol. 1998 Sep;64(9):3376-82. doi: 10.1128/AEM.64.9.3376-3382.1998.

Abstract

A study of the presence of human viruses (adenoviruses, enteroviruses, and hepatitis A viruses [HAVs]) in environmental and shellfish samples was carried out by applying DNA and cDNA amplification techniques by PCR. The detection of human adenoviruses by PCR was also examined as a potential molecular test to monitor viral pollution. The samples studied were urban and slaughterhouse sewage, river water, seawater, and shellfish. Enteroviruses were quantified by PFU in Buffalo green monkey kidney cells and fecal coliforms and phages of Bacteroides fragilis HSP40 were also evaluated in some of the samples. The amplification of viral DNA and cDNA has shown a high prevalence of human viruses that would not be detected by the use of classical techniques, such as the quantification of PFU in cell lines. The results of the analysis of slaughterhouse sewage samples together with the test of farm animal feces indicate that the adenoviruses and the HAVs detected in the environment are mostly of human origin. A significative correlation between the detection of human viruses by PCR and the values of bacteriophages of B. fragilis HSP40 in urban raw sewage was observed. Human adenoviruses were the viruses most frequently detected throughout the year, and all the samples that were positive for enteroviruses or HAVs were also positive for human adenoviruses. The results suggest that the detection of adenoviruses by PCR could be used as an index of the presence of human viruses in the environment where a molecular index is acceptable.

摘要

通过聚合酶链反应(PCR)应用DNA和cDNA扩增技术,对环境和贝类样本中人类病毒(腺病毒、肠道病毒和甲型肝炎病毒 [HAV])的存在情况进行了研究。还对通过PCR检测人类腺病毒作为监测病毒污染的潜在分子检测方法进行了研究。所研究的样本包括城市污水、屠宰场污水、河水、海水和贝类。通过在水牛绿猴肾细胞中进行蚀斑形成单位(PFU)定量来测定肠道病毒,并且还对一些样本中的脆弱拟杆菌HSP40的粪大肠菌群和噬菌体进行了评估。病毒DNA和cDNA的扩增显示人类病毒的高流行率,而使用传统技术(如在细胞系中进行PFU定量)则无法检测到这些病毒。屠宰场污水样本的分析结果以及家畜粪便检测结果表明,环境中检测到的腺病毒和HAV大多源自人类。观察到城市原污水中通过PCR检测人类病毒与脆弱拟杆菌HSP40噬菌体的值之间存在显著相关性。人类腺病毒是全年最常检测到的病毒,所有肠道病毒或HAV呈阳性的样本中人类腺病毒也呈阳性。结果表明,在分子指标可接受的环境中,通过PCR检测腺病毒可作为人类病毒存在的指标。

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