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宏基因组学与病毒发现的未来展望。

Metagenomics and future perspectives in virus discovery.

机构信息

Department of Biology, San Diego State University, San Diego, CA 92182, USA.

出版信息

Curr Opin Virol. 2012 Feb;2(1):63-77. doi: 10.1016/j.coviro.2011.12.004. Epub 2012 Jan 20.

Abstract

Monitoring the emergence and re-emergence of viral diseases with the goal of containing the spread of viral agents requires both adequate preparedness and quick response. Identifying the causative agent of a new epidemic is one of the most important steps for effective response to disease outbreaks. Traditionally, virus discovery required propagation of the virus in cell culture, a proven technique responsible for the identification of the vast majority of viruses known to date. However, many viruses cannot be easily propagated in cell culture, thus limiting our knowledge of viruses. Viral metagenomic analyses of environmental samples suggest that the field of virology has explored less than 1% of the extant viral diversity. In the last decade, the culture-independent and sequence-independent metagenomic approach has permitted the discovery of many viruses in a wide range of samples. Phylogenetically, some of these viruses are distantly related to previously discovered viruses. In addition, 60-99% of the sequences generated in different viral metagenomic studies are not homologous to known viruses. In this review, we discuss the advances in the area of viral metagenomics during the last decade and their relevance to virus discovery, clinical microbiology and public health. We discuss the potential of metagenomics for characterization of the normal viral population in a healthy community and identification of viruses that could pose a threat to humans through zoonosis. In addition, we propose a new model of the Koch's postulates named the 'Metagenomic Koch's Postulates'. Unlike the original Koch's postulates and the Molecular Koch's postulates as formulated by Falkow, the metagenomic Koch's postulates focus on the identification of metagenomic traits in disease cases. The metagenomic traits that can be traced after healthy individuals have been exposed to the source of the suspected pathogen.

摘要

监测病毒性疾病的出现和再现,以控制病毒传播,需要充分的准备和快速反应。确定新疫情的病原体是对疾病爆发做出有效反应的最重要步骤之一。传统上,病毒的发现需要在细胞培养中繁殖病毒,这是一种已被证明的技术,负责识别迄今为止已知的绝大多数病毒。然而,许多病毒不能在细胞培养中轻易繁殖,从而限制了我们对病毒的了解。对环境样本的病毒宏基因组分析表明,病毒学领域只探索了不到 1%的现存病毒多样性。在过去十年中,非依赖培养和非依赖序列的宏基因组方法已经允许在广泛的样本中发现许多病毒。从系统发育上看,其中一些病毒与以前发现的病毒有较远的亲缘关系。此外,在不同的病毒宏基因组研究中产生的序列有 60-99%与已知病毒没有同源性。在这篇综述中,我们讨论了过去十年中病毒宏基因组学领域的进展及其对病毒发现、临床微生物学和公共卫生的相关性。我们讨论了宏基因组学在描述健康社区中正常病毒群和识别通过动物传染病对人类构成威胁的病毒方面的潜力。此外,我们提出了一个新的科赫氏假定模型,称为“宏基因组科赫氏假定”。与原始的科赫氏假定和 Falkow 提出的分子科赫氏假定不同,宏基因组科赫氏假定的重点是在疾病病例中识别宏基因组特征。在健康个体接触疑似病原体来源后,可以追踪到这些宏基因组特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd5/7102772/dc233e94cde2/gr1.jpg

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