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通过高通量测序对A至D种肠道病毒进行全基因组测序:在病毒混合物中的应用

Whole Genome Sequencing of Enteroviruses Species A to D by High-Throughput Sequencing: Application for Viral Mixtures.

作者信息

Joffret Marie-Line, Polston Patsy M, Razafindratsimandresy Richter, Bessaud Maël, Heraud Jean-Michel, Delpeyroux Francis

机构信息

Unité de Biologie des Virus Entériques, Institut Pasteur, Paris, France.

Institut National de la Santé et de la Recherche Médicale, Paris, France.

出版信息

Front Microbiol. 2018 Sep 28;9:2339. doi: 10.3389/fmicb.2018.02339. eCollection 2018.

Abstract

Human enteroviruses (EV) consist of more than 100 serotypes classified within four species for enteroviruses (EV-A to -D) and three species for rhinoviruses, which have been implicated in a variety of human illnesses. Being able to simultaneously amplify the whole genome and identify enteroviruses in samples is important for studying the viral diversity in different geographical regions and populations. It also provides knowledge about the evolution of these viruses. Therefore, we developed a rapid, sensitive method to detect and genetically classify all human enteroviruses in mixtures. Strains of EV-A (15), EV-B (40), EV-C (20), and EV-D (2) viruses were used in addition to 20 supernatants from RD cells infected with stool extracts or sewage concentrates. Two overlapping fragments were produced using a newly designed degenerated primer targeting the conserved CRE region for enteroviruses A-D and one degenerated primer set designed to specifically target the conserved region for each enterovirus species (EV-A to -D). This method was capable of sequencing the full genome for all viruses except two, for which nearly 90% of the genome was sequenced. This method also demonstrated the ability to discriminate, in both spiked and unspiked mixtures, the different enterovirus types present.

摘要

人肠道病毒(EV)由100多种血清型组成,分为肠道病毒的四个种(EV-A至-D)和鼻病毒的三个种,它们与多种人类疾病有关。能够同时扩增样本中的全基因组并鉴定肠道病毒,对于研究不同地理区域和人群中的病毒多样性很重要。这也能提供有关这些病毒进化的知识。因此,我们开发了一种快速、灵敏的方法,用于检测混合物中的所有人类肠道病毒并进行基因分型。除了来自感染粪便提取物或污水浓缩物的RD细胞的20份上清液外,还使用了EV-A(15种)、EV-B(40种)、EV-C(20种)和EV-D(2种)病毒的毒株。使用新设计的针对肠道病毒A-D保守CRE区域的简并引物和一组专门针对每种肠道病毒种(EV-A至-D)保守区域设计的简并引物,产生了两个重叠片段。该方法能够对除两种病毒外的所有病毒进行全基因组测序,对于这两种病毒,测序了近90%的基因组。该方法还证明了在加标和未加标混合物中区分存在的不同肠道病毒类型的能力。

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