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Near-Complete Genome Sequencing of Swine Vesicular Disease Virus Using the Roche GS FLX Sequencing Platform

机译:使用Roche GS FLX测序平台对猪水泡病病毒进行近乎完整的基因组测序

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摘要

Swine vesicular disease virus (SVDV) is an enterovirus that is both genetically and antigenically closely related to human coxsackievirus B5 within the Picornaviridae family. SVDV is the causative agent of a highly contagious (though rarely fatal) vesicular disease in pigs. We report a rapid method that is suitable for sequencing the complete protein-encoding sequences of SVDV isolates in which the RNA is relatively intact. The approach couples a single PCR amplification reaction, using only a single PCR primer set to amplify the near-complete SVDV genome, with deep-sequencing using a small fraction of the capacity of a Roche GS FLX sequencing platform. Sequences were initially verified through one of two criteria; either a match between a de novo assembly and a reference mapping, or a match between all of five different reference mappings performed against a fixed set of starting reference genomes with significant genetic distances within the same species of viruses. All reference mappings used an iterative method to avoid bias. Further verification was achieved through phylogenetic analysis against published SVDV genomes and additional Enterovirus B sequences. This approach allows high confidence in the obtained consensus sequences, as well as provides sufficiently high and evenly dispersed sequence coverage to allow future studies of intra-host variation.
机译:猪水泡性疾病病毒(SVDV)是一种肠道病毒,与Picornaviridae家族的人柯萨奇病毒B5在遗传和抗原上都密切相关。 SVDV是猪中高度传染性(虽然很少致命)的水疱病的病原。我们报告了一种快速的方法,适用于对RNA相对完整的SVDV分离株的完整蛋白质编码序列进行测序。该方法仅使用单个PCR引物组即可扩增接近完整的SVDV基因组,而仅使用Roche GS FLX测序平台的一小部分容量即可进行深度测序,从而实现单个PCR扩增反应。最初通过两个标准之一验证了序列;从头装配和参考图之间的匹配,或对固定组的起始参考基因组进行固定的五个相同参考图之间的匹配,这些起始参考基因组在相同病毒种内具有显着的遗传距离。所有参考映射都使用迭代方法来避免偏差。通过针对已发布的SVDV基因组和其他肠道病毒B序列的系统发育分析,可以进一步验证。这种方法可以使获得的共有序列具有很高的置信度,并且可以提供足够高且均匀分散的序列覆盖率,从而可以对宿主内部变异进行进一步的研究。

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