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Concise and Broadly Applicable Method for Determining the Genomic Sequences of North-American–Type Porcine Reproductive and Respiratory Syndrome Viruses in Various Clusters

机译:简洁而广泛适用的测定北美型猪繁殖与呼吸综合征病毒基因组序列的基因组序列的方法

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References(31) Supplementary materials(2) We developed a concise and broadly applicable method for accurate genomic sequencing of North American genotype (NA-type) porcine reproductive and respiratory syndrome viruses (PRRSVs) that overcomes high genetic variability of the viruses. The method, designated “combination of consensus oligonucleotide reverse transcription and multiple displacement amplification” (CORT-MDA), involves reverse-transcription of viral RNA followed by shotgun sequencing after amplification using only 11 degenerate oligonucleotide primers; these primers were designed against consensus regions within the open reading frames of the 124 NA-type PRRSV strains with reported full-length genomic sequences. Sequencing of the 192 shotgun clones generated per virus showed 80% to 94% coverage on the reported PRRSV genomic sequence, such that only 2 or 3 unread regions had to be resequenced after PCR amplification using custom primers. Direct sequencing of RT-PCR products confirmed absolute consistency between sequences determined by the CORT-MDA method and those from RT-PCR. These results suggest that our method is applicable to diverse NA-type viruses.
机译:参考文献(31)补充材料(2)我们开发了一种简洁且广泛适用的方法,可用于克服北美病毒基因型(NA-type)猪繁殖与呼吸综合征病毒(PRRSV)的准确基因组测序,该方法克服了该病毒的高遗传变异性。该方法称为“共有寡核苷酸逆转录和多置换扩增的组合”(CORT-MDA),涉及病毒RNA的逆转录,然后仅使用11种简并的寡核苷酸引物进行扩增后的shot弹枪测序。这些引物是针对具有报道的全长基因组序列的124个NA型PRRSV菌株的开放阅读框内的共有区域设计的。每种病毒产生的192个shot弹枪克隆的测序表明,在报道的PRRSV基因组序列上有80%至94%的覆盖率,因此,使用定制引物进行PCR扩增后,仅需重新测序2个或3个未读区域。 RT-PCR产物的直接测序证实了通过CORT-MDA方法确定的序列与通过RT-PCR获得的序列之间的绝对一致性。这些结果表明我们的方法适用于多种NA型病毒。

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