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Large-scale evolutionary surveillance of the 2009 H1N1 influenza A virus using resequencing arrays

机译:使用重排阵列对2009 H1N1甲型流感病毒进行大规模进化监测

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In April 2009, a new influenza A (H1N1 2009) virus emerged that rapidly spread around the world. While current variants of this virus have caused widespread disease, particularly in vulnerable groups, there remains the possibility that future variants may cause increased virulence, drug resistance or vaccine escape. Early detection of these virus variants may offer the chance for increased containment and potentially prevention of the virus spread. We have developed and field-tested a resequencing kit that is capable of interrogating all eight segments of the 2009 influenza A(H1N1) virus genome and its variants, with added focus on critical regions such as drug-binding sites, structural components and mutation hotspots. The accompanying base-calling software (EvolSTAR) introduces novel methods that utilize neighbourhood hybridization intensity profiles and substitution bias of probes on the microarray for mutation confirmation and recovery of ambiguous base queries. Our results demonstrate that EvolSTAR is highly accurate and has a much improved call rate. The high throughput and short turn-around time from sample to sequence and analysis results (30 h for 24 samples) makes this kit an efficient large-scale evolutionary biosurveillance tool.
机译:2009年4月,出现了一种新的甲型H1N1流感病毒,并迅速在世界范围内传播。尽管该病毒的当前变体已引起广泛的疾病,尤其是在脆弱人群中,但仍有可能未来的变体可能导致毒力增加,耐药性或疫苗逃逸。对这些病毒变体的早期检测可能会提供更多的机会来遏制并潜在地防止病毒传播。我们已经开发并现场测试了一种重测序试剂盒,该试剂盒能够询问2009年甲型H1N1流感病毒基因组的所有八个片段及其变体,并且重点关注诸如药物结合位点,结构成分和突变热点等关键区域。随附的碱基检出软件(EvolSTAR)引入了新颖的方法,该方法利用邻域杂交强度分布图和微阵列上探针的置换偏差来进行突变确认和不明确碱基查询的恢复。我们的结果表明,EvolSTAR的准确性很高,并且通话率大大提高。从样品到序列和分析结果的高通量和短的处理时间(24个样品需要30 h)使该试剂盒成为高效的大规模进化生物监测工具。

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