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Resequencing Pathogen Microarray (RPM) for Prospective Detectionand Identification of Emergent Pathogen Strains and Variants

机译:重新转移病原体微阵列(RPM),用于术后病原菌菌株和变体的前瞻性检测和鉴定

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High-density resequencing microarrays support simultaneous detection and identification of multiple viral and bacterial pathogens. Because detection and identification using RPM is based upon multiple specimen-specific target pathogen gene sequences generated in the individual test, the test results enable both a differential diagnostic analysis and epidemiological tracking of detected pathogen strains and variants from one specimen to the next. The RPM assay enables detection and identification of pathogen sequences that share as little as 80% sequence similarity to prototype target gene sequences represented as detector tiles on the array. This capability enables the RPM to detect and identify previously unknown strains and variants of a detected pathogen, as in sentinel cases associated with an infectious disease outbreak. We illustrate this capability using assay results from testing influenza A virus vaccines configured with strains that were first defined years after the design of the RPM microarray. Results are also presented from RPM-Flu testing of three specimens independently confirmed to the positive for the 2009 Novel H1N1 outbreak strain of influenza virus.
机译:高密度重新排列微阵列支持同时检测和鉴定多种病毒和细菌病原体。因为使用RPM的检测和识别基于在个体测试中产生的多个样本特异性靶病原体基因序列,所以测试结果使得检测到的病原体菌株和从一个样品到下一个样品的变体能够进行差异诊断分析和流行病学跟踪。 RPM测定能够检测和鉴定分享到80%序列相似性的病原体序列与表示为阵列上的检测器瓦片的原型靶基因序列。这种能力使RPM能够检测和识别检测到的病原体的先前未知的菌株和变体,如与传染病爆发相关的哨兵病例中。我们使用测定结果来说明这种能力,从测试流感病毒疫苗,该病毒疫苗被配置有菌株在RPM微阵列的设计后首次定义的菌株。结果也从RPM - 流感试验中介绍了三种标本,该标本独立证实了2009年新型H1N1爆发血型流感病毒的阳性阳性。

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