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

机译:重测序病原体微阵列(RPM),用于前瞻性检测和鉴定新兴病原体菌株和变体

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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:高密度重测序微阵列支持同时检测和鉴定多种病毒和细菌病原体。由于使用RPM进行检测和鉴定是基于单个测试中生成的多个标本特异的目标病原体基因序列,因此测试结果可以对从一个标本到下一个标本的检测到的病原体菌株和变异进行差异诊断分析和流行病学跟踪。 RPM分析能够检测和鉴定与阵列中检测器图块表示的原型靶基因序列具有低至80%序列相似性的病原体序列。此功能使RPM能够检测和识别以前未知的菌株和检测到的病原体变体,例如在与传染病暴发相关的前哨病例中。我们使用测试的A型流感病毒疫苗的分析结果来说明这种能力,该疫苗配置了在设计RPM微阵列后首次定义的菌株。还将对三个标本进行RPM-Flu测试得出的结果独立确认为2009年新型H1N1流感病毒暴发株为阳性。

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