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A species independent universal bio-detection microarray for pathogen forensics and phylogenetic classification of unknown microorganisms

机译:一种与物种无关的通用生物检测微阵列,用于病原体取证和未知微生物的系统发育分类

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Background The ability to differentiate a bioterrorist attack or an accidental release of a research pathogen from a naturally occurring pandemic or disease event is crucial to the safety and security of this nation by enabling an appropriate and rapid response. It is critical in samples from an infected patient, the environment, or a laboratory to quickly and accurately identify the precise pathogen including natural or engineered variants and to classify new pathogens in relation to those that are known. Current approaches for pathogen detection rely on prior genomic sequence information. Given the enormous spectrum of genetic possibilities, a field deployable, robust technology, such as a universal (any species) microarray has near-term potential to address these needs. Results A new and comprehensive sequence-independent array (Universal Bio-Signature Detection Array) was designed with approximately 373,000 probes. The main feature of this array is that the probes are computationally derived and sequence independent. There is one probe for each possible 9-mer sequence, thus 49 (262,144) probes. Each genome hybridized on this array has a unique pattern of signal intensities corresponding to each of these probes. These signal intensities were used to generate an un-biased cluster analysis of signal intensity hybridization patterns that can easily distinguish species into accepted and known phylogenomic relationships. Within limits, the array is highly sensitive and is able to detect synthetically mixed pathogens. Examples of unique hybridization signal intensity patterns are presented for different Brucella species as well as relevant host species and other pathogens. These results demonstrate the utility of the UBDA array as a diagnostic tool in pathogen forensics. Conclusions This pathogen detection system is fast, accurate and can be applied to any species. Hybridization patterns are unique to a specific genome and these can be used to decipher the identity of a mixed pathogen sample and can separate hosts and pathogens into their respective phylogenomic relationships. This technology can also differentiate between different species and classify genomes into their known clades. The development of this technology will result in the creation of an integrated biomarker-specific bio-signature, multiple select agent specific detection system.
机译:背景技术区分生物恐怖袭击或研究病原体与自然发生的大流行或疾病事件的意外释放的能力,通过采取适当和迅速的应对措施,对于这个国家的安全与保障至关重要。对于来自受感染患者,环境或实验室的样本,至关重要的是要快速而准确地识别出包括自然或工程变体在内的精确病原体,并根据已知病原体对新病原体进行分类。用于病原体检测的当前方法依赖于先前的基因组序列信息。鉴于广泛的遗传可能性,一种可现场部署的强大技术(例如通用(任何物种)微阵列)具有近期满足这些需求的潜力。结果设计了一个新的,全面的序列独立阵列(通用生物特征检测阵列),其中包含约373,000个探针。该阵列的主要特征是探针是计算得出的且与序列无关。每个可能的9-mer序列只有一个探针,因此有4 9 (262,144)个探针。在该阵列上杂交的每个基因组具有对应于这些探针中的每一个的信号强度的独特模式。这些信号强度用于生成信号强度杂交模式的无偏聚类分析,可以轻松地将物种区分为公认的已知植物学关系。在一定范围内,该阵列高度敏感,能够检测出合成的病原体。提出了针对不同布鲁氏菌属物种以及相关宿主物种和其他病原体的独特杂交信号强度模式的示例。这些结果证明了UBDA阵列作为病原体法医学诊断工具的实用性。结论该病原体检测系统快速,准确,可应用于任何物种。杂交模式是特定基因组所特有的,可用于破译混合病原体样品的身份,并可将宿主和病原体分离成各自的亲缘关系。该技术还可以区分不同物种,并将基因组分类为已知的进化枝。该技术的发展将导致创建集成的生物标志物特异性生物特征,多种选择剂特异性检测系统。

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