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用于检测水中诺如病毒并进行基因分型的通用标签阵列的开发与评估

Development and evaluation of a generic tag array to detect and genotype noroviruses in water.

作者信息

Brinkman Nichole E, Fout G Shay

机构信息

U.S. Environmental Protection Agency, Office of Research and Development, National Exposure Research Laboratory, Biohazard Assessment Research Branch, 26 West Martin Luther King Drive, MS 320, Cincinnati, OH 45268, USA.

出版信息

J Virol Methods. 2009 Mar;156(1-2):8-18. doi: 10.1016/j.jviromet.2008.03.010. Epub 2008 May 8.

Abstract

Noroviruses are the leading cause of nonbacterial gastroenteritis outbreaks in the United States, some of which are caused by the ingestion of contaminated water. Detection and genotypic characterization of noroviruses is commonly performed by reverse transcription-polymerase chain reaction (RT-PCR) followed by sequencing. However, sequencing of products amplified from environmental water samples is often hindered by the co-amplification of non-specific cDNA. To overcome this issue, a generic microarray was evaluated to genotype noroviruses by probe hybridization. RT-PCR amplicons are used in a single base extension (SBE) reaction where genotype-specific probes are labeled and then hybridized to an Affymetrix GeneChip GenFlex Tag Array for detection. Using a standardized, multiplex SBE reaction, genotyping of representative strains was accomplished through the identification of genotype-specific patterns of positive hybridization results. Furthermore, the SBE-GenFlex array method was successful in the genotype identification of noroviruses seeded into tap and Ohio River water samples. This study shows the utility of using a microarray to genotype noroviruses in complex environmental matrices.

摘要

诺如病毒是美国非细菌性肠胃炎暴发的主要原因,其中一些是由摄入受污染的水引起的。诺如病毒的检测和基因分型通常通过逆转录聚合酶链反应(RT-PCR)然后进行测序来完成。然而,从环境水样中扩增的产物测序常常受到非特异性cDNA共扩增的阻碍。为了克服这个问题,通过探针杂交评估了一种通用微阵列对诺如病毒进行基因分型。RT-PCR扩增子用于单碱基延伸(SBE)反应,其中对基因型特异性探针进行标记,然后与Affymetrix GeneChip GenFlex Tag Array杂交以进行检测。使用标准化的多重SBE反应,通过鉴定阳性杂交结果的基因型特异性模式完成了代表性菌株的基因分型。此外,SBE-GenFlex阵列方法成功地对接种到自来水和俄亥俄河水样中的诺如病毒进行了基因型鉴定。这项研究表明了使用微阵列对复杂环境基质中的诺如病毒进行基因分型的实用性。

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