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使用多位点聚合酶链反应/电喷雾电离质谱法鉴定细菌性植物病原体

Identification of bacterial plant pathogens using multilocus polymerase chain reaction/electrospray ionization-mass spectrometry.

作者信息

Postinikova E, Baldwin C, Whitehouse C A, Sechler A, Schaad N W, Sampath R, Harpin V, Li F, Melton R, Blyn L, Drader J, Hofstadler S, Schneider W L

机构信息

USDA-ARS, Foreign Disease-Weed Science Research Unit, Fort Detrick, MD, USA.

出版信息

Phytopathology. 2008 Nov;98(11):1156-64. doi: 10.1094/PHYTO-98-11-1156.

Abstract

Polymerase chain reaction/electrospray ionization-mass spectrometry (PCR/ESI-MS, previously known as "TIGER") utilizes PCR with broad-range primers to amplify products from a wide array of organisms within a taxonomic group, followed by analysis of PCR amplicons using mass spectrometry. Computer analysis of precise masses allows for calculations of base compositions for the broad-range PCR products, which can then be compared to a database for identification. PCR/ESI-MS has the benefits of PCR in sensitivity and high-throughput capacity, but also has the distinct advantage of being able to detect and identify organisms with no prior characterization or sequence data. Existing broad range PCR primers, designed with an emphasis on human pathogens, were tested for their ability to amplify DNA of well characterized phytobacterial strains, as well as to populate the existing PCR/ESI-MS bacterial database with base counts. In a blinded panel study, PCR/ESI-MS successfully identified 93% of unknown bacterial DNAs to the genus level and 73% to the species/subspecies level. Additionally, PCR/ESI-MS was capable of detecting and identifying multiple bacteria within the same sample. The sensitivity of PCR/ESI-MS was consistent with other PCR based assays, and the specificity varied depending on the bacterial species. Preliminary tests with real life samples demonstrate a high potential for using PCR/ESI-MS systems for agricultural diagnostic applications.

摘要

聚合酶链反应/电喷雾电离质谱法(PCR/ESI-MS,以前称为“TIGER”)利用带有广谱引物的PCR从分类群中的多种生物体中扩增产物,然后使用质谱法分析PCR扩增子。对精确质量的计算机分析允许计算广谱PCR产物的碱基组成,然后可将其与数据库进行比较以进行鉴定。PCR/ESI-MS具有PCR在灵敏度和高通量能力方面的优点,而且还具有能够检测和鉴定没有先前特征或序列数据的生物体的独特优势。对现有的以人类病原体为重点设计的广谱PCR引物进行了测试,以评估其扩增特征明确的植物细菌菌株DNA的能力,以及用碱基计数填充现有的PCR/ESI-MS细菌数据库的能力。在一项盲法小组研究中,PCR/ESI-MS成功地将93%的未知细菌DNA鉴定到属水平,73%鉴定到种/亚种水平。此外,PCR/ESI-MS能够检测和鉴定同一样本中的多种细菌。PCR/ESI-MS的灵敏度与其他基于PCR的检测方法一致,特异性因细菌种类而异。对实际样本的初步测试表明,使用PCR/ESI-MS系统进行农业诊断应用具有很大潜力。

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