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Development of PCR and TaqMan PCR Assays to Detect Pseudomonas coronafaciens a Causal Agent of Halo Blight of Oats

机译:PCR和TaqMan PCR检测试剂盒的开发用于检测燕麦光环枯萎病的病原体假单胞菌

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摘要

Pseudomonas coronafaciens causes halo blight on oats and is a plant quarantine bacterium in many countries, including the Republic of Korea. Using of the certificated seed is important for control of the disease. Since effective detection method of P. coronafaciens is not available yet, PCR and TaqMan PCR assays for specific detection of P. coronafaciens were developed in this study. PCR primers were designed from the draft genome sequence of P. coronafaciens LMG 5060 which was obtained by the next-generation sequencing in this study. The PCR primer set Pc-12-F/Pc-12-R specifically amplified 498 bp from the 13 strains of P. coronafaciens isolated in the seven different countries (Canada, Japan, United Kingdom, Zimbabwe, Kenya, Germany, and New Zealand) and the nested primer set Pc-12-ne-F/Pc-12-ne-R specifically amplified 298 bp from those strains. The target-size PCR product was not amplified from the non-target bacteria with the PCR and nested primer sets. TaqMan PCR with Pc-12-ne-F/Pc-12-ne-R and a TaqMan probe, Pc-taqman, which were designed inside of the nested PCR amplicon, generated Ct values which in a dose-dependent manner to the amount of the target DNA and the Ct values of all the P. coronafaciens strains were above the threshold Ct value for positive detection. The TaqMan PCR generated positive Ct values from the seed extracts of the artificially inoculated oat seeds above 10 cfu/ml inoculation level. PCR and TaqMan PCR assays developed in this study will be useful tools to detect and identify the plant quarantine pathogen, P. coronafaciens.
机译:假单胞菌(Pseudomonas coronafaciens)在燕麦上引起光环病,在包括大韩民国在内的许多国家中都是植物检疫细菌。使用认证种子对于控制疾病很重要。由于尚无有效的冠状疟原虫检测方法,本研究开发了用于特异性检测冠状疟原虫的PCR和TaqMan PCR检测方法。从Coronafaciens LMG 5060的基因组草图序列设计PCR引物,该序列是通过本研究中的下一代测序获得的。 PCR引物组Pc-12-F / Pc-12-R从七个不同国家(加拿大,日本,英国,津巴布韦,肯尼亚,德国和新西兰)分离的13株冠状疟原虫菌株中特异性扩增了498 bp )和巢式引物组Pc-12-ne-F / Pc-12-ne-R从这些菌株特异性扩增298 bp。使用PCR和嵌套引物对未从非靶标细菌中扩增出目标大小的PCR产物。在嵌套式PCR扩增子内部设计的带有Pc-12-ne-F / Pc-12-ne-R的TaqMan PCR和TaqMan探针Pc-taqman产生的Ct值与剂量成比例关系所有冠状疟原虫菌株的目标DNA的Ct值均高于用于阳性检测的阈值Ct值。 TaqMan PCR从高于10 cfu / ml接种水平的人工接种燕麦种子的种子提取物中产生正Ct值。在这项研究中开发的PCR和TaqMan PCR分析方法将是检测和鉴定植物检疫病原体P. coronafaciens的有用工具。

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