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对用于 PCR 检测沙门氏菌基因组的新特定分子靶标的挖掘和评估。

Mining and evaluation of new specific molecular targets for the PCR detection of Salmonella spp. genome.

机构信息

Key Laboratory of Food Processing and Quality Control, Ministry of Agriculture of China, College of Food Science and Technology, Nanjing Agricultural University, 1 Weigang, Nanjing, 210095, People's Republic of China.

出版信息

World J Microbiol Biotechnol. 2013 Dec;29(12):2219-26. doi: 10.1007/s11274-013-1387-0. Epub 2013 Jun 16.

Abstract

The purpose of this study is to find new molecular targets for the detection of Salmonella. With the online BLAST Program, we compared homology of genomic sequences and specificity in GenBank among Salmonella serovars and non-Salmonella strains and found 98 Salmonella specific target sequences. We selected 33 target sequences of Gene ID from 3335000 to 3337003 for the specificity evaluation, and finally 8 specific fragments screened out, they are 3334138, 3335583, 3335471, 3335211, 3335068, 3336466, 3336736 and 3336998. Primer SC8 of gene 3335583 and SC9 of gene 3335471 were the best in specificity and sensitivity among these primers. The detection sensitivity of Primer SC9 was 1.23 fg/μl for DNA templates and 720 cfu/ml for whole cells, while primer SC8's was 12.3 fg/μl and 720 cfu/ml, respectively. Salmonella could be detected successfully by the PCR method developed in this study after 8 h enrichment when the milk samples were artificially contaminated by this organism at 7 cfu per 10 ml milk.

摘要

本研究旨在寻找用于检测沙门氏菌的新分子靶标。通过在线 BLAST 程序,我们比较了沙门氏菌血清型和非沙门氏菌菌株在 GenBank 中的基因组序列同源性和特异性,发现了 98 个沙门氏菌特异性靶序列。我们从 3335000 到 3337003 个基因 ID 中选择了 33 个目标序列用于特异性评估,最终筛选出 8 个特异性片段,它们是 3334138、3335583、3335471、3335211、3335068、3336466、3336736 和 3336998。基因 3335583 的引物 SC8 和基因 3335471 的引物 SC9 在特异性和敏感性方面表现最佳。引物 SC9 的检测灵敏度为 DNA 模板的 1.23 fg/μl 和全细胞的 720 cfu/ml,而引物 SC8 的分别为 12.3 fg/μl 和 720 cfu/ml。当牛奶样品被该生物体人工污染至每 10 毫升牛奶 7 个菌落时,本研究开发的 PCR 方法在 8 小时富集后可以成功检测到沙门氏菌。

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