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一种基于16S rRNA的、针对伊氏李斯特菌的DNA探针及PCR方法。

A 16S rRNA-based DNA probe and PCR method specific for Listeria ivanovii.

作者信息

Wang R F, Cao W W, Wang H, Johnson M G

机构信息

Department of Food Science and Biotechnology Center, University of Arkansas, Fayetteville, Arkansas 72703.

出版信息

FEMS Microbiol Lett. 1993 Jan 1;106(1):85-92. doi: 10.1111/j.1574-6968.1993.tb05939.x.

Abstract

A 16S rRNA-based DNA probe and polymerase chain reaction (PCR) method was developed for identification and rapid detection of Listeria ivanovii. The probe (R-1) is 5'-GTAGTGACGCATGTCATCAC-3' corresponding to positions 185-204 in the L. ivanovii 16S rRNA sequence. DNA hybridization results indicated that R-1 probe only reacted with L. ivanovii, and not with six other species of Listeria or other bacteria tested. The PCR method using R-1 and a reverse primer, R-2, was positive with all eight strains of L. ivanovii tested but was negative with six other species of Listeria, including nine strains of L. monocytogenes, and 20 other taxonomically related bacteria tested. In our PCR method, starting with whole bacterial cells, only 3 h were required for the PCR assay and 1 h for electrophoresis without any additional time for DNA isolation and DNA hybridization. This PCR method detected as few as 4 cells of L. ivanovii in pure cultures and 4-40 cells of L. ivanovii in inoculated and diluted mouse feed, blood, or faeces samples.

摘要

开发了一种基于16S rRNA的DNA探针和聚合酶链反应(PCR)方法,用于鉴定和快速检测伊氏李斯特菌。该探针(R-1)为5'-GTAGTGACGCATGTCATCAC-3',对应于伊氏李斯特菌16S rRNA序列中的第185至204位。DNA杂交结果表明,R-1探针仅与伊氏李斯特菌反应,而不与其他六种李斯特菌或所测试的其他细菌反应。使用R-1和反向引物R-2的PCR方法对所有八株测试的伊氏李斯特菌呈阳性,但对其他六种李斯特菌呈阴性,其中包括九株单核细胞增生李斯特菌以及20株其他分类学相关细菌。在我们的PCR方法中,从完整细菌细胞开始,PCR检测仅需3小时,电泳需1小时,无需额外的DNA分离和DNA杂交时间。该PCR方法在纯培养物中可检测到低至4个伊氏李斯特菌细胞,在接种和稀释的小鼠饲料、血液或粪便样本中可检测到4至40个伊氏李斯特菌细胞。

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