Datta A R, Wentz B A, Shook D, Trucksess M W
Division of Microbiology, Center for Food Safety and Applied Nutrition, Food and Drug Administration, Washington, D.C. 20204.
Appl Environ Microbiol. 1988 Dec;54(12):2933-7. doi: 10.1128/aem.54.12.2933-2937.1988.
A 500-base-pair DNA fragment of a presumptive beta-hemolysin gene of Listeria monocytogenes has been used to identify this organism by a modified colony hybridization technique. We have cloned this DNA fragment into M13 bacteriophage vectors and sequenced it by a dideoxynucleotide sequencing technique. From this sequencing information, several oligodeoxyribonucleotides were synthesized and used as synthetic probes to identify L. monocytogenes. The probes were specific for L. monocytogenes and did not react with any other Listeria strains in a colony hybridization assay. In particular, one of these probes (AD07) was used to detect L. monocytogenes in artificially contaminated raw-milk and soft-cheese samples.
单核细胞增生李斯特菌假定的β-溶血素基因的一个500个碱基对的DNA片段已被用于通过改良的菌落杂交技术鉴定该微生物。我们已将此DNA片段克隆到M13噬菌体载体中,并通过双脱氧核苷酸测序技术对其进行测序。根据该测序信息,合成了几种寡脱氧核糖核苷酸,并用作合成探针来鉴定单核细胞增生李斯特菌。这些探针对单核细胞增生李斯特菌具有特异性,并且在菌落杂交试验中不与任何其他李斯特菌菌株发生反应。特别是,其中一种探针(AD07)被用于检测人工污染的生乳和软奶酪样品中的单核细胞增生李斯特菌。