Wesley I V, Wesley R D, Heisick J, Harrell F, Wagner D
Physiopathology Research Unit, USDA-Agricultural Research Service, Ames, IA.
Vet Microbiol. 1990 Sep;24(3-4):341-53. doi: 10.1016/0378-1135(90)90182-u.
A synthetic deoxyribonucleotide probe for virulent Listeria monocytogenes, designated ADO7, was evaluated for its ability to identify restriction fragments of L. monocytogenes with nucleic acid sequences homologous with the beta-hemolysin gene by Southern blot hybridization of clinical and food isolates. The synthetic probe hybridized with three restriction fragments (approximately 1.1, 0.86, and 0.76 kb) of the serotype 1/2A isolates. Southern blot hybridization of the serogroup 4B isolates indicated that the nucleic acid sequences homologous with the beta-hemolysin gene probe were limited to a single restriction fragment of approximately 1 kb.
一种用于致病单核细胞增生李斯特菌的合成脱氧核糖核苷酸探针,命名为ADO7,通过对临床和食品分离株进行Southern印迹杂交,评估其识别与β-溶血素基因具有核酸序列同源性的单核细胞增生李斯特菌限制性片段的能力。该合成探针与1/2A血清型分离株的三个限制性片段(约1.1、0.86和0.76 kb)杂交。4B血清群分离株的Southern印迹杂交表明,与β-溶血素基因探针具有核酸序列同源性的序列仅限于一个约1 kb的单一限制性片段。