Lemaître J P, Delcourt A, Rousset A
Faculté de Pharmacie, Université de Bourgogne, Dijon, France.
Lett Appl Microbiol. 1997 Jan;24(1):51-4. doi: 10.1046/j.1472-765x.1997.00346.x.
It is necessary to isolate new phages in order to improve the rate of typeability of Listeria monocytogenes strains. We propose a method which increases the detection of induced phages in the presence of inhibitory substances synthesized or liberated by the cells during phage production. Of the 29 phages isolated, 11 (38%) were detected by the spot-on-the-lawn technique and 18 (62%) were revealed by the soft-agar technique. To increase the rate of phage detection, both techniques appear useful. Listeria cultures were subjected to phage typing procedures utilizing these newly isolated phages and the French International set of phages. It appears that the newly isolated phages are good tools for the differentiation of Listeria strains. Among them, one phage seems to be complementary to the French International set.
为了提高单核细胞增生李斯特菌菌株的分型率,有必要分离新的噬菌体。我们提出了一种方法,该方法可在噬菌体产生过程中细胞合成或释放抑制性物质的情况下增加对诱导噬菌体的检测。在分离出的29种噬菌体中,11种(38%)通过菌苔点滴技术检测到,18种(62%)通过软琼脂技术检测到。为了提高噬菌体检测率,这两种技术似乎都很有用。利用这些新分离的噬菌体和法国国际噬菌体组合对李斯特菌培养物进行噬菌体分型程序。新分离的噬菌体似乎是区分李斯特菌菌株的良好工具。其中,一种噬菌体似乎与法国国际噬菌体组合互补。