Atyeo R F, Oxberry S L, Combs B G, Hampson D J
Division of Veterinary and Biomedical Sciences, Murdoch University, Perth, Australia.
Lett Appl Microbiol. 1998 Feb;26(2):126-30. doi: 10.1046/j.1472-765x.1998.00294.x.
Polymerase chain reaction (PCR) tests were established for detection of Serpulina hyodysenteriae, the agent of swine dysentery, and S. pilosicoli, the agent of intestinal spirochaetosis. Both reactions were specific when tested with DNA from 107 strains of various intestinal spirochaetes. For diagnostic use, faeces were plated to selective medium, and diatomaceous earth extraction used to obtain DNA prior to PCR. This procedure detected 10(3)-10(4) cells of either organism seeded into 0.2 g of faeces. When applied to 63 samples from pigs of eight piggeries naturally infected with either S. hyodysenteriae or S. pilosicoli, both PCRs were specific, more rapid, and detected more positive samples than did routine faecal culture and isolation.
已建立聚合酶链反应(PCR)检测方法,用于检测猪痢疾病原体猪痢疾蛇形螺旋体和肠道螺旋体病病原体毛发蛇形螺旋体。用来自107株各种肠道螺旋体的DNA进行检测时,这两种反应均具有特异性。在诊断应用中,将粪便接种到选择性培养基上,并在PCR之前使用硅藻土提取法获取DNA。该程序可检测接种到0.2克粪便中的10³-10⁴个这两种微生物的细胞。当应用于来自八个猪场自然感染猪痢疾蛇形螺旋体或毛发蛇形螺旋体的猪的63份样本时,两种PCR检测均具有特异性,速度更快,并且比常规粪便培养和分离检测到更多阳性样本。