Songer J G, Kinyon J M, Harris D L
J Clin Microbiol. 1976 Jul;4(1):57-60. doi: 10.1128/jcm.4.1.57-60.1976.
Pure cultures of six pathogenic isolates of Treponema hyodysenteriae, the colonic mucosal scrapings of seven pigs with acute swine dysentery, and feces from seven unaffected pigs were diluted in phosphate-buffered saline and plated on Trypticase soy agar with 5% citrated bovine blood (TSA) and TSA with various levels of spectinomycin (TSA-S). The plates were incubated at 42 degrees C in a vented GasPak jar with a cold palladium catalyst and either 80:20 H2-CO2 by evacuation and refilling or a H2-CO2 generator envelope. Viable cell counts of the six pathogenic isolates were not altered by plating on TSA-S with 400 mug of spectinomycin per ml (TSA-S400) as compared with TSA alone. Dilutions of colonic mucosal scrapings from seven pigs with acute swine dysentery showed numbers of T. hyodysenteriae to be unchanged when plated on TSA-S400. Flora other than T. hyodysenteriae present in acute swine dysentery was inhibited, on the average, by 99.99%. Plating of dilutions of feces of unaffected pigs on TSA-S400 showed inhibition of flora that averaged more than 99.9%. Pathogenicity of T. hyodysenteriae was not altered by isolation or serial passage on TSA-S400.
将猪痢疾密螺旋体的六种致病分离株的纯培养物、七头患有急性猪痢疾的猪的结肠黏膜刮片以及七头未受影响猪的粪便,用磷酸盐缓冲盐水稀释后,接种于含5%枸橼酸化牛血的胰蛋白胨大豆琼脂(TSA)和添加不同水平壮观霉素的TSA(TSA-S)上。平板在42℃下,置于带有冷钯催化剂的通气GasPak罐中培养,通过抽气和重新充气维持80:20的H₂-CO₂混合气体,或使用H₂-CO₂产气袋。与单独使用TSA相比,每毫升含400μg壮观霉素的TSA-S(TSA-S400)平板接种六种致病分离株后,其活菌计数未发生改变。七头患有急性猪痢疾的猪的结肠黏膜刮片稀释液接种于TSA-S400时,猪痢疾密螺旋体数量未变。急性猪痢疾中除猪痢疾密螺旋体以外的菌群平均受到99.99%的抑制。未受影响猪的粪便稀释液接种于TSA-S400时,菌群平均受到超过99.9%的抑制。猪痢疾密螺旋体在TSA-S400上分离或传代后致病性未改变。