Harvey R W, Price T H
J Hyg (Lond). 1981 Oct;87(2):219-24. doi: 10.1017/s0022172400069436.
Six hundred and eighty three samples of chicken giblets were examined for salmonellas. Three hundred and forty nine of these were neck and crop specimens and 224 were combined liver and heart samples. Two hundred and ten, in all, contained salmonellas. The technique of examination included pre-enrichment in buffered peptone water at 37 degrees C for 18 h and subculture to three enrichment media: Muller-Kauffmann tetrathionate, selenite F and Rappaport's magnesium chloride malachite green broth. Inocula from buffered peptone water to 10 ml of tetrathionate and selenite were 1 ml in each case. The inoculum from the pre-enrichment medium to 10 ml of Rappaport was 0.005 ml. Tetrathionate and selenite were incubated at 43 degrees C for 48 h. Rappaport's medium was incubated at 37 degrees C for 48 h. Subcultures from all three enrichment broths were made at 24 h and 48 h to brilliant green MacConkey agar. Selective agars were incubated at 37 degrees C for 24 h. The most successful technique for salmonella isolation used Rappaport's medium, which was significantly more efficient than either tetrathionate or selenite. This finding reinforces results obtained using sewage polluted natural water as test material and it is suggested that routine examination of environment samples for salmonellas could be based on Rappaport's medium alone. If S. typhi, S. dublin or subgenus III salmonellas were likely to be present in the sample, the technique described here would require modification.
对683份鸡内脏样本进行了沙门氏菌检测。其中349份是颈部和嗉囊样本,224份是肝脏和心脏的混合样本。总共有210份样本含有沙门氏菌。检测技术包括在37摄氏度的缓冲蛋白胨水中预富集18小时,然后转接至三种增菌培养基:穆勒 - 考夫曼四硫磺酸盐培养基、亚硒酸盐F培养基和拉帕波特氯化镁孔雀绿肉汤培养基。从缓冲蛋白胨水接种到10毫升四硫磺酸盐和亚硒酸盐培养基中的接种量均为1毫升。从预富集培养基接种到10毫升拉帕波特培养基中的接种量为0.005毫升。四硫磺酸盐和亚硒酸盐培养基在43摄氏度下培养48小时。拉帕波特培养基在37摄氏度下培养48小时。在24小时和48小时时,将所有三种增菌肉汤转接至亮绿麦康凯琼脂平板。选择性琼脂在37摄氏度下培养24小时。分离沙门氏菌最成功的技术是使用拉帕波特培养基,其效率明显高于四硫磺酸盐或亚硒酸盐培养基。这一发现强化了以受污水污染的天然水作为测试材料所获得的结果,建议对环境样本进行沙门氏菌常规检测可仅基于拉帕波特培养基。如果样本中可能存在伤寒沙门氏菌、都柏林沙门氏菌或III亚属沙门氏菌,则此处描述的技术需要修改。