首页> 美国卫生研究院文献>Epidemiology and Infection >Comparison of selenite F Muller-Kauffmann tetrathionate and Rappaports medium for salmonella isolation from chicken giblets after pre-enrichment in buffered peptone water.
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Comparison of selenite F Muller-Kauffmann tetrathionate and Rappaports medium for salmonella isolation from chicken giblets after pre-enrichment in buffered peptone water.

机译:在缓冲蛋白ept水中预先富集后从鸡肉内脏中分离沙门氏菌的亚硒酸盐FMuller-Kauffmann四硫酸盐和Rappaport培养基的比较。

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摘要

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.
机译:检查了六百八十三个鸡内脏样本中的沙门氏菌。其中三百四十九个是颈部和农作物标本,而224个是肝脏和心脏标本。总共有201个含有沙门氏菌。检测技术包括在37摄氏度的蛋白p缓冲水中预富集18 h,然后传代至三种富集培养基:Muller-Kauffmann四硫酸盐,亚硒酸盐F和Rappaport的氯化镁孔雀石绿肉汤。在每种情况下,从缓冲蛋白buffer水中到10毫升四硫代酸盐和亚硒酸盐的接种量均为1毫升。从富集前培养基到10 ml Rappaport的接种量为0.005 ml。将四硫代硫酸盐和亚硒酸盐在43摄氏度下孵育48小时。 Rappaport的培养基在37摄氏度下孵育48小时。将所有三种富集肉汤的亚培养物分别在24小时和48小时制成亮绿色MacConkey琼脂。将选择性琼脂在37℃下孵育24小时。沙门氏菌分离最成功的技术是使用Rappaport培养基,该培养基比四硫酸盐或亚硒酸盐有效得多。这一发现加强了使用污水污染的天然水作为测试材料所获得的结果,并且建议对环境样品中的沙门氏菌进行常规检查可以仅基于Rappaport的培养基。如果样品中可能存在鼠伤寒沙门氏菌,都柏林链球菌或III类沙门氏菌,则此处描述的技术将需要修改。

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