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用葡萄球菌凝聚试验检测产热不稳定肠毒素的产肠毒素性大肠杆菌。

Detection by a staphylococcal coagglutination test of heat-labile enterotoxin-producing enterotoxigenic Escherichia coli.

作者信息

Honda T, Samakoses R, Sornchai C, Takeda Y, Miwatani T

出版信息

J Clin Microbiol. 1983 Apr;17(4):592-5. doi: 10.1128/jcm.17.4.592-595.1983.

Abstract

For detection of heat-labile enterotoxin-producing enterotoxigenic Escherichia coli, the staphylococcal coagglutination test reported by Brill et al. (J. Clin. Microbiol. 9:49-55, 1979) was modified to give better results. Staphylococcal cells were sensitized with anti-heat-labile enterotoxin antiserum and suspended in phosphate-buffered saline containing 0.5% bovine serum albumin, 0.05% Tween 80, 0.01% gelatin, and 0.02% NaN3. The test strain was cultured in 0.25 ml of Biken broth no. 2 in a test tube (12 by 100 mm) stood at an inclination of about 10 degrees to the horizontal. After incubation for 5 h at 37 degrees C, the cells were collected by centrifugation at 2,500 rpm for 15 min and suspended in 50 microliters of polymyxin B solution (20,000 IU/ml). The suspension was then incubated for 1 h at 37 degrees C and centrifuged at 2,500 rpm for 15 min, and 10 microliters of the supernatant was used for the test on a slide. The results of the modified test correlated completely with those obtained by the Biken test. The modifications of the staphylococcal coagglutination test described here allow for detection of heat-labile enterotoxin-producing enterotoxigenic E. coli within 6 to 7 h after inoculation of a test strain.

摘要

为检测产热不稳定肠毒素的产肠毒素大肠杆菌,对布里尔等人(《临床微生物学杂志》9:49 - 55,1979年)报道的葡萄球菌协同凝集试验进行了改进,以获得更好的结果。用抗热不稳定肠毒素抗血清致敏葡萄球菌细胞,并将其悬浮于含0.5%牛血清白蛋白、0.05%吐温80、0.01%明胶和0.02%叠氮化钠的磷酸盐缓冲盐水中。将测试菌株接种于一支(12×100毫米)试管中0.25毫升的二号比肯肉汤中,试管与水平面呈约10度倾斜放置。在37℃孵育5小时后,以2500转/分钟离心15分钟收集细胞,并重悬于50微升多粘菌素B溶液(20000国际单位/毫升)中。然后将该悬液在37℃孵育1小时,再以2500转/分钟离心15分钟,取10微升上清液用于载玻片检测。改进试验的结果与比肯试验完全相关。此处描述的葡萄球菌协同凝集试验的改进方法能够在接种测试菌株后6至7小时内检测出产热不稳定肠毒素的产肠毒素大肠杆菌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e05/272698/9e290900563d/jcm00141-0047-a.jpg

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