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METHOD OF ENTEROCOCCI ISOLATION IN ANAEROBIC CONDITIONS FROM ACCUMULATION MEDIUM

机译:从累积培养基中厌氧条件下肠球菌分离的方法

摘要

FIELD: chemistry.;SUBSTANCE: without grinding, a sample of freshly collected pathological material is put into an accumulation medium - guanosine monophosphate broth with addition of 1% glucose and then cultured in a temperature-controlled cabinet at 37°C for 24 hours. Seeding is then carried out on a Petri dish with agar medium with addition of 5% erythrocytes and on enterococcus agar. The inoculations are kept in a temperature-controlled cabinet for 24-48 hours at 37°C. Samples which failed to grow in aerobic conditions are further inoculated on a Petri dish with agar medium with addition of 5% erythrocytes and then put into an anaerobic jar for 24 hours at 37°C. The inoculations are examined under a microscope and microorganisms are identified from the results using traditional methods.;EFFECT: higher isolation rate of enterococcus in anaerobic conditions at 31,2-36% and possibility of detecting presence of microorganisms in clinical material which do not grow in aerobic conditions.;1 tbl
机译:领域:化学;物质:未经研磨,将新鲜收集的病理物质样品放入蓄积培养基-鸟嘌呤单磷酸鸟嘌呤肉汤中,添加1%葡萄糖,然后在37°C的恒温柜中培养24小时。然后在添加有5%红细胞的琼脂培养基的陪替氏培养皿上和肠球菌琼脂上播种。将接种物在37°C的温度控制柜中保存24-48小时。在需氧条件下不能生长的样品进一步接种在添加有5%红细胞的琼脂培养基的陪替氏培养皿中,然后在37°C的厌氧罐中放置24小时。接种物在显微镜下检查,并使用传统方法从结果中鉴定出微生物。效果:厌氧条件下肠球菌的分离率更高,为31.2-36%,并且有可能在临床材料中检测出不生长的微生物在有氧条件下; 1 tbl

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