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Death and Lysis of Leptospirae When Cultured in Asbestos-Filtered Growth Media

机译:在石棉过滤生长培养基中培养的钩端螺旋体的死亡和溶解

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Death and lysis of leptospirae, when cultured in asbestos-filtered bovine albumin polysorbate 80 media, was quantitated. The pathogens (virulent and avirulent) required 2 × 106 cells/ml to initiate growth in such media, whereas inocula of 2 to 20 cells/ml grew in control medium. Saprophytic leptospirae initiated growth from 2 cells/ml in asbestos-filtered medium as well as control medium. The adverse action of asbestos-filtered medium was not removed by storage of medium for 2 years at 25 C and was not diminished when such medium was frozen at -80 C. Washing with water, HCl and NaHCO3-NaCl, citric acid, and medium components did not remove the lytic activity associated with asbestos-filtered culture medium. Continuous subculture in asbestos-filtered medium was possible from large inocula; however, upon subsequent dilution and reinoculation into asbestos-filtered media, there was no evidence of acquired resistance, and all pathogens failed to grow.
机译:在石棉过滤的牛白蛋白聚山梨酯80培养基中培养时,钩端螺旋体的死亡和溶解被定量。病原体(有毒和无毒)在这种培养基中需要2×106细胞/ ml才能开始生长,而在对照培养基中则需要接种2至20个细胞/ ml的菌种。腐生钩端螺旋体在石棉过滤的培养基和对照培养基中从2个细胞/ ml开始生长。通过在25°C下储存2年,石棉过滤后的介质的不利作用不会被消除,并且当将其在-80°C下冷冻时,这种不利作用也不会减弱。用水,HCl和NaHCO3-NaCl,柠檬酸和介质洗涤成分没有除去与石棉过滤的培养基有关的裂解活性。从大接种物中可以在经石棉过滤的培养基中连续传代培养。但是,在随后稀释并重新接种到石棉过滤的培养基中后,没有获得耐药性的证据,所有病原体均无法生长。

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