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钩端螺旋体在石棉过滤生长培养基中培养时的死亡和裂解。

Death and lysis of leptospirae when cultured in asbestos-filtered growth media.

作者信息

Ellinghausen H C

出版信息

Appl Microbiol. 1973 Dec;26(6):959-68. doi: 10.1128/am.26.6.959-968.1973.

Abstract

Death and lysis of leptospirae, when cultured in asbestos-filtered bovine albumin polysorbate 80 media, was quantitated. The pathogens (virulent and avirulent) required 2 x 10(6) 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 NaHCO(3)-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.

摘要

对钩端螺旋体在经石棉过滤的牛白蛋白聚山梨醇酯80培养基中培养时的死亡和裂解情况进行了定量分析。病原体(有毒力和无毒力的)在这种培养基中起始生长需要2×10⁶个细胞/毫升,而接种量为2至20个细胞/毫升时能在对照培养基中生长。腐生钩端螺旋体在经石棉过滤的培养基以及对照培养基中从2个细胞/毫升开始生长。经石棉过滤的培养基的不利作用不会因在25℃下储存2年而消除,并且当这种培养基在-80℃下冷冻时也不会减弱。用水、盐酸、碳酸氢钠 - 氯化钠、柠檬酸以及培养基成分洗涤并不能去除与经石棉过滤的培养基相关的裂解活性。从大量接种物开始在经石棉过滤的培养基中连续传代培养是可行的;然而,在随后稀释并重新接种到经石棉过滤的培养基中时,没有获得性抗性的证据,并且所有病原体都无法生长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6395/379940/c07f6d117f62/applmicro00035-0150-a.jpg

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