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麻风杆菌在基于透明质酸的培养基上的体外培养。1. 初步报告。

In vitro cultivation of leprosy bacilli on hyaluronic acid based medium. 1. Preliminary report.

作者信息

Skinsnes O K, Matsuo E, Chang P H, Andersson B

出版信息

Int J Lepr Other Mycobact Dis. 1975 Jul-Sep;43(3):193-203.

PMID:767262
Abstract

In vitro cultivation is reported of Mycobacterium leprae on a medium (designated LA-3) based on hyaluronic acid with additional ingredients of yeast extract, bovine albumin and glycerin together with phosphate buffer. The medium is also incorporated with agar or agarose (designated LA-3P) to serve as culture plates. Initial growth in LA-3 in test tubes required about six weeks but subsequently this was speeded up to about two weeks utilizing large quantities of media with aeration by shaking twice a day. Growth on LA-3P yields numerous small orange-yellow colonies in two to three weeks. Facets of the emerging aspects of the life cycle of M. leprae under cultivation are given preliminary report. The bases for the allegation of M. leprae identity of the cultured bacilli are essentially the following six determinations. 1. Pathologic and experimental determined rationale for the essential M. leprae nutrient requirement. 2. Several cultures having the same characteristics have been isolated from LL patients widely separate in time and by geography. 3. Failure of culture isolates to subculture on the usual media employed in the cultivation of mycobacteria at both 37 degrees C and room temperature. 4. 1 degree cultures in liquid medium successfully transferred to 2 degrees liquid medium and to 2 degrees agar medium plates. 5. Bacillary isolates and bacilli of 1 degree and 2 degrees liquid medium cultures all stain with pooled LL serum, FITC coupled, M. leprae specific antibody with which a broad range of other mycobacteria do not react. 6. M. lepraemurium also presents good growth on this medium.

摘要

据报道,麻风分枝杆菌可在一种基于透明质酸的培养基(命名为LA - 3)上进行体外培养,该培养基还添加了酵母提取物、牛白蛋白、甘油以及磷酸盐缓冲液。该培养基还加入了琼脂或琼脂糖(命名为LA - 3P)用作培养平板。在试管中的LA - 3培养基上最初生长需要约六周时间,但随后通过每天振荡通气使用大量培养基,生长速度加快至约两周。在LA - 3P上培养两到三周可产生大量小的橙黄色菌落。初步报道了培养条件下麻风分枝杆菌生命周期新出现方面的情况。认定培养出的杆菌为麻风分枝杆菌的依据主要有以下六项判定。1. 从病理学和实验角度确定了麻风分枝杆菌基本营养需求的理论依据。2. 从广泛分布于不同时间和地域的瘤型麻风患者身上分离出了几种具有相同特征的培养物。3. 培养分离物在37摄氏度和室温下均无法在用于培养分枝杆菌的常用培养基上进行传代培养。4. 液体培养基中的一级培养物成功转移至二级液体培养基和二级琼脂培养基平板上。5. 一级和二级液体培养基培养物中的杆菌分离物和杆菌均能用汇集的瘤型麻风患者血清、异硫氰酸荧光素偶联的麻风分枝杆菌特异性抗体染色,而其他多种分枝杆菌不与该抗体发生反应。6. 鼠麻风杆菌在这种培养基上也生长良好。

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