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肺炎链球菌溶血素对人呼吸道上皮细胞的体外作用

The effect of Streptococcus pneumoniae pneumolysin on human respiratory epithelium in vitro.

作者信息

Feldman C, Mitchell T J, Andrew P W, Boulnois G J, Read R C, Todd H C, Cole P J, Wilson R

机构信息

Department of Thoracic Medicine, National Heart and Lung Institute, London, U.K.

出版信息

Microb Pathog. 1990 Oct;9(4):275-84. doi: 10.1016/0882-4010(90)90016-j.

Abstract

Streptococcus pneumoniae culture filtrates and pneumolysin both slow human ciliary beating and damage respiratory epithelium in vitro. A polyclonal pneumolysin antibody bound to sepharose beads removed pneumolysin from culture filtrates and showed that pneumolysin alone was responsible for the effects on epithelium. In a 48-h organ culture pneumolysin caused ciliary slowing and epithelial disruption in a dose-dependent manner down to 5 ng/ml. Comparison of the ciliary slowing activity and pneumolysin concentration in filtrates in a continuous broth culture showed a maximal effect at 16 h (pneumolysin 7.5 micrograms/ml). Later the activity decreased while the pneumolysin concentration increased (8.8 micrograms/ml). This loss of activity was prevented by neutralisation of the acid pH of the culture medium. Eight different culture filtrates produced significant (P less than 0.05) ciliary slowing which correlated (r = 0.95) with simultaneously measured haemolytic (pneumolysin) activity. Substitution of tryptophan (position 433) by phenylalanine reduced the haemolytic and ciliary slowing activity of pneumolysin, but did not affect its ability to activate complement. There was no correlation between the ciliary slowing produced by the culture filtrate and that produced by the autolysate of a particular strain, nor between ciliary slowing and the extent of autolysis or the serotype of the strain.

摘要

肺炎链球菌培养滤液和肺炎溶血素均可在体外减慢人纤毛摆动并损伤呼吸道上皮。与琼脂糖珠结合的多克隆肺炎溶血素抗体可从培养滤液中去除肺炎溶血素,结果表明仅肺炎溶血素对上皮具有上述作用。在48小时的器官培养中,肺炎溶血素以剂量依赖方式导致纤毛摆动减慢和上皮破坏,最低至5纳克/毫升。在连续肉汤培养中,对滤液中纤毛摆动减慢活性和肺炎溶血素浓度进行比较,结果显示在16小时时作用最大(肺炎溶血素7.5微克/毫升)。随后活性降低,而肺炎溶血素浓度升高(8.8微克/毫升)。通过中和培养基的酸性pH可防止这种活性丧失。八种不同的培养滤液均产生了显著的(P<0.05)纤毛摆动减慢,且与同时测得的溶血(肺炎溶血素)活性相关(r = 0.95)。将色氨酸(第433位)替换为苯丙氨酸可降低肺炎溶血素的溶血和纤毛摆动减慢活性,但不影响其激活补体的能力。培养滤液产生的纤毛摆动减慢与特定菌株自溶产物产生的纤毛摆动减慢之间无相关性,纤毛摆动减慢与自溶程度或菌株血清型之间也无相关性。

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