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从呼吸道和非呼吸道部位分离出的铜绿假单胞菌产物对肺泡巨噬细胞的毒性活性。

Toxic activity against alveolar macrophages of products of Pseudomonas aeruginosa isolated from respiratory and non-respiratory sites.

作者信息

Al-Dujaili A H

出版信息

J Hyg (Lond). 1976 Oct;77(2):211-20. doi: 10.1017/s0022172400024645.

Abstract

The toxic effect of certain products of Pseudomonas aeruginosa on guinea-pig alveolar macrophages has been studied in an attempt to account for the apparent infrequency with which certain strains of this species are associated with respiratory infection. Texts were carried out on strains derived from the respiratory tract, strains from infection at other sites, and strains from the inanimate hospital environment which were believed not to have been responsible for infection ('environmental' strains). Haemolysin, pigments, enzyme-containing fractions, slime and cell-wall fraction all exhibited toxic activity against macrophages in an in vitro system, although for any given strain of Ps. aeruginosa the haemolysin was by far the most potent factor. The activity of this factor against macrophages was directly proportional to its haemolytic activity against human erythrocytes. The haemolysin fractions of environmental strains, which have previously been found to have little activity on erythrocytes, were also less active against macrophages than haemolysin preparations from 'infective' strains. It is therefore postulated that the ability of a strain of Ps. aeruginosa to initiate respiratory infection may be related to the degree of haemolysin production. The activity of other fractions against macrophages is more variable, but they may contribute in different ways to the development of infection once entry into the lung has been achieved.

摘要

为了解释铜绿假单胞菌某些菌株与呼吸道感染关联频率明显较低的现象,研究了该菌某些产物对豚鼠肺泡巨噬细胞的毒性作用。对源自呼吸道的菌株、来自其他部位感染的菌株以及来自医院无生命环境且据信未引发感染的菌株(“环境”菌株)进行了试验。溶血素、色素、含酶组分、黏液和细胞壁组分在体外系统中均对巨噬细胞表现出毒性活性,不过对于任何给定的铜绿假单胞菌菌株而言,溶血素是迄今为止最具活性的因素。该因素对巨噬细胞的活性与其对人红细胞的溶血活性成正比。先前发现对红细胞活性较低的环境菌株的溶血素组分,对巨噬细胞的活性也低于“感染性”菌株的溶血素制剂。因此推测,铜绿假单胞菌菌株引发呼吸道感染的能力可能与溶血素的产生程度有关。其他组分对巨噬细胞的活性变化更大,但一旦进入肺部,它们可能以不同方式促成感染的发展。

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