Observations on Pseudomonas aeruginosa proteolytic and toxic activity in experimentally infected rats.

NIPH annals Pub Date : 1992-12-01
A R Ogaard, P Lausund, B P Berdal
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Abstract

To bypass natural resistance against Pseudomonas aeruginosa infection, a granuloma pouch model to be experimentally infected was established in rats. This experimental model also permitted easy collection of wound exudate. In general, the animals either died or became very ill and were consequently sacrificed within the first 12 days, or they (6 of 16) survived in good condition after 20 days. The virulence of recently isolated strains compared to twelve-months old subcultures of the same strains showed no major differences in clinical pattern. In the first seven days following the start of the infection, all animals presented a fall of elastase activity in the wound exudate. Toxin A was present in the exudate, sometimes in relatively high levels, but there was no correlation between toxin level and the clinical development. As a rule, spontaneous rupture of the granuloma pouch, apparently unrelated to the concentrations of either elastase or toxin A in the exudate, was beneficial to survival. In the present experimental infectious context, neither P. aeruginosa elastase nor toxin A seemed to play any isolated lethal nor pathogenetic role.

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铜绿假单胞菌实验感染大鼠的蛋白水解和毒性活性观察。
为了绕过对铜绿假单胞菌感染的自然抗性,建立了实验性感染的大鼠肉芽肿袋模型。该实验模型还可以方便地收集伤口渗出液。一般来说,这些动物要么在最初的12天内死亡,要么病得很重,因此被处死,要么在20天后(16只中的6只)活得很好。最近分离的菌株的毒力与12个月大的同一菌株的继代培养相比,在临床模式上没有显着差异。在感染开始后的头7天,所有动物的伤口渗出液中弹性蛋白酶活性下降。渗出液中存在毒素A,有时含量较高,但毒素水平与临床发展无相关性。通常,肉芽肿袋的自发破裂,显然与渗出液中弹性蛋白酶或毒素a的浓度无关,有利于存活。在目前的实验感染背景下,铜绿假单胞菌弹性酶和毒素A似乎都没有发挥任何孤立的致死或致病作用。
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Optimalized in vivo production of monoclonal antibodies in mouse ascitic fluid. Time variations in injury incidence. Sogn and Fjordane county community-based injury prevention: evaluation design. Observations on Pseudomonas aeruginosa proteolytic and toxic activity in experimentally infected rats. Abstracts of the Norwegian Virology Symposium IV. Ustaoset, March 19-20, 1992.
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