Matsumoto Koki
Department of Ophthalmology and Visual Science, Kumamoto University Graduate School of Medical Sciences, 1-1-1 Honjo, Kumamoto 860-0811, Japan.
Biol Chem. 2004 Nov;385(11):1007-16. doi: 10.1515/BC.2004.131.
Pseudomonas aeruginosa and Serratia marcescens can cause refractory keratitis resulting in corneal perforation and blindness. These bacteria produce various kinds of proteases. In addition to pseudomonal elastase (LasB) and alkaline protease, LasA protease and protease IV have recently been found to be more important virulence factors of P. aeruginosa . S. marcescens produces a cysteine protease in addition to metalloproteases. These bacterial proteases have a number of biological activities, such as degradation of tissue constituents and host defense-oriented proteins, as well as activation of zymogens (Hageman factor, prekallikrein and pro-matrix metalloproteinases) through limited proteolysis. In this article, the properties of these bacterial proteases are reviewed and the pathogenic roles of these proteases in pseudomonal keratitis are discussed.
铜绿假单胞菌和粘质沙雷氏菌可引起难治性角膜炎,导致角膜穿孔和失明。这些细菌会产生多种蛋白酶。除了铜绿假单胞菌弹性蛋白酶(LasB)和碱性蛋白酶外,最近还发现LasA蛋白酶和蛋白酶IV是铜绿假单胞菌更重要的毒力因子。粘质沙雷氏菌除了产生金属蛋白酶外,还产生一种半胱氨酸蛋白酶。这些细菌蛋白酶具有多种生物学活性,如组织成分和宿主防御相关蛋白的降解,以及通过有限的蛋白水解作用激活酶原(Hageman因子、前激肽释放酶和前基质金属蛋白酶)。本文综述了这些细菌蛋白酶的特性,并讨论了这些蛋白酶在铜绿假单胞菌性角膜炎中的致病作用。