Cover T L
Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-2605, USA.
Mol Microbiol. 1996 Apr;20(2):241-6. doi: 10.1111/j.1365-2958.1996.tb02612.x.
Helicobacter pylori, the causative agent of chronic superficial gastritis and duodenal ulcer disease in humans, produces a unique cytotoxin (VacA) that induces cytoplasmic vacuolation in eukaryotic cells. The structural organization and processing of the vacuolating cytotoxin are characteristic of a family of proteins exemplified by Neisseria gonorrhoeae IgA protease. Although only 50% of H. pylori isolates produce detectable cytotoxin activity in vitro, vacA homologues are present in virtually all isolates. Several families of vacA alleles have been identified, and there is a strong correlation between presence of specific vacA genotypes, cytotoxin activity, and peptic ulceration. Experiments in a mouse model of H. pylori-induced gastric damage indicate that the cytotoxin plays an important role in inducing gastric epithelial necrosis.
幽门螺杆菌是人类慢性浅表性胃炎和十二指肠溃疡病的病原体,它产生一种独特的细胞毒素(VacA),可诱导真核细胞出现细胞质空泡化。空泡化细胞毒素的结构组织和加工过程是一类蛋白质的特征,以淋病奈瑟菌IgA蛋白酶为代表。尽管只有50%的幽门螺杆菌分离株在体外产生可检测到的细胞毒素活性,但实际上所有分离株中都存在vacA同源物。已经鉴定出几个vacA等位基因家族,特定vacA基因型的存在、细胞毒素活性和消化性溃疡之间存在很强的相关性。在幽门螺杆菌诱导的胃损伤小鼠模型中进行的实验表明,该细胞毒素在诱导胃上皮坏死中起重要作用。