Reed S L, Keene W E, McKerrow J H
Department of Medicine, University of California, San Diego 92037.
J Clin Microbiol. 1989 Dec;27(12):2772-7. doi: 10.1128/jcm.27.12.2772-2777.1989.
Expression of the 56-kilodalton (kDa) neutral thiol proteinase has been shown to correlate with the potential of clinical isolates of Entamoeba histolytica to produce invasive disease. A 56-kDa band was identified by gelatin substrate gel electrophoresis in 10 of 10 isolates from patients with colitis or amebic liver abscesses, but in only 1 of 10 isolates from asymptomatic patients. Pathogenic isolates appear capable of releasing significantly larger quantities of the proteinase, as measured by cleavage of a synthetic peptide substrate, ZRR-AMC (benzyloxy-carbonyl-arginine-arginine-4-amino-7-methylcoumarin). We have also shown that the proteinase is released during the course of clinical invasive amebic disease, as demonstrated by the presence of circulating antibodies detectable by enzyme-linked immunosorbent assay. These studies support the importance of the 56-kDa thiol proteinase in the pathogenesis of invasive amebiasis.
已证明,56千道尔顿(kDa)中性巯基蛋白酶的表达与溶组织内阿米巴临床分离株产生侵袭性疾病的可能性相关。通过明胶底物凝胶电泳在10例结肠炎或阿米巴肝脓肿患者的全部10株分离株中鉴定出一条56-kDa条带,但在10例无症状患者的分离株中仅1株出现该条带。通过合成肽底物ZRR-AMC(苄氧羰基-精氨酸-精氨酸-4-氨基-7-甲基香豆素)的裂解测定,致病性分离株似乎能够释放大量的蛋白酶。我们还表明,在临床侵袭性阿米巴病过程中会释放蛋白酶,这通过酶联免疫吸附测定法检测到循环抗体得以证明。这些研究支持了56-kDa巯基蛋白酶在侵袭性阿米巴病发病机制中的重要性。