Wu Z, Milton D, Nybom P, Sjö A, Magnusson K E
Department of Medical Microbiology, Linköping University, Sweden.
Microb Pathog. 1996 Aug;21(2):111-23. doi: 10.1006/mpat.1996.0047.
In this report, we describe the cytotoxic activity of the cholera hemagglutinin/protease (HA/protease). A concentrated protein sample from the 37 degrees C overnight culture supernatant of CVD110, a delta ctxA, delta zot, delta Ace and hlyA::(ctxB mer) mutant of El Tor biotype Ogawa serotype strain E7946 caused morphological changes in cultured MDCK-I epithelial cells and altered their arrangement of filamentous actin (F-actin) and Zonula occludens-associated protein ZO-1. The drastic morphological changes can be inhibited by Zincov, a specific bacterial metalloprotease inhibitor. The cytotoxic fractions of the sample after FPLC gelfiltration fractionation showed two visible protein bands with molecular weights of approximately 34- and 32 kDa. Microsequencing of these two proteins revealed that they were the cholera HA/protease.
在本报告中,我们描述了霍乱血凝素/蛋白酶(HA/蛋白酶)的细胞毒性活性。来自埃尔托生物型小川血清型菌株E7946的ΔctxA、Δzot、ΔAce和hlyA::(ctxB mer)突变体CVD110在37℃过夜培养上清液中的浓缩蛋白样品,导致培养的MDCK-I上皮细胞发生形态变化,并改变了它们的丝状肌动蛋白(F-肌动蛋白)和紧密连接相关蛋白ZO-1的排列。特异性细菌金属蛋白酶抑制剂Zincov可抑制这种剧烈的形态变化。FPLC凝胶过滤分级分离后样品的细胞毒性级分显示出两条可见的蛋白带,分子量约为34 kDa和32 kDa。对这两种蛋白的微量测序表明它们是霍乱HA/蛋白酶。