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胞壁酰二肽/3-脱氧-D-甘露糖庚酮糖合成酶抑制剂与抗菌剂对肠出血性大肠杆菌O157:H7产生和释放维罗毒素的抑制协同作用。

Synergistic effect of CMP/KDO synthase inhibitors with antimicrobial agents on inhibition of production and release of Vero toxin by enterohaemorrhagic Escherichia coli O157:H7.

作者信息

Kondo Ken-ichiro, Doi Hiroyasu, Adachi Hayamitsu, Nishimura Yoshio

机构信息

Microbial Chemistry Research Center, 3-14-23 Kamiosaki, Shinagawa-ku, 141-0021, Tokyo, Japan.

出版信息

Bioorg Med Chem Lett. 2004 Jan 19;14(2):467-70. doi: 10.1016/j.bmcl.2003.10.046.

Abstract

Synergistic effect of CMP/KDO synthase inhibitors in LPS biosynthesis of Gram-negative bacteria with kanamycin (KM) and fosfomycin (FOM) on the production and release of Vero toxins (VTs) by Escherichia coli O157 was evaluated in vitro. While CMP/KDO synthase inhibitors, KM and FOM showed no inhibitory effect on the production/release of VTs by themselves alone, both KM and FOM showed the remarkable inhibition of VT2 release through synergistic collaboration with CMP:KDO synthase inhibitor.

摘要

在体外评估了胞苷一磷酸/3-脱氧-D-甘露-2-辛酮糖酸(CMP/KDO)合酶抑制剂与卡那霉素(KM)和磷霉素(FOM)联合作用对革兰氏阴性菌脂多糖(LPS)生物合成以及大肠杆菌O157产生和释放志贺毒素(VTs)的协同效应。虽然CMP/KDO合酶抑制剂、KM和FOM单独使用时对VTs的产生/释放均无抑制作用,但KM和FOM与CMP/KDO合酶抑制剂协同作用时均显著抑制了VT2的释放。

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