Rice Louis B, Hutton-Thomas Rebecca, Lakticova Viera, Helfand Marion S, Donskey Curtis J
Medical and Research Services, Louis Stokes Cleveland VA Medical Center, The Cleveland Veterans Affairs Research and Education Foundation, and Department of Medicine, Case Western Reserve University, Cleveland, Ohio 44106, USA.
J Infect Dis. 2004 Mar 15;189(6):1113-8. doi: 10.1086/382086. Epub 2004 Mar 1.
We studied the effect of different subcutaneously administered beta-lactam antibiotics on the establishment of gastrointestinal colonization by vancomycin-resistant Enterococcus faecium C68 in a mouse model. Aztreonam, cefazolin, cefepime, and, to a lesser extent, ceftazidime, which neither have significant antienterococcal activity nor are secreted into human bile at high concentrations, did not promote significant vancomycin-resistant enterococci (VRE) colonization. Piperacillin-tazobactam, which has antienterococcal activity and is secreted in human bile at high concentrations, inhibited colonization after limited exposure to the inoculum but was associated with progressively increased VRE colony counts in stool samples after repeated exposure to the VRE inoculum. Ceftriaxone and cefotetan, which lack antienterococcal activity but are secreted into human bile at high concentrations, were associated with rapid and high-level colonization. These data suggest that the risk of VRE colonization varies during exposure to different beta-lactam antimicrobial agents and that the risk is related to biliary concentration and antienterococcal activity of the specific beta-lactam.
我们在小鼠模型中研究了不同皮下注射的β-内酰胺类抗生素对耐万古霉素屎肠球菌C68在胃肠道定植的影响。氨曲南、头孢唑林、头孢吡肟,以及在较小程度上的头孢他啶,既没有显著的抗肠球菌活性,也不会高浓度分泌到人体胆汁中,它们不会促进耐万古霉素肠球菌(VRE)的显著定植。哌拉西林-他唑巴坦具有抗肠球菌活性且高浓度分泌到人体胆汁中,在有限接触接种物后可抑制定植,但在反复接触VRE接种物后,粪便样本中的VRE菌落计数会逐渐增加。头孢曲松和头孢替坦缺乏抗肠球菌活性,但高浓度分泌到人体胆汁中,它们与快速且高水平的定植有关。这些数据表明,在接触不同的β-内酰胺类抗菌药物期间,VRE定植的风险各不相同,且该风险与特定β-内酰胺的胆汁浓度和抗肠球菌活性有关。