Steffee C H, Wasilauskas B L
Department of Pathology, Bowman Gray School of Medicine of Wake Forest University, Winston-Salem, N.C. 27157-1072.
Chemotherapy. 1992;38(5):291-6. doi: 10.1159/000239016.
This study sought to quantitatively describe the spectrum of constitutive and inducible beta-lactamase activity present in a tertiary care center's population of Enterobacter species. beta-Lactamase activity in the absence and presence of 2 recognized beta-lactamase-inducing antibiotics, cefoxitin and imipenem, was measured. The Enterobacter cloacae (n = 35) population was strikingly bimodal, expressing 'all-or-none' cross-resistance to beta-lactams (except imipenem) corresponding to the baseline level of beta-lactamase expression. E. aerogenes (n = 14) displayed a less dichotomous pattern of resistance, and MICs of beta-lactam antibiotics were less strongly related to the magnitude of enzyme activity. We conclude that our nosocomial population of E. cloacae, like strains rendered resistant to beta-lactams in vitro, is largely dependent upon beta-lactamase as a mechanism of this resistance. Furthermore, we document the presence of a large subpopulation of beta-lactam-susceptible isolates possessing inducible beta-lactamase and therefore subject to selection for enzyme derepression.
本研究旨在定量描述一家三级医疗中心分离的肠杆菌属细菌中组成型和诱导型β-内酰胺酶活性的谱型。测定了在不存在和存在两种公认的β-内酰胺酶诱导抗生素(头孢西丁和亚胺培南)的情况下的β-内酰胺酶活性。阴沟肠杆菌(n = 35)群体呈现出明显的双峰模式,对β-内酰胺类抗生素(亚胺培南除外)表现出“全或无”的交叉耐药性,这与β-内酰胺酶表达的基线水平相对应。产气肠杆菌(n = 14)表现出较少的二分耐药模式,β-内酰胺类抗生素的最低抑菌浓度(MIC)与酶活性的大小相关性较弱。我们得出结论,我们医院的阴沟肠杆菌群体,与体外对β-内酰胺类抗生素耐药的菌株一样,很大程度上依赖β-内酰胺酶作为这种耐药性的机制。此外,我们记录了存在大量对β-内酰胺类敏感但具有诱导型β-内酰胺酶的分离株亚群,因此易受酶去阻遏的选择。