Cornaglia G, Mazzariol A, Fontana R, Satta G
Institute of Microbiology, University of Verona, Italy.
Microb Drug Resist. 1996 Summer;2(2):273-6. doi: 10.1089/mdr.1996.2.273.
Scarce information is available on the real mechanism by which carbapenemes penetrate in Enterobacteriaceae, although a considerable amount of evidence suggests that in many species of this family the lack of certain outer membrane proteins is associated with the acquisition of resistance to these antibiotics. The existance of specific pathways for the carbapenems has never been demonstrated, although at times it has been postulated in both wild and mutant strains, on the basis of evident discordances between permeability patterns and suceptibility data. By using the Zimmerman and Rosselet technique, which requires the strain under investigation to harbor a suitable beta-lactamase, the permeability of intact Escherichia coli and Enterobacter cloacae cells to meropenem and imipenem was investigated by transferring a constructed vector carrying the carbapenem hydrolyzing CphA metallo-beta-lactamase gene into the parental strains and their porin-deficient mutants. Reduced amounts of nonspecific porins significantly reduced the penetration of both carbapenems. The virtual absence of porins caused the MICs of meropenem to increase, mostly in Enterobacter cloacae, while it did not affected the MICs of imipenem. No evidence of specific porin pathways of the type described in Pseudomonas aeruginosa was found.
关于碳青霉烯类抗生素在肠杆菌科细菌中的实际渗透机制,目前可获得的信息很少,尽管大量证据表明,在该菌科的许多菌种中,某些外膜蛋白的缺失与对这些抗生素耐药性的获得有关。虽然有时根据野生型和突变菌株的通透性模式与药敏数据之间明显的不一致,推测存在碳青霉烯类抗生素的特定转运途径,但尚未得到证实。通过使用齐默尔曼和罗斯莱特技术(该技术要求被研究菌株携带合适的β-内酰胺酶),将携带碳青霉烯水解CphA金属β-内酰胺酶基因的构建载体转入亲本菌株及其孔蛋白缺陷型突变体,研究了完整的大肠杆菌和阴沟肠杆菌细胞对美罗培南和亚胺培南的通透性。非特异性孔蛋白数量减少显著降低了两种碳青霉烯类抗生素的渗透。几乎没有孔蛋白会导致美罗培南的最低抑菌浓度升高,这在阴沟肠杆菌中最为明显,而对亚胺培南的最低抑菌浓度没有影响。未发现铜绿假单胞菌中描述的那种特定孔蛋白转运途径的证据。