Thiolas Aurélie, Bornet Charléric, Davin-Régli Anne, Pagès Jean-Marie, Bollet Claude
Enveloppe Bactérienne, Perméabilité et Antibiotiques, EA2197, Faculté de Médecine, Université de la Méditerranée, 27 Boulevard Jean Moulin, 13385 Marseille Cedex 05, France.
Biochem Biophys Res Commun. 2004 May 7;317(3):851-6. doi: 10.1016/j.bbrc.2004.03.130.
Enterobacter aerogenes develops increased multidrug resistance via a functional alteration of outer-membrane permeability associated with a decrease in porin function. We have sequenced the gene coding the major porin of Enterobacter aerogenes, omp36. The sequence shows a high similarity with the Klebsiella pneumoniae ompK36 gene and is closely related to the enterobacterial OmpC family. Sequence analysis of several Omp36 issued from clinical strains indicated variability in putative cell-surface exposed domains. Interestingly, substitution Gly112Asp was observed in the conserved eyelet L3 region of the porin produced by two strains, C and 3. This substitution is associated with a high general beta-lactam resistance observed in these isolates and with alteration of pore properties previously described in strain 3 porin [Mol. Microbiol. 41 (2001) 189]. This is the first genetic identification of impermeability-mediated resistance to beta-lactams in various clinical E. aerogenes strains.
产气肠杆菌通过与孔蛋白功能降低相关的外膜通透性功能改变而产生更高的多重耐药性。我们已对产气肠杆菌主要孔蛋白omp36的编码基因进行了测序。该序列与肺炎克雷伯菌ompK36基因高度相似,且与肠杆菌科OmpC家族密切相关。对来自临床菌株的几种Omp36进行序列分析表明,假定的细胞表面暴露结构域存在变异性。有趣的是,在菌株C和3产生的孔蛋白的保守小孔L3区域中观察到Gly112Asp替代。这种替代与这些分离株中观察到的高普遍β-内酰胺耐药性以及先前在菌株3孔蛋白中描述的孔特性改变有关[《分子微生物学》41 (2001) 189]。这是首次对各种临床产气肠杆菌菌株中由通透性介导的β-内酰胺耐药性进行基因鉴定。