Analyses of ampC gene expression in Serratia marcescens reveal new regulatory properties

被引:34
作者
Mahlen, SD [1 ]
Morrow, SS [1 ]
Abdalhamid, B [1 ]
Hanson, ND [1 ]
机构
[1] Creighton Univ, Sch Med, Ctr Res Antiinfect & Biotechnol, Dept Med Microbiol & Immunol, Omaha, NE 68178 USA
关键词
ampC; beta-lactamase; Gram-negative bacteria; regulation;
D O I
10.1093/jac/dkg133
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Serratia marcescens encodes an inducible, chromosomal beta-lactamase, ampC. Studies addressing the regulation of inducible ampC genes have focused primarily on Enterobacter cloacae and Citrobacter freundii. The purpose of this study was to clone and sequence the ampC, ampR and intergenic region of S. marcescens and examine both inducible and basal level ampC expression. Sequence analysis of the S. marcescens ampC gene identified an extended 5' untranslated region (UTR) of 126 nucleotides, which formed a prominent stem-loop structure. Induction of ampC expression required AmpR, and the start of transcription was determined using primer extension analysis. In vivo half-life analysis revealed that the half-life of the S. marcescens ampC transcript was 7 min. Confirmation of the in vivo half-life and the role of the stem-loop structure in the 5' UTR was demonstrated by comparing transcript half-life and luciferase expression between a wild-type (WT) and a 5' UTR stem-loop deletion mutant. These data demonstrated that the stem-loop structure was involved in transcript stability. Taken together, these findings indicate that constitutive expression of S. marcescens ampC is regulated by both transcriptional initiation and post-transcriptional events.
引用
收藏
页码:791 / 802
页数:12
相关论文
共 48 条
[31]   FUNCTIONAL MESSENGER-RNA HALF-LIVES IN ESCHERICHIA-COLI [J].
PEDERSEN, S ;
REEH, S ;
FRIESEN, JD .
MOLECULAR & GENERAL GENETICS, 1978, 166 (03) :329-336
[32]   Detection of plasmid-mediated AmpC β-lactamase genes in clinical isolates by using multiplex PCR [J].
Pérez-Pérez, FJ ;
Hanson, ND .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (06) :2153-2162
[33]   Plasmid-determined AmpC-type β-lactamases [J].
Philippon, A ;
Arlet, G ;
Jacoby, GA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (01) :1-11
[34]   β-lactamases responsible for resistance to expanded-spectrum cephalosporins in Klebsiella pneumoniae, Escherichia coli, and Proteus mirabilis isolates recovered in South Africa [J].
Pitout, JDD ;
Thomson, KS ;
Hanson, ND ;
Ehrhardt, AF ;
Moland, ES ;
Sanders, CC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (06) :1350-1354
[35]   Cloning, sequence analyses, expression, and distribution of ampC-ampR from Morganella morganii clinical isolates [J].
Poirel, L ;
Guibert, M ;
Girlich, D ;
Naas, T ;
Nordmann, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (04) :769-776
[36]   The ACT-1 plasmid-encoded AmpC β-lactamase is inducible:: detection in a complex β-lactamase background [J].
Reisbig, MD ;
Hanson, ND .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 49 (03) :557-560
[37]   COEXISTING STRUCTURES OF AN MESSENGER-RNA STABILITY DETERMINANT - THE 5' REGION OF THE ESCHERICHIA-COLI AND SERRATIA-MARCESCENS-OMPA MESSENGER-RNA [J].
ROSENBAUM, V ;
KLAHN, T ;
LUNDBERG, U ;
HOLMGREN, E ;
VONGABAIN, A ;
RIESNER, D .
JOURNAL OF MOLECULAR BIOLOGY, 1993, 229 (03) :656-670
[38]   TYPE-I BETA-LACTAMASES OF GRAM-NEGATIVE BACTERIA - INTERACTIONS WITH BETA-LACTAM ANTIBIOTICS [J].
SANDERS, CC ;
SANDERS, WE .
JOURNAL OF INFECTIOUS DISEASES, 1986, 154 (05) :792-800
[40]   EMERGENCE OF RESISTANCE TO CEFAMANDOLE - POSSIBLE ROLE OF CEFOXITIN-INDUCIBLE BETA-LACTAMASES [J].
SANDERS, CC ;
SANDERS, WE .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1979, 15 (06) :792-797