The PmrA-regulated pmrC gene mediates phosphoethanolamine modification of lipid A and polymyxin resistance in Salmonella enterica

被引:253
作者
Lee, H
Hsu, FF
Turk, J
Groisman, EA
机构
[1] Washington Univ, Sch Med, Dept Mol Microbiol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Howard Hughes Med Inst, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Internal Med, Div Endocrinol Diabet & Metab, St Louis, MO 63110 USA
关键词
D O I
10.1128/JB.186.13.4124-4133.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The PmrA/PmrB regulatory system of Salmonella enterica controls the modification of lipid A with aminoarabinose and phosphoethanolamine. The aminoarabinose modification is required for resistance to the antibiotic polymyxin B, as mutations of the PmrA-activated pbg operon or ugd gene result in strains that lack aminoarabinose in their lipid A molecules and are more susceptible to polymyxin B. Additional PmrA-regulated genes appear to participate in pollymyxin B resistance, as pbgP and ugd mutants are not as sensitive to polymyxin B as a pmrA mutant. Moreover, the role that the phosphoethanolamine modification of lipid A plays in the resistance to polymyxin B has remained unknown. Here we address both of these questions by establishing that the PmrA-activated pmrC gene encodes an inner membrane protein that is required for the incorporation of phosphoethanolamine into lipid A and for polymyxin B resistance. The PmrC protein consists of an N-terminal region with five transmembrane domains followed by a large periplasmic region harboring the putative enzymatic domain. A pbgP pmrC double mutant resembled a pmrA mutant both in its lipid A profile and in its susceptibility to polymyxin B, indicating that the PmrA-dependent modification of lipid A with aminoarabinose and phosphoethanolamine is responsible for PmrA-regulated polymyxin B resistance.
引用
收藏
页码:4124 / 4133
页数:10
相关论文
共 53 条
[1]  
[Anonymous], 1980, ADV BACTERIAL GENET
[2]   ASSAY OF PROTEINS IN PRESENCE OF INTERFERING MATERIALS [J].
BENSADOUN, A ;
WEINSTEIN, D .
ANALYTICAL BIOCHEMISTRY, 1976, 70 (01) :241-250
[3]   Fe(III)-mediated cellular toxicity [J].
Chamnongpol, S ;
Dodson, W ;
Cromie, MJ ;
Harris, ZL ;
Groisman, EA .
MOLECULAR MICROBIOLOGY, 2002, 45 (03) :711-719
[4]   GENE DISRUPTION IN ESCHERICHIA-COLI - TCR AND KM(R) CASSETTES WITH THE OPTION OF FLP-CATALYZED EXCISION OF THE ANTIBIOTIC-RESISTANCE DETERMINANT [J].
CHEREPANOV, PP ;
WACKERNAGEL, W .
GENE, 1995, 158 (01) :9-14
[5]   MmpL8 is required for sulfolipid-1 biosynthesis and Mycobacterium tuberculosis virulence [J].
Converse, SE ;
Mougous, JD ;
Leavell, MD ;
Leary, JA ;
Bertozzi, CR ;
Cox, JS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (10) :6121-6126
[6]   Phosphorylation of the lipid a region of meningococcal lipopolysaccharide: Identification of a family of transferases that add phosphoethanolamine to lipopolysaccharide [J].
Cox, AD ;
Wright, JC ;
Li, JJ ;
Hood, DW ;
Moxon, ER ;
Richards, JC .
JOURNAL OF BACTERIOLOGY, 2003, 185 (11) :3270-3277
[7]   One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products [J].
Datsenko, KA ;
Wanner, BL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (12) :6640-6645
[8]   Construction of targeted single copy lac fusions using λ Red and FLP-mediated site-specific recombination in bacteria [J].
Ellermeier, CD ;
Janakiraman, A ;
Slauch, JM .
GENE, 2002, 290 (1-2) :153-161
[9]   A SALMONELLA LOCUS THAT CONTROLS RESISTANCE TO MICROBICIDAL PROTEINS FROM PHAGOCYTIC-CELLS [J].
FIELDS, PI ;
GROISMAN, EA ;
HEFFRON, F .
SCIENCE, 1989, 243 (4894) :1059-1062
[10]   Oxygen requirement for the biosynthesis of the S-2-hydroxymyristate moiety in Salmonella typhimurium lipid A -: Function of LpxO, a new Fe2+/α-ketoglutarate-dependent dioxygenase homologue [J].
Gibbons, HS ;
Lin, S ;
Cotter, RJ ;
Raetz, CRH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (42) :32940-32949