|
|
||||||||
The Journal of Medical Microbiology, Vol 46, Issue 11 903-912, Copyright © 1997 by Society for General Microbiology
JOURNAL ARTICLE |
A. Hejazi and F. R. Falkiner
Department of Clinical Microbiology, Trinity College, Dublin, Ireland.
Over the last 30 years, Serratia marcescens has become an important cause of nosocomial infection. There have been many reports concerning the identification, antibiotic susceptibility, pathogenicity, epidemiological investigations and typing of this organism. Accurate identification is important in defining outbreaks. The API 20E system has been used widely, but is not individually satisfactory. The growth of S. marcescens in the environment has been investigated in relation to water, disinfectants and plastics such as blood bags. Certain extracellular products are unique to S. marcescens. Pigment (prodigiosin) biosynthesis by S. marcescens has been investigated fully since the emergence of the organism as a cause of infection. Many other aspects of the pathogenicity and virulence of S. marcescens have been studied, including adherence and hydrophobicity, lipopolysaccharide (LPS) and extracellular products. Two modes of adhesion to host epithelial surfaces have been suggested. These are mannose-resistant (MR) pili and mannose-sensitive (MS) pili. LPS, which is responsible for the biological activity of endotoxin, has been investigated fully and 24 somatic antigens have been described. The production of different enzymes by S. marcescens as virulence factors has also been reported, including chitinase, lipase, chloroperoxidase and an extracellular protein, HasA. Antibiotics used to treat serratia infection include beta-lactam agents, aminoglycosides and fluoroquinolones and a variety of different resistance mechanisms have been demonstrated. Typing methods used to study the epidemiology of S. marcescens include biotyping, bacteriocin typing, phage typing, plasmid analysis, polymerase chain reaction amplification of enterobacterial repetitive intergenic consensus sequences (ERIC-PCR) and ribotyping. Serological typing has also been used and this method seems to be a suitable first-line typing method for S. marcescens, although some strains remain untypable. RAPD-PCR has also been applied to a small number of isolates and seems to be a promising method, especially for rapid monitoring of an outbreak and tracing the source of initial infection.
This article has been cited by other articles:
![]() |
E. J. Kalivoda, N. A. Stella, D. M. O'Dee, G. J. Nau, and R. M. Q. Shanks The Cyclic AMP-Dependent Catabolite Repression System of Serratia marcescens Mediates Biofilm Formation through Regulation of Type 1 Fimbriae Appl. Envir. Microbiol., June 1, 2008; 74(11): 3461 - 3470. [Abstract] [Full Text] [PDF] |
||||
![]() |
C.-C. Lu, H.-C. Lai, S.-C. Hsieh, and J.-K. Chen Resveratrol ameliorates Serratia marcescens-induced acute pneumonia in rats J. Leukoc. Biol., April 1, 2008; 83(4): 1028 - 1037. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Matsuo, J. Chen, Y. Minato, W. Ogawa, T. Mizushima, T. Kuroda, and T. Tsuchiya SmdAB, a Heterodimeric ABC-Type Multidrug Efflux Pump, in Serratia marcescens J. Bacteriol., January 15, 2008; 190(2): 648 - 654. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. E. Castelli, G. V. Fedrigo, A. L. Clementin, M. V. Ielmini, M. F. Feldman, and E. G. Vescovi Enterobacterial Common Antigen Integrity Is a Checkpoint for Flagellar Biogenesis in Serratia marcescens J. Bacteriol., January 1, 2008; 190(1): 213 - 220. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. C. Fineran, N. R. Williamson, K. S. Lilley, and G. P. C. Salmond Virulence and Prodigiosin Antibiotic Biosynthesis in Serratia Are Regulated Pleiotropically by the GGDEF/EAL Domain Protein, PigX J. Bacteriol., November 1, 2007; 189(21): 7653 - 7662. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Makimura, Y. Asai, A. Sugiyama, and T. Ogawa Chemical structure and immunobiological activity of lipid A from Serratia marcescens LPS J. Med. Microbiol., November 1, 2007; 56(11): 1440 - 1446. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Morohoshi, T. Shiono, K. Takidouchi, M. Kato, N. Kato, J. Kato, and T. Ikeda Inhibition of Quorum Sensing in Serratia marcescens AS-1 by Synthetic Analogs of N-Acylhomoserine Lactone Appl. Envir. Microbiol., October 15, 2007; 73(20): 6339 - 6344. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. M Nicasio, R. Quintiliani Jr, C A. DeRyke, J. L Kuti, and D. P Nicolau Treatment of Serratia marcescens Meningitis with Prolonged Infusion of Meropenem Ann. Pharmacother., June 1, 2007; 41(6): 1077 - 1081. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Labbate, H. Zhu, L. Thung, R. Bandara, M. R. Larsen, M. D. P. Willcox, M. Givskov, S. A. Rice, and S. Kjelleberg Quorum-Sensing Regulation of Adhesion in Serratia marcescens MG1 Is Surface Dependent J. Bacteriol., April 1, 2007; 189(7): 2702 - 2711. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Kida, H. Inoue, T. Shimizu, and K. Kuwano Serratia marcescens Serralysin Induces Inflammatory Responses through Protease-Activated Receptor 2 Infect. Immun., January 1, 2007; 75(1): 164 - 174. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. S. Koh, K. W. Lam, M. Alhede, S. Y. Queck, M. Labbate, S. Kjelleberg, and S. A. Rice Phenotypic Diversification and Adaptation of Serratia marcescens MG1 Biofilm-Derived Morphotypes J. Bacteriol., January 1, 2007; 189(1): 119 - 130. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. J. Coulthurst, N. R. Williamson, A. K. P. Harris, D. R. Spring, and G. P. C. Salmond Metabolic and regulatory engineering of Serratia marcescens: mimicking phage-mediated horizontal acquisition of antibiotic biosynthesis and quorum-sensing capacities Microbiology, July 1, 2006; 152(7): 1899 - 1911. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. K. Petty, I. J. Foulds, E. Pradel, J. J. Ewbank, and G. P. C. Salmond A generalized transducing phage ({phi}IF3) for the genomically sequenced Serratia marcescens strain Db11: a tool for functional genomics of an opportunistic human pathogen Microbiology, June 1, 2006; 152(6): 1701 - 1708. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. D. Pham, C. W. Shebelut, M. E. Diodati, C. T. Bull, and M. Singer Mutations affecting predation ability of the soil bacterium Myxococcus xanthus Microbiology, June 1, 2005; 151(6): 1865 - 1874. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. J. Coulthurst, C. L. Kurz, and G. P. C. Salmond luxS mutants of Serratia defective in autoinducer-2-dependent 'quorum sensing' show strain-dependent impacts on virulence and production of carbapenem and prodigiosin Microbiology, June 1, 2004; 150(6): 1901 - 1910. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Mammeri, L. Poirel, P. Bemer, H. Drugeon, and P. Nordmann Resistance to Cefepime and Cefpirome Due to a 4-Amino-Acid Deletion in the Chromosome-Encoded AmpC {beta}-Lactamase of a Serratia marcescens Clinical Isolate Antimicrob. Agents Chemother., March 1, 2004; 48(3): 716 - 720. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Chen, T. Kuroda, M. N. Huda, T. Mizushima, and T. Tsuchiya An RND-type multidrug efflux pump SdeXY from Serratia marcescens J. Antimicrob. Chemother., August 1, 2003; 52(2): 176 - 179. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Kumar and E. A. Worobec Fluoroquinolone resistance of Serratia marcescens: involvement of a proton gradient-dependent efflux pump J. Antimicrob. Chemother., October 1, 2002; 50(4): 593 - 596. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Entcheva, W. Liebl, A. Johann, T. Hartsch, and W. R. Streit Direct Cloning from Enrichment Cultures, a Reliable Strategy for Isolation of Complete Operons and Genes from Microbial Consortia Appl. Envir. Microbiol., January 1, 2001; 67(1): 89 - 99. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| INT J SYST EVOL MICROBIOL | J MED MICROBIOL | MICROBIOLOGY | J GEN VIROL | ALL SGM JOURNALS |