Literature DB >> 12842326

Natural antibiotic susceptibility of strains of Serratia marcescens and the S. liquefaciens complex: S. liquefaciens sensu stricto, S. proteamaculans and S. grimesii.

I Stock1, T Grueger, B Wiedemann.   

Abstract

The natural susceptibility of 77 strains of Serratia marcescens and 41 strains of the S. liquefaciens complex (S. liquefaciens sensu stricto (n=21), S. grimesii (n=10), S. proteamaculans (n=10)) to 70 antibiotics was examined using a microdilution procedure in Isosensitest broth (all strains) and cation-adjusted Mueller Hinton broth (some strains). All species were naturally resistant to benzylpenicillin, oxacillin, cefaclor, cefazolin, cefuroxime, numerous macrolides, lincosamides, streptogramins, glycopeptides, rifampicin and fusidic acid. Uniform natural sensitivity was found to most aminoglycosides, several acylureidopenicillins, ticarcillin, newer cephalosporins, carbapenems, aztreonam, quinolones and antifolates. Species-related differences in susceptibility affecting clinical assessment criteria were found for several agents. S. marcescens was less susceptible to some aminoglycosides than species of the S. liquefaciens group. It was the only species that was uniformly naturally resistant to tetracycline, amoxycillin, amoxycillin/clavulanate and loracarbef. Species of the S. liquefaciens group were naturally resistant and intermediate or naturally intermediate to the latter agents. Differences in susceptibility among the species of the S. liquefaciens complex were generally small. S. proteamaculans was most susceptible to sulphamethoxazole. S. liquefaciens sensu stricto was less susceptible than S. grimesii and S. proteamaculans to tetracyclines, chloramphenicol and nitrofurantoin; it was the only species uniformly naturally resistant to fosfomycin. This study suggested that all species examined probably express chromosomally-encoded AmpC beta-lactamases, but the amount of enzyme may vary from species to species. The naturally-occurring low-level expression of the S. marcescens aminoglycoside 6'-acetyltransferase AAC(6')-Ic and its absence in other Serratia spp. was supported by the data. All species of the S. liquefaciens complex should be considered as probable agents of human diseases.

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Year:  2003        PMID: 12842326     DOI: 10.1016/s0924-8579(02)00163-2

Source DB:  PubMed          Journal:  Int J Antimicrob Agents        ISSN: 0924-8579            Impact factor:   5.283


  25 in total

1.  Plasmid-mediated quinolone resistance in extended-spectrum-β-lactamase- and AmpC β-lactamase-producing Serratia marcescens in China.

Authors:  Hai-Fei Yang; Jun Cheng; Li-Fen Hu; Ying Ye; Jia-Bin Li
Journal:  Antimicrob Agents Chemother       Date:  2012-06-04       Impact factor: 5.191

2.  Identification and characterization of an unusual metallo-β-lactamase from Serratia proteamaculans.

Authors:  Peter Vella; Manfredi Miraula; Emer Phelan; Eleanor W W Leung; Fernanda Ely; David L Ollis; Ross P McGeary; Gerhard Schenk; Nataša Mitić
Journal:  J Biol Inorg Chem       Date:  2013-08-28       Impact factor: 3.358

Review 3.  Efflux-mediated drug resistance in bacteria: an update.

Authors:  Xian-Zhi Li; Hiroshi Nikaido
Journal:  Drugs       Date:  2009-08-20       Impact factor: 9.546

4.  Health care associated infections, antibiotic resistance and clinical outcome: A surveillance study from Sanandaj, Iran.

Authors:  Jafar Soltani; Bahman Poorabbas; Neda Miri; Jalal Mardaneh
Journal:  World J Clin Cases       Date:  2016-03-16       Impact factor: 1.337

5.  Novel tetracycline resistance determinant isolated from an environmental strain of Serratia marcescens.

Authors:  Stuart A Thompson; Elizabeth V Maani; Angela H Lindell; Catherine J King; J Vaun McArthur
Journal:  Appl Environ Microbiol       Date:  2007-02-16       Impact factor: 4.792

Review 6.  Serratia infections: from military experiments to current practice.

Authors:  Steven D Mahlen
Journal:  Clin Microbiol Rev       Date:  2011-10       Impact factor: 26.132

7.  Virulence and prodigiosin antibiotic biosynthesis in Serratia are regulated pleiotropically by the GGDEF/EAL domain protein, PigX.

Authors:  Peter C Fineran; Neil R Williamson; Kathryn S Lilley; George P C Salmond
Journal:  J Bacteriol       Date:  2007-08-31       Impact factor: 3.490

Review 8.  AmpC beta-lactamases.

Authors:  George A Jacoby
Journal:  Clin Microbiol Rev       Date:  2009-01       Impact factor: 26.132

9.  Outbreak of a cluster with epidemic behavior due to Serratia marcescens after colistin administration in a hospital setting.

Authors:  Andrea Karina Merkier; María Cecilia Rodríguez; Ana Togneri; Silvina Brengi; Carolina Osuna; Mariana Pichel; Marcelo H Cassini; Daniela Centrón
Journal:  J Clin Microbiol       Date:  2013-05-22       Impact factor: 5.948

10.  Serratia marcescens ShlA pore-forming toxin is responsible for early induction of autophagy in host cells and is transcriptionally regulated by RcsB.

Authors:  Gisela Di Venanzio; Tatiana M Stepanenko; Eleonora García Véscovi
Journal:  Infect Immun       Date:  2014-06-09       Impact factor: 3.441

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