Literature DB >> 21976608

Serratia infections: from military experiments to current practice.

Steven D Mahlen1.   

Abstract

Serratia species, in particular Serratia marcescens, are significant human pathogens. S. marcescens has a long and interesting taxonomic, medical experimentation, military experimentation, and human clinical infection history. The organisms in this genus, particularly S. marcescens, were long thought to be nonpathogenic. Because S. marcescens was thought to be a nonpathogen and is usually red pigmented, the U.S. military conducted experiments that attempted to ascertain the spread of this organism released over large areas. In the process, members of both the public and the military were exposed to S. marcescens, and this was uncovered by the press in the 1970s, leading to U.S. congressional hearings. S. marcescens was found to be a certain human pathogen by the mid-1960s. S. marcescens and S. liquefaciens have been isolated as causative agents of numerous outbreaks and opportunistic infections, and the association of these organisms with point sources such as medical devices and various solutions given to hospitalized patients is striking. Serratia species appear to be common environmental organisms, and this helps to explain the large number of nosocomial infections due to these bacteria. Since many nosocomial infections are caused by multiply antibiotic-resistant strains of S. marcescens, this increases the danger to hospitalized patients, and hospital personnel should be vigilant in preventing nosocomial outbreaks due to this organism. S. marcescens, and probably other species in the genus, carries several antibiotic resistance determinants and is also capable of acquiring resistance genes. S. marcescens and S. liquefaciens are usually identified well in the clinical laboratory, but the other species are rare enough that laboratory technologists may not recognize them. 16S rRNA gene sequencing may enable better identification of some of the less common Serratia species.

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Year:  2011        PMID: 21976608      PMCID: PMC3194826          DOI: 10.1128/CMR.00017-11

Source DB:  PubMed          Journal:  Clin Microbiol Rev        ISSN: 0893-8512            Impact factor:   26.132


  385 in total

1.  Nonpigmented Serratia marcescens.

Authors:  E Clayton; A Von Graevenitz
Journal:  JAMA       Date:  1966-09-26       Impact factor: 56.272

2.  Contraindication for use of Serratia marcescens as tracer organisms in research.

Authors:  H H Thayer
Journal:  J Dent Res       Date:  1966 May-Jun       Impact factor: 6.116

3.  Fimbria-mediated adherence of Serratia marcescens strain US5 to human urinary bladder surface.

Authors:  T Yamamoto; A Ariyoshi; K Amako
Journal:  Microbiol Immunol       Date:  1985       Impact factor: 1.955

4.  A three-phase in-vitro system for studying Pseudomonas aeruginosa adhesion and biofilm formation upon hydrogel contact lenses.

Authors:  Claudia Rändler; Rutger Matthes; Andrew J McBain; Bernd Giese; Martin Fraunholz; Rabea Sietmann; Thomas Kohlmann; Nils-Olaf Hübner; Axel Kramer
Journal:  BMC Microbiol       Date:  2010-11-09       Impact factor: 3.605

5.  Smaqnr, a new chromosome-encoded quinolone resistance determinant in Serratia marcescens.

Authors:  C Velasco; J M Rodríguez-Martínez; A Briales; P Díaz de Alba; J Calvo; A Pascual
Journal:  J Antimicrob Chemother       Date:  2009-11-26       Impact factor: 5.790

6.  Serratia marcescens bacteremia - an indicator for outbreak management and heightened surveillance.

Authors:  Elizabeth E Gillespie; Jennifer Bradford; Judith Brett; Despina Kotsanas
Journal:  J Perinat Med       Date:  2007       Impact factor: 1.901

Review 7.  AmpC beta-lactamases.

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

8.  Molecular characterization of an enterobacterial metallo beta-lactamase found in a clinical isolate of Serratia marcescens that shows imipenem resistance.

Authors:  E Osano; Y Arakawa; R Wacharotayankun; M Ohta; T Horii; H Ito; F Yoshimura; N Kato
Journal:  Antimicrob Agents Chemother       Date:  1994-01       Impact factor: 5.191

9.  The role of the Serratia marcescens SdeAB multidrug efflux pump and TolC homologue in fluoroquinolone resistance studied via gene-knockout mutagenesis.

Authors:  Sanela Begic; Elizabeth A Worobec
Journal:  Microbiology       Date:  2008-02       Impact factor: 2.777

10.  Serratia marcescens outbreak in a paediatric oncology unit traced to contaminated chlorhexidine.

Authors:  T A McAllister; C E Lucas; H Mocan; R H Liddell; B E Gibson; I M Hann; D J Platt
Journal:  Scott Med J       Date:  1989-10       Impact factor: 0.729

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  157 in total

1.  Fetal exposures and perinatal influences on the stool microbiota of premature infants.

Authors:  Diana A Chernikova; Devin C Koestler; Anne Gatewood Hoen; Molly L Housman; Patricia L Hibberd; Jason H Moore; Hilary G Morrison; Mitchell L Sogin; Muhammad Zain-Ul-Abideen; Juliette C Madan
Journal:  J Matern Fetal Neonatal Med       Date:  2015-09-04

2.  EepR Mediates Secreted-Protein Production, Desiccation Survival, and Proliferation in a Corneal Infection Model.

Authors:  Kimberly M Brothers; Nicholas A Stella; Eric G Romanowski; Regis P Kowalski; Robert M Q Shanks
Journal:  Infect Immun       Date:  2015-08-31       Impact factor: 3.441

3.  Photodynamic inactivation diminishes quorum sensing-mediated virulence factor production and biofilm formation of Serratia marcescens.

Authors:  Zahra Fekrirad; Nasim Kashef; Ehsan Arefian
Journal:  World J Microbiol Biotechnol       Date:  2019-11-25       Impact factor: 3.312

4.  Pseudohemoptysis due to Serratia marcescens.

Authors:  Stephanie Parks Taylor; Brice Taylor
Journal:  J Gen Intern Med       Date:  2013-11-02       Impact factor: 5.128

5.  Identification of SlpB, a Cytotoxic Protease from Serratia marcescens.

Authors:  Robert M Q Shanks; Nicholas A Stella; Kristin M Hunt; Kimberly M Brothers; Liang Zhang; Patrick H Thibodeau
Journal:  Infect Immun       Date:  2015-05-04       Impact factor: 3.441

6.  An IgaA/UmoB Family Protein from Serratia marcescens Regulates Motility, Capsular Polysaccharide Biosynthesis, and Secondary Metabolite Production.

Authors:  Nicholas A Stella; Kimberly M Brothers; Jake D Callaghan; Angelina M Passerini; Cihad Sigindere; Preston J Hill; Xinyu Liu; Daniel J Wozniak; Robert M Q Shanks
Journal:  Appl Environ Microbiol       Date:  2018-03-01       Impact factor: 4.792

7.  Serratia marcescens arn, a PhoP-regulated locus necessary for polymyxin B resistance.

Authors:  Quei Yen Lin; Yi-Lin Tsai; Ming-Che Liu; Wei-Cheng Lin; Po-Ren Hsueh; Shwu-Jen Liaw
Journal:  Antimicrob Agents Chemother       Date:  2014-06-23       Impact factor: 5.191

8.  Coproduction of KPC-2 and IMP-10 in Carbapenem-Resistant Serratia marcescens Isolates from an Outbreak in a Brazilian Teaching Hospital.

Authors:  Kesia Esther Silva; Rodrigo Cayô; Cecilia Godoy Carvalhaes; Flávia Patussi Correia Sacchi; Fernanda Rodrigues-Costa; Ana Carolina Ramos da Silva; Julio Croda; Ana Cristina Gales; Simone Simionatto
Journal:  J Clin Microbiol       Date:  2015-04-15       Impact factor: 5.948

9.  Structure of glycerol dehydrogenase from Serratia.

Authors:  Paul Musille; Eric Ortlund
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2014-01-21       Impact factor: 1.056

10.  CpxR-Dependent Thermoregulation of Serratia marcescens PrtA Metalloprotease Expression and Its Contribution to Bacterial Biofilm Formation.

Authors:  Roberto E Bruna; María Victoria Molino; Martina Lazzaro; Javier F Mariscotti; Eleonora García Véscovi
Journal:  J Bacteriol       Date:  2018-03-26       Impact factor: 3.490

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