Literature DB >> 9303951

Clinical importance and antibiotic resistance of Acinetobacter spp. Proceedings of a symposium held on 4-5 November 1996 at Eilat, Israel.

K J Towner1.   

Abstract

Members of the genus Acinetobacter, particularly multiresistant strains of A. baumannii, are implicated in a wide spectrum of nosocomial infections, including bacteraemia, secondary meningitis and urinary tract infection, but have now assumed a particularly important role as agents of nosocomial pneumonia in intensive care units (ICUs). Rapid genotyping methods for the identification and typing of these organisms have allowed a better appreciation of the epidemiology and survival of these organisms in the hospital environment. Their emergence as significant pathogens seems to be related partly to their survival ability and partly to their ability to develop resistance rapidly to the major groups of antibiotics, resulting in a considerable selective advantage in environments (such as ICUs) with widespread and heavy uses of antibiotics. Molecular and biochemical mechanisms of resistance to the major beta-lactam, aminoglycoside and quinolone groups of antibiotics have now been elucidated in some detail for these organisms, and experimental models, including a mouse model of A. baumannii pneumonia, have been developed to examine the efficacy of different therapeutic regimens for difficult-to-treat-infections caused by these bacteria. 'Non-classic' antibiotic combinations--such as ticarcillin with clavulanic acid and sulbactam--seem to show promise for treating systemic infections caused by otherwise multiresistant strains, but revised screening procedures in the pharmaceutical industry may be required in the near future to select novel compounds with activity against multiresistant Acinetobacter spp. and other emerging gram-negative, non-fermentative bacilli in general.

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Year:  1997        PMID: 9303951     DOI: 10.1099/00222615-46-9-721

Source DB:  PubMed          Journal:  J Med Microbiol        ISSN: 0022-2615            Impact factor:   2.472


  21 in total

1.  Generation and serological characterization of murine monoclonal antibodies against O antigens from Acinetobacter reference strains.

Authors:  R Pantophlet; L Brade; H Brade
Journal:  Clin Diagn Lab Immunol       Date:  2001-07

2.  Identification of Acinetobacter baumannii strains with monoclonal antibodies against the O antigens of their lipopolysaccharides.

Authors:  R Pantophlet; L Brade; H Brade
Journal:  Clin Diagn Lab Immunol       Date:  1999-05

3.  Control of an Acinetobacter [corrected] baumannii outbreak in a neonatal ICU without suspension of service: a devastating outbreak in Diyarbakir, Turkey.

Authors:  S Hosoglu; M Hascuhadar; E Yasar; S Uslu; B Aldudak
Journal:  Infection       Date:  2011-09-01       Impact factor: 3.553

Review 4.  The epidemiology of antimicrobial resistance in hospital acquired infections: problems and possible solutions.

Authors:  M J Struelens
Journal:  BMJ       Date:  1998-09-05

5.  Antibiotic resistance in Acinetobacter spp. isolated from sewers receiving waste effluent from a hospital and a pharmaceutical plant.

Authors:  L Guardabassi; A Petersen; J E Olsen; A Dalsgaard
Journal:  Appl Environ Microbiol       Date:  1998-09       Impact factor: 4.792

6.  Acinetobacter spp as Nosocomial Pathogen : Clinical Significance and Antimicrobial Sensitivity.

Authors:  K K Lahiri; N S Mani; S S Purai
Journal:  Med J Armed Forces India       Date:  2011-07-21

7.  Functions of the mismatch repair gene mutS from Acinetobacter sp. strain ADP1.

Authors:  D M Young; L N Ornston
Journal:  J Bacteriol       Date:  2001-12       Impact factor: 3.490

8.  Autoantibodies to brain components and antibodies to Acinetobacter calcoaceticus are present in bovine spongiform encephalopathy.

Authors:  H Tiwana; C Wilson; J Pirt; W Cartmell; A Ebringer
Journal:  Infect Immun       Date:  1999-12       Impact factor: 3.441

9.  O-antigen diversity among Acinetobacter baumannii strains from the Czech Republic and Northwestern Europe, as determined by lipopolysaccharide-specific monoclonal antibodies.

Authors:  R Pantophlet; A Nemec; L Brade; H Brade; L Dijkshoorn
Journal:  J Clin Microbiol       Date:  2001-07       Impact factor: 5.948

10.  Microbial synergy via an ethanol-triggered pathway.

Authors:  Michael G Smith; Shelley G Des Etages; Michael Snyder
Journal:  Mol Cell Biol       Date:  2004-05       Impact factor: 4.272

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