Document Detail


Characterization of the importance of Staphylococcus epidermidis autolysin and polysaccharide intercellular adhesin in the pathogenesis of intravascular catheter-associated infection in a rat model.
MedLine Citation:
PMID:  11237828     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A rat central venous catheter (CVC) infection model was used to assess the importance of the proteinacious autolysin (AtlE) and the polysaccharide intercellular adhesin (PIA) in the pathogenesis of Staphylococcus epidermidis CVC-associated infection. Wild-type (wt) S. epidermidis O-47 was significantly more likely to cause a CVC infection than was either of the isogenic mutant strains (AtlE-negative [O-47mut1] or PIA-negative [O-47mut2]). Bacteria were retrieved from the explanted catheters of 87.5% of rats inoculated with S. epidermidis O-47, compared with 25% of rats challenged with either S. epidermidis O-47mut1 or O-47mut2 (P=.007). Peripheral bacteremia was documented in 75% of rats challenged with S. epidermidis O-47, compared with 12.5% and 25% challenged with O-47mut1 and O-47mut2, respectively (P=.009). Metastatic disease was more common in rats inoculated with wt S. epidermidis, compared with AtlE- or PIA-deficient mutants. These results confirm the importance of initial adherence, associated with AtlE, and biofilm production, mediated by PIA, in the pathogenesis of S. epidermidis experimental CVC infection.
Authors:
M E Rupp; P D Fey; C Heilmann; F Götz
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Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, U.S. Gov't, Non-P.H.S.     Date:  2001-03-01
Journal Detail:
Title:  The Journal of infectious diseases     Volume:  183     ISSN:  0022-1899     ISO Abbreviation:  J. Infect. Dis.     Publication Date:  2001 Apr 
Date Detail:
Created Date:  2001-03-12     Completed Date:  2001-05-10     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0413675     Medline TA:  J Infect Dis     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1038-42     Citation Subset:  AIM; IM    
Affiliation:
Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE 68198-4031, USA. merupp@unmc.edu
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MeSH Terms
Descriptor/Qualifier:
Animals
Bacteremia
Bacterial Adhesion
Catheterization, Central Venous / adverse effects*
Disease Models, Animal
Male
Mutation
N-Acetylmuramoyl-L-alanine Amidase / deficiency,  genetics,  physiology*
Polysaccharides, Bacterial / genetics,  physiology*
Rats
Rats, Sprague-Dawley
Staphylococcal Infections / microbiology*,  mortality
Staphylococcus epidermidis* / metabolism,  pathogenicity
Virulence
Viscera / microbiology
Chemical
Reg. No./Substance:
0/Polysaccharides, Bacterial; 0/polysaccharide intercellular adhesin; EC 3.5.1.28/N-Acetylmuramoyl-L-alanine Amidase

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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