Previous Article | Next Article ![]()
Infect Immun, June 1998, p. 2778-2781, Vol. 66, No. 6
Institute of Medical Microbiology and Hygiene,
Received 9 October 1997/Returned for modification 29 December
1997/Accepted 31 March 1998
The abilities of a parent and mutant pair of Staphylococcus
epidermidis strains, the slime-producing parent RP62A and its slime-negative mutant, to establish endocarditis in a rabbit model of
aortic valve endocarditis and to accumulate and adhere to surfaces in
vitro were compared. Vegetation titer and infection rate depended on
the presence or absence of a catheter (P = 0.020) and
on inoculum size (P < 0.001) but not on the infecting
strain. The ability of the parent strain vis-à-vis its mutant to
accumulate in vitro on surfaces as demonstrated in a slime test did not
correlate with any enhancement in the development of endocarditis in
the rabbit model. In vitro initial adherence rates were identical. Both
isolates accumulated to the same reduced extent in vitro in the
presence of serum, albumin, or gelatin. Adhesion was equally promoted
by addition of fibronectin. These data suggest that the in vitro
phenomenon of accumulation described as slime production in the absence
of serum may not be an important virulence determinant in vivo.
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
The Abilities of a Staphylococcus
epidermidis Wild-Type Strain and Its Slime-Negative Mutant To
Induce Endocarditis in Rabbits Are Comparable
*
Corresponding author. Mailing address: San Francisco
General Hospital, 1001 Potrero Ave., Building 100, Room 301, San
Francisco, CA 94110. Phone: (415) 206-8971. Fax: (415) 206-4360. E-mail: francoise{at}epi-center.ucsf.edu.
Infect Immun, June 1998, p. 2778-2781, Vol. 66, No. 6
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»