Infect Immun, June 1998, p. 3024-3027, Vol. 66, No. 6
Structural Biochemistry Program, SAIC
Frederick, National Cancer Institute-Frederick Cancer Research and
Development Center, Frederick, Maryland
21702-12011;
Department of Research,
York Hospital, York, Pennsylvania
17405-71982;
Department of Microbiology,
Philadelphia College of Osteopathic Medicine, Philadelphia,
Pennsylvania 19131-16963; and
Microbiology Group, Department of Biological Sciences,
Illinois State University, Normal, Illinois
61790-41204
Received 13 January 1998/Returned for modification 6 March
1998/Accepted 31 March 1998
Antibodies to Staphylococcus aureus heat shock proteins
(Hsps) are present in the sera of patients with S. aureus endocarditis (M. W. Qoronfleh, W. Weraarchakul, and
B. J. Wilkinson, Infect. Immun. 61:1567-1570, 1993). Although
these proteins are immunogenic, their role in infection has not been
established. We developed a cell culture system as a model to examine
the potential involvement of staphylococcal Hsps in the initial events
of infection. This study supports a model in which a clinical
endocarditis isolate responds to host cell signals by selectively
regulating the synthesis of numerous proteins, including the stress
proteins Hsp60 (GroEL homolog) and Hsp70 (DnaK homolog) and a unique
58-kDa protein.
0019-9567/98/$00.00+0
Enhanced Levels of Staphylococcus aureus Stress
Protein GroEL and DnaK Homologs Early in Infection of Human
Epithelial Cells
*
Corresponding author. Mailing address: SAIC Frederick,
National Cancer Institute-Frederick Cancer Research and Development Center (NCI-FCRDC), Structural Biochemistry Program (SBP), Bldg. 320, P.O. Box B, Frederick, MD 21702-1201. Phone: (301) 846-1996. Fax: (301)
846-6875. E-mail: ooronfle{at}ncifcrf.gov.
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