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Infection and Immunity, September 2000, p. 5385-5392, Vol. 68, No. 9
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Staphylococcus aureus RN6390 Replicates
and Induces Apoptosis in a Pulmonary Epithelial Cell Line
Barbara C.
Kahl,1
Mark
Goulian,2
Willem
van
Wamel,3
Mathias
Herrmann,4
Sanford M.
Simon,2
Gilla
Kaplan,5
Georg
Peters,4 and
Ambrose
L.
Cheung3,*
Laboratory of Bacterial Pathogenesis and
Immunology,1 Laboratory of Cellular
Biophysics,2 and Laboratory of Cellular
Physiology and Immunology,5 Rockfeller
University, New York, New York 10021; Department of
Microbiology, Dartmouth Medical School, Hanover, New Hampshire
032553; and Medical Microbiology,
Westfälische Wilhelms Universität Münster, D-48149
Münster, Germany4
Received 20 March 2000/Returned for modification 10 May
2000/Accepted 26 May 2000
Staphylococcus aureus frequently colonizes the airways
of patients with compromised airway defenses (e.g., cystic fibrosis [CF] patients) for extended periods. Persistent and relapsing infections may be related to live S. aureus bacteria
actively residing inside epithelial cells. In this study, we infected a respiratory epithelial cell line, which was derived from a CF patient,
with S. aureus RN6390. Internalization of S. aureus was found to be time and dose dependent and could be
blocked by cytochalasin D. Transmission electron microscopy revealed
that internalized bacteria resided within endocytic vacuoles without
any evidence of lysosomal fusion in a 24-h period. The results of
internalization experiments and time-lapse fluorescence microscopy of
epithelial cells infected with green fluorescent S. aureus
indicate that, after an initial lag period of 7 to 9 h,
intracellular bacteria began to replicate, with three to five divisions
in a 24-h period, leading to apoptosis of infected cells. Induction of
apoptosis required bacterial internalization and is associated with
intracellular replication. The slow and gradual replication of S. aureus inside epithelial cells hints at the role of host factors
or signals in bacterial growth and further suggests possible cross talk
between host cells and S. aureus.
*
Corresponding author. Mailing address: Department of
Microbiology, Dartmouth Medical School, Hanover, NH 03255. Phone: (603) 650-1340. Fax: (603) 650-1318. E-mail:
Ambrose.Cheung{at}Dartmouth.edu.
Infection and Immunity, September 2000, p. 5385-5392, Vol. 68, No. 9
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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