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Infection and Immunity, April 2000, p. 2129-2134, Vol. 68, No. 4
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Group B Streptococci and Other Gram-Positive Cocci
Bind to Cytokeratin 8
Glen S.
Tamura* and
Aphakorn
Nittayajarn
Children's Hospital and Medical Center and
the University of Washington, Seattle, Washington
Received 2 November 1999/Returned for modification 27 December
1999/Accepted 19 January 2000
Group B streptococci (GBS) adhere to surface receptors present on
epithelial cells; these receptors include fibronectin and laminin. To
identify other possible receptors, plasma membranes from A549 cells, a
respiratory tract epithelial cell line, were prepared. These plasma
membranes were tested in a protein blot analysis using radiolabeled GBS
as a probe. GBS adhered to two species, with molecular masses of 50 kDa
(p50) and 57 kDa (p57). We concluded that p50 and p57 correspond to two
forms of cytokeratin 8 (CK8) on the basis of the following results: (i)
protein blot results demonstrated that p50 and p57 exactly comigrated
with two forms of CK8 after separation by sodium dodecyl
sulfate-polyacrylamide gel electrophoresis (PAGE); (ii) p50 and p57
exactly comigrated with CK8 after separation by two-dimensional PAGE;
(iii) CK8 in solution bound to GBS, as demonstrated by immunoblot
analysis of proteins from A549 lysates that bound to GBS in a
liquid-phase assay; and (iv) radiolabeled GBS bound to A549
lysate-derived CK8 that had been captured in anti-CK8-coated microtiter
wells. CK8 bound to COH1-13, an acapsular mutant of COH1, demonstrating that adherence is not mediated by capsular polysaccharide.
Trypsin-treated GBS did not bind to CK8, indicating that adherence is
mediated via a protein on the surface of GBS. Soluble CK8 bound to six of six GBS strains tested. Soluble CK8 also bound to
Staphylococcus aureus, Lactococcus lactis,
Enterococcus faecalis, and Streptococcus pyogenes. We hypothesize that adherence of GBS to cytokeratin may
be important for maintenance of colonization at sites of keratinized epithelium, such as the vagina, or for adherence of these bacteria to
damaged epithelial cells at other sites.
*
Corresponding author. Mailing address: Children's
Hospital and Regional Medical Center, P.O. Box 5371, 4800 Sand Point
Way N.E., Seattle, WA 98105-0371. Phone: (206) 526-2073. Fax: (206) 527-3890. E-mail: gtamura{at}u.washington.edu.
Infection and Immunity, April 2000, p. 2129-2134, Vol. 68, No. 4
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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