Hyaluronic acid capsule and the role of streptococcal entry into keratinocytes in invasive skin infection.

It has been suggested that entry of pathogenic bacteria, including streptococci, into epithelial cells may represent an early stage of invasive infections. We found that poorly encapsulated wild-type strains and unencapsulated mutants of group A Streptococcus entered cultured human keratinocytes with high efficiency, while strains that produced large amounts of hyaluronic acid capsule did not, regardless of M-protein type or clinical source of the isolate. However, encapsulated streptococci produced extensive local necrosis and systemic infection in a mouse model of skin infection, while an isogenic acapsular strain did not. The results implicate the hyaluronic acid capsule as a virulence factor in soft tissue infection. Entry of poorly encapsulated group A Streptococcus into human epithelial cells does not appear to represent an initial step in invasive disease; rather, the capacity of encapsulated strains to avoid uptake by epithelial cells is associated with enhanced virulence in skin and soft tissue infection.

[1]  M. Wessels,et al.  Hyaluronate capsule and surface M protein in resistance to opsonization of group A streptococci , 1996, Infection and immunity.

[2]  D L Stevens,et al.  Streptococcal infections of skin and soft tissues. , 1996, The New England journal of medicine.

[3]  G. Donnarumma,et al.  Invasion of cultured human cells by Streptococcus pyogenes. , 1995, Research in microbiology.

[4]  M. Wessels,et al.  Critical role of the group A streptococcal capsule in pharyngeal colonization and infection in mice. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[5]  E. Chi,et al.  Group A streptococci efficiently invade human respiratory epithelial cells. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[6]  P. Hotez,et al.  Hyaluronidases of the gastrointestinal invasive nematodes Ancylostoma caninum and Anisakis simplex: possible functions in the pathogenesis of human zoonoses. , 1994, The Journal of infectious diseases.

[7]  J. Goldberg,et al.  Effects on virulence of mutations in a locus essential for hyaluronic acid capsule expression in group A streptococci , 1994, Infection and immunity.

[8]  M. Boyle,et al.  Association between expression of immunoglobulin G-binding proteins by group A streptococci and virulence in a mouse skin infection model , 1993, Infection and immunity.

[9]  E. Chi,et al.  Respiratory epithelial cell invasion by group B streptococci , 1992, Infection and immunity.

[10]  B. Kruskal,et al.  Phagocytic chimeric receptors require both transmembrane and cytoplasmic domains from the mannose receptor , 1992, The Journal of experimental medicine.

[11]  Dwight R. Johnson,et al.  Epidemiologic analysis of group A streptococcal serotypes associated with severe systemic infections, rheumatic fever, or uncomplicated pharyngitis. , 1992, The Journal of infectious diseases.

[12]  D. Stevens Invasive group A streptococcus infections. , 1992, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[13]  J. Rheinwald,et al.  Variable expression of retinoic acid receptor (RAR beta) mRNA in human oral and epidermal keratinocytes; relation to keratin 19 expression and keratinization potential. , 1991, Differentiation; research in biological diversity.

[14]  J. Goldberg,et al.  Hyaluronic acid capsule is a virulence factor for mucoid group A streptococci. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[15]  S. Falkow Bacterial entry into eukaryotic cells , 1991, Cell.

[16]  R. Isberg,et al.  Discrimination between intracellular uptake and surface adhesion of bacterial pathogens. , 1991, Science.

[17]  J. Rheinwald,et al.  Three distinct keratinocyte subtypes identified in human oral epithelium by their patterns of keratin expression in culture and in xenografts. , 1990, Differentiation; research in biological diversity.

[18]  A. Gee,et al.  [10] Measurement of leukocyte chemotaxis in vivo , 1988 .

[19]  A. Gee,et al.  Measurement of leukocyte chemotaxis in vivo. , 1988, Methods in enzymology.

[20]  J. Rheinwald,et al.  Tumorigenic keratinocyte lines requiring anchorage and fibroblast support cultured from human squamous cell carcinomas. , 1981, Cancer research.

[21]  R. Edstrom,et al.  A sensitive method for the assay of hyaluronidase activity. , 1977, Analytical biochemistry.