| Title |
Severity of nonbullous Staphylococcus aureus impetigo in children is associated with strains harboring genetic markers for exfoliative toxin B, Panton-Valentine leukocidin, and the multidrug resistance plasmid pSK41 |
| Published in |
Journal of Clinical Microbiology. ISSN 0095-1137. |
| Author |
Koning, S. (Sander); Belkum, van A.F. (Alex); Snijders, S.V. (Susan); Nouwen, J.L. (Jan); Veld, op 't M.; Wouden, van der J.C. (Hans); Verduin, C.M. (Cees); Verbrugh, H.A. (Henri); Leeuwen, van W.B. (Willem); Suijlekom-Smit, van L.W.A. (Lisette) |
| Date |
2003-01-01 |
| Language |
English |
| Type |
article |
| Abstract |
Nonbullous impetigo is a common skin infection in children and is
frequently caused by Staphylococcus aureus. Staphylococcal toxins and
especially exfoliative toxin A are known mediators of bullous impetigo in
children. It is not known whether this is also true for nonbullous
impetigo. We set out to analyze clonality among clinical isolates of S.
aureus from children with nonbullous impetigo living in a restricted
geographical area in The Netherlands. We investigated whether
staphylococcal nasal carriage and the nature of the staphylococcal strains
were associated with the severity and course of impetigo. Bacterial
isolates were obtained from the noses and wounds of children suffering
from impetigo. Strains were genetically characterized by pulsed-field gel
electrophoresis-mediated typing and binary typing, which was also used to
assess toxin gene content. In addition, a detailed clinical questionnaire
was filled in by each of the participating patients. Staphylococcal nasal
carriage seems to predispose the patients to the development of impetigo,
and 34% of infections diagnosed in the Rotterdam area are caused by one
clonal type of S. aureus. The S. aureus strains harbor the exfoliative
toxin B (ETB) gene as a specific virulence factor. In particular, the
numbers (P = 0.002) and sizes (P < 0.001) of the lesions were increased in
patients infected with an ETB-positive strain. Additional predictors of
disease severity and development could be identified. The presence of a
staphylococcal plasmid encoding multiple antibiotic resistance traits, as
detected by binary typing, was associated with a reduction in the cure
rate. Our results recognize that a combination of staphylococcal virulence
and resistance genes rather than a single gene determines the development
and course of nonbullous impetigo. The identification of these microbial
genetic markers, which are predictive of the severity and the course of
the disease, will facilitate guided individualized antimicrobial therapy
in the future. |
| Publication |
http://hdl.handle.net/1765/10189 |
| Persistent Identifier |
urn:NBN:nl:ui:15-1765/10189 |
| Metadata |
XML |
| Repository |
Erasmus University Rotterdam |