Colonization With Staphylococcus aureus in Atopic Dermatitis Patients: Attempts to Reveal the Unknown
Atopic dermatitis (AD) patients are massively colonized with ( ) in lesional and non-lesional skin. A skin infection may become systemic if left untreated. Of interest, the incidence of multi-drug resistant (MRSA) in AD patients is higher as compared to a healthy population, which makes treatment ev...
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Published in | Frontiers in microbiology Vol. 11; p. 567090 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
11.01.2021
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Subjects | |
Online Access | Get full text |
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Summary: | Atopic dermatitis (AD) patients are massively colonized with
(
) in lesional and non-lesional skin. A skin infection may become systemic if left untreated. Of interest, the incidence of multi-drug resistant
(MRSA) in AD patients is higher as compared to a healthy population, which makes treatment even more challenging. Information on the specific genetic background of
accompanying and/or causing AD flares would be of great importance in terms of possible treatment option development. In this review, we summarized the data on the prevalence of
in general in AD skin, and the prevalence of specific clones that might be associated with flares of eczema. We put our special interest in the presence and role of staphylococcal enterotoxins as important virulence factors in the epidemiology of AD-derived
. Also, we summarize the present and potentially useful future anti-staphylococcal treatment. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 Edited by: Fabian Cieplik, University Medical Center Regensburg, Germany Reviewed by: Teruaki Nakatsuji, University of California, San Diego, United States; Michael Otto, National Institutes of Health (NIH), United States This article was submitted to Antimicrobials, Resistance and Chemotherapy, a section of the journal Frontiers in Microbiology |
ISSN: | 1664-302X 1664-302X |
DOI: | 10.3389/fmicb.2020.567090 |