Toxin in bullous impetigo and staphylococcal scalded-skin syndrome targets desmoglein 1

M Amagai, N Matsuyoshi, ZH Wang, C Andl… - Nature medicine, 2000 - nature.com
M Amagai, N Matsuyoshi, ZH Wang, C Andl, JR Stanley
Nature medicine, 2000nature.com
Exfoliative toxin A, produced by Staphylococcus aureus, causes blisters in bullous impetigo
and its more generalized form, staphylococcal scalded-skin syndrome 1, 2, 3. The toxin
shows exquisite specificity in causing loss of cell adhesion only in the superficial epidermis.
Although exfoliative toxin A has the structure of a serine protease, a target protein has not
been identified 4, 5. Desmoglein (Dsg) 1, a desmosomal cadherin that mediates cell–cell
adhesion, may be the target of exfoliative toxin A, because it is the target of autoantibodies in …
Abstract
Exfoliative toxin A, produced by Staphylococcus aureus, causes blisters in bullous impetigo and its more generalized form, staphylococcal scalded-skin syndrome 1, 2, 3. The toxin shows exquisite specificity in causing loss of cell adhesion only in the superficial epidermis. Although exfoliative toxin A has the structure of a serine protease, a target protein has not been identified 4, 5. Desmoglein (Dsg) 1, a desmosomal cadherin that mediates cell–cell adhesion, may be the target of exfoliative toxin A, because it is the target of autoantibodies in pemphigus foliaceus, in which blisters form with identical tissue specificity and histology. We show here that exfoliative toxin A cleaved mouse and human Dsg1, but not closely related cadherins such as Dsg3. We demonstrate this specific cleavage in cell culture, in neonatal mouse skin and with recombinant Dsg1, and conclude that Dsg1 is the specific receptor for exfoliative toxin A cleavage. This unique proteolytic attack on the desmosome causes a blister just below the stratum corneum, which forms the epidermal barrier, presumably allowing the bacteria in bullous impetigo to proliferate and spread beneath this barrier.
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