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JAMA Dermatol. 2014 Mar;150(3):260-5. doi: 10.1001/jamadermatol.2013.8627.

The presence and impact of biofilm-producing staphylococci in atopic dermatitis.

Author information

1
Department of Dermatology, Drexel University College of Medicine, Philadelphia, Pennsylvania.
2
Surgical Infections Research and Bacterial Pathogenesis Program, Drexel University College of Medicine, Philadelphia, Pennsylvania.
3
Department of Dermatology, Drexel University College of Medicine, Philadelphia, Pennsylvania2Surgical Infections Research and Bacterial Pathogenesis Program, Drexel University College of Medicine, Philadelphia, Pennsylvania.

Abstract

IMPORTANCE:

Atopic dermatitis (AD) is thought to be a double-hit phenomenon with an unknown environmental component and a genetic abnormality likely centered on the filaggrin gene. Biologically, the presence of Staphylococcus aureus in AD was reported more than 2 decades ago, but the relationship to AD has been elusive.

OBJECTIVE:

To explore the bacteria that produce the biofilms in the lesions of AD and the response of the innate immune system to these biofilm occlusions of the sweat ducts by specifically evaluating Toll-like receptor 2.

DESIGN, SETTING, AND PARTICIPANTS:

University hospital dermatologic clinic study involving the environmental component related to the characterization, correlation, and impact of staphylococci and their biofilms in AD. We processed routine skin swabs from lesional and nonlesional skin from 40 patients with AD and performed scrapings and biopsies. We also obtained 20 samples from controls (10 inflamed skin samples and 10 normal skin samples).

EXPOSURES:

Gram staining, bright-field microscopy, hematoxylin and eosin, periodic acid-Schiff, Congo red, and light microscopy.

MAIN OUTCOMES AND MEASURES:

Association of staphylococcal biofilms with AD pathogenesis.

RESULTS:

All AD-affected samples contained multidrug-resistant staphylococci, with S aureus (42.0%) and Staphylococcus epidermidis (20.0%) as the predominant species. All isolates were positive for extracellular polysaccharide and biofilm (85.0% strong biofilm producers and 15.0% moderately to weakly positive). Polymerase chain reaction revealed the biofilm-mediating icaD (93.0%) and aap (12.5%) genes in the isolates (some contained both). We also examined tissues for microbial identification, extracellular biomass formation, biofilm formation, and staphylococcal biofilm in skin tissues. Occlusion of sweat ducts with periodic acid-Schiff-positive and Congo red-positive material was noted on microscopic tissue examination. Toll-like receptor 2 was shown to be activated in AD lesional skin (immediately proximal to the sweat ducts), which likely led to the initiation of proteinase-activated receptor 2-mediated pruritus and MyD88-mediated spongiosis.

CONCLUSIONS AND RELEVANCE:

Biofilm formation by AD-associated staphylococci almost certainly plays a major role in the occlusion of sweat ducts and leads to inflammation and pruritus. We believe the environmental hit in AD relates to staphylococci and their biofilms, which occlude sweat ducts.

PMID:
24452476
DOI:
10.1001/jamadermatol.2013.8627
[Indexed for MEDLINE]

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