Staphylococcal communities on skin are associated with atopic dermatitis and disease severity.
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Staphylococcal communities on skin are associated with atopic dermatitis and disease severity. / Edslev, Sofie Marie; Olesen, Caroline Meyer; Nørreslet, Line Brok; Ingham, Anna Cäcilia; Iversen, Søren; Lilje, Berit; Clausen, Maja Lisa; Jensen, Jørgen Skov; Stegger, Marc; Agner, Tove; Andersen, Paal Skytt.
I: Microorganisms, Bind 9, Nr. 2, 432, 2021, s. 1-17.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Staphylococcal communities on skin are associated with atopic dermatitis and disease severity.
AU - Edslev, Sofie Marie
AU - Olesen, Caroline Meyer
AU - Nørreslet, Line Brok
AU - Ingham, Anna Cäcilia
AU - Iversen, Søren
AU - Lilje, Berit
AU - Clausen, Maja Lisa
AU - Jensen, Jørgen Skov
AU - Stegger, Marc
AU - Agner, Tove
AU - Andersen, Paal Skytt
PY - 2021
Y1 - 2021
N2 - The skin microbiota of atopic dermatitis (AD) patients is characterized by increased Staphylococcus aureus colonization, which exacerbates disease symptoms and has been linked to reduced bacterial diversity. Skin bacterial communities in AD patients have mostly been described at family and genus levels, while species‐level characterization has been limited. In this study, we investigated the role of the bacteria belonging to the Staphylococcus genus using targeted sequencing of the tuf gene with genus‐specific primers. We compared staphylococcal communities on lesional and non‐lesional skin of AD patients, as well as AD patients with healthy controls, and determined the absolute abundance of bacteria present at each site. We observed that the staphylococcal community, bacterial alpha diversity, and bacterial densities were similar on lesional and non-lesional skin, whereas AD severity was associated with significant changes in staphylococcal composition. Increased S. aureus, Staphylococcus capitis, and Staphylococcus lugdunensis abundances were correlated with increased severity. Conversely, Staphylococcus hominis abundance was negatively correlated with severity. Furthermore, S. hominis relative abundance was reduced on AD skin compared to healthy skin. In conclusion, various staphylococcal species appear to be important for skin health.
AB - The skin microbiota of atopic dermatitis (AD) patients is characterized by increased Staphylococcus aureus colonization, which exacerbates disease symptoms and has been linked to reduced bacterial diversity. Skin bacterial communities in AD patients have mostly been described at family and genus levels, while species‐level characterization has been limited. In this study, we investigated the role of the bacteria belonging to the Staphylococcus genus using targeted sequencing of the tuf gene with genus‐specific primers. We compared staphylococcal communities on lesional and non‐lesional skin of AD patients, as well as AD patients with healthy controls, and determined the absolute abundance of bacteria present at each site. We observed that the staphylococcal community, bacterial alpha diversity, and bacterial densities were similar on lesional and non-lesional skin, whereas AD severity was associated with significant changes in staphylococcal composition. Increased S. aureus, Staphylococcus capitis, and Staphylococcus lugdunensis abundances were correlated with increased severity. Conversely, Staphylococcus hominis abundance was negatively correlated with severity. Furthermore, S. hominis relative abundance was reduced on AD skin compared to healthy skin. In conclusion, various staphylococcal species appear to be important for skin health.
KW - 16S rRNA amplicon sequencing
KW - 16S rRNA qPCR
KW - Atopic dermatitis
KW - Coagulase-negative staphylococci
KW - S. aureus
KW - Skin microbiome
KW - Skin microbiota
KW - Staphylococcus
KW - Tuf amplicon sequencing
U2 - 10.3390/microorganisms9020432
DO - 10.3390/microorganisms9020432
M3 - Journal article
C2 - 33669791
AN - SCOPUS:85100924013
VL - 9
SP - 1
EP - 17
JO - Microorganisms
JF - Microorganisms
SN - 2076-2607
IS - 2
M1 - 432
ER -
ID: 257875968