The Effect of Systemic Antibiotics for Suppurative Skin and Soft Tissue Infections on the Skin Microbiome.

antibiotics longitudinal cohort microbiome skin infection treatment

Journal

Open forum infectious diseases
ISSN: 2328-8957
Titre abrégé: Open Forum Infect Dis
Pays: United States
ID NLM: 101637045

Informations de publication

Date de publication:
May 2022
Historique:
received: 07 12 2021
accepted: 21 03 2022
entrez: 22 4 2022
pubmed: 23 4 2022
medline: 23 4 2022
Statut: epublish

Résumé

Skin and soft tissue infections (SSTIs) are very common bacterial infections. There are few data on the microbiome of persons with and without SSTIs and the effects of systemic antibiotic therapy. We sampled the skin microbiome from 10 outpatients with acute suppurative SSTI before and after systemic antibiotic therapy and enrolled 10 matched controls. Samples were collected at 6 skin body sites (occipital scalp, axilla, interdigital hand web spaces, gluteal crease, inguinal creases, and popliteal fossa), 2 mucosal sites (throat, anterior nares), and the site of skin infection (for case subjects) at baseline and a week later after abscess incision, drainage, and oral antibiotics. Among 10 SSTI cases, mean age was 41.5 years and 3 had diabetes mellitus. The gluteal crease at baseline had higher α-diversity in controls vs cases ( We surprisingly found no significant differences in microbiome comparing noninfected skin sites before and after systemic SSTI antibiotic therapy nor significant differences at noninfected skin sites between SSTI cases and uninfected controls. We also found minimal significant differences between microbiome diversity and bacterial signatures at noninfected skin sites between patients with acute skin infection and uninfected controls. Our findings challenge the dogma that systemic antibiotics impact the skin microbiome.

Sections du résumé

Background UNASSIGNED
Skin and soft tissue infections (SSTIs) are very common bacterial infections. There are few data on the microbiome of persons with and without SSTIs and the effects of systemic antibiotic therapy.
Methods UNASSIGNED
We sampled the skin microbiome from 10 outpatients with acute suppurative SSTI before and after systemic antibiotic therapy and enrolled 10 matched controls. Samples were collected at 6 skin body sites (occipital scalp, axilla, interdigital hand web spaces, gluteal crease, inguinal creases, and popliteal fossa), 2 mucosal sites (throat, anterior nares), and the site of skin infection (for case subjects) at baseline and a week later after abscess incision, drainage, and oral antibiotics.
Result UNASSIGNED
Among 10 SSTI cases, mean age was 41.5 years and 3 had diabetes mellitus. The gluteal crease at baseline had higher α-diversity in controls vs cases (
Conclusions UNASSIGNED
We surprisingly found no significant differences in microbiome comparing noninfected skin sites before and after systemic SSTI antibiotic therapy nor significant differences at noninfected skin sites between SSTI cases and uninfected controls. We also found minimal significant differences between microbiome diversity and bacterial signatures at noninfected skin sites between patients with acute skin infection and uninfected controls. Our findings challenge the dogma that systemic antibiotics impact the skin microbiome.

Identifiants

pubmed: 35450081
doi: 10.1093/ofid/ofac141
pii: ofac141
pmc: PMC9017368
doi:

Types de publication

Journal Article

Langues

eng

Pagination

ofac141

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR001881
Pays : United States

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

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Auteurs

Alfred A Chan (AA)

Division of Dermatology, Department of Medicine, Lundquist Research Institute at Harbor-University of California, Los Angeles Medical Center, Torrance, California, USA.

Evelyn A Flores (EA)

Division of Infectious Diseases, Department of Medicine, Lundquist Research Institute at Harbor-University of California, Los Angeles Medical Center, Torrance, California, USA.

Marian Navarrete (M)

Division of Dermatology, Department of Medicine, Lundquist Research Institute at Harbor-University of California, Los Angeles Medical Center, Torrance, California, USA.

Donna Phan Tran (D)

Division of Infectious Diseases, Department of Medicine, Lundquist Research Institute at Harbor-University of California, Los Angeles Medical Center, Torrance, California, USA.

Delphine J Lee (DJ)

Division of Dermatology, Department of Medicine, Lundquist Research Institute at Harbor-University of California, Los Angeles Medical Center, Torrance, California, USA.
David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, USA.

Loren G Miller (LG)

Division of Infectious Diseases, Department of Medicine, Lundquist Research Institute at Harbor-University of California, Los Angeles Medical Center, Torrance, California, USA.
David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, USA.

Classifications MeSH