Longitudinal Dynamics of Skin Bacterial Communities in the Context of Staphylococcus aureus Decolonization.


Journal

Microbiology spectrum
ISSN: 2165-0497
Titre abrégé: Microbiol Spectr
Pays: United States
ID NLM: 101634614

Informations de publication

Date de publication:
27 04 2022
Historique:
pubmed: 7 4 2022
medline: 30 4 2022
entrez: 6 4 2022
Statut: ppublish

Résumé

Decolonization with topical antimicrobials is frequently prescribed in health care and community settings to prevent Staphylococcus aureus infection. However, effects on commensal skin microbial communities remains largely unexplored. Within a household affected by recurrent methicillin-resistant S. aureus skin and soft tissue infections (SSTI), skin swabs were collected from the anterior nares, axillae, and inguinal folds of 14 participants at 1- to 3-month intervals over 24 months. Four household members experienced SSTI during the first 12-months (observational period) and were prescribed a 5-day decolonization regimen with intranasal mupirocin and bleach water baths at the 12-month study visit. We sequenced the 16S rRNA gene V1-V2 region and compared bacterial community characteristics between the pre- and post-intervention periods and between younger and older subjects. The median Shannon diversity index was stable during the 12-month observational period at all three body sites. Bacterial community characteristics (diversity, stability, and taxonomic composition) varied with age. Among all household members, not exclusively among the four performing decolonization, diversity was unstable throughout the year post-intervention. In the month after decolonization, bacterial communities were changed. Although communities largely returned to their baseline states, relative abundance of some taxa remained changed throughout the year following decolonization (e.g., more abundant

Identifiants

pubmed: 35384711
doi: 10.1128/spectrum.02672-21
pmc: PMC9045213
doi:

Substances chimiques

Anti-Bacterial Agents 0
Anti-Infective Agents, Local 0
RNA, Ribosomal, 16S 0
Water 059QF0KO0R
Mupirocin D0GX863OA5
Chlorhexidine R4KO0DY52L

Types de publication

Journal Article Research Support, U.S. Gov't, P.H.S. Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0267221

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR002345
Pays : United States

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Auteurs

Stephanie A Fritz (SA)

Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.

Todd N Wylie (TN)

Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
McDonnell Genome Institute, Washington University School of Medicine, St. Louis, Missouri, USA.

Haley Gula (H)

Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.

Patrick G Hogan (PG)

Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.

Mary G Boyle (MG)

Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.

Carol E Muenks (CE)

Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.

Melanie L Sullivan (ML)

Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.

Carey-Ann D Burnham (CD)

Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri, USA.
Department of Pathology & Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.

Kristine M Wylie (KM)

Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
McDonnell Genome Institute, Washington University School of Medicine, St. Louis, Missouri, USA.

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Classifications MeSH