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Gut microbiome alpha diversity decreases in relation to body weight, antibiotic exposure, and infection with multidrug-resistant organisms.
Panzer, Jonathan J; Maples, Catherine; Meyer, Monica P; Tillotson, Glenn; Theis, Kevin R; Chopra, Teena.
Afiliación
  • Panzer JJ; Department of Biochemistry, Microbiology, and Immunology, Wayne State University School of Medicine, Detroit, MI.
  • Maples C; Department of Infectious Diseases, Wayne State University, Detroit, MI.
  • Meyer MP; Civilian Health Solutions, Leidos, Inc., Bethesda, MD.
  • Tillotson G; GST Micro LLC, North, VA.
  • Theis KR; Department of Biochemistry, Microbiology, and Immunology, Wayne State University School of Medicine, Detroit, MI. Electronic address: ktheis@med.wayne.edu.
  • Chopra T; Department of Infectious Diseases, Wayne State University, Detroit, MI. Electronic address: tchopra@med.wayne.edu.
Am J Infect Control ; 52(6): 707-711, 2024 Jun.
Article en En | MEDLINE | ID: mdl-38176539
ABSTRACT

BACKGROUND:

The human gastrointestinal tract is home to a dense and diverse microbiome, predominated by bacteria. Despite the conservation of critical functionality across most individuals, the composition of the gut microbiome is highly individualized, leading to differential responses to perturbations such as oral antibiotics or multidrug-resistant organism (MDRO) infection. Herein, subject responses to these perturbations based on their body weight were evaluated.

METHODS:

Fecal samples were collected from 45 subjects at the Detroit Medical Center to evaluate the effects of perturbations on subjects' gut microbiome composition. Bacterial profiling was completed using 16S rRNA gene sequencing.

RESULTS:

Subjects with multiple MDROs, subjects weighing greater than 80 kg infected with MDRO E coli, and subjects weighing less than 80 kg with exposure to vancomycin and carbapenem antibiotics during hospitalization had significantly decreased gut microbiome richness.

CONCLUSIONS:

Both administration of oral antibiotics and MDRO infections decreased gut microbiome alpha diversity, but the magnitude of these gut microbiome perturbations was body weight dependent.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Peso Corporal / ARN Ribosómico 16S / Farmacorresistencia Bacteriana Múltiple / Heces / Microbioma Gastrointestinal / Antibacterianos Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: Am J Infect Control Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Peso Corporal / ARN Ribosómico 16S / Farmacorresistencia Bacteriana Múltiple / Heces / Microbioma Gastrointestinal / Antibacterianos Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: Am J Infect Control Año: 2024 Tipo del documento: Article