Persistence and Sexual Dimorphism of Gut Dysbiosis and Pathobiome after Sepsis and Trauma

Author:

Munley Jennifer A.1,Park Gwoncheol2,Kelly Lauren S.1,Kannan Kolenkode B.1,Mankowski Robert T.3,Casadesus Gemma4,Chakrabarty Paramita5,Wallet Shannon M.6,Maile Robert1,Bible Letitia E.1,Wang Bo7,Moldawer Lyle L.1,Mohr Alicia M.1,Nagpal Ravinder2,Efron Philip A.1

Affiliation:

1. Department of Surgery and Sepsis and Critical Illness Research Center, University of Florida College of Medicine, Gainesville, Florida, U.S.A

2. The Gut Biome Lab, Department of Health, Nutrition and Food Sciences, Florida State University, Tallahassee, FL, U.S.A

3. Division of Gerontology, Geriatrics and Palliative Care, Department of Medicine, University of Alabama, Birmingham, Alabama, U.S.A

4. Department of Pharmacology and Therapeutics, University of Florida College of Medicine, Gainesville, Florida, U.S.A

5. Department of Neuroscience, University of Florida College of Medicine, Gainesville, Florida, U.S.A

6. Department of Oral Biology, University of Florida College of Medicine, Gainesville, Florida, U.S.A

7. Department of Biomedical and Chemical Engineering and Sciences, Florida Institute of Technology, Melbourne, FL, U.S.A

Abstract

Objective: To evaluate the persistence of intestinal microbiome dysbiosis and gut-plasma metabolomic perturbations following severe trauma or sepsis weeks after admission in patients experiencing chronic critical illness (CCI). Summary: Trauma and sepsis can lead to gut dysbiosis and alterations in the plasma and fecal metabolome. However, the impact of these perturbations and correlations between gut dysbiosis and the plasma metabolome in chronic critical illness have not been studied. Methods: A prospective observational cohort study was performed with healthy subjects, severe trauma patients, patients with sepsis residing in an intensive care unit (ICU) for 2-3 weeks. A high-throughput multi-omics approach was utilized to evaluate the gut microbial and gut-plasma metabolite responses in critically ill trauma and sepsis patients 14-21 days after ICU admission. Results: Patients in the sepsis and trauma cohorts demonstrated strikingly depleted gut microbiome diversity, with significant alterations and specific pathobiome patterns in the microbiota composition compared to healthy subjects. Further subgroup analyses based on sex revealed resistance to changes in microbiome diversity among female trauma patients compared to healthy counterparts. Sex-specific changes in fecal metabolites were also observed after trauma and sepsis, while plasma metabolite changes were similar in both males and females. Conclusions: Dysbiosis induced by trauma and sepsis persists up to 14-21 days after onset and is sex-specific, underscoring the implication of pathobiome and entero-septic microbial-metabolite perturbations in post-sepsis and post-trauma CCI. This indicates resilience to infection or injury in females’ microbiome and should inform and facilitate future precision/personalized medicine strategies in the intensive care unit.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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