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Repeated enema administration in rhesus macaques is not sufficient to promote bacterial dysbiosis or gastrointestinal dysfunction

  1. Author:
    Ortiz, Alexandra M
    Casta, Fabiola Castello
    Bodykevich, Elizabeth G
    Flynn, Jacob K
    Carmody,Christine
    Brooks, Kelsie
    Ruiz, Delmy
    Yee, Debra S
    Simpson, Jennifer
    Rahmberg, Andrew R
    Keele,Brandon
    Brenchley, Jason M
  2. Author Address

    Barrier Immunity Section, Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA., AIDS and Cancer Virus Program, Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA., Barrier Immunity Section, Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA. Electronic address: jbrenchl@niaid.gov.,
    1. Year: 2025
    2. Date: Jun 07
    3. Epub Date: 2025 06 07
  1. Journal: Mucosal Immunology
  2. Type of Article: Article
  1. Abstract:

    Chronic gastrointestinal diseases are a significant global health burden that can require the use of gastrointestinal-cleansing regimens for diagnostics or therapeutic treatment. These regimens are beneficial for facilitating surgical preparation, drug delivery, colorectal cancer screenings, and personal use is common among proponents of natural health and among certain populations at high risk of HIV acquisition. It remains unclear, however, whether repeated clearance of the colonic microbiome induces persistent changes in the microbiome, intestinal immunity, and viral disease susceptibility. We addressed these parameters by repeatedly administering iso-osmolar enemas to rhesus macaques prior to low-dose intra-rectal challenge with simian immunodeficiency virus (SIV). Considering both longitudinal and cross-sectional analyses, we observed no consistent changes in the fecal microbiome or intestinal immune parameters of treated animals, nor were significant differences observed in susceptibility to SIV acquisition. Unexpectedly, enema-treated animals exhibited significantly lower setpoint viral loads after infection, although we were unable to clearly identify attributing causes. Our study demonstrates that repeated microbiome clearance using clinically administered iso-osmolar enemas is not sufficient to restructure the fecal microbiome, perturb intestinal immune parameters, or increase susceptibility to mucosal SIV challenge. This research framework serves as a model for the development of colonic-administered diagnostics and interventions. Copyright © 2025. Published by Elsevier Inc.

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External Sources

  1. DOI: 10.1016/j.mucimm.2025.06.002
  2. PMID: 40490097
  3. PII : S1933-0219(25)00058-3

Library Notes

  1. Fiscal Year: FY2024-2025
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