Butyrate-producing gut bacteria and viral infections in kidney transplant recipients: A pilot study. Academic Article uri icon

Overview

abstract

  • BACKGROUND: The gut microbiome is being associated increasingly with development of infections besides Clostridium difficile infection. A recent study found an association between butyrate-producing gut (BPG) bacteria and less frequent development of lower respiratory viral infections in allogeneic hematopoietic stem cell transplant recipients (Haak et al, Blood 131(26): 2978, 2018). In this investigation, we examine the relationship between the abundance of BPG bacteria and the development of viral infections in a cohort of kidney transplant recipients. METHODS: We recruited 168 kidney transplant recipients who provided 510 fecal specimens in the first 3 months after transplantation and profiled the gut microbiota using 16S rRNA gene sequencing of the V4-V5 hypervariable region. We classified the kidney transplant recipients into higher BPG Bacteria Group and lower BPG Bacteria Group using the same criteria of 1% relative gut abundance of BPG bacteria as the Haak et al study. RESULTS: Administration of antibiotics against anaerobes was associated with a significant decrease in the relative gut abundance of BPG bacteria. The higher BPG Bacteria Group was associated with less development of respiratory viral infections (Hazard Ratio [HR]: 0.28, P = .01) but not with less development of CMV viremia (HR: 0.38, P = .13) or BK viremia (HR: 1.02, P = .98) at 2 years post transplantation. CONCLUSION: Our pilot investigation supports future validation of the relationship between high relative gut abundance of BPG bacteria and decreased risk for development of respiratory viral infections.

publication date

  • October 8, 2019

Research

keywords

  • Bacteria
  • Gastrointestinal Microbiome
  • Kidney Transplantation
  • Respiratory Tract Infections
  • Virus Diseases

Identity

PubMed Central ID

  • PMC6917841

Scopus Document Identifier

  • 85076492927

Digital Object Identifier (DOI)

  • 10.1111/tid.13180

PubMed ID

  • 31544324

Additional Document Info

volume

  • 21

issue

  • 6