Peritoneal Microbiome in End-Stage Renal Disease Patients and the Impact of Peritoneal Dialysis Therapy

Liliana Simões-Silva1,2,3, Ricardo Araujo1,2,4, Manuel Pestana1,2,5,6

  • 1i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-180 Porto, Portugal.

Microorganisms
|January 30, 2020
PubMed

Insights

Peritoneal dialysis (PD) may alter the unique microbiome within the peritoneal cavity of end-stage kidney disease (ESKD) patients. This study characterizes the ESKD peritoneal microbiome, revealing potential links to infection risk during PD therapy.

Area of Science:

  • Microbiology
  • Nephrology
  • Human Microbiome Research

Background:

  • Peritoneal dialysis (PD)-related infections remain a significant clinical challenge.
  • Emerging research highlights the role of microbiomes in previously sterile body sites.
  • Understanding the peritoneal microbiome is crucial for managing infections in end-stage kidney disease (ESKD) patients.

Purpose of the Study:

  • To characterize the peritoneal microbiome in ESKD patients without PD therapy.
  • To investigate alterations in the peritoneal microbiome of ESKD patients undergoing PD therapy.
  • To explore the potential impact of PD on the peritoneal microbiome and infection risk.

Main Methods:

  • Cross-sectional study analyzing peritoneal tissue microbiomes.
  • 16S rRNA sequencing approach used for microbial analysis.
  • Comparison between ESKD patients not on PD (n=11) and those on PD (n=9).

Main Results:

  • The peritoneal microbiome in ESKD patients is low-abundance, dominated by Proteobacteria, Firmicutes, Actinobacteria, and Bacteroidetes.
  • PD therapy was associated with reduced species richness in the peritoneal microbiome.
  • Pseudomonadaceae and Prevotelaceae families were dominant in PD patients.

Conclusions:

  • This study presents the first characterization of the peritoneal microbiome in ESKD patients.
  • PD therapy may induce significant alterations in the peritoneal microbiome composition.
  • Further research is needed to elucidate the clinical relevance of these microbiome changes in PD-related infections.

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