Blood, Gut, and Oral Microbiome in Kidney Transplant Recipients

Author:

Sampaio Susana1234,Araujo Ricardo12,Merino-Riba Ana12567,Lelouvier Benjamin8,Servant Florence8,Quelhas-Santos Janete12,Pestana Manuel1234,Sampaio-Maia Benedita19

Affiliation:

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

2. INEB - Instituto de Engenharia Biomédica, Universidade do Porto, Rua Alfredo Allen, 208, 4200- 180 Porto, EPE, Portugal

3. Faculty of Medicine, University of Porto, EPE, Portugal

4. Department of Nephrology, São João Hospital Center, EPE, Portugal

5. Universitat Autònoma de Barcelona, Barcelona, Spain

6. Nephrology Department, Hospital Universitari Germans Trias i Pujol, Badalona, Spain

7. Hospital Universitari Doctor Josep Trueta, Girona, Spain

8. Vaiomer, Labège, France

9. Faculty of Dental Medicine, University of Porto, Porto, Portugal

Abstract

Background and Objective: Recent reports describe the existence of a blood microbiome profile not associated with an infection state. Given the high impact that the dysbiotic human microbiome appears to have in chronic kidney disease and, in particular, in the outcome of kidney transplant recipients (KTRs), we aimed to explore the variations and correlations of the gut, oral, and blood microbiome of recipients, 3 months after kidney transplantation. Materials and Methods: We conducted a cross-sectional study where the microbiome of stool, saliva, and blood collected from recipients 3 months after kidney transplantation (N = 6) was analyzed by polymerase chain reaction (PCR) amplification and sequencing of the V3–V4 hypervariable regions of the 16S rRNA gene using MiSeq Illumina® technology. Results: Blood of KTRs harbors a distinct low-abundance microbiome dominated by Proteobacteria and Firmicutes. Gut and oral microbiome of KTRs also present distinct profiles. The existence of a proportion of shared operational taxonomic units among the different body sites is reported, mainly classified as Proteobacteria and Firmicutes. Conclusions: This study provides evidence of existence a blood microbiome in KTRs, different from the gut and the oral microbiome profiles, with a small number of operational taxonomic units representing a shared microbiome. The clinical relevance of this observation should be further explored in these patients.

Publisher

Medknow

Subject

Nephrology

Reference23 articles.

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