Gut microbiota dysbiosis and diarrhea in kidney transplant recipients.

TitleGut microbiota dysbiosis and diarrhea in kidney transplant recipients.
Publication TypeJournal Article
Year of Publication2019
AuthorsLee JRichard, Magruder M, Zhang L, Westblade LF, Satlin MJ, Robertson A, Edusei E, Crawford C, Ling L, Taur Y, Schluter J, Lubetzky M, Dadhania D, Pamer E, Suthanthiran M
JournalAm J Transplant
Volume19
Issue2
Pagination488-500
Date Published2019 02
ISSN1600-6143
KeywordsAdult, Bacteria, Case-Control Studies, Cohort Studies, Diarrhea, Dysbiosis, Feces, Female, Follow-Up Studies, Gastrointestinal Microbiome, Glomerular Filtration Rate, Graft Rejection, Graft Survival, Humans, Kidney Failure, Chronic, Kidney Function Tests, Kidney Transplantation, Male, Middle Aged, Postoperative Complications, Prognosis, Risk Factors, RNA, Ribosomal, 16S
Abstract

Posttransplant diarrhea is associated with kidney allograft failure and death, but its etiology remains unknown in the majority of cases. Because altered gut microbial ecology is a potential basis for diarrhea, we investigated whether posttransplant diarrhea is associated with gut dysbiosis. We enrolled 71 kidney allograft recipients for serial fecal specimen collections in the first 3 months of transplantation and profiled the gut microbiota using 16S ribosomal RNA (rRNA) gene V4-V5 deep sequencing. The Shannon diversity index was significantly lower in 28 diarrheal fecal specimens from 25 recipients with posttransplant diarrhea than in 112 fecal specimens from 46 recipients without posttransplant diarrhea. We found a lower relative abundance of 13 commensal genera (Benjamini-Hochberg adjusted P ≤ .15) in the diarrheal fecal specimens including the same 4 genera identified in our prior study. The 28 diarrheal fecal specimens were also evaluated by a multiplexed polymerase chain reaction (PCR) assay for 22 bacterial, viral, and protozoan gastrointestinal pathogens, and 26 specimens were negative for infectious etiologies. Using PICRUSt (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States) to predict metagenomic functions, we found that diarrheal fecal specimens had a lower abundance of metabolic genes. Our findings suggest that posttransplant diarrhea is not associated with common infectious diarrheal pathogens but with a gut dysbiosis.

DOI10.1111/ajt.14974
Alternate JournalAm J Transplant
PubMed ID29920927
PubMed Central IDPMC6301138
Grant ListK23 AI124464 / AI / NIAID NIH HHS / United States
P30 CA008748 / CA / NCI NIH HHS / United States
R37 AI051652 / AI / NIAID NIH HHS / United States
/ / Chinese American Medical Society / International
Related Faculty: 
Lars Westblade, Ph.D.

Pathology & Laboratory Medicine 1300 York Avenue New York, NY 10065 Phone: (212) 746-6464
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