A Distinct Nasal Microbiota Signature in Peritoneal Dialysis Patients

Author:

Khan Iman,Wu Sylvia,Hudson Anika,Hughes Clayton,Stryjniak Gabriel,Westblade Lars F.,Satlin Michael J.,Tedrow Nicholas,Uhlemann Anne-Catrin,Kraft Colleen,Dadhania Darshana M.,Silberzweig Jeffrey,De Vlaminck Iwijn,Li Carol,Srivatana Vesh,Lee John Richard

Abstract

ABSTRACTRationale & ObjectiveThe nasal passages harbor both commensal and pathogenic bacteria. In this study, we sought to characterize the anterior nasal microbiota in PD patients using 16S rRNA gene sequencing.Study DesignCross-sectional.Setting & ParticipantsWe recruited 32 PD patients, 37 kidney transplant (KTx) recipients, 22 living donor/healthy control (HC) participants and collected anterior nasal swabs at a single point in time.PredictorsWe performed 16S rRNA gene sequencing of the V4-V5 hypervariable region to determine the nasal microbiota.OutcomesNasal microbiota profiles were determined at the genus level as well as the amplicon sequencing variant level.Analytical ApproachWe compared nasal abundance of common genera among the 3 groups using Wilcoxon rank sum testing with Benjamini-Hochberg adjustment. DESeq2 was also utilized to compare the groups at the ASV levels.ResultsIn the entire cohort, the most abundant genera in the nasal microbiota included:Staphylococcus, Corynebacterium, Streptococcus, andAnaerococcus. Correlational analyses revealed a significant inverse relationship between the nasal abundance ofStaphylococcusand that ofCorynebacterium. PD patients have a higher nasal abundance ofStreptococcusthan KTx recipients and HC participants. PD patients have a more diverse representation ofStaphylococcusandStreptococcusthan KTx recipients and HC participants. PD patients who concurrently have or who developed futureStaphylococcusperitonitis had a numerically higher nasal abundance ofStaphylococcusthan PD patients who did not developStaphylococcusperitonitis.Limitations16S RNA gene sequencing provides taxonomic information to the genus level.ConclusionsWe find a distinct nasal microbiota signature in PD patients compared to KTx recipients and HC participants. Given the potential relationship between the nasal pathogenic bacteria and infectious complications, further studies are needed to define the nasal microbiota associated with these infectious complications and to conduct studies on the manipulation of the nasal microbiota to prevent such complications.

Publisher

Cold Spring Harbor Laboratory

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