Fungal and Bacterial Microbiome in Sinus Mucosa of Patients with and without Chronic Rhinosinusitis

Author:

Lee Jivianne T.12ORCID,Simpson Carra A.3,Yang Hong‐Ho4ORCID,Suh Jeffrey D.1,Wang Marilene B.12ORCID,Lagishetty Venu3,Liang Fengting3,Jacobs Jonathan P.5ORCID

Affiliation:

1. Department of Head & Neck Surgery, David Geffen School of Medicine University of California Los Angeles Los Angeles California U.S.A.

2. Department of Surgery VA Greater Los Angeles Healthcare System Los Angeles California U.S.A.

3. Vatche and Tamar Manoukian Division of Digestive Diseases, Department of Medicine, David Geffen School of Medicine University of California Los Angeles Los Angeles California U.S.A.

4. David Geffen School of Medicine University of California Los Angeles Los Angeles California U.S.A.

5. Division of Gastroenterology, Hepatology and Parenteral Nutrition VA Greater Los Angeles Healthcare System Los Angeles California U.S.A.

Abstract

ObjectivesDysbiosis of the sinonasal microbiome has been implicated in the pathogenesis of chronic rhinosinusitis (CRS). However, the mycobiome remains largely understudied, and microbial alterations associated with specific CRS subtypes have yet to be delineated. The objective of this study is to investigate the fungal and bacterial microbiome of sinus mucosa in CRS patients with and without nasal polyposis (CRSwNP and CRSsNP) versus healthy controls.MethodsSinus mucosa was obtained from 92 patients (31 CRSsNP, 31 CRSwNP, and 30 controls) undergoing endoscopic sinus/skull base surgery. Data regarding demographics, Lund‐MacKay scores, and histopathology were collected. Fungal and bacterial microbiome analysis was performed utilizing internal transcribed spacer amplicon and 16S rRNA sequencing.ResultsBeta diversity of the sinonasal mycobiome differed significantly between CRS and controls (p = 0.001) and between CRSwNP and controls (p = 0.049), but not between CRSwNP and CRSsNP (p = 0.32) nor between CRSsNP and controls (p = 0.06). With respect to the bacterial microbiome, significantly lower alpha diversity was observed between CRS and controls (p < 0.001), CRSwNP versus controls (p < 0.001), and CRSsNP versus controls (p < 0.001). Beta diversity was also significantly different at the genus level between CRSwNP and CRSsNP (p = 0.019), CRSwNP and controls (p = 0.002)), and CRSsNP and controls (p < 0.001). However, alpha and beta diversity did not differ significantly between CRS patients with/without eosinophils or correlate with Lund‐MacKay scores.ConclusionsDifferences in mycobiota diversity in CRS patients in comparison with controls suggest that alterations in the mycobiome may contribute to disease pathogenesis. Our findings also confirmed that diminished diversity among bacterial communities is associated with CRS and that significant differences are present in microbial composition between CRSwNP and CRSsNP.Level of Evidence3 Laryngoscope, 2023

Publisher

Wiley

Subject

Otorhinolaryngology

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