Microbial lineages in sarcoidosis. A metagenomic analysis tailored for low–microbial content samples

Clarke, Erik L, Lauder, Abigail P, Hofstaedter, Casey E, Hwang, Young, Fitzgerald, Ayannah S, Imai, Ize, Biernat, Wojciech, Rękawiecki, Bartłomiej, Majewska, Hanna, Dubaniewicz, Anna, Litzky, Leslie A, Feldman, Michael D, Bittinger, Kyle, Rossman, Milton D, Patterson, Karen C, Bushman, Frederic D and Collman, Ronald G (2018) Microbial lineages in sarcoidosis. A metagenomic analysis tailored for low–microbial content samples. American Journal of Respiratory and Critical Care Medicine, 197 (2). pp. 225-234. ISSN 1073-449X

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RATIONALE: The etiology of sarcoidosis is unknown, but microbial agents are suspected as triggers.

OBJECTIVES: We sought to identify bacterial, fungal, or viral lineages in specimens from patients with sarcoidosis enriched relative to control subjects using metagenomic DNA sequencing. Because DNA from environmental contamination contributes disproportionately to samples with low authentic microbial content, we developed improved methods for filtering environmental contamination.

METHODS: We analyzed specimens from subjects with sarcoidosis (n = 93), control subjects without sarcoidosis (n = 72), and various environmental controls (n = 150). Sarcoidosis specimens consisted of two independent sets of formalin-fixed, paraffin-embedded lymph node biopsies, BAL, Kveim reagent, and fresh granulomatous spleen from a patient with sarcoidosis. All specimens were analyzed by bacterial 16S and fungal internal transcribed spacer ribosomal RNA gene sequencing. In addition, BAL was analyzed by shotgun sequencing of fractions enriched for viral particles, and Kveim and spleen were subjected to whole-genome shotgun sequencing.

MEASUREMENTS AND MAIN RESULTS: In one tissue set, fungi in the Cladosporiaceae family were enriched in sarcoidosis compared with nonsarcoidosis tissues; in the other tissue set, we detected enrichment of several bacterial lineages in sarcoidosis but not Cladosporiaceae. BAL showed limited enrichment of Aspergillus fungi. Several microbial lineages were detected in Kveim and spleen, including Cladosporium. No microbial lineage was enriched in more than one sample type after correction for multiple comparisons.

CONCLUSIONS: Metagenomic sequencing revealed enrichment of microbes in single types of sarcoidosis samples but limited concordance across sample types. Statistical analysis accounting for environmental contamination was essential to avoiding false positives.

Item Type: Article
Keywords: sarcoidosis, metagenomic, microbiome, bacterial 16Sribosomal RNA, fungal internal transcribed spacer ribosomal RNA
Schools and Departments: Brighton and Sussex Medical School > Clinical and Experimental Medicine
Depositing User: Lisa Costick
Date Deposited: 05 Apr 2019 10:26
Last Modified: 03 Feb 2021 15:45
URI: http://sro.sussex.ac.uk/id/eprint/83040

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