House dust metagenome and pulmonary function in a US farming population

• Published in: Microbiome Vol. 12; no. 1; pp. 129 - 14
• Main Authors: Lee, Mikyeong, Kaul, Abhishek, Ward, James M, Zhu, Qiyun, Richards, Marie, Wang, Ziyue, González, Antonio, Parks, Christine G, Beane Freeman, Laura E, Umbach, David M, Motsinger-Reif, Alison A, Knight, Rob, London, Stephanie J
• Format: Journal Article
• Language: English
• Published: England BioMed Central 18.07.2024; BMC
• Subjects: Adult; Agriculture; Bacteria - classification; Bacteria - genetics; Bacteria - isolation & purification; Dust - analysis; Female; Forced Expiratory Volume; Humans; Lung - microbiology; Male; Metagenome; Metagenomics - methods; Microbiome; Microbiota; Microbiota - genetics; Middle Aged; Respiratory Function Tests; Spirometry; United States; Vital Capacity; Whole genome sequencing; United States; Spirometry; Microbiota; Whole genome sequencing; Metagenome; Microbiome; Respiratory function tests
• ISSN: 2049-2618; 2049-2618
• DOI: 10.1186/s40168-024-01823-y

Chronic exposure to microorganisms inside homes can impact respiratory health. Few studies have used advanced sequencing methods to examine adult respiratory outcomes, especially continuous measures. We aimed to identify metagenomic profiles in house dust related to the quantitative traits of pulmonary function and airway inflammation in adults. Microbial communities, 1264 species (389 genera), in vacuumed bedroom dust from 779 homes in a US cohort were characterized by whole metagenome shotgun sequencing. We examined two overall microbial diversity measures: richness (the number of individual microbial species) and Shannon index (reflecting both richness and relative abundance). To identify specific differentially abundant genera, we applied the Lasso estimator with high-dimensional inference methods, a novel framework for analyzing microbiome data in relation to continuous traits after accounting for all taxa examined together. Pulmonary function measures (forced expiratory volume in one second (FEV ), forced vital capacity (FVC), and FEV /FVC ratio) were not associated with overall dust microbial diversity. However, many individual microbial genera were differentially abundant (p-value < 0.05 controlling for all other microbial taxa examined) in relation to FEV , FVC, or FEV /FVC. Similarly, fractional exhaled nitric oxide (FeNO), a marker of airway inflammation, was unrelated to overall microbial diversity but associated with differential abundance for many individual genera. Several genera, including Limosilactobacillus, were associated with a pulmonary function measure and FeNO, while others, including Moraxella to FEV /FVC and Stenotrophomonas to FeNO, were associated with a single trait. Using state-of-the-art metagenomic sequencing, we identified specific microorganisms in indoor dust related to pulmonary function and airway inflammation. Some were previously associated with respiratory conditions; others were novel, suggesting specific environmental microbial components contribute to various respiratory outcomes. The methods used are applicable to studying microbiome in relation to other continuous outcomes. Video Abstract.