Characterization of the lung microbiome and inflammatory cytokine levels in women exposed to environmental risk factors: A pilot study

Author:

Morales‐González Fernando1,Lira‐Lucio Juan A.1,Falfán‐Valencia Ramcés1ORCID,Márquez‐García José E.2,Abarca‐Rojano Edgar3,Ramírez‐Venegas Alejandra4,Sansores Raúl H.5,García‐Gómez Leonor4,Hernández‐Pérez Andrea4,Pérez‐Rubio Gloria1ORCID

Affiliation:

1. HLA Laboratory, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas Mexico City Mexico

2. Subdirección de Investigación Biomédica, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas Mexico City Mexico

3. Sección de Estudios de Posgrado e Investigación, Escuela Superior de Medicina, Instituto Politécnico Nacional Mexico City Mexico

4. Department of Tobacco Smoking and COPD Research Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas Mexico City Mexico

5. Clínica de Enfermedades Respiratorias, Fundación Médica Sur Mexico City Mexico

Abstract

AbstractIntroductionLung microbiome dysbiosis affects the immune system balance and promotes lung inflammation. We aimed to characterize and compare the lung bacteriome composition and the cytokine profile in women with normal lung function exposed to risk factors for chronic lung diseases (tobacco smoking and biomass‐burning smoke exposure).MethodsWe included women with biomass‐burning smoke exposure (BE, n = 11) and current smokers women (TS, n = 10). The bacteriome composition was performed in induced sputum, sequencing the 16 rRNA gene. Cytokine levels were measured using enzyme‐linked immunosorbent assay multiplex assay in the supernatant of induced sputum. For quantitative variables, we used medians and minimum and maxim values. For the amplicon sequence variants (ASV) differential abundance testing between groups.ResultsAt the taxa level, the phylum Proteobacteria was found in a higher proportion in the TS group concerning BE (p = .045); however, after the false discovery rate adjustment, this difference was not retained (p = .288). We found a higher concentration of IL‐1β in the TS group than in the BE group (248.6 vs. 177.9 pg/mL, p = .010). Women with high biomass‐burning smoke exposure in an hour per day had a positive correlation with the abundance of Bacteroidota (ρ = 0.71, p = .014) and Fusobacteriota (ρ = 0.73, p = .011). FEV1/FVC had a positive correlation with an abundance of Bacteroidota, Proteobacteria, and Fusobacteria (ρ = 0.74, p = .009, ρ = 0.85, p = .001, and ρ = 0.83, p = .001, respectively). In tobacco smoking, women had a positive correlation (ρ = 0.77, p = .009) between cigarettes per day and Firmicutes' abundance.ConclusionCompared to biomass‐burning smoke‐exposed women, current smokers have poor lung function and high levels of IL‐1β in sputum. Women with biomass‐burning smoke exposure present an increased abundance of Bacteroidota and Fusobacteriota.

Publisher

Wiley

Subject

Immunology,Immunology and Allergy

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