Täubel Martin, Jalanka Jonna, Kirjavainen Pirkka V, Tuoresmäki Pauli, Hyvärinen Anne, Skevaki Chrysanthi, Piippo-Savolainen Eija, Pekkanen Juha, Karvonen Anne M
Department of Health Security, Finnish Institute for Health and Welfare, Kuopio, Finland.
Institute of Public Health and Clinical Nutrition, University of Eastern Finland, Kuopio, Finland.
Ann Am Thorac Soc. 2023 Oct;20(10):1456-1464. doi: 10.1513/AnnalsATS.202303-187OC.
Fungal exposure has been associated with predisposing and protective effects on the development of childhood asthma. To study whether early-life house dust mycobiota composition is associated with the development of asthma. Mycobiota were determined by amplicon sequencing from 382 dust samples collected from living room floors 2 months after birth in homes of the LUKAS cohort. Asthma status by 10.5 years of age was defined from questionnaires and assigned as ever asthma ( = 68) or current asthma ( = 27). Inhalant atopy was clinically determined at the same age. β-composition was analyzed using PERMANOVA-S, and asthma and atopy analyses were performed using discrete time hazard models and logistic regression, respectively. The house dust mycobiota composition based on Bray-Curtis distance was different in the homes of children who later did or did not develop asthma. The first and the fourth axes scores of principal coordinates analysis based on Bray-Curtis were associated with ever asthma. Of the genera with the strongest correlation with these axes, the relative abundance of , , , , and showed protective associations with asthma. None of these associations remained significant after mutual adjustment among the five genera or when mutually adjusted for other microbial cell wall markers and previously identified asthma-protective bacterial indices. Neither fungal α-diversity nor load was associated with asthma in the whole population, but higher fungal richness was a risk factor among children on farms. Higher fungal loads (measured via quantitative polymerase chain reaction) in house dust were associated with the risk of inhalant atopy. The results of our analyses from this well-characterized birth cohort suggest that the early-life house dust mycobiota in Finnish homes, characterized via DNA amplicon sequencing, do not have strong predisposing or protective effects on asthma development.
接触真菌与儿童哮喘的易感性和保护作用有关。为了研究生命早期室内灰尘真菌群落组成是否与哮喘的发生有关。通过对LUKAS队列中出生后2个月从客厅地板收集的382份灰尘样本进行扩增子测序来确定真菌群落。根据问卷确定10.5岁时的哮喘状态,并将其分为曾患哮喘(n = 68)或现患哮喘(n = 27)。在同一年龄临床确定吸入性特应性。使用PERMANOVA-S分析β-组成,分别使用离散时间风险模型和逻辑回归进行哮喘和特应性分析。基于Bray-Curtis距离的室内灰尘真菌群落组成在后来患或未患哮喘的儿童家中有所不同。基于Bray-Curtis的主坐标分析的第一和第四轴得分与曾患哮喘有关。在与这些轴相关性最强的属中,曲霉属、青霉属、枝孢属、镰刀菌属和链格孢属的相对丰度与哮喘呈保护关联。在这五个属之间相互调整后,或者在与其他微生物细胞壁标记物和先前确定的哮喘保护细菌指标相互调整后,这些关联均不再显著。在整个人口中,真菌α-多样性和载量均与哮喘无关,但在农场儿童中,较高的真菌丰富度是一个风险因素。室内灰尘中较高的真菌载量(通过定量聚合酶链反应测量)与吸入性特应性风险相关。我们对这个特征明确的出生队列的分析结果表明,通过DNA扩增子测序表征的芬兰家庭生命早期室内灰尘真菌群落对哮喘的发生没有强烈的易感性或保护作用。