Aydin Malik, Weisser Cornelius, Rué Olivier, Mariadassou Mahendra, Maaß Sandra, Behrendt Ann-Kathrin, Jaszczyszyn Yan, Heilker Tatje, Spaeth Maximilian, Vogel Silvia, Lutz Sören, Ahmad-Nejad Parviz, Graf Viktoria, Bellm Aliyah, Weisser Christoph, Naumova Ella A, Arnold Wolfgang H, Ehrhardt Anja, Meyer-Bahlburg Almut, Becher Dörte, Postberg Jan, Ghebremedhin Beniam, Wirth Stefan
Laboratory of Experimental Pediatric Pneumology and Allergology, Faculty of Health, Center for Biomedical Education and Research, School of Life Sciences, Witten/Herdecke University, Witten, Germany.
Center for Child and Adolescent Medicine, Helios University Hospital Wuppertal, Witten/Herdecke University, Wuppertal, Germany.
Front Allergy. 2021 May 31;2:667562. doi: 10.3389/falgy.2021.667562. eCollection 2021.
Although the nose, as a gateway for organism-environment interactions, may have a key role in asthmatic exacerbation, the rhinobiome of exacerbated children with asthma was widely neglected to date. The aim of this study is to understand the microbiome, the microbial immunology, and the proteome of exacerbated children and adolescents with wheeze and asthma. Considering that a certain proportion of wheezers may show a progression to asthma, the comparison of both groups provides important information regarding clinical and phenotype stratification. Thus, deep nasopharyngeal swab specimens, nasal epithelial spheroid (NAEsp) cultures, and blood samples of acute exacerbated wheezers (WH), asthmatics (AB), and healthy controls (HC) were used for culture ( = 146), 16 S-rRNA gene amplicon sequencing ( = 64), and proteomic and cytokine analyses. Interestingly, were over-represented in WH, whereas and were associated with AB. In contrast, commonly colonized HCs. Moreover, , and were significantly more abundant in AB compared to WH and HC. The α-diversity analyses demonstrated an increase of bacterial abundance levels in atopic AB and a decrease in WH samples. Microbiome profiles of atopic WH differed significantly from atopic AB, whereby atopic samples of WH were more homogeneous than those of non-atopic subjects. The NAEsp bacterial exposure experiments provided a disrupted epithelial cell integrity, a cytokine release, and cohort-specific proteomic differences especially for cultures. This comprehensive dataset contributes to a deeper insight into the poorly understood plasticity of the nasal microbiota, and, in particular, may enforce our understanding in the pathogenesis of asthma exacerbation in childhood.
尽管鼻子作为机体与环境相互作用的通道,可能在哮喘急性发作中起关键作用,但迄今为止,哮喘急性发作儿童的鼻腔生物群一直被广泛忽视。本研究的目的是了解喘息和哮喘急性发作儿童及青少年的微生物组、微生物免疫学和蛋白质组。鉴于一定比例的喘息患者可能会发展为哮喘,两组的比较为临床和表型分层提供了重要信息。因此,对急性发作的喘息患者(WH)、哮喘患者(AB)和健康对照者(HC)的深部鼻咽拭子标本、鼻上皮球体(NAEsp)培养物和血液样本进行培养(n = 146)、16S - rRNA基因扩增子测序(n = 64)以及蛋白质组和细胞因子分析。有趣的是,[具体微生物名称1]在WH中过度富集,而[具体微生物名称2]和[具体微生物名称3]与AB相关。相比之下,[具体微生物名称4]常见于HC中。此外,与WH和HC相比,[具体微生物名称5]、[具体微生物名称6]和[具体微生物名称7]在AB中显著更为丰富。α多样性分析表明,特应性AB中的细菌丰度水平增加,而WH样本中的细菌丰度水平降低。特应性WH的微生物组谱与特应性AB有显著差异,其中特应性WH样本比非特应性受试者的样本更具同质性。NAEsp细菌暴露实验显示上皮细胞完整性受损、细胞因子释放以及特定队列的蛋白质组差异,尤其是对于[具体培养类型]培养物。这个综合数据集有助于更深入地了解人们了解较少的鼻腔微生物群的可塑性,特别是可能加强我们对儿童哮喘急性发作发病机制的理解。