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Citizen-science based study of the oral microbiome in Cystic fibrosis and matched controls reveals major differences in diversity and abundance of bacterial and fungal species

机译:基于科学的囊性纤维化和匹配对照中的口腔微生物组的研究揭示了细菌和真菌物种的多样性和丰度的主要差异

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摘要

Introduction: Cystic fibrosis (CF) is an autosomal genetic disease, associated with the production of excessively thick mucosa and with life-threatening chronic lung infections. The microbiota of the oral cavity can act as a reservoir or as a barrier for infectious microorganisms that can colonize the lungs. However, the specific composition of the oral microbiome in CF is poorly understood.Methods: In collaboration with CF associations in Spain, we collected oral rinse samples from 31 CF persons (age range 7-47) and matched controls, and then performed 16S rRNA metabarcoding and high-throughput sequencing, combined with culture and proteomics-based identification of fungi to survey the bacterial and fungal oral microbiome.Results: We found that CF is associated with less diverse oral microbiomes, which were characterized by higher prevalence of Candida albicans and differential abundances of a number of bacterial taxa that have implications in both the connection to lung infections in CF, as well as potential oral health concerns, particularly periodontitis and dental caries.Conclusion: Overall, our study provides a first global snapshot of the oral microbiome in CF. Future studies are required to establish the relationships between the composition of the oral and lung microbiomes in CF.
机译:介绍:囊性纤维化(CF)是常染色体遗传疾病,与过厚的粘膜产生和危及生命的慢性肺部感染相关。口腔的微生物可作为储层或作为可能殖民植入肺部的传染性微生物的屏障。然而,CF中的口腔微生物组的特定组成是较差的。方法:与西班牙的CF关联合作,我们从31种CF人(年龄范围7-47)和匹配的对照组中收集口腔冲洗样品,然后进行16S rRNA沟通和高通量测序,结合培养和蛋白质组学的真菌鉴定,调查细菌和真菌口腔微生物。结果:我们发现CF与较少不同的口腔微生物瘤相关,其特征是念珠菌肽的患病率较高许多细菌分类群的差异丰度,这些分类在CF中的肺部感染以及潜在的口腔健康问题,特别是牙周炎和牙科龋。结论:总体而言,我们的研究提供了口腔微生物组的第一个全局快照在CF.未来的研究是建立口腔和肺部微生物组成之间的关系。

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