Department of Bacteriology, University of Wisconsin-Madison, Madison, WI, USA.
Microbiology Doctoral Training Program, University of Wisconsin-Madison, Madison, WI, USA.
Microbiome. 2024 Oct 18;12(1):206. doi: 10.1186/s40168-024-01940-8.
Alterations in upper respiratory microbiomes have been implicated in shaping host health trajectories, including by limiting mucosal pathogen colonization. However, limited comparative studies of respiratory microbiome development and functioning across age groups have been performed. Herein, we perform shotgun metagenomic sequencing paired with pathogen inhibition assays to elucidate differences in nasal and oral microbiome composition and intermicrobial interactions across healthy 24-month-old infant (n = 229) and adult (n = 100) populations.
We find that beta diversity of nasal and oral microbiomes varies with age, with nasal microbiomes showing greater population-level variation compared to oral microbiomes. Infant microbiome alpha diversity was significantly lower across nasal samples and higher in oral samples, relative to adults. Accordingly, we demonstrate significant differences in genus- and species-level composition of microbiomes between sites and age groups. Antimicrobial resistome patterns likewise varied across body sites, with oral microbiomes showing higher resistance gene abundance compared to nasal microbiomes. Biosynthetic gene clusters encoding specialized metabolite production were found in higher abundance across infant oral microbiomes, relative to adults. Investigation of pathogen inhibition revealed greater inhibition of gram-negative and gram-positive bacteria by oral commensals, while nasal isolates had higher antifungal activity.
In summary, we identify significant differences in the microbial communities inhabiting nasal and oral cavities of healthy infants relative to adults. These findings inform our understanding of the interactions impacting respiratory microbiome composition and functions related to colonization resistance, with important implications for host health across the lifespan. Video Abstract.
上呼吸道微生物组的改变与宿主健康轨迹有关,包括通过限制粘膜病原体定植来实现。然而,针对不同年龄组的呼吸道微生物组发育和功能的比较研究有限。在此,我们通过 shotgun 宏基因组测序和病原体抑制试验,阐明了健康 24 月龄婴儿(n=229)和成人(n=100)鼻和口腔微生物组组成和微生物间相互作用的差异。
我们发现鼻和口腔微生物组的 beta 多样性随年龄而变化,与口腔微生物组相比,鼻微生物组的群体水平变化更大。与成人相比,婴儿鼻腔样本的微生物组 alpha 多样性明显较低,而口腔样本的微生物组 alpha 多样性较高。相应地,我们在属和种水平上证明了微生物组在不同部位和年龄组之间的组成存在显著差异。抗菌药物耐药组模式也随身体部位而变化,与鼻腔微生物组相比,口腔微生物组的耐药基因丰度更高。与成人相比,我们发现婴儿口腔微生物组中编码特殊代谢产物生产的生物合成基因簇的丰度更高。对病原体抑制的研究表明,口腔共生菌对革兰氏阴性菌和革兰氏阳性菌的抑制作用更强,而鼻腔分离物的抗真菌活性更高。
总之,我们确定了健康婴儿与成人鼻腔和口腔微生物群之间存在显著差异。这些发现为我们了解影响定植抵抗的呼吸道微生物组组成和功能的相互作用提供了信息,对整个生命周期内宿主健康具有重要意义。视频摘要。