Russo Edda, Di Gloria Leandro, Cerboneschi Matteo, Smeazzetto Serena, Baruzzi Gian Paolo, Romano Francesca, Ramazzotti Matteo, Amedei Amedeo
Department of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.
Department of Biomedical, Experimental and Clinical Sciences "Mario Serio" University of Florence, 50134 Florence, Italy.
Biomedicines. 2023 Feb 23;11(3):684. doi: 10.3390/biomedicines11030684.
In this exploratory study, we investigate the variation in the facial skin microbiome architecture through aging and their functional association with host genetic factors in a cohort of healthy women, living in the same area and without cutaneous diseases. Notably, facial skin microbiota (SM) samples were collected from a cohort of 15 healthy Caucasian females, firstly divided into three age groups (younger women aged 20-35 years old; middle aged women of 36-52 years old; and older women aged 53-68 years old). Then, the recruited cohort was divided into two groups based on their facial hydration level (dry and normal skin). The facial SM revealed a different composition in the three analyzed aging groups and between normal and dry skins. The middle-aged women also revealed functional variations associated with collagen biosynthesis and oxidative stress damage repair. Otherwise, the association between selected host SNPs (single nucleotide polymorphisms) and the facial SM profile showed significant associations, suggesting a negative correlation with collagen metabolism and ROS damage protection. Finally, the composition and functionality of the facial SM seemed to affect the aging process through the two aging-correlated pathways of host ROS damage repair and collagen metabolism. Our exploratory data could be useful for future studies characterizing the structure, function, and dynamics of the SM in the aging process to design personalized therapeutic agents focusing on potential genomic targets, microbes, and their metabolites.
在这项探索性研究中,我们调查了居住在同一地区且无皮肤疾病的健康女性队列中,面部皮肤微生物群结构随年龄的变化及其与宿主遗传因素的功能关联。值得注意的是,从15名健康的白种女性队列中采集了面部皮肤微生物群(SM)样本,这些女性首先被分为三个年龄组(20 - 35岁的年轻女性;36 - 52岁的中年女性;以及53 - 68岁的老年女性)。然后,根据面部水合水平(干性和正常皮肤)将招募的队列分为两组。面部SM在三个分析的年龄组以及正常皮肤和干性皮肤之间显示出不同的组成。中年女性还显示出与胶原蛋白生物合成和氧化应激损伤修复相关的功能变化。此外,所选宿主单核苷酸多态性(SNP)与面部SM谱之间的关联显示出显著相关性,表明与胶原蛋白代谢和ROS损伤保护呈负相关。最后,面部SM的组成和功能似乎通过宿主ROS损伤修复和胶原蛋白代谢这两条与衰老相关的途径影响衰老过程。我们的探索性数据可能有助于未来的研究,以表征衰老过程中SM的结构、功能和动态,从而设计针对潜在基因组靶点、微生物及其代谢产物的个性化治疗药物。