Neighborhood deadwood and yard rewilding modulate commensal microbiomes and inflammatory signals among urbanites.

IF 14.9 1区 生物学 Q1 MICROBIOLOGY
Marja I Roslund, Laura Uimonen, Laura Kummola, Damiano Cerrone, Ann Ojala, Anna Luukkonen, Ella Holopainen, Aku Korhonen, Reijo Penttilä, Mika Saarenpää, Martti Venäläinen, Hanna Haveri, Juho Rajaniemi, Olli H Laitinen, Aki Sinkkonen, The Biwe Research Group
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Abstract

Background: Urbanization and biodiversity loss reduce human exposure to diverse microbiomes. Current evidence suggests that the vanishing microbiomes in industrialized populations are a central factor in the rising prevalence of non-communicable immune-mediated diseases. Rewilding has been proposed as an approach to diversify urban microbial communities and promote immunological resilience.

Results: We rewilded 21 urban private yards with deadwood, vegetation, and microbially rich soil. Control yards (15) were analyzed for comparison. We analyzed skin bacteria and oral microbiomes and used vegetation and deadwood inventories, satellite data, and questionnaires to determine the effects of rewilding, living environment, and lifestyle factors on skin and oral microbiota, functional gene pathways, and cytokine levels (IL-6, IL-10). Neighborhood deadwood within 200-m radii around home yards was used as an indicator of environmental biodiversity. Samples were collected before the rewilding in summer and three months later in autumn. Skin microbial diversity stayed constant and was associated with plant richness in the rewilding group, despite the normal seasonal decline and reduced outdoor time in autumn. Rewilding was associated with a decrease in tetrahydrofolate biosynthesis and salvage, and L-histidine degradation gene pathways and other changes in oral microbiota. In the rewilding group in autumn, picking of berries and fruits was directly associated with immunoregulatory IL-10 and pleiotropic IL-6 in saliva, and neighborhood deadwood abundance with the fatty acid biosynthesis superpathway in oral microbiomes. When groups were analyzed jointly, the diversity of oral microbial functional gene pathways was negatively correlated with IL-6 levels, and neighborhood deadwood abundance was directly linked to skin Gammaproteobacterial taxa, and typically soil-derived Cytobacillus sp. CY-G and Streptomyces sp. HSG2 in saliva.

Conclusions: Our findings are consistent with the biodiversity hypothesis, suggesting that biodiversity exposure may influence commensal microbiomes and biological pathways involved in host-microbe interactions. Our results suggest that the amount of decaying deadwood in the neighborhood, in addition to conventional measures of greenness and vegetation diversity, may provide advantageous information in studies examining human-environment microbiome interactions. This may inform biodiversity-related ecosystem services related to impacts on human health. Our findings provide an incentive for future studies and strategic investments for rewilding urban microbiomes to support planetary health. Video Abstract.

社区枯木和庭院放归调节城市居民的共生微生物群和炎症信号。
背景:城市化和生物多样性丧失减少了人类对不同微生物群的暴露。目前的证据表明,工业化人口中微生物群的消失是非传染性免疫介导疾病患病率上升的一个核心因素。野化被认为是使城市微生物群落多样化和提高免疫恢复能力的一种方法。结果:我们将21个城市私人庭院重新野化,其中有枯木,植被和微生物丰富的土壤。对照码(15个)进行分析比较。我们分析了皮肤细菌和口腔微生物群,并使用植被和枯木调查、卫星数据和问卷调查来确定野化、生活环境和生活方式因素对皮肤和口腔微生物群、功能基因通路和细胞因子水平(IL-6、IL-10)的影响。以家庭庭院周围200 m范围内的社区枯木作为环境生物多样性的指标。在夏季放养前和秋季放养3个月后分别采集样本。在野化组中,皮肤微生物多样性保持不变,并与植物丰富度相关,尽管正常的季节性下降和秋季户外时间减少。野化与四氢叶酸生物合成和回收减少、l -组氨酸降解基因途径减少以及口腔微生物群的其他变化有关。在秋季的野化组中,浆果和水果的采摘与唾液中免疫调节IL-10和多效性IL-6直接相关,而邻近枯木的丰度与口腔微生物群中脂肪酸生物合成超途径直接相关。当组间联合分析时,口腔微生物功能基因通路的多样性与IL-6水平呈负相关,邻域枯木丰度与皮肤γ -变形菌类群直接相关,唾液中典型的是土壤来源的胞芽孢杆菌CY-G和链霉菌sp. HSG2。结论:我们的研究结果与生物多样性假说一致,表明生物多样性暴露可能影响宿主-微生物相互作用的共生微生物组和生物学途径。我们的研究结果表明,除了传统的绿化和植被多样性测量外,附近腐烂枯木的数量可能为研究人类与环境微生物组的相互作用提供有利的信息。这可能为影响人类健康的与生物多样性有关的生态系统服务提供信息。我们的发现为未来的研究和战略投资提供了动力,以重新野生城市微生物群,以支持地球健康。视频摘要。
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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